#METABOLOMICS WORKBENCH lamitinalab_20250519_094345 DATATRACK_ID:5927 STUDY_ID:ST004039 ANALYSIS_ID:AN006678 PROJECT_ID:PR002531 VERSION 1 CREATED_ON July 11, 2025, 12:21 pm #PROJECT PR:PROJECT_TITLE Soma to neuron communication links stress adaptation to stress avoidance PR:PROJECT_TITLE behavior PR:PROJECT_SUMMARY In multicellular organisms, signaling from the nervous system to the peripheral PR:PROJECT_SUMMARY tissues can activate physiological responses to stress. Here, we show that PR:PROJECT_SUMMARY inter-tissue stress communication can also function in reverse, i.e. from the PR:PROJECT_SUMMARY peripheral tissue to the nervous system. osm-8 mutants, which activate the PR:PROJECT_SUMMARY osmotic stress response in the C. elegans skin, also exhibit defective osmotic PR:PROJECT_SUMMARY avoidance behavior, which is regulated by the ASH neuronal avoidance circuit. PR:PROJECT_SUMMARY osm-8 osmotic avoidance behavior is completely suppressed by mutation of the PR:PROJECT_SUMMARY Patched/NPC1 homolog ptr-23. The function of osm-8 and ptr-23 in the hypodermal PR:PROJECT_SUMMARY epithelial cells is both necessary and sufficient for directing neuronal osmotic PR:PROJECT_SUMMARY avoidance behavior. Endogenously tagged alleles of osm-8 and ptr-23 co-localize PR:PROJECT_SUMMARY exclusively in the hypodermal lysosomes. Unbiased lipidomic analysis shows that PR:PROJECT_SUMMARY osm-8 leads to a ptr-23-dependent elevation of the lysosome specific lipid PR:PROJECT_SUMMARY bis(monoacylglycero)phosphate (BMP) and expansion of the pool of hypodermal PR:PROJECT_SUMMARY lysosomes. Just as genetic activation of the osmotic stress response by loss of PR:PROJECT_SUMMARY osm-8 in the hypodermis causes an Osm phenotype, acute physiological exposure to PR:PROJECT_SUMMARY osmotic stress also confers a reversible Osm phenotype. Behavioral plasticity PR:PROJECT_SUMMARY requires glycerol production, as mutations in the glycerol biosynthetic enzymes PR:PROJECT_SUMMARY gpdh-1 and gpdh-2 are defective in acquired Osm behavior. While the osm-8 PR:PROJECT_SUMMARY induced Osm behavior requires ptr-23, physiologically induced Osm behavior does PR:PROJECT_SUMMARY not. Instead, both genetic and physiologically induced Osm phenotypes require PR:PROJECT_SUMMARY the unusual non-neuronal lysosomal V-ATPase subunit vha-5, which is also PR:PROJECT_SUMMARY critical for organismal osmotic stress survival. Together, these data reveal PR:PROJECT_SUMMARY that genetic or physiological activation of stress signaling from the skin PR:PROJECT_SUMMARY elicits lysosome-associated signals that modulate the function of a sensory PR:PROJECT_SUMMARY neuron circuit. Such ‘body-brain’ interoceptive communication may allow PR:PROJECT_SUMMARY organisms to better match neuronal decision-making with organismal physiological PR:PROJECT_SUMMARY state. PR:INSTITUTE University of Pittsburgh PR:DEPARTMENT Pediatrics and Cell Biology PR:LABORATORY Lamitina Lab PR:LAST_NAME Lamitina PR:FIRST_NAME Todd PR:ADDRESS Childrens Hospital of Pittsburgh PR:EMAIL stl52@pitt.edu PR:PHONE 267-439-0330 PR:FUNDING_SOURCE NIH R01GM135577; NIH S10OD023402 #STUDY ST:STUDY_TITLE Soma to neuron communication links stress adaptation to stress avoidance ST:STUDY_TITLE behavior ST:STUDY_SUMMARY In multicellular organisms, signaling from the nervous system to the peripheral ST:STUDY_SUMMARY tissues can activate physiological responses to stress. Here, we show that ST:STUDY_SUMMARY inter-tissue stress communication can also function in reverse, i.e. from the ST:STUDY_SUMMARY peripheral tissue to the nervous system. osm-8 mutants, which activate the ST:STUDY_SUMMARY osmotic stress response in the C. elegans skin, also exhibit defective osmotic ST:STUDY_SUMMARY avoidance behavior, which is regulated by the ASH neuronal avoidance circuit. ST:STUDY_SUMMARY osm-8 osmotic avoidance behavior is completely suppressed by mutation of the ST:STUDY_SUMMARY Patched/NPC1 homolog ptr-23. The function of osm-8 and ptr-23 in the hypodermal ST:STUDY_SUMMARY epithelial cells is both necessary and sufficient for directing neuronal osmotic ST:STUDY_SUMMARY avoidance behavior. Endogenously tagged alleles of osm-8 and ptr-23 co-localize ST:STUDY_SUMMARY exclusively in the hypodermal lysosomes. Unbiased lipidomic analysis shows that ST:STUDY_SUMMARY osm-8 leads to a ptr-23-dependent elevation of the lysosome specific lipid ST:STUDY_SUMMARY bis(monoacylglycero)phosphate (BMP) and expansion of the pool of hypodermal ST:STUDY_SUMMARY lysosomes. Just as genetic activation of the osmotic stress response by loss of ST:STUDY_SUMMARY osm-8 in the hypodermis causes an Osm phenotype, acute physiological exposure to ST:STUDY_SUMMARY osmotic stress also confers a reversible Osm phenotype. Behavioral plasticity ST:STUDY_SUMMARY requires glycerol production, as mutations in the glycerol biosynthetic enzymes ST:STUDY_SUMMARY gpdh-1 and gpdh-2 are defective in acquired Osm behavior. While the osm-8 ST:STUDY_SUMMARY induced Osm behavior requires ptr-23, physiologically induced Osm behavior does ST:STUDY_SUMMARY not. Instead, both genetic and physiologically induced Osm phenotypes require ST:STUDY_SUMMARY the unusual non-neuronal lysosomal V-ATPase subunit vha-5, which is also ST:STUDY_SUMMARY critical for organismal osmotic stress survival. Together, these data reveal ST:STUDY_SUMMARY that genetic or physiological activation of stress signaling from the skin ST:STUDY_SUMMARY elicits lysosome-associated signals that modulate the function of a sensory ST:STUDY_SUMMARY neuron circuit. Such ‘body-brain’ interoceptive communication may allow ST:STUDY_SUMMARY organisms to better match neuronal decision-making with organismal physiological ST:STUDY_SUMMARY state. ST:INSTITUTE University of Pittsburgh ST:DEPARTMENT Pediatrics and Cell Biology ST:LABORATORY Lamitina Lab ST:LAST_NAME Lamitina ST:FIRST_NAME Todd ST:ADDRESS 4401 Penn Ave, Rangos 7122 ST:EMAIL stl52@pitt.edu ST:PHONE 12674390330 ST:NUM_GROUPS 3 ST:TOTAL_SUBJECTS 18 ST:PUBLICATIONS https://doi.org/10.1101/2025.05.07.652728 #SUBJECT SU:SUBJECT_TYPE Invertebrate SU:SUBJECT_SPECIES Caenorhabditis elegans SU:TAXONOMY_ID 6239 SU:GENOTYPE_STRAIN Wild type, osm-8(dr170), osm-8(dr170); ptr-23(dr180) SU:AGE_OR_AGE_RANGE Day 1 adults SU:GENDER Hermaphrodite #SUBJECT_SAMPLE_FACTORS: SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data SUBJECT_SAMPLE_FACTORS 1 N2_1 Sample source:C.Elegans tissue | Genotype:Wild type RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_1.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_1.mzXML SUBJECT_SAMPLE_FACTORS 2 N2_2 Sample source:C.Elegans tissue | Genotype:Wild type RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_2.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_2.mzXML SUBJECT_SAMPLE_FACTORS 3 N2_3 Sample source:C.Elegans tissue | Genotype:Wild type RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_3.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_3.mzXML SUBJECT_SAMPLE_FACTORS 4 N2_4 Sample source:C.Elegans tissue | Genotype:Wild type RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_4.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_4.mzXML SUBJECT_SAMPLE_FACTORS 5 N2_5 Sample source:C.Elegans tissue | Genotype:Wild type RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_5.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_5.mzXML SUBJECT_SAMPLE_FACTORS 6 N2_6 Sample source:C.Elegans tissue | Genotype:Wild type RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_6.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_6.mzXML SUBJECT_SAMPLE_FACTORS 7 dr170_1 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_7.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_7.mzXML SUBJECT_SAMPLE_FACTORS 8 dr170_2 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_8.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_8.mzXML SUBJECT_SAMPLE_FACTORS 9 dr170_3 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_9.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_9.mzXML SUBJECT_SAMPLE_FACTORS 10 dr170_4 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_10.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_10.mzXML SUBJECT_SAMPLE_FACTORS 11 dr170_5 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_11.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_11.mzXML SUBJECT_SAMPLE_FACTORS 12 dr170_6 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_12.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_12.mzXML SUBJECT_SAMPLE_FACTORS 13 dr170 dr180_1 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_13.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_13.mzXML SUBJECT_SAMPLE_FACTORS 14 dr170 dr180_2 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_14.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_14.mzXML SUBJECT_SAMPLE_FACTORS 15 dr170 dr180_3 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_15.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_15.mzXML SUBJECT_SAMPLE_FACTORS 16 dr170 dr180_4 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_16.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_16.mzXML SUBJECT_SAMPLE_FACTORS 17 dr170 dr180_5 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_17.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_17.mzXML SUBJECT_SAMPLE_FACTORS 18 dr170 dr180_6 Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) RAW_FILE_NAME_PositivePolarity=013025_Lamitina_CElegans_Lipid_Pos_18.mzXML; RAW_FILE_NAME_NegtivePolarity=013025_Lamitina_CElegans_Lipid_Neg_18.mzXML #COLLECTION CO:COLLECTION_SUMMARY For each replicate, N2, osm-8(dr170), and osm-8(dr170); ptr-23(dr180) animals CO:COLLECTION_SUMMARY were seeded on 3x15 cm NGM plate with a lawn of OP50 as starved L1s. Animals CO:COLLECTION_SUMMARY were grown at 20ºC until animals were day 1 adults. We collected a total of six CO:COLLECTION_SUMMARY replicates for each genotype for analysis. Worms were washed off plates using M9 CO:COLLECTION_SUMMARY buffer, pelleted in a swinging bucket centrifuge at 2,000xg for 1 minute, and CO:COLLECTION_SUMMARY then washed three times. Worm pellets were resuspended in 10ml of M9 buffer and CO:COLLECTION_SUMMARY incubated at 20ºC with rocking for 15 minutes to evacuate OP50 bacteria from CO:COLLECTION_SUMMARY the intestine. Worms were pelleted and the density of worms per microliter was CO:COLLECTION_SUMMARY calculated for each strain. For each sample, ~5,000 worms were pipetted into CO:COLLECTION_SUMMARY 2.0ml tubes containing a MP Bio Matrix A (garnet/ceramic sphere) and frozen at CO:COLLECTION_SUMMARY -80ºC prior to processing. CO:SAMPLE_TYPE Worms CO:STORAGE_CONDITIONS -80℃ CO:COLLECTION_VIALS 2.0ml tubes CO:ADDITIVES MP Bio Matrix A #TREATMENT TR:TREATMENT_SUMMARY No treatment. All strains were grown under identical isotonic plate conditions TR:TREATMENT_SUMMARY (51mM NaCl NGM plates). The only variable was genotype. #SAMPLEPREP SP:SAMPLEPREP_SUMMARY Metabolic quenching, lysis, and lipid extraction was performed by adding 0.5mL SP:SAMPLEPREP_SUMMARY ice cold phosphate buffered saline. Samples were homogenized in MP Biomatrix A SP:SAMPLEPREP_SUMMARY tubes at 60 Hz for 1 minute. Uncleared supernatant (400 µL) was transferred to SP:SAMPLEPREP_SUMMARY a clean glass tube containing 10 µL of LipidSplash, deuterated internal SP:SAMPLEPREP_SUMMARY standards (Avanti Polar Lipids. Alabaster, AL) and subjected to Folch SP:SAMPLEPREP_SUMMARY extraction. Samples were rested on ice for 10 minutes before phase separation SP:SAMPLEPREP_SUMMARY via centrifugation at 2500 x g for 15 minutes. The organic phase (0.7 mL) was SP:SAMPLEPREP_SUMMARY transferred to a clean glass vial and dried to completion under N2. Samples were SP:SAMPLEPREP_SUMMARY resuspended in 100 µL of 1:1 acetonitrile:isopropanol and 3µL was injected for SP:SAMPLEPREP_SUMMARY online LC-HRMS analysis. #CHROMATOGRAPHY CH:CHROMATOGRAPHY_SUMMARY Briefly, samples were injected via a Thermo Vanquish UHPLC and separated over a CH:CHROMATOGRAPHY_SUMMARY reversed phase Thermo Accucore C-18 column (2.1×100mm, 5μm particle size) CH:CHROMATOGRAPHY_SUMMARY maintained at 55°C. For the 30 minute LC gradient, the mobile phase consisted CH:CHROMATOGRAPHY_SUMMARY of the following: solvent A (50:50 H2O:ACN 10 mM ammonium acetate/0.1% acetic CH:CHROMATOGRAPHY_SUMMARY acid) and solvent B (90:10 IPA:ACN 10 mM ammonium acetate/0.1% acetic acid). The CH:CHROMATOGRAPHY_SUMMARY gradient started at 30% B and increased to 43%B over 2 minutes followed by an CH:CHROMATOGRAPHY_SUMMARY increase to 55%B in 0.1 minute. The organic increased to 65%B over the next 10 CH:CHROMATOGRAPHY_SUMMARY minutes, followed by an increase to 85%B over 6 minutes. For column washing the CH:CHROMATOGRAPHY_SUMMARY gradient increased to 100%B over 2 minutes and was held for 5 minutes followed CH:CHROMATOGRAPHY_SUMMARY by 5 minutes of equilibration at 30%B. CH:CHROMATOGRAPHY_TYPE Reversed phase CH:INSTRUMENT_NAME Thermo Vanquish CH:COLUMN_NAME Thermo Accucore Vanquish C18+ UHPLC (100 x 2.1mm, 1.5um) CH:SOLVENT_A 50% water/50% acetonitrile; 10 mM ammonium acetate; 0.1% acetic acid CH:SOLVENT_B 90% isopropanol/10% acetonitrile; 10 mM ammonium acetate; 0.1% acetic acid CH:FLOW_GRADIENT 30% B and increased to 43%B over 2 minutes followed by an increase to 55%B in CH:FLOW_GRADIENT 0.1 minute. The organic increased to 65%B over the next 10 minutes, followed by CH:FLOW_GRADIENT an increase to 85%B over 6 minutes. For column washing the gradient increased to CH:FLOW_GRADIENT 100%B over 2 minutes and was held for 5 minutes followed by 5 minutes of CH:FLOW_GRADIENT equilibration at 30%B CH:FLOW_RATE 0.260mL/min CH:COLUMN_TEMPERATURE 55 #ANALYSIS AN:ANALYSIS_TYPE MS #MS MS:INSTRUMENT_NAME Thermo Orbitrap ID-X Tribrid MS:INSTRUMENT_TYPE Orbitrap MS:MS_TYPE ESI MS:ION_MODE NEGATIVE MS:MS_COMMENTS The Thermo ID-X tribrid mass spectrometer was operated in both positive and MS:MS_COMMENTS negative ESI mode. A data-dependent MS2 method was used with scanning in Full MS MS:MS_COMMENTS mode from 200 to 1500 m/z at 120,000 resolution with an AGC target of 5e4 for MS:MS_COMMENTS triggering MS2 fragmentation using stepped HCD collision energies at 20, 40, and MS:MS_COMMENTS 60% in the Orbitrap at 15,000 resolution. Source ionization settings were 3.5kV MS:MS_COMMENTS and 2.4kV spray voltage, respectively for positive and negative mode. Source gas MS:MS_COMMENTS parameters were 35 sheath gas, 5 auxiliary gas at 300°C, and 1 sweep gas. MS:MS_COMMENTS Calibration was performed prior to analysis using the PierceTM FlexMix Ion MS:MS_COMMENTS Calibration Solutions (Thermo Fisher Scientific). Internal standard peak areas MS:MS_COMMENTS were then extracted manually using Quan Browser (Thermo Fisher Xcalibur ver. MS:MS_COMMENTS 4.4), normalized to weight and internal standard peak area, then graphed using MS:MS_COMMENTS GraphPad PRISM (ver 9.0). Untargeted differential comparisons were performed MS:MS_COMMENTS using LipidSearch 5.1 (Thermo Fisher) to generate a ranked list of significant MS:MS_COMMENTS lipid compounds at the class and species-specific levels. #MS_METABOLITE_DATA MS_METABOLITE_DATA:UNITS Normalized Peak area MS_METABOLITE_DATA_START Samples N2_1 N2_2 N2_3 N2_4 N2_5 N2_6 dr170_1 dr170_2 dr170_3 dr170_4 dr170_5 dr170_6 dr170 dr180_1 dr170 dr180_2 dr170 dr180_3 dr170 dr180_4 dr170 dr180_5 dr170 dr180_6 Factors Sample source:C.Elegans tissue | Genotype:Wild type Sample source:C.Elegans tissue | Genotype:Wild type Sample source:C.Elegans tissue | Genotype:Wild type Sample source:C.Elegans tissue | Genotype:Wild type Sample source:C.Elegans tissue | Genotype:Wild type Sample source:C.Elegans tissue | Genotype:Wild type Sample source:C.Elegans tissue | Genotype:osm-8(dr170) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) Sample source:C.Elegans tissue | Genotype:osm-8(dr170) ptr-23(dr180) LBPA(17:1_18:3)-H_1 8.09E-05 3.40E-05 3.62E-05 2.92E-05 2.54E-05 5.94E-05 0.000440014 0.001268263 0.000965664 0.000756002 0.000769106 0.000645344 NF NF NF 3.28E-08 NF NF LBPA(15:0_17:0)-H 0.000112997 0.000203625 2.84E-05 4.76E-05 5.62E-05 0.000119313 2.83E-05 0.00024092 0.00125295 0.000286731 0.002748093 0.000330637 NF NF NF NF NF NF LBPA(17:1_18:3)-H_2 0.000136305 5.79E-05 5.42E-05 6.61E-05 0.000103364 0.000145378 0.000912505 0.001946358 0.001546058 0.001410732 0.001432266 0.00142877 NF NF NF 2.82E-05 NF NF LBPA(17:1_20:3)-H 0.000173865 7.33E-05 4.83E-05 0.000192563 0.000115791 0.000154302 0.001553773 0.001701225 0.001729181 0.001654658 0.001961711 0.001361119 NF NF NF NF NF NF LBPA(15:0_16:0)-H 0.000412303 0.000696609 0.000215735 0.000283901 0.000340246 0.000381066 4.01E-05 0.000157079 0.001435604 0.000492346 0.006189713 0.000154666 NF NF NF NF NF NF PG(17:1_18:3)-H 0.000135596 5.77E-05 5.59E-05 6.76E-05 0.000103835 0.000145733 0.000917217 0.00204975 0.001561611 0.001374461 0.001641724 0.001383914 NF NF NF 2.77E-05 NF NF PG(16:0_20:5)-H 0.000247508 0.000209485 0.000160479 0.000158943 0.000198612 0.000295127 0.001722316 0.002057225 0.001826523 0.001337742 0.002001211 0.001113737 NF NF 6.62E-05 NF NF NF PG(15:0_20:5)-H 0.000472469 0.000292233 0.00029887 0.000299357 0.00030777 0.000439685 0.000883364 0.002587893 0.002067761 0.00129256 0.001862857 0.001511258 3.79E-05 NF NF NF NF NF LBPA(16:1_17:1)-H 0.000104545 6.47E-05 2.93E-05 9.50E-05 7.58E-05 0.000131603 0.002012904 0.002291928 0.00215174 0.002036132 0.002240866 0.001850277 4.61E-05 5.85E-05 7.14E-05 6.51E-05 6.98E-05 4.73E-05 PC(14:0_15:1)+CH3COO 0.000798233 0.000795645 0.000576614 0.000734601 0.000648712 0.000813232 0.000281006 0.000393043 0.000352668 0.000266635 0.000339018 0.000227526 0.001040729 0.001061141 0.001020118 0.001012749 0.001054396 0.000997344 LBPA(19:1_19:1)-H 5.80E-05 0.000122282 1.65E-10 0.000117306 0.000129146 0.00024569 0.001482591 0.001341574 0.001313396 0.001397898 0.001436095 0.001188137 0.00021315 0.0002056 0.000119427 0.00010044 0.000176003 6.75E-05 LBPA(17:1_17:1)-H 0.000366318 0.00014446 0.00026317 0.000174537 0.000330634 0.000354954 0.003606728 0.003039386 0.002690766 0.003004082 0.002874874 0.002994501 3.19E-05 0.000144337 0.000156418 0.000126695 0.000190724 0.000128956 PC(15:0_17:0)+CH3COO 0.008223804 0.008305292 0.007487236 0.008740249 0.008605234 0.009196601 0.002694296 0.003971337 0.003654511 0.003306967 0.003826258 0.003277194 0.00711353 0.006873785 0.007272065 0.006857382 0.00699632 0.00710032 PC(O-18:1_20:3)+CH3COO 0.000634808 0.000609564 0.000550686 0.000588792 0.000566402 0.000428693 0.000157402 0.00018246 0.000121332 8.65E-05 0.000117912 0.000185781 0.000543043 0.000644167 0.000539404 0.000542691 0.000589221 0.000533018 PC(15:1_18:4)+CH3COO 0.005856257 0.00498023 0.004579776 0.005980755 0.005783097 0.00617035 0.000813055 0.001766287 0.001474054 0.001124021 0.001369034 0.000725715 0.00450413 0.00454467 0.004840059 0.004146389 0.00458042 0.004379796 PG(17:1_18:1)-H 0.001725712 0.001599049 0.001175202 0.001726167 0.00184716 0.002479589 0.007648254 0.009804811 0.009548797 0.009357003 0.010783006 0.010885031 0.00126347 0.001277923 0.001458813 0.001311844 0.001269873 0.001285166 LBPA(18:1_19:1)-H 0.001058907 0.000808841 0.000945781 0.001167841 0.001173633 0.001634418 0.00466937 0.006711223 0.00652491 0.006142271 0.006483907 0.005775662 0.000695202 0.000776939 0.000765423 0.000682751 0.000756897 0.000722142 PC(18:0_20:3)+CH3COO 0.011613868 0.011690865 0.011043527 0.011488416 0.01027533 0.01286514 0.004373826 0.005625971 0.005228287 0.003901732 0.005189478 0.003522232 0.010430319 0.010254842 0.010656712 0.010597841 0.010435359 0.010554235 LBPA(17:1_18:1)-H 0.002014692 0.001594531 0.001205666 0.002086234 0.001772587 0.002469644 0.00769406 0.01009164 0.011263188 0.009479263 0.010997272 0.008997798 0.001255818 0.001383031 0.001394042 0.001278397 0.00137247 0.001243417 LPC(14:0)+CH3COO 0.003108852 0.002748185 0.001932519 0.002833107 0.002429024 0.003149721 0.000700011 0.000875534 0.000766909 0.000652303 0.001042319 0.000752605 0.00215285 0.002300653 0.002589499 0.002469007 0.002376115 0.002055794 PE(18:1_19:1)-H_1 0.00573948 0.031552495 0.033209496 0.006850518 0.012527295 0.033758855 0.001616407 0.002467068 0.005712634 0.001940877 0.002842711 0.001341495 0.020485572 0.018171295 0.018930476 0.021608015 0.019436971 0.01536007 PC(17:1_20:3COOH)+CH3COO 0.001154667 0.000317404 0.001358687 0.001278395 0.000856295 0.000850869 0.000454305 0.000735444 0.000600486 0.000449385 0.000462699 0.000329719 0.001649053 0.001752333 0.001503369 0.001721727 0.001785709 0.001498096 PC(14:0_16:1)+CH3COO 0.003992423 0.004038067 0.004176582 0.003776593 0.00383226 0.004060396 0.002758378 0.003008364 0.002989052 0.002266446 0.002827531 0.002350808 0.005726528 0.005523289 0.005985302 0.005135924 0.005681223 0.005083124 PC(17:1_20:3)+CH3COO 0.052826932 0.062444602 0.058493249 0.064406623 0.058940356 0.063124531 0.029062834 0.035217041 0.03094013 0.030253592 0.032710147 0.02715415 0.056845195 0.057743109 0.052603097 0.051209589 0.052294761 0.052441173 LBPA(19:1_20:4)-H_1 4.21E-05 1.89E-10 6.71E-05 4.44E-09 5.30E-09 0.000975767 0.001292948 0.001187185 0.001055292 0.00118919 0.000898429 3.09E-05 1.98E-10 2.38E-10 1.47E-10 2.06E-05 PC(14:0_20:5)+CH3COO 0.039498009 0.046288227 0.036154168 0.045482414 0.037863225 0.0438905 0.005077667 0.011226961 0.009670225 0.005152826 0.008600943 0.005547395 0.022249128 0.024999123 0.025797204 0.024033826 0.024807859 0.024034711 PC(12:0_20:5)+CH3COO_1 0.00198235 0.001761954 0.002154438 0.001921655 0.00192744 0.001742576 0.000465858 0.000750717 0.000766182 0.000494772 0.000301919 0.00040155 0.001740938 0.00205712 0.00180803 0.001867154 0.002089305 0.001771757 PC(20:3_20:3)+CH3COO 0.014548602 0.015385071 0.013044747 0.012694589 0.01272456 0.014584592 0.00477419 0.006575203 0.005490973 0.004011691 0.005930347 0.003658446 0.013027956 0.015066752 0.014162874 0.013380474 0.012164023 0.01332572 PC(17:1_20:4COOH)+CH3COO_1 0.00323452 0.001105447 0.004660893 0.00364217 0.003794127 0.003217282 0.000679839 0.001764546 0.001399301 0.001127321 0.001537374 0.000684551 0.003556564 0.004046133 0.004064664 0.003780426 0.003861078 0.003897042 PC(14:0_20:4)+CH3COO_1 0.007123121 0.007165138 0.006372046 0.007581422 0.007148134 0.007603149 0.001982888 0.004015741 0.002992071 0.00207182 0.002948709 0.001967384 0.00681363 0.007258527 0.007248023 0.007246768 0.007339124 0.00732881 LPC(20:4)+CH3COO_1 0.004150554 0.006301097 0.003669843 0.003540225 0.004251175 0.004256903 0.002233988 0.003082406 0.002317528 0.002070798 0.003133859 0.001825845 0.006733157 0.0064089 0.008135251 0.007401448 0.007400503 0.008251543 Cer(t18:1_24:0)-H_1 0.047029434 0.046083445 0.04433875 0.05267773 0.047510619 0.053784042 0.008105413 0.010697536 0.011031132 0.006322942 0.008744372 0.006357494 0.023402949 0.02991789 0.030169354 0.026807404 0.026118731 0.024801394 PC(14:0_15:0)+CH3COO 0.002705697 0.001870682 0.002346623 0.002632349 0.002359349 0.002481182 0.000645382 0.000934379 0.001094537 0.00061078 0.000818957 0.00068023 0.002030667 0.002204248 0.002458625 0.002609816 0.002560322 0.002319391 PC(18:0_18:3)+CH3COO_1 0.004660292 0.0049184 0.004530751 0.004530728 0.004297959 0.005600372 0.001621439 0.00237506 0.002369325 0.001655643 0.002110742 0.001856345 0.003983189 0.004715968 0.004725063 0.004402598 0.004285722 0.004802649 PC(20:3_20:4)+CH3COO_1 0.025661231 0.029284286 0.025282007 0.026807043 0.025098642 0.026532778 0.007908623 0.011053086 0.009612153 0.007006196 0.010496103 0.006195156 0.019892731 0.020629958 0.021447112 0.022604889 0.019365781 0.020796734 PC(20:4_20:5)+CH3COO_1 0.133358403 0.142770431 0.118262514 0.124548183 0.137042426 0.137035332 0.041959928 0.066111393 0.05362516 0.037513121 0.053813396 0.034041317 0.123852009 0.117232596 0.125280363 0.113824773 0.113801128 0.129719746 Cer(d17:0_24:0)-H 0.002093973 0.001971231 0.001444891 0.001769011 0.001576786 0.00193458 5.83E-05 0.000227762 0.000200572 7.11E-05 0.000215485 6.50E-05 0.000601694 0.000595307 0.000634915 0.000570494 0.000677867 0.000605961 PC(15:1_20:4)+CH3COO 0.004432902 0.005548981 0.004509358 0.00500984 0.005072305 0.007057592 0.002054594 0.003748284 0.003027259 0.002078215 0.00294412 0.00202622 0.006302778 0.006562458 0.006879733 0.00717397 0.007026482 0.006511941 PC(17:1_18:2)-CH3_1 0.012084832 0.008873905 0.007958742 0.010312999 0.010512114 0.012260331 0.00010604 0.001048228 0.000654627 0.000632905 0.000888303 0.000571644 0.002611733 0.002758317 0.003077228 0.003290744 0.00263059 0.002745973 LBPA(16:0_18:2)-H 0.000198516 0.000159008 0.0001161 0.000214726 0.000123303 0.000311206 0.001463226 0.002075685 0.001322293 0.001911884 0.00197188 0.001474252 5.99E-08 2.32E-06 9.50E-07 0.000119569 1.11E-06 9.94E-07 Cer(t17:0_23:1)-H_1 0.080027193 0.078069069 0.07209286 0.07808379 0.071932738 0.079546279 0.018531034 0.023630298 0.02669015 0.016858968 0.021008339 0.01721345 0.047810595 0.052359722 0.049948516 0.043286787 0.046323602 0.04436644 Cer(t18:1_24:0)-H_2 0.035284423 0.030873842 0.027491024 0.032655726 0.028273548 0.032831611 0.005786705 0.007643321 0.007335172 0.004810682 0.007997563 0.004471513 0.021529122 0.030844298 0.031480165 0.026140862 0.025901191 0.02511365 PC(20:4_20:4)+CH3COO_1 0.007559752 0.00830587 0.006992572 0.00770549 0.007264738 0.007852122 0.006512712 0.008413611 0.006143734 0.005211776 0.00634485 0.004437635 0.014241932 0.014891804 0.014919812 0.012778719 0.013697245 0.015076432 LPC(20:3)+CH3COO 0.009059843 0.008599983 0.007112673 0.008484786 0.006737937 0.011359519 0.00276646 0.004524411 0.003525117 0.002447465 0.004364344 0.002560412 0.008973785 0.008745168 0.009256838 0.007893683 0.00950407 0.009787994 PC(15:1_20:5)+CH3COO_1 0.01028629 0.01107471 0.009132101 0.011916831 0.010300824 0.011240692 0.004311732 0.006583501 0.005311149 0.003251827 0.004461104 0.003269799 0.012202879 0.01405911 0.013506294 0.011104121 0.012456518 0.013029938 PC(20:4COOH_20:5)+CH3COO_1 0.00921076 0.004553638 0.012486377 0.009106536 0.009204534 0.008476257 0.000378804 0.002152789 0.001239884 0.000631603 0.001374869 0.000454727 0.004813368 0.006329415 0.006608515 0.006669186 0.00644223 0.005459816 PC(17:0_20:4)+CH3COO 0.002442439 0.003127392 0.002943585 0.003395689 0.002736888 0.003254848 0.001855902 0.001971184 0.00167026 0.001290655 0.001437971 0.001007119 0.003997801 0.003635481 0.003519673 0.003474857 0.003546174 0.003436837 PG(18:1_20:4)-H_1 0.000152777 6.01E-05 4.39E-10 5.79E-05 9.36E-05 2.61E-10 0.001486563 0.002294222 0.001919308 0.001824662 0.002588954 0.00173854 2.62E-10 2.73E-10 1.50E-10 1.26E-10 3.66E-10 5.48E-10 PC(14:0_17:1)+CH3COO_1 0.008143139 0.007949107 0.007091738 0.008266067 0.007668995 0.008020413 0.005738604 0.006194912 0.005228453 0.004332649 0.005159799 0.004480245 0.0093491 0.009750953 0.009821778 0.01113202 0.010815714 0.009736744 PC(13:0_20:5)+CH3COO 0.005856257 0.00498023 0.004579776 0.005980755 0.005783097 0.00617035 0.000813055 0.002240587 0.001474054 0.000521713 0.001369034 0.000725715 0.00450413 0.00454467 0.004840059 0.004146389 0.00458042 0.004379796 Cer(d12:1_16:0_21:3)+HCOO_1 0.001285892 0.001167467 0.000952869 0.001186471 0.0011693 0.001147655 0.000706416 0.000777551 0.00063467 0.000527575 0.000773894 0.000531445 0.001310016 0.001690821 0.00160471 0.001457857 0.001459601 0.001527494 PC(18:2_21:3COOH)+HCOO_1 0.003561995 0.000693677 0.00289821 0.001903395 0.002002354 0.001618474 0.000751841 0.001173473 0.001210427 0.000915646 0.001347363 0.000768312 0.003957142 0.003774529 0.003333995 0.002924794 0.003857977 0.003060019 PC(20:3_21:4COOH)+HCOO 0.003176095 0.001232147 0.004300751 0.00468512 0.003504019 0.002781059 0.000426679 0.001235844 0.000728229 0.000435754 0.00097695 0.000399141 0.004848073 0.003180038 0.003891363 0.004356196 0.004466896 0.003699567 PC(15:0_18:3)+CH3COO_1 0.021705886 0.025321973 0.023161212 0.022706758 0.024002724 0.026491979 0.008871451 0.016368169 0.011335776 0.009472338 0.009780223 0.009900084 0.025403373 0.026807442 0.028897075 0.024821273 0.025197642 0.02635066 OAHFA(2:0_24:0)-H_1 0.11136308 0.118624525 0.087985499 0.112529406 0.09984441 0.126324226 0.008665459 0.02256068 0.022254162 0.014746985 0.019640923 0.012169893 0.044132938 0.055120201 0.054898253 0.055369692 0.054672398 0.048509071 PC(15:1_20:5)+CH3COO_2 0.01028629 0.01107471 0.009132101 0.011916831 0.010300824 0.011240692 0.004011488 0.006583501 0.005311149 0.003251827 0.004461104 0.002793334 0.012202879 0.01405911 0.013506294 0.011104121 0.012456518 0.013029938 PC(18:0_20:4)+CH3COO_1 0.010753874 0.011962891 0.009773863 0.011221088 0.009993283 0.011405948 0.003052863 0.004385292 0.004230731 0.003079896 0.004782419 0.002618587 0.007859358 0.009403558 0.009565462 0.009178213 0.008686315 0.008610515 PC(14:0_18:3)+CH3COO_1 0.004492606 0.005020629 0.004793046 0.00565993 0.004710532 0.004662634 0.001546025 0.002522267 0.001886313 0.001427822 0.001861464 0.001444717 0.004563007 0.004224346 0.005526801 0.004439046 0.004760389 0.004691156 PC(18:1_20:3COOH)+CH3COO 0.003062064 0.00075423 0.004082568 0.002743285 0.002050075 0.00216927 0.000678239 0.001084338 0.001322075 0.000801736 0.001102686 0.000736219 0.003764896 0.00324157 0.003077611 0.003104705 0.002895678 0.002639811 PC(14:0_18:4)+CH3COO 0.002763244 0.003019506 0.003352178 0.003618594 0.003051325 0.003411234 0.000790168 0.001427199 0.001129818 0.000657862 0.00105404 0.000917159 0.002914191 0.002754622 0.003337368 0.002892831 0.003160349 0.002473397 Cer(d14:1_28:0)-H_1 0.000893755 0.001000409 0.000889272 0.000959846 0.000697463 0.000920316 9.90E-05 0.000125054 0.000162817 6.17E-05 0.000123179 1.99E-05 0.000403724 0.000417345 0.000553434 0.000485956 0.000494312 0.000423582 PC(19:1COOH_20:5)+HCOO 0.005809778 0.001919713 0.006550054 0.005823237 0.004780399 0.003933616 0.001046856 0.002919875 0.001825165 0.001194445 0.002099176 0.001418956 0.005856734 0.006722106 0.005773152 0.005235239 0.006171253 0.005432644 PE(17:0_20:4COOH)-H_1 0.002038565 0.000901729 0.002155731 0.001919914 0.001777771 0.001740938 0.000291753 0.000706188 0.000765998 0.000494083 0.000467467 0.000402563 0.001564007 0.002051577 0.001666653 0.001949486 0.002097723 0.00176589 Cer(t17:0_24:1)-H_1 0.052414312 0.048881757 0.036146472 0.046376448 0.042638164 0.047955363 0.010317815 0.013187429 0.013527337 0.009853304 0.013014024 0.00772845 0.029600419 0.036284907 0.038714285 0.030615523 0.029690622 0.030641429 Cer(d17:1_24:0)-H_1 0.001272889 0.001100858 0.00076238 0.001297013 0.000800638 0.000996963 3.45E-05 0.000214547 0.000189079 8.84E-05 9.42E-05 0.000132977 0.000776032 0.000779781 0.000963029 0.000673968 0.000634729 0.000699798 PC(15:0_16:0)+CH3COO_1 0.003532156 0.003350956 0.003533287 0.003969838 0.003630199 0.003699343 0.002012781 0.002002237 0.002271779 0.001473259 0.002167177 0.001681625 0.003329372 0.003602156 0.003996256 0.003905729 0.0037165 0.003856139 PG(17:1_17:1)-H 0.000365423 0.000143629 0.000262937 0.000176145 0.000329468 0.000354265 0.003576502 0.003059326 0.002758848 0.004585343 0.002894019 0.002954358 3.31E-05 0.000143913 0.000156647 0.00016649 0.000189295 0.000127339 PC(16:0_20:3)+CH3COO 0.014298366 0.014885583 0.012587535 0.014998556 0.014733025 0.01516761 0.007217895 0.009403237 0.006969542 0.005969131 0.006288086 0.006177673 0.01270012 0.01483629 0.015102508 0.013694122 0.014001149 0.013795459 PC(18:2_20:5)-CH3_1 0.012512571 0.013220158 0.010297439 0.013164049 0.011956355 0.014518782 9.19E-07 0.000823439 0.000575822 0.00041976 0.000708675 0.00036828 0.002126682 0.002226516 0.002737584 0.0028808 0.002180006 0.002491993 PC(20:0_20:3)+CH3COO 0.001560333 0.001379102 0.001458726 0.001645751 0.001378969 0.00144768 0.000276423 0.000483314 0.000441108 0.000403122 0.000649235 0.00034335 0.001267053 0.00173402 0.001473044 0.001340039 0.001266556 0.001445228 Cer(t19:0_24:0)-H 0.001200291 0.001067176 0.000896364 0.001088422 0.000968919 0.001130181 0.000114557 0.000183917 0.000323313 7.60E-05 0.00026904 0.000154673 0.000705046 0.000792276 0.000925242 0.000713201 0.000692015 0.00075168 PC(18:1COOH_20:5)+CH3COO 0.00551777 0.001962642 0.006504014 0.005780451 0.004866723 0.003898381 0.001035274 0.002913091 0.001801831 0.001170839 0.002241752 0.001444563 0.005376259 0.006663086 0.005884386 0.005161027 0.006091634 0.005553666 Cer(t17:0_26:1)-H_1 0.011615713 0.010133729 0.007324571 0.010857334 0.009106848 0.01089891 0.002514395 0.003596238 0.003904812 0.002328024 0.003431821 0.002166491 0.007706434 0.00931257 0.01113327 0.008993583 0.008599201 0.00874716 PC(15:0_15:0)+CH3COO 0.004534095 0.00420748 0.004507236 0.004872906 0.004588882 0.004619324 0.001526241 0.002179858 0.002835164 0.001712599 0.001954144 0.001725731 0.004176145 0.004268256 0.004635168 0.004481261 0.004190729 0.004049012 PC(15:0_20:4COOH)+CH3COO_1 0.003113987 0.001120745 0.004994652 0.003633521 0.003447518 0.002384684 0.000834988 0.002010906 0.001425643 0.00164246 0.00160554 0.000570845 0.00428916 0.00444255 0.003755697 0.003757074 0.004225443 0.003947056 LBPA(18:1_20:3)-H 0.000590735 0.000263248 0.000310806 0.000445831 0.000458647 0.00048205 0.001122596 0.001886797 0.00156081 0.001767196 0.001810325 0.00129591 0.000232498 0.000266752 0.000209308 0.000200861 0.000191642 0.000217309 LBPA(17:1_19:1)-H 0.000441908 0.000383505 0.000365865 0.00047624 0.000489267 0.000754867 0.003173208 0.004665184 0.004739564 0.003998635 0.004701153 0.002991689 0.000595003 0.000632074 0.000468285 0.000463558 0.00057901 0.000511021 PC(17:0_18:3)+CH3COO_1 0.009706757 0.008924924 0.008693515 0.01011294 0.009215139 0.010532784 0.00214294 0.00248161 0.004708809 0.002521474 0.002963377 0.00119172 0.008016136 0.008231819 0.007753556 0.007638394 0.008799597 0.007704358 PC(15:1_15:1)+CH3COO 0.001061844 0.000817834 0.001020389 0.000877347 0.000763971 0.001027016 0.001276737 0.000789286 0.000688685 0.000737052 0.000926892 0.00081779 0.002033115 0.00224856 0.001999734 0.001758979 0.002193534 0.002122958 PE(O-19:1_20:4)-H_1 0.004473053 0.005593059 0.005151681 0.005157037 0.005806681 0.005382821 0.001566181 0.00228427 0.001985011 0.001214491 0.001272214 0.001178222 0.00405106 0.004025739 0.003830946 0.004112696 0.004561314 0.003549513 PC(18:2_18:2)-CH3 0.00517755 0.004337581 0.003099295 0.004181284 0.003940714 0.004792136 3.03E-05 0.000551336 0.000232712 0.000295716 0.000263397 9.41E-05 0.001149341 0.001172388 0.001487619 0.00127893 0.001127242 0.001448359 PC(20:0_20:4)+CH3COO_1 0.000873475 0.000867423 0.000728085 0.00089221 0.000842386 0.00099805 0.000143723 0.000298258 0.000322482 0.000143055 0.000425839 0.000286845 0.000768842 0.001031435 0.000859982 0.000876756 0.00098962 0.000852971 PC(20:0_20:4)+CH3COO_2 0.001423885 0.001255595 0.001768703 0.001412948 0.000933614 0.00152293 0.000234726 0.000390944 0.000378875 0.000296958 0.000478557 0.000165146 0.000815779 0.00103951 0.00100651 0.000936527 0.000981962 0.00085756 PC(16:0_18:3)+CH3COO_1 0.01187339 0.01209741 0.012561276 0.012738053 0.012029127 0.012675358 0.006535868 0.007236477 0.004122245 0.004956506 0.006170673 0.006062469 0.010176188 0.011540596 0.012208869 0.011659166 0.012034984 0.011961419 PC(18:0_20:4)+CH3COO_2 0.005742817 0.005834933 0.004582825 0.005237472 0.005067477 0.005718418 0.002482786 0.003476765 0.003058964 0.002142691 0.003121171 0.001953401 0.005908024 0.007597551 0.007610389 0.006536924 0.0062234 0.007574526 Cer(t16:0_22:1)-H 0.00292441 0.002561821 0.002161568 0.003071249 0.002453556 0.002894139 0.000499208 0.00069757 0.000346941 0.000421012 0.000553212 0.000511307 0.001374019 0.001300261 0.001785753 0.001882923 0.001611847 0.001580646 Cer(t17:0_23:1)-H_2 0.011816093 0.009895545 0.008793724 0.010236484 0.008669974 0.009884066 0.002123862 0.00319978 0.003032819 0.002304864 0.003252624 0.001789877 0.007040013 0.008757622 0.007954272 0.006497736 0.006590065 0.006689578 PC(18:2_20:4COOH)+CH3COO_1 0.001721341 0.000521698 0.002403775 0.002029606 0.001565179 0.001360093 0.000294597 0.000789087 0.000525768 0.000378235 0.000489767 0.000615245 0.001796505 0.002366352 0.001726656 0.001619423 0.002023897 0.001730634 Cer(t18:1_26:0)-H 0.011944867 0.009258994 0.007337659 0.010319515 0.00995341 0.010596605 0.001657609 0.003943903 0.003605087 0.002660387 0.003513265 0.002336911 0.006878443 0.007967436 0.009370523 0.007754439 0.007589605 0.008108285 PC(16:0_20:4)+CH3COO_1 0.01382366 0.016073645 0.013860988 0.015735959 0.013699418 0.017811815 0.00668235 0.008511231 0.007674597 0.00726943 0.008449678 0.005115049 0.012072184 0.014142079 0.014095364 0.014919773 0.013918439 0.013855624 PC(16:0_20:4)+CH3COO_2 0.005610579 0.005016532 0.004847217 0.005085314 0.004856129 0.004628475 0.003489717 0.00336277 0.002905781 0.00185831 0.002792593 0.001960968 0.006122692 0.006448959 0.006352752 0.005260598 0.006504066 0.006632774 PG(20:4_20:5)-H_1 0.000563756 0.000517633 0.00031768 0.000354425 0.000590406 0.000521555 0.002592597 0.004095277 0.003004303 0.002462959 0.003714863 0.00233304 4.22E-05 3.76E-05 7.94E-05 8.16E-05 9.59E-05 7.95E-05 PC(20:4_20:5)+CH3COO_2 0.193587765 0.212804939 0.181720045 0.182096343 0.183201603 0.204054901 0.036044257 0.067898331 0.061320436 0.035079407 0.059720826 0.031893212 0.11470382 0.116846122 0.120713274 0.12018729 0.108942097 0.123980539 LPC(15:0)+CH3COO_1 0.015225197 0.013347782 0.010124404 0.014560226 0.009688708 0.01479343 0.002904038 0.005767363 0.005559383 0.003991807 0.005117794 0.004572066 0.009938476 0.010024538 0.011113572 0.011029923 0.010204012 0.008856715 Cer(t16:0_24:1)-H 0.001603269 0.001615325 0.000920095 0.001737518 0.001162659 0.001911366 0.000219934 0.000290881 0.000248897 0.00016215 0.000259214 0.000239741 0.000775131 0.000598357 0.000810893 0.00094669 0.000782143 0.00066221 PC(21:3COOH_20:4)+HCOO_1 0.003176095 0.001232147 0.00326698 0.00468512 0.002241845 0.002781059 0.000426679 0.001235844 0.000728229 0.000404353 0.00097695 0.000397591 0.003372017 0.003180038 0.003891363 0.004777052 0.004466896 0.003204362 PC(O-18:1_20:5)+CH3COO_1 0.002860839 0.003097076 0.002534464 0.002401673 0.002542721 0.002547538 0.00042676 0.000892723 0.000733349 0.000556387 0.000586251 0.000377533 0.001592997 0.002079346 0.002100764 0.001581236 0.001725593 0.00179599 PC(O-18:1_20:5)+CH3COO_2 0.002860839 0.003097076 0.002534464 0.002401673 0.002542721 0.002547538 0.00042676 0.000892723 0.000733349 0.000556387 0.000586251 0.000377533 0.001592997 0.002079346 0.002100764 0.001581236 0.001725593 0.00179599 Cer(d12:0_16:0_16:0)+HCOO_1 0.053702891 0.046786031 0.033453033 0.049596788 0.045204104 0.054632955 0.011445347 0.016279357 0.015675897 0.011146266 0.015491391 0.00981408 0.032183205 0.048125898 0.051688238 0.04299505 0.04316917 0.039521152 PC(20:4_20:4COOH)+CH3COO 0.007722076 0.002837148 0.00847021 0.007703167 0.006289809 0.005114654 0.00049036 0.002340094 0.001096194 0.000784143 0.001557166 0.00061838 0.005094144 0.007119889 0.007220902 0.005795773 0.007770957 0.005415826 Cer(t18:1_24:0)+HCOO 0.002923201 0.003205452 0.002857995 0.003108148 0.003035748 0.002972086 0.000569807 0.000746945 0.000613384 0.000590165 0.000888101 0.000592992 0.001511389 0.002101633 0.001833133 0.001900027 0.001779438 0.001459312 PC(17:0_18:0)+CH3COO_1 0.007426462 0.006763021 0.005089071 0.006976269 0.006224962 0.006901763 0.002191584 0.002769082 0.002975527 0.002077913 0.002965214 0.001797174 0.004897051 0.005547489 0.005747068 0.004623853 0.005004284 0.004912643 PC(18:1_20:4)-CH3_1 0.006920713 0.006088782 0.004564721 0.006049042 0.00583278 0.006367518 2.34E-05 0.000364059 0.00021232 0.000236202 0.000398163 9.04E-05 0.001363675 0.001416175 0.001769123 0.001803838 0.001079271 0.001371328 LPE(17:1)-H_1 0.011256387 0.008434238 0.008148061 0.011867451 0.012639906 0.011534438 0.005819786 0.008768838 0.007920213 0.006163942 0.007011412 0.007554686 0.017219268 0.015724715 0.017915241 0.014251427 0.019949209 0.015048052 LBPA(17:1_20:5)-H 0.000390502 0.000240052 0.000177009 0.000115587 0.000282943 0.000200854 0.000897774 0.001124324 0.0012082 0.00062749 0.001018195 0.00100643 7.49E-07 9.65E-07 4.55E-08 4.52E-08 3.38E-05 PC(17:2_20:3)+CH3COO 0.005198173 0.005697138 0.008674358 0.005727974 0.003905829 0.005491463 0.001996869 0.002799939 0.002069204 0.001653109 0.001933713 0.001559179 0.006055429 0.005088223 0.004728991 0.004317632 0.005265722 0.004528815 Cer(d17:1_24:0)+HCOO 0.002186259 0.001860567 0.001900875 0.002391073 0.002195447 0.001960294 0.000262343 0.000435956 0.000492697 0.000301339 0.000401878 0.000242092 0.001141988 0.001276498 0.0012337 0.001336663 0.000840642 0.001098873 LBPA(20:4_20:5)-H_1 0.000563814 0.000517697 0.000317902 0.000353722 0.000593598 0.000526269 0.002595005 0.004351649 0.002998032 0.00243157 0.003150314 0.002341156 6.61E-05 3.64E-05 7.78E-05 7.94E-05 9.66E-05 7.80E-05 PC(18:1_20:4)+CH3COO_1 0.039192509 0.038495165 0.039077172 0.038827941 0.036728786 0.039688002 0.01806141 0.03000831 0.02585372 0.020480538 0.028045411 0.018464429 0.050655455 0.055072279 0.051502653 0.042944103 0.046415652 0.051313204 PC(18:0_20:5)+CH3COO_1 0.038096602 0.041664908 0.027632884 0.035213161 0.035251451 0.040029834 0.007647251 0.012383974 0.011416612 0.007178833 0.010775186 0.006267835 0.02052664 0.025853339 0.027617506 0.022881452 0.021393947 0.025044043 PC(16:0_20:5)+CH3COO_1 0.001785659 0.002383927 0.001364567 0.001971938 0.002095749 0.002190402 0.000660687 0.000910453 0.000902863 0.000918574 0.000950703 0.000776119 0.002147795 0.002019442 0.001496887 0.002027317 0.001887746 0.001712203 PC(22:0_20:5)+CH3COO 0.00309392 0.002906956 0.002618178 0.00270766 0.002287653 0.002929641 9.35E-05 0.000688137 0.000602229 0.000341193 0.000506849 0.000215664 0.001243767 0.001546854 0.001707189 0.001646976 0.001406694 0.001566686 PC(22:0_18:1)+CH3COO 0.002677568 0.002636775 0.002096142 0.002321067 0.002058468 0.00230847 0.000562418 0.000575807 0.000695275 0.000430791 0.000670143 0.000370845 0.001187768 0.001442651 0.001741177 0.001555853 0.001310529 0.001432221 PC(17:1_18:1)+HCOO 0.002045147 0.00270853 0.002768962 0.001907037 0.002117577 0.002439604 0.002097566 0.002123197 0.002134757 0.001994973 0.002189341 0.001647595 0.002813645 0.002810777 0.002893274 0.002939292 0.002985152 0.00274412 PC(17:1_18:3)+CH3COO_1 0.038855218 0.040091527 0.040010348 0.038340265 0.040914439 0.039988896 0.021257293 0.035064969 0.028483714 0.024654066 0.028246115 0.023505556 0.045380693 0.047469807 0.045549397 0.044237727 0.047282348 0.047040617 PC(14:0_20:4)+CH3COO_2 0.017739753 0.021763607 0.016594808 0.018279907 0.017386003 0.019222305 0.004974221 0.011459849 0.009830885 0.007196703 0.010215685 0.007111813 0.017341235 0.017730024 0.020713773 0.018606401 0.019334631 0.019308264 PC(21:0_20:5)+CH3COO 0.001901841 0.002182976 0.002098343 0.002179919 0.001917208 0.002029953 0.000476132 0.000585623 0.000745585 0.000417933 0.000437056 0.000417867 0.001597811 0.001488668 0.001582687 0.00117235 0.001206138 0.001294393 PC(20:5_20:5)+CH3COO 0.369501757 0.387507543 0.336290994 0.379986218 0.367989591 0.363368283 0.076556626 0.137755181 0.125971422 0.078701482 0.115469057 0.073452678 0.207998665 0.225512939 0.249628318 0.218631373 0.211116062 0.236626742 Cer(d12:1_16:0_21:3)+HCOO_2 0.003779673 0.003565211 0.003047746 0.003523896 0.00334567 0.003730661 0.000986698 0.00122694 0.001097864 0.000954364 0.001414725 0.0007913 0.001877186 0.002103934 0.002396554 0.002289282 0.002082971 0.0021446 PC(20:4_20:5)+HCOO_1 0.001485946 0.001573078 0.001238324 0.001518653 0.001449645 0.00149786 0.00039778 0.000682974 0.000494218 0.000499653 0.000634681 0.000357043 0.00140319 0.001310318 0.001588202 0.001463358 0.001031392 0.001422504 PC(20:5_20:5)+HCOO_1 0.004327248 0.005064077 0.003819179 0.004354176 0.003864171 0.004454912 0.001145155 0.001765066 0.001455511 0.000866954 0.001359215 0.000975254 0.002609767 0.002774393 0.002806595 0.003023598 0.00243273 0.002667414 PC(19:4_20:5)+CH3COO_1 0.009610077 0.012870668 0.009834069 0.013331446 0.011732264 0.013088504 0.002297738 0.004171276 0.00414988 0.001779337 0.002448681 0.002225386 0.00905433 0.006735679 0.007517187 0.008571411 0.008632796 0.007445636 PC(18:3_20:3)+CH3COO 0.02564587 0.025221533 0.023153093 0.023129699 0.02476102 0.025305374 0.005794712 0.012829273 0.009189465 0.007418654 0.010104431 0.006505513 0.023541099 0.025747852 0.025974416 0.026043616 0.024808225 0.034970102 PC(18:1CHO_20:5)+CH3COO_1 0.001522804 0.001479105 0.001742093 0.00187543 0.00127006 0.001635494 0.000192258 0.000506855 0.000524247 0.000549676 0.000328633 0.000259817 0.000950948 0.001110432 0.001188127 0.001085211 0.000955394 0.001090666 PC(15:0_20:4COOH)+CH3COO_2 0.001798827 0.000526065 0.002250689 0.002194249 0.00153962 0.001504632 0.000406978 0.001000816 0.000873747 0.000572786 0.000798238 0.000329131 0.00198156 0.002148745 0.00204949 0.002129688 0.002011064 0.001536444 PC(18:1CHO_20:5)+CH3COO_2 0.001522804 0.001479105 0.001968935 0.00187543 0.00127006 0.001635494 0.000192316 0.000509279 0.000524247 0.000549676 0.000328633 0.000259875 0.000950948 0.001110432 0.001188127 0.001085211 0.000955394 0.001090666 Cer(t17:0_22:1)-H_1 0.003941447 0.00345992 0.002934916 0.003592069 0.003254231 0.003533642 0.000854467 0.001617361 0.001112945 0.00119883 0.001759017 0.001032522 0.003361095 0.003851416 0.003106058 0.003097306 0.002988216 0.002746961 PC(20:4_21:4COOH)+HCOO_1 0.001342343 0.00053369 0.001706921 0.001752876 0.001415345 0.001121167 2.86E-05 0.000526084 0.000338454 4.06E-05 0.000336242 0.000125611 0.001119425 0.001828097 0.001422839 0.001614745 0.00142644 0.001229531 PG(19:1_20:5)-H 0.001178393 0.000668795 0.00057724 0.000803199 0.000883722 0.001023532 0.006079108 0.009895363 0.008183316 0.00622209 0.00794559 0.005667021 3.60E-08 5.17E-05 3.65E-05 2.86E-09 2.67E-05 PC(17:0_18:4)+CH3COO 0.003754422 0.003614017 0.003127662 0.004127258 0.003639717 0.003379111 0.001718914 0.002363116 0.002054306 0.001368509 0.001679496 0.001419346 0.003491213 0.003238079 0.003106056 0.003508566 0.003814459 0.003512821 Cer(d17:0_22:0)-H 0.004080894 0.003742062 0.002845676 0.00427164 0.002915895 0.004012937 0.000313303 0.000812989 0.000772118 0.000331382 0.000489799 0.000336907 0.001239312 0.001504029 0.001615153 0.001568183 0.001461097 0.001481295 PC(19:1_20:5)+CH3COO_1 0.029083139 0.035659577 0.032623512 0.033587912 0.031904539 0.018773878 0.007385255 0.012226837 0.011358161 0.008361093 0.008044139 0.006863541 0.019934069 0.021036057 0.020829326 0.016613169 0.020429338 0.018003065 PC(16:0_20:4COOH)+CH3COO 0.001742787 0.000511088 0.002122403 0.001985355 0.001857244 0.001273733 0.000890271 0.001526406 0.001151382 0.001095213 0.001343362 0.000964035 0.00230139 0.002792634 0.002634732 0.003008497 0.002682258 0.002171187 PE(O-18:1_20:4)-H_1 0.066153761 0.070029124 0.056374918 0.061939886 0.068698064 0.065956279 0.016952905 0.035230584 0.026370518 0.019843081 0.030154102 0.018425241 0.050803477 0.055544907 0.066339662 0.064461915 0.060590684 0.055656465 PE(O-19:1_20:5)-H_1 0.016320244 0.021573958 0.019167215 0.018474591 0.020654274 0.019777223 0.002690107 0.00546702 0.004940283 0.002713905 0.002827966 0.002948634 0.009136824 0.008844019 0.00892826 0.009823972 0.010282024 0.00781024 PC(20:2_20:4)+CH3COO_1 0.002231165 0.002031662 0.002888336 0.001587429 0.001659395 0.001863697 0.000767373 0.001009545 0.00071519 0.001023256 0.000696229 0.000470603 0.002003642 0.002832061 0.002669099 0.002077223 0.002334773 0.001961694 PC(18:2_21:3COOH)+HCOO_2 0.002773303 0.000693677 0.00289821 0.001903395 0.002002354 0.001618474 0.000414619 0.001173473 0.001210427 0.000915646 0.001347363 0.000768312 0.002496943 0.003774529 0.003333995 0.002924794 0.003857977 0.003060019 PC(20:0_20:5)+CH3COO 0.00460594 0.004840216 0.003882175 0.004585472 0.00412158 0.005041139 0.000704735 0.001391534 0.001416205 0.000864088 0.001456014 0.000768415 0.0026496 0.003105737 0.003532762 0.002749216 0.00257767 0.002885521 LBPA(18:2_20:5)-H 0.001125758 0.000586498 0.000532637 0.000626426 0.000589009 0.0006925 0.003147338 0.006685485 0.004404797 0.003807336 0.004528616 0.003897694 2.66E-10 3.33E-05 7.17E-05 3.34E-05 2.07E-09 2.31E-10 PE(22:3COOH_17:1)-H 0.000493178 0.000887381 0.000982647 0.000757608 0.001219309 0.000687493 0.002267319 0.002983565 0.003010033 0.002973575 0.003169659 0.002826114 0.001575945 0.000993427 0.001129883 0.001682975 0.001531794 0.001198415 PC(14:0_18:3)+CH3COO_2 0.004719925 0.004348476 0.004954676 0.004784916 0.004496035 0.004804316 0.001225628 0.002465503 0.002112945 0.001759416 0.001757977 0.001589456 0.003741988 0.003828463 0.003588687 0.003123049 0.003895621 0.003690748 PE(O-20:2_20:4)-H 0.000867135 0.000877959 0.000950388 0.000840523 0.000938803 0.000883966 0.000146974 0.000453198 0.00025537 0.00017827 0.000386355 0.000243114 0.000830727 0.000738996 0.0009894 0.00090746 0.000754183 0.000771452 PC(18:1_20:5)+CH3COO_1 0.019528061 0.023392576 0.020519721 0.022620441 0.020987106 0.021238242 0.006229206 0.008928523 0.00995722 0.004615382 0.007984285 0.005395734 0.014629756 0.014683851 0.014752286 0.014682895 0.014588981 0.014805975 PC(18:3_20:5)+CH3COO_1 0.152139171 0.17729612 0.141347793 0.15608833 0.151275069 0.1531552 0.026081588 0.076126419 0.052681159 0.035587719 0.051676734 0.031380172 0.122179524 0.108775667 0.111048267 0.125817576 0.127968564 0.138694296 Cer(d17:0_21:0)-H 0.000778255 0.000702201 0.000346829 0.000890337 0.000584205 0.000771632 3.87E-05 6.69E-05 3.06E-05 6.64E-05 7.63E-05 0.000282225 0.000190604 0.000296295 0.000252389 0.000291695 0.000218364 PC(19:1_20:3)+CH3COO_1 0.038658057 0.037319839 0.0331594 0.035914602 0.034073635 0.03946031 0.024207239 0.029052327 0.0240709 0.02045915 0.024589963 0.01777035 0.035987163 0.041241484 0.03799358 0.040540362 0.037474422 0.039499149 PE(O-19:0_20:4)-H 0.002263399 0.002714482 0.002320122 0.002774936 0.003227082 0.003073727 0.001160133 0.001506291 0.001671171 0.001083921 0.001223298 0.001140624 0.002113894 0.002247647 0.002221141 0.002415373 0.002443933 0.002146185 PC(18:0_19:0)+CH3COO 0.000755982 0.000941439 0.000786622 0.000937824 0.000724327 0.00087902 0.000216034 0.000272111 0.00025474 7.77E-05 0.000161744 0.000139504 0.000479779 0.000545182 0.000620889 0.000587111 0.000575755 0.000444475 LBPA(20:4_20:5)-H_2 0.00079607 0.000680259 0.000403783 0.0004532 0.0005352 0.000734944 0.002093321 0.003491594 0.003071182 0.001779083 0.002944319 0.001942298 4.30E-05 3.43E-09 0.000164904 5.36E-05 3.46E-05 8.43E-05 Cer(t17:0_26:1)-H_2 0.036913456 0.033458381 0.025670232 0.03212826 0.031409542 0.034509362 0.004769498 0.006460458 0.007083187 0.00403456 0.007242291 0.004015265 0.011867185 0.01539105 0.018391312 0.015147445 0.013550158 0.014763893 PC(15:0_20:4)+CH3COO 0.024675755 0.026693402 0.024657776 0.027744208 0.026161348 0.026000641 0.005445626 0.01004963 0.011502749 0.006223142 0.009532028 0.007098664 0.017340817 0.01600012 0.017480383 0.018699408 0.017158714 0.016859584 LBPA(17:1_20:4)-H 7.03E-05 3.43E-05 5.71E-05 4.11E-09 6.82E-05 2.43E-05 0.000861145 0.00138155 0.001289325 0.00096992 0.001073998 0.000956676 4.23E-08 2.10E-10 2.14E-05 3.63E-08 PC(18:1_18:2COOH)+CH3COO_1 0.001148141 0.000320571 0.001554588 0.001290784 0.001076282 0.000698789 0.0005027 0.00071701 0.000877496 0.000555829 0.001050678 0.000847117 0.002160319 0.001999514 0.001865795 0.001959254 0.00177765 0.001454376 PE(20:4_20:5)-H_1 0.003562949 0.003888636 0.002762458 0.003210562 0.003142643 0.003612279 0.000750608 0.001877263 0.001501567 0.001140974 0.001322654 0.000789407 0.002739056 0.002846126 0.003580934 0.003020147 0.003060881 0.003005567 PC(17:0_18:0)+CH3COO_2 0.00168053 0.00191289 0.00148607 0.001938971 0.001597112 0.001931245 0.001110816 0.000815635 0.000791134 0.000553235 0.000719562 0.000629502 0.001722088 0.001506524 0.001499983 0.001468678 0.001458209 0.001495247 PC(20:3_20:5)+HCOO 0.00180703 0.002219685 0.002015985 0.001947836 0.001875029 0.001785189 0.000796214 0.000960268 0.000828452 0.000392282 0.000915922 0.00058258 0.00154198 0.001902725 0.001597012 0.001892553 0.001530751 0.001755417 PC(15:1_17:1)+CH3COO 0.00529051 0.005205233 0.005250057 0.004946383 0.006284559 0.005159027 0.00893473 0.005973493 0.006456736 0.005531363 0.006288358 0.00496846 0.010960965 0.011465793 0.010983482 0.011008941 0.012071451 0.011966429 PC(20:4_20:5)+HCOO_2 0.002519421 0.002513674 0.002041313 0.002804211 0.002632634 0.002545331 0.00046721 0.000825875 0.000724261 0.000414851 0.000782799 0.000345207 0.001363443 0.001473985 0.001829857 0.001640264 0.00146128 0.001410442 LPC(17:1)+CH3COO 0.043234329 0.037972051 0.027152692 0.038837668 0.033108493 0.042775431 0.01966169 0.025185609 0.023359107 0.019338925 0.023868389 0.019115087 0.035264001 0.038537537 0.045211353 0.037950775 0.03893849 0.033676355 PG(20:5_20:5)-H 0.003161077 0.002268867 0.001512083 0.002060509 0.002147443 0.002791785 0.006728631 0.011367957 0.009235068 0.005623609 0.008767331 0.005796851 0.000166199 0.00019602 0.00015793 0.000204032 9.97E-05 0.000137875 Cer(d12:1_16:0_16:0)+HCOO 0.00375852 0.003948738 0.003420333 0.003979459 0.003707749 0.004400045 0.00057314 0.001162965 0.001038025 0.000882116 0.001218487 0.000678607 0.002291085 0.002500349 0.002590065 0.002124719 0.001915796 0.001969148 PC(14:0_18:2)+CH3COO 0.021458758 0.02161027 0.023156776 0.020027135 0.020387636 0.025488588 0.007057783 0.012375937 0.008638346 0.0082318 0.009448572 0.007675604 0.021317825 0.019240781 0.021771796 0.014936192 0.021237011 0.019933498 PC(O-18:1_18:2)+CH3COO 0.001082173 0.001041017 0.001027629 0.000814259 0.00089443 0.001129183 3.52E-05 0.000336547 0.000285984 0.000118611 0.000221718 0.00022935 0.000780087 0.000744937 0.000906418 0.000580106 0.000669667 0.000825615 PC(15:0_18:3)+CH3COO_2 0.015865184 0.017157459 0.018736778 0.015561611 0.017114969 0.017169673 0.002723239 0.006635766 0.006131074 0.004617693 0.005239622 0.004424413 0.009937036 0.0117904 0.011617166 0.009322044 0.010767072 0.011290405 LBPA(18:1_18:2)-H 0.001185375 0.000904383 0.001145138 0.001057127 0.001117362 0.001269728 0.002544883 0.006455905 0.005112283 0.005093956 0.005436801 0.004275001 0.000365234 0.000335609 0.000231035 0.000384749 0.000236933 0.000263192 PC(17:1_18:3)+CH3COO_2 0.043839599 0.042823752 0.043245041 0.041291236 0.043264062 0.044543854 0.0119817 0.025472572 0.020884449 0.015436759 0.018934818 0.014027297 0.036672493 0.036990655 0.038652948 0.032574634 0.036408087 0.035270284 Cer(d17:1_24:0)-H_2 0.004705182 0.004697746 0.003124531 0.004838427 0.003956586 0.004691841 0.000474699 0.000676736 0.001006677 0.000554533 0.000820036 0.000490077 0.002041951 0.00279213 0.002962628 0.002208816 0.001893485 0.002077483 PC(18:1_20:3)-CH3 0.006665975 0.005686319 0.00442404 0.005994016 0.005403821 0.006513168 8.93E-05 0.000329332 0.000276021 0.000189183 0.000307043 7.50E-05 0.001116069 0.001000771 0.001304246 0.001702784 0.000993803 0.001091171 PE(O-19:1_20:4)-H_2 0.005968928 0.006175246 0.005468636 0.00633837 0.00702393 0.006629804 0.001085501 0.001996295 0.001807873 0.001108584 0.001440464 0.000961882 0.002758523 0.002942979 0.002885375 0.003220544 0.003086002 0.002812024 LPC(16:0)+CH3COO_1 0.006030678 0.005870503 0.00403189 0.006795675 0.004932049 0.006279409 0.002544131 0.002698856 0.002917905 0.001856831 0.002976151 0.001940578 0.004693664 0.005747166 0.006543264 0.005113444 0.005214082 0.00478229 PE(16:0_20:4COOH)-H 0.001115415 0.000327888 0.001500159 0.00184126 0.001096457 0.00100861 0.000315141 0.000670137 0.000392845 0.000362637 0.000612436 0.000486178 0.001603749 0.001247356 0.001313666 0.00178913 0.001421975 0.001139555 PC(18:3_20:4)+CH3COO 0.012867817 0.01355822 0.013154752 0.012704077 0.012393624 0.013377489 0.001402077 0.004554754 0.003465401 0.002703174 0.00402639 0.002273978 0.006884315 0.007085292 0.007583058 0.007327873 0.006882436 0.006923226 PC(19:1_20:4)+CH3COO_1 0.001481752 0.005928914 0.006029668 0.008099983 0.006535911 0.004422727 0.001973918 0.002580364 0.001290821 0.001927924 0.00160921 0.001144113 0.004105461 0.004950063 0.00407873 0.004151088 0.003413045 0.004322013 PC(15:0_18:0)+CH3COO 0.006552015 0.004776582 0.005417549 0.006266426 0.005637513 0.005837279 0.003055956 0.003434362 0.003571736 0.002175299 0.002819606 0.002312615 0.005545552 0.006124376 0.00597088 0.004533924 0.005688849 0.005599008 LPC(17:2)+CH3COO_1 0.001232079 0.001254471 0.000836469 0.001654158 0.001354191 0.001409675 0.000543817 0.000814096 0.000641395 0.000363144 0.000497008 0.000527824 0.001386515 0.001147747 0.001414162 0.001171066 0.001232897 0.001088807 LPC(17:2)+CH3COO_2 0.001232079 0.001254471 0.000836469 0.001654158 0.001354191 0.001409675 0.000543817 0.000814096 0.000641395 0.000363144 0.000497008 0.000527824 0.001386515 0.001147747 0.001414162 0.001171066 0.001232897 0.001088807 PC(19:3_20:3)+CH3COO 0.002562442 0.003435501 0.002075517 0.003138901 0.002880778 0.003037413 0.001034151 0.001192315 0.001383595 0.000308206 0.000846926 0.000633573 0.002697612 0.002350926 0.002144438 0.002552325 0.002833916 0.002277437 PE(17:0_18:1COOH)-H_1 0.001502516 0.000353435 0.001593075 0.001695833 0.001468892 0.001321802 0.000433719 0.000550153 0.000753796 0.000568846 0.000531686 0.000604498 0.001528892 0.001494817 0.001197174 0.001349082 0.001573348 0.001035592 PE(17:0_18:1COOH)-H_2 0.001502516 0.000353435 0.001593075 0.001695833 0.001468892 0.001321802 0.000433719 0.000550153 0.000753796 0.000568846 0.000531686 0.000604498 0.001528892 0.001494817 0.001197174 0.001349082 0.001573348 0.001035592 Cer(d12:0_16:0_16:0)+HCOO_2 0.167936103 0.147218991 0.120436213 0.162860704 0.155370171 0.174097626 0.022116097 0.032543286 0.033455263 0.022032775 0.036198028 0.019210552 0.055800003 0.082178964 0.084449337 0.071297822 0.067151072 0.06531284 PC(15:0_17:1)+CH3COO_1 0.035876647 0.041866751 0.040430029 0.038007045 0.040807541 0.038598785 0.0274608 0.030041068 0.02979097 0.02284034 0.027819547 0.021100607 0.046850435 0.044980975 0.048645664 0.041849884 0.045837709 0.037917602 PC(17:1_18:1)+CH3COO_1 0.003792588 0.003495101 0.003378082 0.003165885 0.003169285 0.002046693 0.002115227 0.002041197 0.002330691 0.001897101 0.002315906 0.002146277 0.003148615 0.003091101 0.003398634 0.002999729 0.002804307 0.002846099 PC(15:0_20:3)+CH3COO 0.031967148 0.032787695 0.033982811 0.034789107 0.032884142 0.033852865 0.015597739 0.022303733 0.021979292 0.015105257 0.016689699 0.016524144 0.036227459 0.032010029 0.030154695 0.028606847 0.031586978 0.031473587 LBPA(17:1_18:2)-H 0.000371114 0.000254697 0.000203295 0.000206093 0.000219363 0.000255569 0.002282832 0.004384486 0.003631137 0.003339127 0.003428056 0.003178342 2.69E-05 2.57E-10 3.03E-05 2.80E-05 LPC(17:0)+CH3COO_1 0.000906826 0.001072492 0.000968736 0.000984462 0.001000504 0.001083767 0.000114843 0.000302579 0.000229857 0.000310343 0.000317122 0.000364605 0.000579277 0.000666649 0.000681055 0.000544497 0.000619041 0.000716895 PC(18:4_20:5)+CH3COO 0.06913038 0.082990119 0.062305137 0.067749031 0.067186571 0.072279267 0.004994943 0.019725535 0.015855531 0.010023601 0.014473202 0.009189761 0.029928136 0.02998965 0.039692653 0.034043982 0.032442217 0.036983881 PC(20:5_20:5)+HCOO_2 0.013884458 0.01886672 0.012479317 0.01855366 0.015913668 0.02104421 0.001104036 0.002755356 0.003416711 0.00123762 0.001643427 0.001120404 0.005463872 0.004718797 0.005077023 0.006002766 0.005853444 0.005408125 PE(18:0_20:4COOH)-H 0.00203472 0.000500084 0.002315086 0.002313725 0.001948762 0.001572714 0.000691025 0.001256023 0.001218687 0.001037732 0.001343883 0.000642282 0.001962077 0.002637448 0.002677789 0.002528614 0.002698398 0.002141865 PC(19:1_20:5)+CH3COO_2 0.005172576 0.005883767 0.00545741 0.005190248 0.006989439 0.004068199 0.002567011 0.002451213 0.002323797 0.001547538 0.001948858 0.001666165 0.006807116 0.00627707 0.005084977 0.004260238 0.004890768 0.005300103 PC(19:1_18:3)+CH3COO 0.031124639 0.029994743 0.032615044 0.035144347 0.029232203 0.028952758 0.015259442 0.023860534 0.021253014 0.017045526 0.019521113 0.015302325 0.031965174 0.032607863 0.029778021 0.028751977 0.03113481 0.030865317 PG(17:1_20:5)-H 0.000879821 0.000437509 0.000370086 0.0005495 0.000721937 0.000567872 0.003953801 0.007410816 0.005858764 0.003985206 0.005683116 0.004615743 8.22E-05 6.95E-05 3.69E-05 6.66E-05 0.000103779 PC(15:0_17:1)-CH3 0.002471822 0.001861392 0.001765487 0.002285046 0.002131198 0.002492643 3.35E-05 9.21E-05 8.56E-05 9.81E-05 7.05E-05 3.78E-10 0.000561147 0.000478117 0.000761094 0.001036198 0.000698174 0.000673905 PC(18:1_20:4COOH)+CH3COO 0.008188282 0.002982666 0.011304284 0.00890287 0.006868768 0.006181569 0.00112233 0.004005496 0.002968697 0.001859155 0.003809618 0.001826396 0.007743403 0.009248371 0.010057292 0.008040916 0.008507331 0.006252684 PE(23:0_20:5)-H 0.000789644 0.000860861 0.000645842 0.000754588 0.000781717 0.000864718 0.000222974 0.000450111 0.000365503 0.000219937 0.000328 0.000233093 0.000702339 0.00056343 0.000660191 0.000655163 0.000656284 0.000621748 PC(19:3_20:4)+CH3COO 0.001486618 0.001767335 0.001789126 0.002259077 0.00184632 0.002100158 0.000587353 0.000647429 0.000689959 0.000252419 0.000498979 0.000423082 0.001497719 0.000971797 0.001369305 0.001509515 0.001416911 0.001292195 PC(18:1_20:4CHO)+CH3COO_1 0.001930104 0.001020159 0.002371806 0.001830483 0.001919801 0.001588736 0.000624316 0.001069335 0.0007563 0.000780088 0.000911101 0.000562369 0.001832841 0.002341577 0.001939073 0.00172644 0.001495641 0.001837465 PG(20:4_20:5)-H_2 0.000796512 0.000658921 0.000403956 0.000455082 0.000526307 0.000740343 0.002084727 0.003706536 0.003076583 0.001772643 0.002981416 0.001877868 4.22E-05 3.25E-09 0.000163511 5.23E-05 3.65E-05 8.37E-05 Cer(t17:0_24:1)-H_2 0.230129831 0.230551412 0.212551161 0.215680904 0.209193996 0.219810646 0.06126088 0.085991074 0.088608283 0.058118917 0.082146862 0.053126273 0.120519448 0.143934064 0.153120958 0.137808098 0.125165838 0.13125562 PC(18:1_13:3CHO)+CH3COO 0.001394372 0.000413206 0.001583615 0.001664394 0.001252461 0.001240901 0.000754638 0.000719799 0.000853033 0.000476167 0.000814915 0.000632051 0.00172666 0.001877778 0.001958134 0.001955083 0.00128797 0.001451171 PC(18:4_20:5)+HCOO_1 0.000824346 0.000901773 0.00050731 0.000878695 0.000749252 0.000840372 3.14E-10 0.000107442 4.02E-05 5.94E-05 4.03E-10 0.000191312 0.000292222 0.000309937 0.000272977 0.000289889 0.00033137 LPC(18:0)+CH3COO_1 0.000591915 0.000546368 0.000398958 0.000587321 0.000475586 0.000521851 0.000103328 0.000208131 0.00027482 0.000133384 0.000138571 0.000133219 0.000424307 0.000492847 0.000402658 0.000369021 0.000504553 0.000402978 PC(18:2_20:4COOH)+CH3COO_2 0.005971671 0.001973379 0.006708953 0.006346835 0.004713551 0.003554535 0.00094567 0.003243805 0.002057399 0.001052839 0.002126168 0.000973741 0.00569547 0.007833683 0.006642228 0.005534669 0.007488826 0.005043698 PC(18:2_20:3)+CH3COO 0.028002167 0.036815639 0.025774995 0.160183369 0.025458866 0.033788366 0.012013725 0.023605023 0.017502075 0.016860042 0.013068651 0.013447475 0.035659584 0.038986298 0.036366217 0.027728256 0.033127647 0.038256252 PC(20:4_20:5)-CH3_1 0.003330356 0.003119687 0.002289568 0.00309494 0.002524614 0.004033145 3.46E-05 0.000103018 0.000107637 4.89E-05 0.000152685 7.30E-05 0.000487805 0.000454489 0.000690722 0.000880004 0.000532019 0.000600448 PC(19:2_20:5)+CH3COO 0.009356956 0.011686891 0.010291689 0.011624813 0.010747417 0.01167432 0.003250588 0.005116917 0.004793959 0.002439 0.003137731 0.002892842 0.009055067 0.007431152 0.007124468 0.007296971 0.008244035 0.007491531 PC(20:1_20:3)+CH3COO 0.003354075 0.004132745 0.003211608 0.003273565 0.003201812 0.003527254 0.00053559 0.001434291 0.0011487 0.000977441 0.001386545 0.000745815 0.002247216 0.002968938 0.00262607 0.002352974 0.002336887 0.002275162 PC(15:0_16:1)+CH3COO_1 0.009973369 0.010373386 0.009581672 0.010775949 0.009753258 0.01070916 0.003755505 0.006136734 0.006712206 0.004721701 0.006221903 0.004233873 0.010769535 0.010003508 0.010214193 0.008775139 0.009428021 0.009303367 PE(20:2_20:4)-H 0.002066069 0.002284329 0.001593191 0.001765606 0.001991313 0.001820026 0.000206469 0.000549394 0.000513219 0.000337168 0.000596055 0.000198376 0.000970735 0.001084942 0.001341923 0.001172475 0.00107918 0.000979921 PC(18:4_20:5)+HCOO_2 0.001011287 0.001373019 0.000839384 0.001339387 0.001324923 0.001502951 3.72E-05 0.000177643 0.000119197 7.97E-05 0.000113123 0.000509551 0.0003249 0.000551271 0.000428776 0.000492633 0.000417744 PE(18:1_20:2COOH)-H 0.002291107 0.002875578 0.003426611 0.002293057 0.003321508 0.002368867 0.005012647 0.005774492 0.006791662 0.005484807 0.006419975 0.006487842 0.004094759 0.003519504 0.003667012 0.003863612 0.003717668 0.003354756 PC(17:2_20:4)+CH3COO 0.003709868 0.004331583 0.003887892 0.005083246 0.00446134 0.004418612 0.001495179 0.002418228 0.001857658 0.00113695 0.001447611 0.001335897 0.003864792 0.00317711 0.003107904 0.003688526 0.003750722 0.003078112 LPC(18:1)+CH3COO_1 0.008482674 0.007469053 0.006613644 0.007879765 0.007259592 0.009322871 0.002299508 0.004088085 0.003750808 0.002954113 0.00439006 0.003432805 0.006384645 0.008184454 0.00781467 0.007606383 0.006545802 0.009295957 PC(20:4CHO_20:5)+CH3COO_1 0.001165076 0.000631832 0.001787372 0.00161432 0.001394105 0.001432165 0.000217875 0.000603571 0.00021653 0.000307789 0.000278922 0.000243716 0.000870309 0.001311994 0.00133236 0.001239304 0.001542811 0.000978819 PG(17:0_20:5)-H 0.00054657 0.00046243 0.00036197 0.000620688 0.000546384 0.000481689 0.002486322 0.004328038 0.004328478 0.003286287 0.003917988 0.002949711 3.43E-05 1.97E-10 2.27E-05 2.95E-05 PC(20:5_21:5CHO)+HCOO 0.000779688 0.000214776 0.000820622 0.000962479 0.000704951 0.000783299 4.19E-05 0.000286873 0.000241018 8.30E-05 9.35E-05 0.000101297 0.000416102 0.000547359 0.000454398 0.000609002 0.000565071 0.000533908 PC(17:1COOH_18:2)-CH3 0.000548983 0.000708971 0.000998395 0.000794698 0.001093 0.000608519 0.002261669 0.002343998 0.002451117 0.002119493 0.002474419 0.00224064 0.00144173 0.001020328 0.001284064 0.001790206 0.00152106 0.001197718 PI(18:0_18:2)-H 0.000421159 0.000409407 0.000652811 0.000463916 0.000531398 0.000401179 0.001865763 0.001470016 0.001832314 0.001771459 0.002001249 0.00170655 0.000923218 0.001016804 0.000834569 0.001133038 0.001260777 0.000819965 PE(O-17:1_20:5)-H 0.010136673 0.012222597 0.010613252 0.012888132 0.012127075 0.012449119 0.001479109 0.003660327 0.003281447 0.001588075 0.001893385 0.001765667 0.005875924 0.005291804 0.00566691 0.007150849 0.006708721 0.0054065 LPC(18:2)+CH3COO_1 0.027450719 0.023641434 0.016110787 0.022662074 0.019765964 0.027241571 0.005316203 0.011711844 0.009048889 0.008020682 0.010183601 0.007328213 0.017997947 0.022834902 0.023169099 0.015950105 0.020531156 0.01859286 PG(18:2_20:5)-H 0.001072569 0.000584349 0.000532395 0.000627766 0.000591287 0.000691865 0.002493848 0.006731478 0.004883086 0.003729255 0.005407343 0.004092414 2.53E-10 3.42E-05 7.42E-05 3.32E-05 3.20E-05 2.22E-10 PC(14:0_18:0)+CH3COO 0.00133757 0.001485147 0.001238414 0.001342549 0.001185687 0.001547932 0.001321338 0.00082737 0.000720514 0.000651786 0.000855796 0.000621824 0.001580734 0.001864975 0.001993216 0.001728377 0.001627224 0.001741579 PC(17:0_20:3)+CH3COO_1 0.02510949 0.022711216 0.021332039 0.01861276 0.021177291 0.021022492 0.008274937 0.012116733 0.009987406 0.009527706 0.009809667 0.009725277 0.021026771 0.025817245 0.022345419 0.015825823 0.019958665 0.019628126 PE(O-19:1_20:3)-H_1 0.004972566 0.00635946 0.005564001 0.005220839 0.006054081 0.006164055 0.001980292 0.001995334 0.001845305 0.001317972 0.001176672 0.001318761 0.003397916 0.003208162 0.002934737 0.003805594 0.003873014 0.002873053 PC(22:4COOH_20:5)-CH3 0.014337694 0.019042332 0.012475167 0.01854785 0.016221573 0.020156557 0.001042135 0.002816806 0.003384415 0.001237316 0.001644134 0.001120147 0.0052945 0.004709647 0.004975795 0.005994409 0.005910116 0.004998545 PC(17:0_20:3)+CH3COO_2 0.02510949 0.022711216 0.021332039 0.01861276 0.021177291 0.021022492 0.008274937 0.012116733 0.009987406 0.009527706 0.009809667 0.007458661 0.021026771 0.025817245 0.022345419 0.015825823 0.019958665 0.019628126 PC(O-18:1_18:1)+CH3COO_1 0.003849219 0.003610142 0.002846651 0.003372973 0.003182575 0.003986568 0.000775904 0.001541836 0.00134161 0.001293394 0.001570342 0.001016769 0.003036403 0.003706051 0.003820377 0.00253271 0.002604913 0.00331223 PC(17:1_19:1COOH)+HCOO_1 0.005002558 0.00134159 0.005732812 0.004839902 0.003584813 0.003024591 0.003341391 0.004047208 0.004747261 0.00521508 0.004951786 0.003964201 0.009668983 0.008582159 0.00769715 0.007390349 0.008428188 0.006896525 PC(20:4COOH_20:5)+CH3COO_2 0.002951064 0.001397444 0.003611469 0.00367099 0.003082636 0.002935369 0.000131448 0.000774957 0.00058643 0.000289502 0.000555921 0.000208735 0.0013392 0.002303892 0.002284315 0.002198178 0.002608266 0.001638336 PC(17:2_20:5)+CH3COO_1 0.006725421 0.007215155 0.006663773 0.007617263 0.006574009 0.007803202 0.002291674 0.004155942 0.003530518 0.002230741 0.002515414 0.002366933 0.005332365 0.005047824 0.005471889 0.00554965 0.005745749 0.005248678 Cer(t17:0_20:1)-H 0.016905135 0.01535756 0.012080681 0.015337765 0.013357768 0.015296198 0.002829215 0.004967613 0.004886257 0.003685457 0.005272905 0.00315699 0.007579636 0.007950691 0.009544367 0.008083193 0.008086259 0.007273489 PC(16:0_17:0)+CH3COO_1 0.001002588 0.001003887 0.001017019 0.001227712 0.001103888 0.000980381 0.000883892 0.000631382 0.00058086 0.000366049 0.000501454 0.0003997 0.001257184 0.001208487 0.001076232 0.001201136 0.001350067 0.001124111 PC(21:1_20:3)+CH3COO 0.001180397 0.000982355 0.001055007 0.001420982 0.000932599 0.001024812 0.000388294 0.000347639 0.000473748 0.000296427 0.000397973 0.000274937 0.000660735 0.000860913 0.000793292 0.000706706 0.00059261 0.000769346 LPC(15:1)+CH3COO 0.001706628 0.001423469 0.000741046 0.001378913 0.001413193 0.001575434 0.001342001 0.001287261 0.001136119 0.000899307 0.00132127 0.000987748 0.002348991 0.002772196 0.003340302 0.002290705 0.002797234 0.002145527 PC(17:0_18:1)+CH3COO_1 0.02037254 0.022891529 0.02176582 0.023112972 0.021623478 0.024256302 0.011717683 0.012412022 0.013769237 0.008480818 0.010015897 0.008791586 0.019155146 0.017886086 0.017665545 0.017951893 0.018068129 0.016271386 PE(21:0_20:5)-H 0.005622536 0.006771753 0.006221823 0.005979807 0.00615501 0.005442298 0.002115797 0.003549317 0.003327695 0.001915329 0.002357096 0.002348249 0.005337449 0.004844019 0.005327381 0.004776178 0.005076371 0.004311792 PC(17:0_20:5)+CH3COO_1 0.083702384 0.088970034 0.079535647 0.08861582 0.079891341 0.087512806 0.035009802 0.053784131 0.049066164 0.032822637 0.037818773 0.03890683 0.0705684 0.074392313 0.06689399 0.068788853 0.06264832 0.071954512 PE(14:0_18:2)-H 0.016577844 0.015077631 0.012950313 0.013742519 0.014656927 0.015526036 0.001213912 0.003696946 0.003073921 0.002115225 0.002852486 0.002342254 0.005753789 0.005143449 0.006923032 0.007378428 0.006334893 0.005607589 PE(17:0_17:1)-H_1 0.007339027 0.008743473 0.006856964 0.010567394 0.010614998 0.009129646 0.003663256 0.003645843 0.002662071 0.003105284 0.002588538 0.003418454 0.006598099 0.004835235 0.005553052 0.006402338 0.006498253 0.005223194 PC(20:1_20:5)+CH3COO_1 0.015065671 0.016999519 0.014558521 0.013904885 0.013727752 0.015568125 0.001438096 0.004283501 0.003813317 0.002602237 0.003716197 0.002328404 0.007084357 0.008560966 0.00900684 0.006911236 0.00624777 0.007570178 PE(15:0_18:2)-H 0.02424676 0.020833198 0.024826624 0.024646152 0.028387236 0.026065501 0.006686528 0.007904148 0.007675424 0.005407431 0.006415213 0.004882306 0.01106279 0.010223171 0.012951715 0.012963632 0.012620163 0.010528791 PE(20:4_20:5)-H_2 0.016285249 0.017650136 0.014153939 0.015413781 0.016014474 0.017519501 0.002001062 0.005361001 0.004367668 0.002774165 0.004270246 0.00224823 0.007605796 0.008117008 0.010706943 0.009603057 0.008374208 0.008450812 PC(19:1_20:4)-CH3_1 0.003183222 0.00259263 0.001974464 0.003160775 0.002714669 0.003435076 9.98E-05 0.000304843 0.000121313 9.12E-05 6.37E-05 0.00016854 0.000576515 0.000592428 0.000910408 0.001062988 0.000734557 0.00071032 PC(20:4_21:4COOH)+HCOO_2 0.004275607 0.001618776 0.00532948 0.006410406 0.003780808 0.003786791 0.00049048 0.002073536 0.000859144 0.000783495 0.001665873 0.000618071 0.003871186 0.004907521 0.005941446 0.00709569 0.007569581 0.004949333 PC(20:1_20:4)+CH3COO_1 0.002734002 0.0024211 0.002387005 0.0025053 0.002493312 0.002626809 0.000648634 0.001326715 0.001030157 0.000688778 0.001099244 0.00051935 0.00234094 0.002749586 0.002371277 0.002087735 0.001834689 0.002008198 PC(13:1_20:5)+CH3COO 0.003494442 0.001281631 0.004071932 0.003174194 0.002755695 0.00269588 0.000557145 0.002003427 0.001618647 0.001090429 0.001838018 0.000812793 0.003183173 0.003107732 0.003155309 0.003434479 0.003536115 0.002852926 PC(17:0_18:0)+HCOO 0.002746251 0.002998397 0.002734444 0.003595801 0.002827708 0.003334367 0.001220224 0.001189581 0.001496353 0.000804121 0.001206046 0.000801668 0.002278857 0.002134857 0.002148098 0.001944817 0.002144473 0.001798131 PC(17:1_18:3)-CH3_1 0.004819292 0.00387151 0.003135094 0.004167585 0.004149132 0.004692163 0.000264119 0.000135262 0.000136331 0.00032227 0.000126633 0.000857225 0.000923283 0.001161026 0.001462675 0.000906539 0.000990814 PC(18:2_20:4)+CH3COO 0.053693613 0.054224067 0.053845058 0.050215159 0.050575396 0.052675036 0.014016227 0.030195894 0.024848361 0.019104679 0.02401613 0.016592818 0.043371168 0.046962254 0.046130844 0.035655946 0.041692508 0.043663958 PE(18:0_18:1COOH)-H 0.004617951 0.003210523 0.004309971 0.004974517 0.004855772 0.004473306 0.001118034 0.002526024 0.00230342 0.001712147 0.002500345 0.001445323 0.003499432 0.003997499 0.004509767 0.00393832 0.004622439 0.00393308 PC(18:2_18:3)+CH3COO 0.043013204 0.041675343 0.046674202 0.039744242 0.040529698 0.043124926 0.006289242 0.021386645 0.015952128 0.01366634 0.018603438 0.010755503 0.029719214 0.03602935 0.033950618 0.029021524 0.033320796 0.032338755 PC(19:1_20:4)+CH3COO_2 0.007951858 0.008992536 0.008634733 0.009263512 0.008278441 0.010139281 0.003700584 0.004072673 0.004054584 0.002770099 0.003168513 0.002628826 0.007781935 0.007739669 0.007078462 0.006297401 0.006845874 0.005208987 Cer(d12:1_17:0_21:3)+HCOO 0.001371985 0.001074555 0.001021967 0.001229898 0.001251525 0.001264275 0.000302286 0.000810683 0.000653331 0.000570137 0.000696334 0.000507982 0.001213874 0.001150192 0.001550841 0.001254826 0.001252068 0.001164342 PC(18:1_20:4CHO)+CH3COO_2 0.002058726 0.000935053 0.002408152 0.002017372 0.001703716 0.001887904 0.000436064 0.001228693 0.001049095 0.000674903 0.001112865 0.000627413 0.001763882 0.002385719 0.0019282 0.001960394 0.002180493 0.001841547 PC(20:0_19:1)+CH3COO 0.003906893 0.00387108 0.002916694 0.003335156 0.00314091 0.003491291 0.001097366 0.001636751 0.001526571 0.000985973 0.001595151 0.000909175 0.002129833 0.002668205 0.002727406 0.002593885 0.002392198 0.002323329 PC(18:3_20:5)-CH3 0.005859468 0.004024456 0.003358599 0.005421129 0.005284265 0.004802574 6.52E-07 0.000315417 0.000289857 0.000107908 0.000260669 0.00011081 0.000687026 0.000669498 0.001092962 0.001116454 0.000775842 0.000851069 LPC(18:0)+CH3COO_2 0.006091301 0.005429059 0.003992751 0.005583896 0.004804911 0.006186161 0.001670959 0.002576042 0.002375568 0.001440846 0.002268195 0.001587192 0.003313699 0.003969811 0.004692108 0.004004267 0.003887688 0.003651588 PC(21:0_18:1)+CH3COO 0.003144206 0.00351603 0.003063366 0.003122388 0.0030341 0.003325108 0.000623568 0.00098497 0.001144451 0.000553655 0.000773958 0.000573528 0.001973635 0.00254236 0.001822619 0.001991866 0.002059815 0.001518086 PC(19:1_18:2)+CH3COO_1 0.008247341 0.008459881 0.007786696 0.009682903 0.00528553 0.009738519 0.004069684 0.005058442 0.004657095 0.00407495 0.004301635 0.002755385 0.007839582 0.008963706 0.006628311 0.006828668 0.007820206 0.007153248 PC(16:0_18:0)+CH3COO 0.00268268 0.002335194 0.002390216 0.002886539 0.002270193 0.00241692 0.002183428 0.00099587 0.001423474 0.0012873 0.001777788 0.001001138 0.002933667 0.002955153 0.002912049 0.002624485 0.002761834 0.002928504 PE(18:1_20:4COOH)-H 0.004053764 0.001309362 0.004860044 0.004056364 0.003470304 0.003294582 0.000557798 0.002125881 0.001605911 0.001104694 0.001503036 0.000591658 0.003133327 0.0032362 0.003595022 0.004059094 0.003544326 0.002881907 PC(17:0_17:0)+CH3COO_1 0.004740853 0.004912524 0.003719408 0.004715803 0.004327758 0.004791717 0.000992168 0.001751607 0.002126139 0.001251088 0.00193002 0.001194609 0.003198599 0.00375338 0.003482466 0.00273247 0.003006805 0.003195107 PE(17:0_20:4)-H_1 0.023760879 0.023992279 0.019532975 0.020645803 0.026973363 0.023221652 0.00874606 0.017055179 0.014420132 0.011310206 0.014330049 0.010373042 0.021472 0.021057381 0.024677055 0.022897795 0.024172599 0.021783408 PC(14:1_18:2)+CH3COO 0.002231671 0.002349567 0.002662718 0.002430851 0.002439859 0.002563964 0.00118177 0.002497324 0.002015744 0.001755289 0.002411211 0.001418895 0.004239505 0.003559064 0.004099122 0.003213931 0.003789936 0.003660295 PC(18:3_18:4)+CH3COO_1 0.017312709 0.01853046 0.017648649 0.016871325 0.017092217 0.01916325 0.002128814 0.009456834 0.005943185 0.00358819 0.005875133 0.003870337 0.011958596 0.012205297 0.01538645 0.01450773 0.013196523 0.014676743 PE(17:0_18:1COOH)-H_3 0.002252888 0.001834356 0.002444792 0.002347633 0.002221117 0.002060782 0.000977333 0.002078846 0.001542614 0.001441018 0.002156983 0.001487294 0.003223109 0.002872721 0.003303079 0.002795369 0.00298195 0.00293884 PC(15:0_20:5)-CH3_1 0.009286894 0.008423307 0.006060355 0.008545383 0.007776783 0.009913451 8.60E-05 0.000416548 0.000181484 0.000172271 0.000270369 0.000181724 0.001085734 0.001180048 0.001515691 0.002104235 0.001068021 0.00157353 PE(20:3_20:5)-H 0.01411083 0.014064449 0.012711969 0.012294226 0.012961277 0.012973799 0.002487974 0.006839153 0.004537684 0.003571654 0.004772743 0.003057548 0.00848211 0.00920499 0.011761596 0.010067965 0.009350673 0.009572718 PC(18:4_18:4)+CH3COO 0.003065145 0.009634361 0.002224647 0.008126076 0.008240829 0.008451848 0.000380249 0.002281321 0.001892486 0.000937466 0.002194975 0.001141694 0.003902767 0.003677173 0.005673647 0.005326321 0.0045882 0.00544791 PC(18:2_20:4COOH)+CH3COO_3 0.005971671 0.001973379 0.006708953 0.006346835 0.004713551 0.004262175 0.00094567 0.003813083 0.002057399 0.001052839 0.002126168 0.00140556 0.00569547 0.007833683 0.006642228 0.005534669 0.007488826 0.005043698 PC(18:1_18:1)+HCOO 0.003153859 0.003398064 0.003249166 0.003131988 0.003066244 0.003316011 0.001967787 0.002060902 0.002152102 0.001702338 0.002252468 0.001967189 0.003239308 0.003016587 0.003132791 0.002656017 0.002780563 0.002672197 PE(17:0_20:3)-H 0.019618263 0.024421964 0.020697171 0.023322491 0.025760361 0.024521129 0.004962755 0.011131701 0.009979133 0.006448021 0.008236742 0.007395427 0.014085304 0.015074237 0.017285312 0.019375424 0.017871958 0.015988574 PE(O-18:1_20:5)-H_1 0.216277497 0.232995504 0.198182816 0.202925202 0.228244936 0.217529862 0.028101862 0.074012249 0.06090205 0.038714715 0.06211159 0.036473508 0.096895561 0.107738234 0.133915195 0.124104572 0.11464734 0.108096503 PC(17:1_18:1COOH)+CH3COO_1 0.00439629 0.001339207 0.005727428 0.004393476 0.003990673 0.003228337 0.003220332 0.004035936 0.005321849 0.004219966 0.004930615 0.004135154 0.009458193 0.010221298 0.008307158 0.006960858 0.009422825 0.007282763 PE(O-17:1_20:4)-H_1 0.002871055 0.003239628 0.003322845 0.00353018 0.003870775 0.004573853 0.000722743 0.001206791 0.001052391 0.000683579 0.000818907 0.000649642 0.001916581 0.001680935 0.001979571 0.002425141 0.002261066 0.001600199 PE(O-19:1_18:3)-H 0.001655656 0.001794405 0.001753843 0.001683801 0.001822296 0.00191293 0.000369042 0.000631242 0.000508929 0.000289219 0.000388193 0.000283315 0.000965994 0.0008105 0.001010207 0.001210292 0.001328239 0.001053723 PC(19:1_18:2)+CH3COO_2 0.008247341 0.008459881 0.007786696 0.009682903 0.007657752 0.009738519 0.004069684 0.005058442 0.004815751 0.00407495 0.004301635 0.002755385 0.007839582 0.008963706 0.006628311 0.006828668 0.007820206 0.007153248 PS(18:0_20:5)-H_1 0.00129581 0.001768852 0.002624898 0.001559243 0.002420917 0.002157574 2.28E-07 0.000732636 0.00024996 0.000194061 0.000416433 0.000318072 0.001022628 0.001223137 0.001516663 0.001379638 0.001148664 0.001734368 PC(20:3CHO_20:5)+CH3COO_1 0.002299926 0.000818345 0.002958321 0.002767642 0.001996427 0.002161087 0.000299439 0.00097988 0.000556971 0.000604349 0.000887199 0.000338353 0.00139532 0.002358354 0.001951992 0.001729752 0.002039921 0.001644156 PC(20:3CHO_20:5)+CH3COO_2 0.002299926 0.000818345 0.002958321 0.002767642 0.001996427 0.002161087 0.000299439 0.00097988 0.000556971 0.000604349 0.000887199 0.000338353 0.00139532 0.002358354 0.001951992 0.001729752 0.002039921 0.001644156 LPC(18:4)+CH3COO_1 0.002368462 0.001848732 0.00134845 0.001296676 0.001909223 0.002152458 0.000269491 0.001096189 0.000925446 0.000581058 0.00096079 0.000622419 0.00161201 0.001843429 0.00187507 0.001501407 0.001761148 0.001645131 LPC(18:4)+CH3COO_2 0.002368462 0.001848732 0.001348082 0.001296676 0.001909223 0.002152458 0.000269466 0.001096189 0.000925446 0.000581058 0.00096079 0.000622419 0.00161201 0.001843429 0.00187507 0.001501407 0.001761148 0.001645131 PC(17:1_20:5)+HCOO_1 0.003212509 0.002294631 0.002800902 0.002654507 0.002748428 0.002467158 0.001048667 0.001648104 0.001197605 0.000887448 0.001125079 0.000759667 0.002045122 0.00201351 0.002106678 0.002035861 0.001848412 0.002086386 PE(18:1_18:2)-H_1 0.005304528 0.004580657 0.006418091 0.003811612 0.005675214 0.004293549 0.000318642 0.001636466 0.001300407 0.001655172 0.001738615 0.001267865 0.002640821 0.003038752 0.003194268 0.003766112 0.003928242 0.003686053 PC(17:1_20:4COOH)+CH3COO_2 0.000810286 0.000167069 0.000370165 0.000888795 0.000725676 0.000681195 0.000220421 0.00037244 0.000185444 0.000456529 0.000243773 0.000221232 0.00076073 0.000848653 0.000988206 0.000850086 0.001133432 0.000622252 PC(17:1_20:4COOH)+CH3COO_3 0.000810286 0.000167069 0.000370165 0.000888795 0.000725676 0.000681195 0.000220421 0.00037244 0.000185444 0.000456529 0.000243773 0.000221232 0.00076073 0.000848653 0.000988206 0.000850086 0.001133432 0.000622252 Cer(t17:1_24:1)-H_1 0.001250836 0.001198693 0.000849969 0.000958593 0.000915529 0.001187278 0.000120203 0.000112979 9.08E-05 0.000131245 0.000162917 6.22E-05 0.000383924 0.000459746 0.000459122 0.000456044 0.000254022 0.000296381 PC(20:4CHO_20:5)+CH3COO_2 0.001451698 0.000629917 0.001169944 0.001377478 0.001304833 0.001280618 0.000140829 0.000455677 0.000521984 4.34E-05 0.000117992 0.000168755 0.00091299 0.001377812 0.000781396 0.001239321 0.000980064 0.001077232 PC(15:0_20:5)-CH3_2 0.009682343 0.00877284 0.006417639 0.009179685 0.00808935 0.0104524 8.62E-05 0.000417815 0.000222487 0.00017205 0.000308949 0.000180896 0.001178419 0.001179789 0.001566173 0.002229002 0.001071724 0.001620284 PG(17:1_18:2)-H 0.00036746 0.00025382 0.000203652 0.000207312 0.000218264 0.000264627 0.002288379 0.004393838 0.003788775 0.003377936 0.003435764 0.002390034 2.01E-10 2.31E-10 1.99E-10 4.42E-07 PC(17:1_18:2)+CH3COO_1 0.142121117 0.132309238 0.134024269 0.123648622 0.129107068 0.13786914 0.066910595 0.107673842 0.084139223 0.078667381 0.085033503 0.066293132 0.139022532 0.144531019 0.137589252 0.113107075 0.130366061 0.144191615 Cer(d17:1_22:0)-H 0.012939619 0.013911269 0.011791412 0.013255478 0.01052196 0.012210951 0.001981827 0.003922887 0.00414078 0.002697503 0.003772545 0.002145686 0.006198004 0.007186405 0.006955824 0.006818137 0.005465308 0.005704303 PC(20:5_20:3)+CH3COO 0.168730517 0.177362029 0.124813947 0.170445073 0.141175876 0.177972432 0.002254211 0.075395509 0.063205078 0.041586975 0.065785579 0.039104974 0.124947451 0.121939742 0.146766701 0.115241194 0.124293476 0.12653413 LBPA(19:1_20:4)-H_2 8.37E-05 5.50E-05 2.53E-10 5.08E-05 6.53E-05 0.001043073 0.001317729 0.001221605 0.000852399 0.00113316 0.000824188 2.57E-05 2.89E-05 2.41E-05 PC(20:3_20:5)+CH3COO 0.168730517 0.177362029 0.124813947 0.170445073 0.141175876 0.177972432 0.002254211 0.075395509 0.063205078 0.043461078 0.065785579 0.039104974 0.124947451 0.121939742 0.146766701 0.115241194 0.124293476 0.12653413 LPC(20:4)+CH3COO_2 0.017463643 0.012113707 0.007486493 0.015349812 0.011090742 0.015409418 0.003757595 0.006135225 0.005332573 0.003474058 0.004944652 0.003836845 0.007179942 0.010668914 0.010325752 0.00997076 0.009382584 0.008210215 PC(16:0_18:1)+CH3COO_1 0.046780805 0.049084749 0.044726123 0.047096405 0.04779592 0.052840151 0.03598799 0.038209009 0.04219161 0.030486883 0.036472042 0.028637822 0.051531838 0.052942376 0.054074846 0.046426033 0.049277558 0.052490914 Cer(t17:0_21:1)-H 0.088920126 0.091838731 0.078670155 0.091531679 0.086974614 0.097878003 0.023105981 0.039204671 0.040258406 0.025558117 0.029408107 0.026945082 0.059424423 0.06211622 0.055594627 0.051640243 0.056276856 0.047444315 PC(19:1_19:1)+CH3COO_1 0.008430809 0.007717786 0.009045884 0.009081021 0.008036593 0.00814288 0.007280733 0.005896605 0.004921907 0.005337165 0.006105022 0.004203309 0.011905447 0.013686462 0.011877488 0.008955188 0.010033504 0.010236796 PC(16:0_20:5)-CH3_1 0.004078104 0.003351546 0.002591438 0.003655067 0.002924418 0.004047311 4.06E-05 0.000293794 0.000301333 0.000140381 0.000259159 9.13E-05 0.000710062 0.000632851 0.000814204 0.001167759 0.000737698 0.000707555 PC(18:2_20:5)+HCOO 0.0043405 0.003423252 0.004189574 0.004159143 0.003249184 0.004465947 0.000791906 0.001882358 0.001690015 0.001316622 0.001644173 0.00092326 0.003024464 0.002684797 0.002959255 0.002509588 0.00246767 0.003076452 PE(20:5_20:5)-H_1 0.016690712 0.017824962 0.014142541 0.015433803 0.016544476 0.016841704 0.001680452 0.005308827 0.003870233 0.002694555 0.003872455 0.00202261 0.006309219 0.00804274 0.00926677 0.008379974 0.007223515 0.007983822 OAHFA(2:0_26:0)-H 0.01442684 0.013614543 0.0080963 0.015619157 0.015120577 0.017683582 0.003041743 0.009156123 0.008816021 0.005345689 0.006770757 0.005347742 0.011694773 0.013429179 0.01548086 0.013792307 0.014226477 0.013080878 PE(18:3_20:5)-H_1 0.012431594 0.012833066 0.010680326 0.011432705 0.012328507 0.012396405 0.001610027 0.005552362 0.003849734 0.002628264 0.004145135 0.002311842 0.006872734 0.007143326 0.008926673 0.007636636 0.008148457 0.007779342 PC(17:0COOH_16:1)-CH3 0.000659634 0.000269948 0.000860159 0.000739395 0.000390864 0.000420775 0.000192299 1.08E-06 0.00030666 0.000216135 0.000241035 8.43E-07 0.001070167 0.000860921 0.000897203 0.000468523 0.000998584 0.000740169 Cer(d17:0_23:0)-H 0.000830373 0.000914908 0.000567335 0.00097478 0.000679413 0.000773096 4.13E-05 8.38E-05 5.37E-05 5.10E-05 7.07E-05 3.69E-05 0.000253042 0.00015196 0.000187382 0.000319474 0.000316925 0.000245139 LBPA(17:0_18:1)-H_1 0.001122753 0.00109988 0.001141643 0.001280596 0.001277336 0.00129038 0.001030837 0.002584005 0.002640111 0.002035024 0.002680628 0.001989962 0.000344102 0.000474771 0.000440965 0.000541855 0.000431651 0.000358453 PC(18:1CHO_20:4)+CH3COO 0.001871926 0.000773368 0.002026332 0.002244351 0.001800074 0.001799035 0.000586143 0.00136388 0.001124095 0.000798527 0.001463884 0.000817422 0.002093426 0.002556613 0.002030437 0.00215555 0.002140658 0.00189234 PC(18:1_20:4CHO)+CH3COO_3 0.001871926 0.000773368 0.002026332 0.002244351 0.001800074 0.001799035 0.000586143 0.00136388 0.001124095 0.000798527 0.001463884 0.000817422 0.002093426 0.002556613 0.002030437 0.00215555 0.002140658 0.00189234 PC(15:0_18:1COOH)+CH3COO 0.00150264 0.000348256 0.001931769 0.001649559 0.001212211 0.000983561 0.00075613 0.000963077 0.001080211 0.001004387 0.001195565 0.001177036 0.002858766 0.002622691 0.002049616 0.001814418 0.00228835 0.001870568 PC(20:4CHO_20:5)+CH3COO_3 0.002982083 0.001191629 0.003091303 0.003304336 0.002806355 0.003026607 0.000282864 0.001020431 0.000738534 0.000150924 0.000558586 0.000330031 0.001537281 0.002880593 0.001845921 0.002275832 0.00213909 0.00175903 PE(O-20:2_20:5)-H 0.002364334 0.002786234 0.003009856 0.002476491 0.002677792 0.002534909 0.000139594 0.0008403 0.000715203 0.000487553 0.000896411 0.000425953 0.001451482 0.001573222 0.00210068 0.00160261 0.001667452 0.001359303 PE(17:0_22:0)-H 0.000804822 0.000740201 0.000769324 0.000829416 0.000937553 0.000866979 0.000241502 0.000370868 0.000347366 0.00026547 0.000298548 0.000174479 0.000470539 0.000495468 0.000551075 0.000610129 0.000503022 0.000496346 PC(16:0_20:5)+CH3COO_2 0.041676563 0.046293442 0.041275872 0.043078939 0.040242666 0.04392505 0.019804079 0.025764159 0.024206784 0.014061204 0.019877172 0.013361966 0.036612774 0.034235057 0.043113086 0.032930562 0.03454201 0.040859198 PC(17:1_21:4COOH)+HCOO 0.000851694 0.000159378 0.001355508 0.0008419 0.000691283 0.000948034 0.000212428 0.00036865 0.00018112 0.00047083 0.000254658 0.000212888 0.000724267 0.000909972 0.001017341 0.00084008 0.001083542 0.000593831 PC(17:1_20:5)+CH3COO_1 0.039846685 0.03639384 0.045191891 0.047482983 0.034952069 0.038043578 0.014407098 0.018877952 0.020050965 0.009748307 0.013676609 0.010342537 0.033172245 0.031141487 0.023151365 0.028136971 0.031627943 0.029266058 LBPA(16:1_18:1)-H 0.000715576 0.000888377 0.000616945 0.000732063 0.000439473 0.00089739 0.001469842 0.002637075 0.002884001 0.002375006 0.003709754 0.00185754 0.000278858 0.000489732 0.000400753 0.000162746 0.000429191 0.000286355 PE(17:1_21:3COOH)-H 0.000527278 0.000660646 0.001041956 0.000624805 0.000952344 0.00061195 0.00160197 0.002525126 0.002647451 0.001886392 0.002309095 0.002307165 0.001212227 0.000750605 0.000951024 0.001218732 0.001144106 0.000844739 PE(O-18:1_18:3)-H_1 0.017752323 0.019126855 0.017758333 0.016754109 0.020021702 0.018411711 0.004117418 0.010301423 0.006828193 0.006053901 0.007832474 0.005573952 0.012536556 0.012621887 0.016816426 0.017115197 0.015297211 0.013722248 PE(17:0_18:2)-H 0.097034716 0.083316042 0.090408763 0.080915919 0.09716169 0.086976179 0.015387418 0.038618153 0.031761936 0.028515275 0.032839982 0.027415759 0.057745313 0.048514538 0.058177117 0.049736117 0.053772881 0.049679715 PE(O-19:2_18:2)-H_1 0.004278275 0.00372925 0.004817047 0.004181132 0.005026657 0.005136549 0.001182291 0.002583885 0.002305143 0.001320634 0.001463489 0.001203146 0.003646072 0.003470641 0.003398938 0.003745342 0.004251777 0.003124422 PE(18:2_20:4)-H 0.006399875 0.005972582 0.00534945 0.006038783 0.006192058 0.006214389 0.000716871 0.002053474 0.00143853 0.001227932 0.001608564 0.001100344 0.002631977 0.002556541 0.002909216 0.003053257 0.002764701 0.002445176 PC(18:3_20:4COOH)+CH3COO 0.004523897 0.001416569 0.004814089 0.004355103 0.003276245 0.002886139 0.000568458 0.001636591 0.001145376 0.001019253 0.001173774 0.000748675 0.002768427 0.004921801 0.003192851 0.003049689 0.003565936 0.002897772 PC(12:0_18:2)+CH3COO 0.002170945 0.001833693 0.002506398 0.002399513 0.002249047 0.002116373 0.000948371 0.002126533 0.00162565 0.001475959 0.002152204 0.001188823 0.003216221 0.002828883 0.003296961 0.002788219 0.003081289 0.00286472 PE(18:0_18:2)-H_1 0.134499782 0.124471904 0.119074636 0.121084904 0.1430548 0.131682049 0.031244744 0.061858291 0.051546964 0.043098275 0.059212983 0.037873972 0.077403674 0.081315623 0.094138655 0.088447571 0.086305843 0.077846319 PC(18:1_19:2COOH)+HCOO 0.001665934 0.000652518 0.003281335 0.001883408 0.001437681 0.001648931 0.001175357 0.001878794 0.00170392 0.001789506 0.001826229 0.001624241 0.004487343 0.003593417 0.002479479 0.004095009 0.00428535 0.003443523 PI(18:0_18:1)-H 0.000584266 0.00052251 0.00092948 0.000935687 0.001270745 0.001011974 0.002957621 0.004680725 0.004247068 0.004524671 0.005164025 0.005069336 0.00203488 0.002323837 0.001974705 0.002494537 0.002474992 0.002105591 PE(21:0_20:3)-H 0.00254844 0.004096284 0.003023004 0.003574153 0.004002105 0.002961788 0.001966636 0.002091846 0.002115031 0.001410173 0.001852092 0.001735157 0.003154162 0.00263053 0.003104183 0.003571512 0.003690177 0.002808527 PE(17:0_10:2CHO)-H 0.001592178 0.00026493 0.00156662 0.001984161 0.002012029 0.001036828 0.000580206 0.000552968 0.001077241 0.000499808 0.000744049 0.000509122 0.001454787 0.001728701 0.001311214 0.001432055 0.001564457 0.001166204 PE(16:0_20:4)-H_1 0.014015497 0.014376222 0.012692844 0.013399734 0.01485855 0.014378618 0.008231909 0.01157795 0.008983694 0.007195713 0.009573016 0.00645222 0.013579488 0.013197829 0.017501917 0.016378314 0.01628426 0.014737772 PC(18:0_18:0)+CH3COO 0.002601643 0.002444633 0.002370306 0.002483399 0.001688354 0.002297954 0.001193479 0.000615828 0.001292989 0.000844247 0.001320827 0.000769443 0.001703005 0.002300356 0.002426188 0.002054408 0.001983233 0.001905661 PE(18:0_20:4)-H_1 0.01903371 0.019819868 0.017712438 0.019002592 0.020651221 0.019670795 0.011780616 0.018298057 0.01366351 0.013023894 0.015867543 0.009978576 0.020587481 0.02193962 0.025898922 0.025888778 0.025498354 0.022349232 PC(19:0_19:1)+CH3COO 0.003403444 0.003817406 0.00306165 0.003579235 0.003188784 0.003778465 0.001582835 0.001602875 0.00210606 0.000963976 0.0013308 0.001266261 0.002635759 0.002646448 0.002714091 0.002512976 0.002536898 0.00231412 PC(14:1_20:5)+CH3COO_1 0.004328018 0.005344997 0.00436578 0.004036244 0.003310013 0.003976214 0.000454703 0.002201528 0.00220828 0.000829973 0.002032075 0.000643838 0.003703924 0.004120789 0.004825284 0.003682005 0.004359722 0.005787581 PC(18:2_18:4)+CH3COO 0.015913023 0.017216285 0.018034113 0.014169113 0.015234328 0.015248941 0.002459165 0.011631467 0.008245837 0.006132235 0.008092881 0.005067173 0.017045752 0.019871681 0.016219703 0.014070708 0.015762932 0.016147638 LPE(20:5)-H 0.027230108 0.01729105 0.023686985 0.026699729 0.025200678 0.025522464 0.006385791 0.01185569 0.01379873 0.009492102 0.013483333 0.009275716 0.01932001 0.020566638 0.022287288 0.022573353 0.022232039 0.016184607 PE(O-17:1_20:3)-H 0.008839554 0.008884205 0.005942023 0.011501417 0.010063135 0.007348921 0.002661999 0.004322985 0.004022436 0.002192248 0.002781402 0.002644847 0.006874269 0.005703748 0.007438245 0.008799395 0.007589816 0.005539342 PG(16:1_18:1)-H 0.000717116 0.000864879 0.000624415 0.000700439 0.000436458 0.000934318 0.001442138 0.002626408 0.003027798 0.001824702 0.003696758 0.002268045 0.000278552 0.000489797 0.000414887 0.000161005 0.000428489 0.000285824 LBPA(18:1_20:4)-H 0.000845707 0.000545568 0.000649296 0.000766972 0.000647019 0.000538841 0.001121292 0.002813478 0.003072607 0.002660398 0.003209391 0.001523993 0.000241881 1.27E-09 0.000313291 0.000242873 2.26E-09 2.99E-09 PC(17:1_17:1)+CH3COO_1 0.091560881 0.082978677 0.088319547 0.087607643 0.084096452 0.085147305 0.100927147 0.090071418 0.086157124 0.07309064 0.084973956 0.066494983 0.112346385 0.117437987 0.116741587 0.113317322 0.117971497 0.117147533 PC(20:4COOH_20:5)+CH3COO_3 0.002288626 0.000830106 0.002295522 0.00250919 0.002434182 0.002189647 5.55E-05 0.000641729 0.000333662 0.000103307 0.000194426 0.000115787 0.000648379 0.001564718 0.001325995 0.001720593 0.001559839 0.001394656 PC(16:1_18:3)+CH3COO 0.006821158 0.007336243 0.006781446 0.006733279 0.00757893 0.007458937 0.002066995 0.005649967 0.004501142 0.003807046 0.004729284 0.003075725 0.008178284 0.007823555 0.008912386 0.006409136 0.007837519 0.008040619 PE(O-18:1_20:2)-H_1 0.031568595 0.031770388 0.032062518 0.02680451 0.032101098 0.029656912 0.012366002 0.017298533 0.013239466 0.012591266 0.014425229 0.010013727 0.018638613 0.024281484 0.023914888 0.021264652 0.021996567 0.020048439 LBPA(16:1_20:5)-H 0.000256699 0.00011085 0.000125977 0.000164267 0.000357466 0.000161461 0.001024832 0.00200041 0.00183153 0.001345038 0.002300835 0.001089101 0.000113974 2.55E-10 2.57E-10 2.72E-10 1.77E-10 PE(17:0_20:5)-H_1 0.08298385 0.095447832 0.081532271 0.090213745 0.095548837 0.094159859 0.028055784 0.039994652 0.036123667 0.02081199 0.02404063 0.023330074 0.052748809 0.047000332 0.05312359 0.060649894 0.062159482 0.048282465 PC(18:1_18:3)+CH3COO_1 0.059544214 0.052942222 0.06744962 0.067372568 0.066617784 0.053258738 0.021317679 0.046812926 0.034993998 0.026476376 0.036895839 0.026894868 0.053008827 0.065336966 0.055748325 0.056811326 0.064632247 0.06898099 LPC(18:2)+CH3COO_2 0.027427656 6.05E-05 0.000282531 0.023215248 0.02117791 0.00056096 0.000120682 0.000240307 0.000254739 0.000134097 6.89E-05 0.00010016 0.000444695 0.000520325 0.000532738 0.000300636 0.000540016 0.000413718 LBPA(17:0_20:5)-H 0.00054821 0.000483832 0.00036369 0.000649175 0.000543845 0.000486166 0.002663697 0.004488553 0.004444093 0.002849234 0.004110123 0.002406925 3.47E-05 2.10E-10 2.36E-05 3.00E-05 PC(17:0_20:5)+CH3COO_2 0.020422859 0.024725199 0.022776145 0.024205959 0.020095777 0.022256319 0.00799758 0.013144846 0.010266175 0.004815779 0.00793423 0.005853745 0.017163469 0.01719077 0.017150569 0.016160452 0.016560727 0.014471701 PC(16:1_18:2)+CH3COO_1 0.030965823 0.030842386 0.030567115 0.028526324 0.028729695 0.029847667 0.011459638 0.024992009 0.019977615 0.016725752 0.020400851 0.014472902 0.035380983 0.036136245 0.037200186 0.026348014 0.032971723 0.033977134 PC(17:2_18:2)+CH3COO 0.008523332 0.009380685 0.00711303 0.009538442 0.008182396 0.010446144 0.002430058 0.005370801 0.003599196 0.003487884 0.00296088 0.003330672 0.008540179 0.007341237 0.006850458 0.005663503 0.007761065 0.006510838 PC(16:2_20:5)+CH3COO 0.003966319 0.003922358 0.002777651 0.004523151 0.003815174 0.003970455 0.000875132 0.001991891 0.002237925 0.001625661 0.002607632 0.00136763 0.003237672 0.003764086 0.004167268 0.003155675 0.003730478 0.003675759 PC(17:1_20:5)+CH3COO_2 0.187037084 0.209414845 0.19766524 0.204011669 0.199989565 0.207111916 0.067627657 0.12126408 0.098236064 0.07737728 0.098794625 0.06817923 0.137033692 0.143181111 0.163559401 0.145819133 0.141882304 0.149849223 Cer(d17:1_17:0)-H 0.000657576 0.000578526 0.00054175 0.000616254 0.000557977 0.000609292 5.14E-05 0.000213932 7.16E-05 9.61E-05 3.52E-05 0.000302841 0.000346988 0.0002798 0.000283597 0.000319733 0.000268945 PC(18:3_20:5)+HCOO_1 0.002682053 0.001982139 0.001738057 0.002164609 0.001698059 0.001988216 0.000283166 0.001080836 0.000488272 0.000315282 0.000741899 0.000402161 0.001301399 0.001647938 0.001271349 0.00164602 0.001446541 0.001901136 PC(16:1_20:5)-CH3_1 0.003090346 0.002580473 0.002218867 0.003172736 0.002670178 0.003292259 0.000100818 0.000332668 0.000403991 0.000192796 0.000453516 0.000222353 0.000709406 0.00085213 0.001151168 0.001129208 0.000922372 0.000660118 PE(17:0_20:5)-H_2 0.183989479 0.201417497 0.167405429 0.17732344 0.19330211 0.190736498 0.030860425 0.087395495 0.069424176 0.051201963 0.064028567 0.04498439 0.097143071 0.109237045 0.127234781 0.118071287 0.11723154 0.113958969 PE(20:3_20:4)-H 0.001943522 0.00222161 0.001678406 0.001894226 0.002060517 0.001945065 0.000348696 0.000705058 0.000455908 0.000347977 0.000628648 0.00032938 0.000984386 0.001281294 0.001351464 0.001836097 0.001165894 0.001168523 PC(17:1_20:5)+CH3COO_3 0.187037084 0.212040004 0.200012029 0.204011669 0.199989565 0.207111916 0.070481704 0.122679694 0.099549744 0.07737728 0.100099473 0.070396425 0.137033692 0.143181111 0.163559401 0.145819133 0.141882304 0.149849223 PE(18:3_20:4)-H 0.002353615 0.002574455 0.002386022 0.002338476 0.002442039 0.002267567 0.000332882 0.000998873 0.000662829 0.000450291 0.000830093 0.000413181 0.001396365 0.001249099 0.001837824 0.001920042 0.001548839 0.001361899 PC(15:0_18:2)+CH3COO 0.053146505 0.049950499 0.051383521 0.04928112 0.052360399 0.051612194 0.035875678 0.027127918 0.02178097 0.017422733 0.018678515 0.015193645 0.045057758 0.051038025 0.047376276 0.037966204 0.043175272 0.042877954 PE(19:0_20:4)-H 0.002118641 0.002476309 0.002055167 0.002444286 0.002489645 0.002452231 0.001034524 0.00160609 0.001443598 0.000777851 0.000989218 0.000932791 0.002258484 0.001971494 0.002064237 0.002278527 0.002420778 0.001752893 PC(17:1_20:5)-CH3_1 0.012692398 0.010826507 0.008143182 0.011032573 0.010338442 0.013820783 4.60E-09 0.000680384 0.000499095 0.000279375 0.000566321 0.000369653 0.001549971 0.001514124 0.002155884 0.002973844 0.001552016 0.001792189 PC(17:1_21:6)-CH3 0.006498601 0.006232562 0.005793289 0.004964649 0.005492848 0.0055777 0.001008782 0.003197352 0.002023104 0.00185944 0.002459254 0.0013659 0.00378815 0.004548657 0.005040132 0.003969996 0.003915808 0.004106283 Cer(d17:1_22:0)+HCOO 0.005351783 0.005716419 0.004500147 0.005860663 0.004714221 0.005162715 0.000887274 0.002110695 0.002013102 0.001361511 0.002021663 0.001167237 0.002968026 0.003379852 0.003467522 0.00305787 0.002748001 0.002786437 PC(22:0_18:3)+CH3COO 0.000369225 0.000350324 0.000333403 0.000499543 0.000367677 0.000727458 8.79E-07 0.000100461 1.82E-06 5.67E-08 4.32E-05 0.000140132 0.000440463 0.000265395 0.00058077 0.000433995 0.000347614 0.000250179 PE(14:0_15:0)-H 0.00424877 0.004083567 0.003506163 0.004591676 0.004413311 0.004457417 0.000401801 0.00107226 0.000787494 0.000411244 0.000783197 0.000801739 0.001857688 0.00155676 0.002135574 0.002998761 0.002312383 0.001784988 PC(17:2_18:3)+CH3COO_1 0.001844183 0.002589908 0.001879763 0.003054307 0.002719044 0.002937935 0.000368212 0.000995936 0.000795375 0.000495442 0.000576783 0.000586899 0.001571024 0.001385376 0.001189458 0.001213051 0.001462557 0.001133568 PE(O-19:1_20:5)-H_2 0.002870368 0.003265441 0.002749042 0.002679276 0.002926149 0.002717763 0.000548266 0.001279182 0.001226314 0.00053809 0.001100359 0.000651272 0.001615717 0.001887285 0.002145965 0.001692122 0.001946031 0.001804717 PC(19:1_20:4)+CH3COO_3 0.02838743 0.03105736 0.025649292 0.027003232 0.026142115 0.029827706 0.021492499 0.026974998 0.020474044 0.015850096 0.020616429 0.015855918 0.031883424 0.038598995 0.03426567 0.029293735 0.030521059 0.0372635 PC(20:5_20:5)-CH3_1 0.008690532 0.00898306 0.005920655 0.008066442 0.007837391 0.011184743 0.000137912 0.000383761 0.000372864 0.000126473 0.000349018 0.000109175 0.000791585 0.000714718 0.001150064 0.001437061 0.000810104 0.000971231 PE(O-18:1_20:4)-H_2 0.053637014 0.058188921 0.051542356 0.052233238 0.060432989 0.055797573 0.008885435 0.01939069 0.016808678 0.011399251 0.018105027 0.010076942 0.023432508 0.026752912 0.033363511 0.037219932 0.033616879 0.028696841 PE(20:4_20:4)-H 0.001192636 0.001037185 0.000875972 0.001040469 0.001129151 0.001056075 5.27E-05 0.000167356 0.000155209 2.12E-09 0.00023189 7.56E-05 0.000297906 0.000482667 0.000608043 0.000645831 0.000439592 0.000427201 PC(17:0_18:1)+CH3COO_2 0.052299588 0.054136174 0.050739627 0.049929447 0.049488319 0.051781811 0.017358497 0.028200754 0.026619239 0.020129871 0.025853593 0.017088402 0.037968472 0.042975786 0.039619083 0.033580616 0.033812038 0.035767397 LPE(19:1)-H_1 0.012357112 0.006894246 0.00768023 0.010877028 0.013428068 0.011007076 0.013268853 0.008902062 0.010980909 0.007423494 0.009738856 0.00862188 0.016326695 0.019427252 0.017811403 0.013876863 0.019992145 0.015991892 PC(20:3CHO_20:5)+CH3COO_3 0.000839355 0.000808722 0.001393995 0.001156166 0.001121863 0.001103474 0.000103897 0.000414713 0.000445383 0.000249746 0.000374907 0.000122335 0.000747901 0.001013904 0.000622381 0.001038661 0.000753061 0.000754465 PE(O-18:1_20:3)-H 0.093708131 0.094343272 0.085973999 0.090253182 0.122548373 0.091951997 0.023402247 0.04263124 0.034649376 0.026225356 0.041298682 0.024444989 0.054313634 0.056177714 0.071006594 0.077354977 0.062956174 0.055362581 PC(20:2_20:3)+CH3COO 0.003117835 0.003516408 0.002891397 0.002668812 0.002556336 0.002730014 0.001073362 0.001466251 0.001247216 0.000983503 0.001236664 0.00082095 0.002709751 0.003723664 0.002783113 0.001852358 0.002415579 0.002691737 PC(20:5_22:5)+CH3COO 0.001514868 0.001839119 0.001438685 0.001687909 0.001543203 0.001553517 0.000121745 0.000122954 0.000116538 3.13E-05 0.000116258 0.000318683 0.000514198 0.000660859 0.000391408 0.00038101 0.000516773 PC(19:1_20:1)+CH3COO_1 0.001542786 0.001461886 0.001299559 0.0016481 0.001290078 0.001395281 0.000441792 0.000618107 0.000644723 0.000487929 0.000739913 0.000375588 0.0014701 0.001471505 0.001139874 0.000943077 0.001091685 0.001019169 PE(18:0_20:5)-H_1 0.243296648 0.251298615 0.222205206 0.228217348 0.243425317 0.238951736 0.066979333 0.131938709 0.10502021 0.079508393 0.108698449 0.068930912 0.144705605 0.15856128 0.18411252 0.179121301 0.170507466 0.154549998 PC(18:2_21:4COOH)+HCOO 0.006141173 0.001705761 0.005840571 0.004996091 0.004752064 0.00398166 0.00100228 0.003145773 0.002053783 0.001036306 0.002595378 0.000851813 0.004285227 0.006546114 0.006709604 0.004680134 0.006561535 0.004217617 PE(18:1_20:2)-H 0.014313075 0.019272071 0.013104431 0.011066891 0.014735678 0.013206268 0.002667983 0.005973574 0.004379535 0.003745211 0.005870131 0.003258097 0.009826509 0.011495731 0.011189044 0.009897254 0.006688541 0.008702877 LBPA(18:1_18:3)-H 0.000243946 0.000207336 0.000221473 0.000243126 0.000195893 0.000253143 0.001375608 0.003471178 0.002940367 0.00246744 0.003491237 0.00250679 3.56E-05 2.38E-05 2.69E-05 5.14E-05 PC(18:1_20:3)+CH3COO 0.004421591 0.004933641 0.004311624 0.00498596 0.004165496 0.004632981 0.002418199 0.003222148 0.003107246 0.001250812 0.002643735 0.001937654 0.004423632 0.004544654 0.003983027 0.00462763 0.004372965 0.003979148 PE(O-17:1_20:4)-H_2 0.003355353 0.003971883 0.00374202 0.004156802 0.004484434 0.00437725 0.001175923 0.002272343 0.002382915 0.001023727 0.001283142 0.000997303 0.003505162 0.00270987 0.003511349 0.003969675 0.003951194 0.00301588 PC(19:1_20:4)+CH3COO_4 0.00240471 0.00310964 0.002309927 0.002245358 0.002105782 0.001903732 0.001917639 0.002492078 0.002109566 0.002139646 0.001687594 0.001234236 0.002895453 0.003906493 0.002992687 0.003374394 0.003856669 0.003213719 PE(22:0_20:4)-H_1 0.001021729 0.001407795 0.000853139 0.001236053 0.000965797 0.000837348 0.000456442 0.001061212 0.000812417 0.000824727 0.000729864 0.000624465 0.001138719 0.001409386 0.001532935 0.001612535 0.001463796 0.001232489 PE(20:2_20:5)-H 0.006582646 0.006214515 0.005535887 0.004463244 0.005463829 0.005487971 0.001008355 0.003187086 0.002101243 0.001806269 0.002461324 0.001364329 0.003683696 0.004488679 0.004787487 0.00373345 0.003895319 0.004095823 PG(18:1_18:3)-H 0.000240931 0.000207259 0.000221473 0.000243912 0.000239435 0.000254708 0.001373737 0.003583925 0.00280624 0.002494695 0.003509289 0.002624655 3.56E-05 2.38E-05 2.69E-05 5.14E-05 PC(20:4_20:4)+CH3COO_2 0.013505209 0.01490465 0.013455542 0.015513158 0.013691611 0.014328559 0.003840818 0.006048558 0.005364886 0.003362515 0.006659492 0.003076483 0.008520087 0.008750481 0.010272912 0.011837515 0.00842798 0.008968812 PC(18:3_20:5)+CH3COO_2 0.16685232 0.180901172 0.15510052 0.167332752 0.164868138 0.172852087 0.028509971 0.093847289 0.05323108 0.003477773 0.055681257 0.035414581 0.108942973 0.112306251 0.130199138 0.118824499 0.118092584 0.129192018 PC(17:1_18:1)+CH3COO_2 0.227510634 0.223574317 0.22229916 0.216774541 0.21155412 0.22162324 0.139710916 0.2011265 0.177636902 0.151208497 0.186589985 0.142865659 0.24063807 0.228361169 0.243065468 0.215317131 0.227039325 0.23053226 PC(18:1_20:5)+CH3COO_2 0.403586471 0.418947853 0.40028686 0.393322315 0.393022061 0.402845244 0.104513109 0.229215706 0.198145214 0.143429231 0.198470251 0.132869622 0.275039152 0.298380207 0.311910626 0.270279512 0.271575249 0.296078814 PC(18:0_20:5)+CH3COO_2 0.003056089 0.003378465 0.004161965 0.006175807 0.004036289 0.00268939 0.00044019 0.001696298 0.001245553 0.000506764 0.001214067 0.000523656 0.002227157 0.002289384 0.002686682 0.003050053 0.003223696 0.002059347 PC(20:4_21:4COOH)+HCOO_3 0.003436164 0.00136468 0.00458621 0.002968776 0.003542721 0.002436049 0.000489144 0.000848084 0.000859144 0.000667337 0.001121977 0.000615933 0.0017179 0.003758656 0.001934769 0.003448738 0.002697973 0.003391267 PC(20:4CHO_20:5)+CH3COO_4 0.001294727 0.000676269 0.00162405 0.001488194 0.001509322 0.001210554 4.71E-05 0.000343557 0.00013464 6.85E-05 6.24E-05 4.88E-10 0.000483021 0.000639991 0.000659751 0.00066357 0.001037956 0.000487681 PE(22:0_20:5)-H 0.00573754 0.006217506 0.005315196 0.005004913 0.006557114 0.006107661 0.001568447 0.00368125 0.002959315 0.002218777 0.003109537 0.001926651 0.004562873 0.004837828 0.006139163 0.005519781 0.004701225 0.004373426 LBPA(19:1_18:2)-H 0.000240528 0.000185658 0.0001525 0.000170241 0.000183638 0.000210425 0.001481233 0.002663979 0.00273547 0.001921085 0.001999857 0.00184186 2.20E-10 4.95E-05 2.88E-10 PE(19:0_20:5)-H_1 0.017936628 0.020764786 0.019689438 0.019331231 0.02141464 0.02123877 0.005935851 0.009932105 0.008483001 0.005225248 0.006027068 0.006379483 0.012347413 0.011065237 0.011325638 0.012291805 0.01328505 0.010588731 PE(21:0_20:4)-H 0.002994214 0.002921469 0.003274882 0.003185011 0.00296769 0.003181494 0.001019059 0.001690848 0.001778819 0.001066308 0.00129018 0.001334463 0.002194201 0.002172919 0.002497782 0.002961314 0.002494385 0.002114632 PC(17:1_20:4)+CH3COO_1 0.046504932 0.046212618 0.046587194 0.047418895 0.04497682 0.047830037 0.019715632 0.031921647 0.024714037 0.018378031 0.027050234 0.017110576 0.041993464 0.045716966 0.039926694 0.048728846 0.034665581 0.036983116 PC(18:1_18:1)-CH3_1 0.017189342 0.010135838 0.009559568 0.016576114 0.010393127 0.009797352 0.000127396 0.00166831 0.001811198 0.001145824 0.001881765 0.001008667 0.003512456 0.002666266 0.003575376 0.00413279 0.002780072 0.003067094 PE(22:2CHO_20:4)-H 0.00147382 0.002257078 0.002459873 0.001767596 0.002099132 0.00181249 0.001476892 0.002559166 0.001704413 0.001686983 0.001983526 0.001558901 0.002485659 0.002829764 0.002954745 0.002877536 0.003039177 0.002966098 PE(18:0_20:3)-H_1 0.038255975 0.038996304 0.032998701 0.037707338 0.041166884 0.0379239 0.014691042 0.02020373 0.019930862 0.013135993 0.022922449 0.012126441 0.029477123 0.027719799 0.034618743 0.038465036 0.031077998 0.027562593 PC(21:4COOH_20:5)-CH3 0.004784992 0.006748397 0.004510932 0.005355268 0.005102355 0.006345871 0.000156911 0.000889801 0.001109866 0.000399704 0.000924011 0.000399977 0.001435513 0.001446703 0.002025306 0.001817877 0.001654417 0.001628174 PE(O-20:3_18:1)-H 0.003577636 0.00352547 0.006014487 0.004565436 0.005306402 0.005148459 0.000708715 0.001606789 0.001622933 0.001919922 0.002869477 0.001360764 0.005335319 0.004577737 0.004403228 0.003738305 0.003497605 0.003248539 PC(18:1_19:3)+CH3COO 0.007563077 0.009344446 0.009193191 0.009729345 0.00798204 0.009696762 0.003982049 0.005770406 0.004226294 0.003053247 0.005377722 0.003495885 0.010073465 0.009337082 0.006466675 0.006936871 0.009028027 0.008600264 PC(19:1_19:1)+CH3COO_2 0.026232331 0.026517742 0.024519692 0.026487942 0.023982105 0.028912396 0.011781167 0.012938181 0.015510133 0.009265846 0.0134908 0.012432984 0.023172912 0.025435477 0.019913841 0.021261236 0.021501242 0.016150062 PC(18:0_17:1)+CH3COO_1 0.020913204 0.020032619 0.019261948 0.02055271 0.019051515 0.021827308 0.016757199 0.016269362 0.016349593 0.011671635 0.014094162 0.010492223 0.018567791 0.023094591 0.023326908 0.022350887 0.020907809 0.021588268 PC(15:1_16:2)+CH3COO_1 0.003710877 0.00218264 0.002397032 0.00252262 0.00245094 0.001820997 0.001453159 0.002531679 0.002972967 0.001702465 0.001436487 0.001756446 0.004310849 0.003203755 0.004152422 0.003813199 0.003233963 0.004029525 PE(16:0_20:5)-H 0.100513843 0.105030835 0.096477062 0.102487634 0.107649342 0.101845858 0.040109318 0.06191709 0.049246438 0.03605685 0.049030077 0.032470916 0.068324429 0.066771974 0.089610559 0.081467422 0.080564651 0.073643798 PE(17:0_20:4)-H_2 0.007538519 0.008713177 0.007671154 0.008087547 0.009078717 0.007758683 0.006657905 0.007312633 0.006419778 0.004310272 0.004429593 0.00444189 0.009541032 0.008287085 0.009244949 0.01039355 0.010498531 0.00836724 PE(15:0_17:0)-H 0.019761545 0.019067058 0.01814915 0.019617719 0.023300512 0.021051531 0.002642154 0.007257444 0.006189645 0.005023756 0.006367348 0.005174954 0.009750287 0.009544805 0.008725321 0.008993651 0.011205358 0.011496604 PE(23:0_18:1)-H 0.002346686 0.0024497 0.00227186 0.002230163 0.002643017 0.002915454 0.000857787 0.001319629 0.00107226 0.000876808 0.00125587 0.000856766 0.001708314 0.001754304 0.001956136 0.002006808 0.001725292 0.001358288 PS(18:0_20:5)-H_2 0.001942709 0.002005627 0.001005162 0.002262764 0.003280062 0.003498838 1.47E-09 9.38E-05 5.59E-08 8.88E-05 5.59E-05 4.23E-05 0.000488938 0.000639499 0.001102541 0.001352228 0.00064647 0.000665543 PC(20:1_20:4)+CH3COO_2 0.003881918 0.004595034 0.003918303 0.00391448 0.0034506 0.00399744 0.000463936 0.00161249 0.001187284 0.000974102 0.00153035 0.000755764 0.001974393 0.002624845 0.002882362 0.002283046 0.002081141 0.002348286 PC(18:0_18:1)+CH3COO 0.052870169 0.049940622 0.043741374 0.047268321 0.043044281 0.053497243 0.023571617 0.031673919 0.033074685 0.024185591 0.031441388 0.021408754 0.04110931 0.047466097 0.048435215 0.036781204 0.040015392 0.044212137 PC(18:2_20:5)+CH3COO_1 0.288795515 0.254518381 0.273160475 0.246034558 0.249188038 0.271708742 0.060014351 0.154667674 0.113541807 0.087199741 0.104789431 0.077887401 0.229120236 0.213300039 0.251776522 0.155113239 0.187461497 0.254065722 Cer(d14:0_4:0)-H 0.02088132 0.009446201 0.016677796 0.014134237 0.011095849 0.014327165 0.021020093 0.023796377 0.022711027 0.026788501 0.016608521 0.021613427 0.012036214 0.015755779 0.012010944 0.005076857 0.011621917 0.008586404 PC(19:1_20:4COOH)+CH3COO 0.002261938 0.000882191 0.003973876 0.003349278 0.002107229 0.001977257 0.000711097 0.001933387 0.001361926 0.00114608 0.001187271 0.000792444 0.002788031 0.004150621 0.002383075 0.003907215 0.003040896 0.002521967 PE(17:0_18:3)-H_1 0.012340979 0.013638907 0.01305253 0.014578332 0.015770989 0.014438798 0.003296286 0.006035216 0.004956305 0.003566047 0.003825121 0.003676954 0.00808605 0.00634366 0.008741853 0.010124938 0.010005788 0.007181865 Cer(t17:0_24:0)-H 0.003080926 0.002763636 0.002106551 0.00332854 0.002630252 0.003352756 0.000328645 0.000811026 0.001082915 0.000487135 0.00087185 0.000439098 0.001477674 0.001321485 0.002043271 0.001703384 0.001800002 0.001307662 PC(18:1_20:4CHO)+CH3COO_4 0.001133516 0.000323839 0.00158562 0.001069535 0.000797572 0.000878758 0.000579159 0.000922316 0.001070568 0.000703582 0.001101327 0.000718624 0.001819742 0.001840707 0.00168801 0.001521393 0.001565596 0.001148922 LPC(18:1)+HCOO 0.001018922 0.001062197 0.00076581 0.001006507 0.000592642 0.001021095 0.000231262 0.000679111 0.000301696 0.000249074 0.00030116 0.000346051 0.000638396 0.000727161 0.000985689 0.000834387 0.000813964 0.000833012 LPC(16:2)+CH3COO 0.000685575 0.00051536 0.00033762 0.000573171 0.000360184 0.00064406 0.000172408 0.000443409 0.0004003 0.000228342 0.000485708 0.000320391 0.000673786 0.000614784 0.000935466 0.000760345 0.000840272 0.000621405 PC(19:1_18:2)+HCOO 0.001186073 0.000919259 0.001581449 0.000924595 0.001044845 0.001020671 0.000495469 0.000805952 0.000417036 0.000472593 0.000602776 0.00064866 0.000977556 0.001295286 0.001177083 0.000941805 0.001152655 0.000852077 PC(14:1_20:5)+CH3COO_2 0.001818993 0.001549871 0.001749017 0.001643239 0.00188977 0.001923474 0.000553295 0.001074814 0.000555554 0.000322904 0.000445698 0.000377569 0.001376661 0.00166915 0.001384306 0.001663976 0.000959124 0.001325373 PC(17:1_20:4)-CH3 0.004146121 0.003207245 0.002534839 0.003709028 0.003109727 0.003165903 8.30E-08 0.000351356 0.000172969 0.000127055 0.000139404 8.62E-05 0.000479586 0.000523646 0.000842655 0.001118895 0.000653718 0.000773252 PC(18:2_20:4)-CH3 0.003973165 0.003138147 0.002399126 0.003507893 0.003029824 0.004108337 9.47E-05 4.51E-05 0.000112258 6.82E-09 5.87E-05 0.000409931 0.000364481 0.000667832 0.000808915 0.00039092 0.000623389 PC(21:3COOH_20:5)+HCOO 0.000771631 0.000215305 0.000683098 0.000848456 0.000541077 0.000327068 4.35E-08 0.000218848 1.47E-06 9.00E-08 1.01E-06 4.79E-07 0.000578008 0.000828745 0.001041219 0.000461686 0.001201444 0.000458456 PC(17:1_20:5)-CH3_2 0.002287716 0.002059774 0.002338753 0.002516796 0.002194317 0.002948439 8.17E-05 0.000359582 0.000313929 2.10E-08 0.000197787 0.000229461 0.000487799 0.000551617 0.00076455 0.000569646 0.00071184 0.000488956 PE(18:0_10:2CHO)-H 0.000869684 0.00021668 0.000943698 0.001154487 0.001160277 0.000903849 0.000294732 0.000441825 0.000526778 0.000393982 0.000798312 0.000347729 0.000880119 0.001001523 0.000824269 0.000935805 0.001229349 0.000983278 LPE(20:4)-H_1 0.006211233 0.00402065 0.005037331 0.006691206 0.005993038 0.005601365 0.003418468 0.004567987 0.005165837 0.003865828 0.004144968 0.00388479 0.006491649 0.007355164 0.007979567 0.007733943 0.007697849 0.004980427 PC(19:0_20:5)+CH3COO 0.002659096 0.003301365 0.002689449 0.003156508 0.002859652 0.003116378 0.001093652 0.001494765 0.001228736 0.000461154 0.000800307 0.000940266 0.001738003 0.00185334 0.001744438 0.002009419 0.001830095 0.001785379 PG(18:1_20:4)-H_2 0.000901058 0.000516482 0.000661766 0.000764629 0.000641286 0.000638677 0.001330944 0.003799201 0.002396889 0.002016187 0.002107243 0.00150756 0.000239731 0.000287845 0.000277833 0.000202349 0.000225903 0.0002243 PE(O-18:1_18:2)-H_1 0.271062435 0.271595535 0.259435024 0.229942757 0.288156956 0.262937433 0.06841207 0.14777513 0.11208724 0.090715818 0.12007669 0.078573612 0.15375099 0.178769725 0.206849925 0.176039282 0.188269699 0.170008461 PC(18:1CHO_20:5)+CH3COO_3 0.00156686 0.001226965 0.001404052 0.001303235 0.001384076 0.001415737 0.000385577 0.000557801 0.000731735 0.000661991 0.000552098 0.000549944 0.001117336 0.001135076 0.000806019 0.000882811 0.001200187 0.000928156 PE(O-19:0_20:5)-H_1 0.006158748 0.006959064 0.005887013 0.00668268 0.006454444 0.007271454 0.001566891 0.003137391 0.00228457 0.001621541 0.002028374 0.001318275 0.003350257 0.003642672 0.003798585 0.004133415 0.003889057 0.003127077 PC(15:1_20:5)+CH3COO_3 0.002052665 0.00233361 0.002509067 0.001933954 0.002556591 0.002382827 0.000522559 0.001392051 0.000625286 0.000590528 0.000718647 0.000733677 0.001738819 0.001637869 0.00210682 0.002172238 0.00169261 0.00127156 PC(18:1_20:4)-CH3_2 0.008106901 0.008410317 0.006789872 0.008051333 0.0082805 0.009111748 0.000370805 0.000192662 6.84E-05 0.000298215 9.66E-05 0.001037458 0.000779215 0.001456545 0.001686836 0.000874173 0.001052942 PC(17:1_19:1)+CH3COO_1 0.030384439 0.030821972 0.032506628 0.033075942 0.027218795 0.024839298 0.019781226 0.022501344 0.019833402 0.016977466 0.015968801 0.014244532 0.028370119 0.032965731 0.033164991 0.02711235 0.026742333 0.023765624 PE(O-16:0_18:1)-H 0.018703788 0.0143181 0.013455124 0.015613778 0.015730892 0.017305867 0.007157731 0.010079075 0.009945119 0.00792449 0.010287926 0.007680604 0.01297734 0.011367052 0.014548795 0.014102575 0.012833108 0.011806845 PC(19:1_19:1)-CH3 0.001008629 0.000883411 0.000873833 0.000921239 0.000868934 0.000973189 8.99E-05 0.000199551 0.000130817 0.000127351 0.000146337 9.34E-05 0.000337488 0.0002833 0.000238118 0.000229134 0.000214208 0.000303025 Cer(t17:1_24:0)-H 0.001375851 0.000966185 0.000780972 0.000989886 0.001234027 0.001724355 0.00018649 0.000277181 0.000279062 0.000180468 0.0002879 0.000118639 0.000451246 0.000856761 0.000947469 0.000586404 0.000583161 0.000568783 PI(18:0_19:4)-H 0.000143725 9.59E-05 0.000169131 0.00014769 0.000215801 0.000167492 0.000614474 0.00058959 0.000518692 0.000549289 0.000553011 0.000581392 0.000330472 0.000291739 0.000383563 0.000512093 0.000423649 0.00032986 PC(15:1_20:5)+CH3COO_4 0.001746047 0.002362626 0.003062152 0.002206569 0.002192659 0.002673664 0.000522991 0.00130943 0.000625286 0.000591743 0.000718647 0.000733677 0.001887543 0.001830385 0.002440386 0.001412494 0.00169261 0.001418339 PS(18:0_20:5)-H_3 0.001375304 0.001865963 0.001455057 0.001621694 0.001529683 0.00241516 1.32E-09 6.51E-05 5.59E-08 3.91E-05 5.59E-05 4.23E-05 0.000380357 0.000210375 0.000779496 0.000825638 0.000490115 0.000612737 PC(20:1_20:2)+CH3COO 0.001084406 0.001417563 0.001490782 0.000809224 0.000998732 0.000979255 0.000199178 0.000344573 0.000394686 0.000320941 0.000465164 0.00020926 0.000927796 0.001258777 0.000966972 0.000627985 0.000622205 0.000901884 PE(O-18:1_14:0)-H 0.002438045 0.00258923 0.002137593 0.00227483 0.002713368 0.002822742 0.000648809 0.001322062 0.001112582 0.000627976 0.001116036 0.000849833 0.001388674 0.001517822 0.001970872 0.002016859 0.001962185 0.001797271 PE(18:4_20:5)-H 0.003355187 0.004126468 0.003050173 0.003303604 0.003222917 0.004140726 0.000209876 0.001254372 0.000889835 0.000517259 0.000812597 0.000425942 0.001272031 0.00153786 0.001897846 0.001612161 0.00172539 0.001581134 PI(18:1_18:2)-H 0.00036258 0.000386617 0.000843746 0.000551068 0.000701736 0.000515951 0.001272388 0.001806417 0.001738832 0.002022107 0.001863154 0.002019251 0.001087368 0.000992159 0.000977519 0.001349218 0.001239816 0.000925628 PE(18:2_20:5)-H_1 0.004192904 0.003729371 0.002494065 0.004073753 0.003884938 0.003621542 0.000749288 0.00174295 0.0011395 0.000879902 0.001296109 0.000786257 0.001726197 0.001969335 0.002725467 0.002198858 0.002400366 0.002171437 PC(19:1_20:3)+CH3COO_2 0.002264915 0.001912568 0.002049373 0.002073192 0.001820092 0.001801076 0.001733213 0.001106109 0.000922802 0.001380847 0.001302202 0.000790905 0.002746299 0.002839688 0.002462029 0.001789746 0.001932518 0.002485013 LPE(17:1)-H_2 0.016126982 0.007621341 0.012825311 0.019459411 0.016320463 0.01636444 0.017340296 0.011279267 0.016039265 0.012331577 0.020428476 0.011408308 0.029634132 0.025191767 0.02828859 0.020878686 0.028095469 0.022522505 PE(22:0_18:2)-H 0.018437459 0.018716873 0.016902982 0.015625291 0.018735485 0.017207848 0.004324743 0.009614496 0.008193884 0.007198244 0.00858926 0.006217228 0.011268299 0.012354898 0.013322799 0.011814351 0.011364807 0.010838806 PE(O-18:0_20:4)-H_1 0.018769273 0.019299483 0.015749199 0.017173758 0.018646745 0.022335782 0.008228458 0.015551678 0.011242885 0.00885302 0.012385375 0.007919692 0.016052333 0.017244716 0.021837814 0.018050582 0.019074984 0.017673243 PE(O-18:2_20:5)-H 0.004110421 0.004576464 0.004120578 0.003803947 0.004207355 0.004278859 8.18E-05 0.001570673 0.001154121 0.000823875 0.001386656 0.000668043 0.002114915 0.002047228 0.002827834 0.002667605 0.002083512 0.002134233 LPC(20:2)+CH3COO 0.002120218 0.001778963 0.00161135 0.001386158 0.001551315 0.002064592 0.000319373 0.000691604 0.000355502 0.000534745 0.000652981 0.000407472 0.000925128 0.001439818 0.001592146 0.000915232 0.001555463 0.001054212 PE(18:0_18:3)-H_1 0.024737618 0.024684844 0.023299642 0.024162063 0.027895385 0.025685735 0.006762955 0.013927601 0.011741134 0.010027151 0.013502051 0.008592848 0.016620246 0.015559427 0.021096302 0.021745714 0.019609848 0.017874032 PC(19:4_20:5)+CH3COO_2 0.002351926 0.003785017 0.003050811 0.00415256 0.004018503 0.004384613 0.000774186 0.001321193 0.001456681 0.000503794 0.000865511 0.000612811 0.002082392 0.001700306 0.001797946 0.002280009 0.00244296 0.001659038 PE(16:0_18:3)-H_1 0.026741032 0.02719349 0.027188746 0.027477577 0.032120593 0.027980813 0.006528655 0.013852251 0.010149328 0.008572745 0.011470751 0.00800787 0.015820002 0.014050809 0.021118163 0.022638674 0.019503682 0.018540937 PC(18:1_18:3)+CH3COO_2 0.004246854 0.004585653 0.015235507 0.003169494 0.003365772 0.004686898 0.007706729 0.010137446 0.009348541 0.005898806 0.008930249 0.002144636 0.012848797 0.014528269 0.015129072 0.014452455 0.013218095 0.013331731 PE(16:0_18:2)-H 0.0641075 0.062483159 0.062681261 0.06430939 0.069523444 0.064735627 0.014881837 0.031673776 0.025312039 0.020602352 0.025397658 0.016896739 0.03710589 0.032903221 0.043837536 0.042264166 0.041758229 0.034608893 PE(22:0_20:3)-H 0.002948847 0.003383795 0.002877754 0.002887632 0.003575696 0.003259416 0.001211489 0.002285157 0.00189493 0.00130311 0.002058774 0.001436754 0.002788402 0.002924506 0.003363371 0.003854816 0.002779986 0.002618875 Cer(t17:0_22:1)-H_2 0.310291196 0.297903322 0.283938714 0.287463962 0.275540302 0.294195861 0.075687345 0.13661653 0.138860938 0.100802155 0.134815796 0.086001032 0.172736784 0.204049694 0.203731087 0.173330018 0.163158476 0.174449293 PC(15:1_16:1)+CH3COO 0.004502854 0.004505446 0.006478273 0.004561676 0.00529883 0.005562448 0.006954632 0.008307675 0.006837253 0.0059867 0.007006813 0.005358584 0.010371308 0.00952137 0.010165463 0.008187634 0.009840476 0.008838512 PC(20:0_18:1)+CH3COO 0.006780599 0.007033741 0.006052794 0.006270245 0.005692038 0.006358907 0.002087888 0.003179994 0.003764831 0.002311207 0.003136525 0.002037154 0.004286629 0.005137906 0.004707509 0.003904039 0.004486243 0.004350255 PE(22:2COOH_18:1)-H 0.003244443 0.004685367 0.004540088 0.003880884 0.004358682 0.002956797 0.005625551 0.006236751 0.006620906 0.005654783 0.007074786 0.006102245 0.005263866 0.004437958 0.004863007 0.005207149 0.004575367 0.004378716 PE(O-19:1_18:2)-H 0.002768085 0.00303457 0.003533666 0.002947493 0.003525619 0.00320699 0.000787548 0.001830778 0.001783958 0.001257073 0.00139471 0.001199678 0.002752587 0.00248967 0.002231573 0.002334869 0.002310415 0.002001993 Cer(d17:1_26:0)-H 0.000661042 0.00070434 0.00041393 0.000764805 0.000718531 0.000635056 0.000100001 8.02E-05 6.50E-05 5.56E-05 0.000377557 0.000522267 0.000333038 0.000402295 0.000275866 0.000257718 PE(15:0_18:3)-H_1 0.010834781 0.010293457 0.010045983 0.010161672 0.011989794 0.010450046 0.00137837 0.004601917 0.003938887 0.002686908 0.003754534 0.002837201 0.006134759 0.004875036 0.006698923 0.007400732 0.007335029 0.005718947 PC(16:1_18:4)+CH3COO 0.005472872 0.005713058 0.006014548 0.005715472 0.005949674 0.006030842 0.001369891 0.004538304 0.003425272 0.002654575 0.002437383 0.002355552 0.005369291 0.006551803 0.009814814 0.005239877 0.008574931 0.008245432 PE(23:0_18:2)-H 0.001042621 0.001082941 0.000809024 0.000933499 0.000715542 0.000617025 0.000493761 0.000539596 0.000437386 0.000377382 0.00034671 0.000363832 0.000822264 0.000869974 0.000563307 0.000768145 0.000692447 0.000620232 PC(17:1_20:4CHO)+CH3COO 0.000947131 0.000313733 0.000916079 0.001093929 0.000924338 0.000690603 0.000214419 0.000501847 0.00051311 0.000457491 0.00062462 0.000549119 0.001039861 0.000845676 0.000930287 0.001045343 0.001182179 0.000669604 LPE(18:3)-H_1 0.005472482 0.001699317 0.004970224 0.005085528 0.005302754 0.002331294 0.001852748 0.00277015 0.002929007 0.002701085 0.004079556 0.003564179 0.004483282 0.005549889 0.006890455 0.005518372 0.006450831 0.004536578 PE(15:0_20:5)-H 0.016641802 0.017135785 0.015200413 0.016284973 0.016693987 0.016499023 0.001466146 0.006222407 0.004789892 0.003510277 0.004251381 0.003022482 0.007000824 0.006623763 0.00872943 0.009680446 0.008447269 0.007558379 PC(18:2_20:5)-CH3_2 0.001850205 0.001384778 0.000987017 0.001584055 0.001923472 0.001850083 4.09E-05 0.000254804 0.000110658 0.000211442 0.000311074 0.000120399 0.000511869 0.0003732 0.000473493 0.000507617 0.000455006 0.000318661 PC(18:1_18:2COOH)+CH3COO_2 0.003253691 0.000712722 0.00533204 0.002627049 0.002219272 0.001913816 0.002057929 0.002774329 0.003329831 0.003079279 0.003882615 0.002333907 0.008923198 0.007782204 0.006483927 0.005219615 0.005235019 0.005179086 PC(17:0_17:0)+CH3COO_2 0.002937251 0.002990043 0.002812671 0.003310584 0.002776901 0.00328559 0.001222759 0.001189687 0.001708199 0.000802348 0.001160225 0.000764458 0.00215818 0.001811577 0.002149802 0.001850965 0.001925195 0.001744434 PC(12:0_20:5)+CH3COO_2 0.002350883 0.000365051 0.001255667 0.001710748 0.001190685 0.00172403 0.000245298 0.000837997 0.000586093 0.000297701 0.000368104 0.000319405 0.000862489 0.000896687 0.000999399 0.000964904 0.001287097 0.001032625 PI(19:1_20:5)-H_1 0.005395453 0.004768012 0.00647374 0.005439337 0.009456347 0.006413772 0.011200838 0.013521518 0.011132524 0.010268177 0.012032054 0.009953586 0.005589924 0.005653903 0.006037544 0.010080639 0.007635099 0.006283449 PE(15:0_16:0)-H_1 0.01698988 0.015422343 0.015634201 0.017131405 0.018507435 0.01752028 0.003834829 0.006681476 0.006248363 0.004361479 0.00629721 0.00474523 0.008556793 0.007585093 0.011030839 0.012749787 0.011532361 0.009246051 PC(15:0_20:5)+HCOO 0.001858144 0.001534192 0.002089914 0.001657216 0.001420085 0.001607606 0.000409039 0.000945317 0.000689726 0.000321048 0.000379962 0.000413035 0.001217421 0.001019038 0.001159103 0.001206567 0.000938888 0.000976451 PC(9:2CHO_20:5)+CH3COO 0.001373615 0.000433565 0.001386956 0.001563544 0.001163026 0.000441967 0.000525815 0.000701436 0.000691185 0.000572289 0.000715575 0.000494126 0.001307419 0.001564563 0.001562737 0.001329125 0.001760574 0.000736169 PC(18:1_10:2CHO)+CH3COO_1 0.002577121 0.000770279 0.002826031 0.003314342 0.002011525 0.002065546 0.000960457 0.001464383 0.001841536 0.001255665 0.002194186 0.001167297 0.003166926 0.002955596 0.002671188 0.002658608 0.002755908 0.002035561 PC(19:1_20:4)+CH3COO_5 0.041682262 0.042096267 0.036112179 0.040938413 0.038495349 0.044225917 0.021419102 0.030514547 0.025772633 0.019939754 0.026684312 0.018145528 0.031124693 0.035496003 0.034339797 0.03535109 0.032555585 0.035515562 PE(21:0_18:3)-H 0.0022138 0.00255804 0.002555228 0.002477115 0.002754132 0.002649974 0.000703463 0.001820512 0.001474253 0.000930259 0.00128277 0.001171098 0.002131488 0.001828692 0.00229936 0.002450506 0.002166974 0.002030997 PC(19:1COOH_18:2)+HCOO_1 0.003233994 0.00073369 0.005511257 0.002586514 0.002272787 0.002329521 0.001989428 0.002315574 0.003560975 0.00303206 0.002862035 0.002429844 0.008820008 0.007866587 0.006440198 0.004507794 0.005188655 0.005268518 PC(19:1_20:5)-CH3_1 0.019127253 0.016448659 0.011618035 0.016961727 0.016090267 0.018840082 0.000151874 0.001139727 0.000632104 0.000429534 0.000950274 0.00035666 0.001789032 0.001706251 0.002268404 0.003710723 0.002081137 0.002163542 PE(18:1_20:3)-H 0.026488046 0.026332227 0.027167162 0.027749965 0.03122048 0.028776137 0.005895462 0.014868904 0.012858849 0.010383155 0.015807088 0.00900855 0.019299188 0.018669796 0.023199377 0.025422557 0.021169886 0.018434412 PC(18:2CHO_20:5)+CH3COO 0.001229165 0.000449279 0.001398728 0.001336014 0.001141506 0.000998061 0.00022257 0.000716748 0.000278401 0.000367135 0.000502524 0.000290558 0.000699856 0.001273545 0.000822869 0.001161912 0.001254048 0.000894932 PC(19:1_19:2)+CH3COO 0.002395577 0.003080886 0.003132219 0.003235185 0.003203188 0.003530902 0.00141069 0.001785411 0.001991725 0.001159385 0.001453659 0.00111397 0.003276861 0.003005155 0.002537368 0.00199573 0.002545713 0.00245613 PG(15:0_17:1)-H 0.001243288 0.001627591 0.001399912 0.001295309 0.00132827 0.002152929 0.001258409 0.002042717 0.003212796 0.001579923 0.00258145 0.001686565 0.000595003 0.000743926 0.000639982 0.000583254 0.000472717 0.000430097 PE(15:0_20:4)-H 0.008157136 0.008418784 0.006108906 0.00888641 0.007405864 0.008678215 0.000538931 0.001568222 0.001648471 0.001002043 0.001697515 0.001115346 0.00207918 0.002016306 0.003094211 0.003331885 0.003052705 0.002703199 PC(16:1_20:5)-CH3_2 0.003090346 0.002580473 0.002218867 0.002939441 0.002670178 0.003292259 6.40E-05 0.000332553 0.000402205 0.000191596 0.000426041 0.000200371 0.000934107 0.00085213 0.00056809 0.000508151 0.000922372 0.000660118 PC(20:4CHO_20:4)+CH3COO 0.001125597 0.000293121 0.00098846 0.00081744 0.000724282 0.00076581 5.17E-05 0.000415635 0.000181406 0.000250155 0.000310222 0.000167852 0.000667557 0.001046385 0.000927779 0.000473726 0.000558976 0.000994303 LPC(20:5)+HCOO_1 0.001148238 0.000963303 0.000632718 0.001060673 0.000770825 0.001028008 0.000165558 0.000429288 0.000275803 0.000148053 0.000420225 0.000186564 0.000466623 0.000668504 0.000801707 0.000911234 0.000727958 0.000545715 PC(15:0_20:4)-CH3 0.001844332 0.001664622 0.001360975 0.002074147 0.001697902 0.002045116 0.000195705 0.000169292 6.92E-05 0.000108019 3.33E-05 0.000278806 0.000522987 0.000464258 0.000548064 0.000299788 0.000375218 PC(20:2_20:5)+CH3COO 0.051292954 0.053783255 0.046086643 0.044225953 0.044284147 0.049263644 0.000637348 0.02333262 0.016746543 0.01187535 0.019655209 0.008226599 0.044202695 0.049916934 0.045437368 0.039201195 0.019734847 0.044806447 PC(17:0_18:1)-CH3_1 0.001729156 0.001727971 0.001374168 0.001661324 0.001801682 0.002103023 8.64E-07 4.24E-07 0.000272951 8.70E-05 0.000105214 8.96E-05 0.000590226 0.00035649 0.000451768 0.000683222 0.000267549 0.000401514 PE(O-18:1_18:4)-H 0.002104041 0.002076892 0.001826313 0.001411418 0.002244226 0.002039618 0.000242449 0.00104716 0.000596355 0.000498247 0.000808521 0.00060335 0.001040098 0.001110287 0.00137205 0.001333751 0.001496195 0.001304604 PE(O-17:1_18:1)-H_1 0.011149265 0.005432076 0.007073959 0.005597379 0.009442308 0.006553709 0.001548175 0.003875721 0.003636591 0.002502329 0.003915474 0.002996131 0.004750113 0.005214488 0.006838312 0.005317165 0.006220387 0.004922379 LPC(18:2)+CH3COO_3 0.005687953 0.005051104 0.004396861 0.004409443 0.003732947 0.005229214 0.000962438 0.003095747 0.001419378 0.001179323 0.00228158 0.001323606 0.003584287 0.003707305 0.003932003 0.002757174 0.00367873 0.003485951 PC(20:4_21:4COOH)+HCOO_4 0.002961555 0.001245077 0.002897848 0.002515855 0.002737952 0.003090206 0.000133531 0.001296863 0.000405934 0.000129527 0.000355615 0.000126752 0.001094886 0.003236174 0.002031262 0.003159759 0.003899485 0.00226187 LPC(16:1)+CH3COO 0.004390923 0.003739406 0.002643737 0.003759431 0.003449701 0.004238739 0.00227621 0.003613648 0.003433204 0.0023663 0.003698792 0.00263534 0.004360443 0.004641093 0.005658394 0.00457134 0.00489341 0.004054957 PC(15:1_18:3)+CH3COO 0.009234589 0.006771462 0.009444874 0.005560974 0.007538526 0.007414548 0.003391323 0.007995549 0.005953564 0.002875642 0.007283788 0.002849565 0.009464829 0.010431458 0.014126908 0.009370664 0.015465973 0.014520355 PC(17:0_19:0)+CH3COO_1 0.00094565 0.000848575 0.000633664 0.000942447 0.000817609 0.000842757 3.81E-05 0.000128707 0.000256016 1.18E-07 0.000281611 0.00011647 0.000331797 0.000475637 0.000324781 0.000468768 0.000364665 0.000506982 PS(18:0_20:5)-H_4 0.000744297 0.00118384 0.001187237 0.000810035 0.00101179 0.000692892 0.000180679 0.000797703 0.000360885 0.000357561 0.000381879 0.000495289 0.00093652 0.000730853 0.001101955 0.001022342 0.000958858 0.000789497 PE(18:2_20:5)-H_2 0.024597047 0.023420645 0.021529956 0.019545753 0.021311465 0.021382044 0.003250774 0.012774544 0.008307119 0.006885699 0.00818678 0.005564507 0.013384608 0.01412379 0.017519328 0.012928352 0.015160695 0.014463265 PE(20:5_20:5)-H_2 0.000778155 0.01954567 0.015948749 0.000685935 0.001015906 0.001246317 8.33E-05 0.000247828 0.00019482 0.000157279 0.000142737 0.000114894 0.000479823 0.000413337 0.000489638 0.000516216 0.00067435 0.00099368 PC(18:0_20:5)-CH3 0.002102726 0.001810866 0.001564553 0.001905807 0.001688604 0.002183417 0.000325115 0.000139887 0.000155595 4.02E-09 0.000280526 1.99E-05 0.000325994 0.000462351 0.000573241 0.000561462 0.000475297 0.000424699 PC(18:1_21:4COOH)+HCOO 0.003371521 0.000688854 0.004083151 0.001973651 0.002341974 0.001076677 0.000567634 0.001108174 0.001078226 0.001040922 0.001684795 0.000679876 0.003569867 0.003316775 0.003949328 0.00214215 0.002414661 0.001857427 PC(O-18:0_20:3)+CH3COO 0.001723547 0.001444172 0.001270073 0.001441845 0.001146095 0.001483361 0.000371777 0.000557582 0.000477366 0.000355656 0.00051978 0.000260281 0.000638574 0.000753618 0.000789803 0.000610798 0.000626033 0.000742892 PE(19:1_20:3)-H_1 0.003434196 0.003260658 0.002373595 0.003349226 0.003082122 0.003839046 7.83E-05 0.00028979 0.000188665 0.000206354 0.000279565 0.000105662 0.000581938 0.00067327 0.000992008 0.001345773 0.000527167 0.000790679 PE(O-18:1_17:1)-H_1 0.003208706 0.005134033 0.00163191 0.007074232 0.00287039 0.007236501 0.001240988 0.003560997 0.000395761 0.002630759 0.003912993 0.000431958 0.004755624 0.004822921 0.006416359 0.005488822 0.005532323 0.004874724 PI(18:1_18:1)-H 0.001199089 0.00100584 0.002212596 0.001495129 0.002243082 0.001553611 0.003728631 0.005626806 0.006086216 0.006333634 0.007662 0.006131396 0.003089864 0.002644986 0.002592937 0.004249746 0.003512868 0.002384514 PC(17:1_22:4COOH)-H 0.03246308 0.038773053 0.035905355 0.039599647 0.036339773 0.037854861 0.011971532 0.019458292 0.020915663 0.009187623 0.013249037 0.011111697 0.029875392 0.024459414 0.022975021 0.02315752 0.025015609 0.023769669 PE(18:1_18:1COOH)-H_1 0.0046483 0.000856627 0.003369881 0.004278338 0.003851309 0.002565266 0.000754635 0.001492097 0.002593903 0.001786174 0.002766083 0.001661161 0.004579512 0.003764729 0.004022806 0.004036286 0.003587428 0.002633253 PC(O-19:0_18:1)+HCOO 0.003338258 0.00358422 0.003684676 0.003718614 0.00326857 0.003404125 0.001630533 0.002289071 0.002692549 0.001794174 0.002108916 0.0017916 0.003114487 0.0032215 0.002919821 0.002593486 0.003426828 0.002827344 PE(O-18:1_18:3)-H_2 0.009474065 0.009790306 0.00993454 0.008869679 0.011190792 0.00953064 0.00155016 0.004512805 0.003790076 0.002851444 0.003940661 0.002362955 0.005088858 0.005514917 0.007451694 0.005617105 0.006601892 0.005411117 PC(18:0_19:1)+CH3COO 0.019931316 0.011877308 0.012885112 0.014440084 0.017361636 0.014525865 0.011089393 0.012856901 0.012650081 0.009246135 0.011908473 0.007472658 0.013781268 0.017632446 0.016349196 0.016014928 0.015882186 0.014763352 PE(16:0_18:4)-H 0.005605882 0.005587205 0.005769395 0.005283787 0.006242802 0.005558241 0.001143585 0.002975097 0.002233869 0.00146704 0.002969871 0.001462998 0.003712002 0.00298073 0.004468171 0.004337625 0.004166718 0.0038873 PE(19:1_20:1)-H 0.001355446 0.001093885 0.001436657 0.001366948 0.001714885 0.001548382 0.000209193 0.000461573 0.000468167 0.000293142 0.000341295 0.000389285 0.000824576 0.000726451 0.000939877 0.000754967 0.00064865 0.000469206 PC(18:1_19:1COOH)+HCOO_1 0.00130482 0.000330439 0.001913018 0.001163891 0.000878337 0.001000579 0.001027852 0.000995999 0.001931891 0.001751041 0.001961691 0.001412299 0.003262193 0.002891248 0.002640172 0.002862425 0.002544653 0.001982276 PC(17:0_17:1)+CH3COO_1 0.006480996 0.007180709 0.006983392 0.007678554 0.007174028 0.007677979 0.006844598 0.006562931 0.00546568 0.00354686 0.004068398 0.004347164 0.008623361 0.007384987 0.007805276 0.008112 0.008337258 0.007453204 PC(17:2_20:5)+CH3COO_2 0.017412641 0.023246061 0.020336279 0.023160366 0.021918459 0.021756967 0.005081607 0.010043941 0.007876234 0.004398364 0.005314513 0.005629636 0.007662057 0.013906565 0.014287819 0.014980892 0.016907332 0.014864246 PE(19:1_19:1)-H_1 0.013339501 0.013464685 0.011786811 0.01381017 0.01613086 0.013581123 0.006357215 0.007562487 0.006199667 0.005963305 0.006526581 0.007128236 0.011501444 0.009043443 0.009873014 0.011514436 0.01373324 0.008237196 PC(17:1_18:2)-CH3_2 0.000911125 0.000731914 0.000495423 0.000714001 0.001010025 0.000908583 1.93E-06 4.98E-05 5.29E-05 3.81E-05 0.000176328 4.88E-05 0.000169802 0.000306123 0.000391993 0.000332146 0.000184258 0.000221031 PC(18:2_18:2)+CH3COO 0.04422084 0.037893645 0.049678486 0.037626246 0.043067437 0.040088144 0.014155704 0.036354206 0.023670897 0.023489036 0.021129231 0.014889331 0.043799575 0.056996348 0.042597108 0.030610809 0.047931214 0.0530982 PC(21:0_18:2)+CH3COO_1 0.001924771 0.00205516 0.002340756 0.001957698 0.001243884 0.000967533 0.000772944 0.000558605 0.000800038 0.000526974 0.000567812 0.000481218 0.001408895 0.001945113 0.001525781 0.000815014 0.001517973 0.001157378 LPC(18:1)+CH3COO_2 0.060302428 0.057452146 0.041256978 0.058714988 0.052243058 0.060414255 0.016482239 0.033384983 0.028873567 0.02168813 0.033912543 0.022324482 0.042721688 0.043643875 0.056740355 0.039620522 0.045669585 0.038671875 PC(20:4CHO_20:5)+CH3COO_5 0.001013789 0.000526097 0.001335098 0.001374452 0.000945469 0.001167927 0.000178988 0.000435174 0.000481468 7.69E-05 0.000289642 0.000163731 0.000462922 0.001003897 0.0008591 0.001288517 0.001104756 0.000730362 PC(19:1_20:2)+CH3COO_1 0.014798602 0.015153438 0.012780332 0.010820444 0.011440827 0.013315853 0.005752797 0.00834411 0.006623289 0.006199811 0.006905244 0.00421639 0.010023845 0.014160285 0.012067151 0.008274719 0.010322601 0.0108701 PC(21:1_20:4)+CH3COO 0.001099612 0.000951079 0.000758813 0.001014993 0.000827854 0.001031653 0.000271977 0.000535811 0.00035675 0.000358796 0.000428879 0.000279478 0.000528966 0.000599495 0.00054211 0.000608197 0.000598452 0.000717715 PE(17:0_20:4COOH)-H_2 0.001593714 0.000604845 0.001826582 0.002007945 0.00185888 0.001335743 0.000388679 0.000533725 0.000911255 0.000235658 0.000262859 0.000319779 0.001456475 0.001146992 0.002359243 0.001484321 0.001740675 0.000897143 PC(18:1_20:5)+HCOO 0.004632262 0.005053794 0.004373931 0.005361935 0.005083672 0.005294311 0.001554793 0.003051761 0.002439088 0.001898316 0.002498201 0.00168404 0.003374927 0.003484322 0.003450913 0.003589839 0.002998905 0.003185985 PE(19:1_20:2)-H_1 0.009380422 0.009720571 0.007935073 0.008227512 0.010560121 0.009736517 0.002653931 0.005279753 0.004381164 0.00355921 0.004599225 0.00341657 0.005524027 0.006367272 0.006992992 0.006748965 0.005866562 0.005403488 PE(17:0_18:1)-H_1 0.163522633 0.152219394 0.139804224 0.160690943 0.186845009 0.164862224 0.032128641 0.076981917 0.084554364 0.059030654 0.081260527 0.055155523 0.104795914 0.100181008 0.116021557 0.123496063 0.108088599 0.092987729 PE(O-17:1_18:2)-H 0.016811285 0.020752432 0.020466375 0.021045975 0.023100746 0.026031137 0.007042974 0.013697261 0.011326801 0.006591338 0.006048124 0.008563253 0.016200966 0.013249013 0.015403736 0.016299678 0.018159148 0.013673593 PC(18:1_18:2)+CH3COO 0.189348927 0.182866018 0.178382949 0.165598533 0.164070438 0.177678785 0.060898338 0.130216782 0.109223493 0.095111112 0.10966559 0.081330768 0.161869837 0.175399887 0.162445512 0.120236043 0.152634258 0.158045198 PC(17:0_20:5)-CH3_1 0.006942634 0.006148457 0.004740695 0.006038391 0.00573562 0.006819428 0.000624913 0.000387436 0.000293805 0.000568432 0.00098476 0.000512842 0.001114828 0.001009881 0.001249206 0.001845878 0.001182138 0.00122639 PE(25:0_18:2)-H 0.000806324 0.000882206 0.000677328 0.000701396 0.000991525 0.000842752 0.000128067 0.000318006 0.000332283 0.000220362 0.000279031 0.000203074 0.0004099 0.00044783 0.000529359 0.000561892 0.000415335 0.00035098 PC(18:1_20:5CHO)+CH3COO_1 0.002232571 0.000646656 0.002614361 0.002392471 0.001966196 0.001866991 0.000604787 0.001574005 0.001515046 0.001527844 0.00160748 0.001100138 0.001860424 0.003112821 0.002906027 0.002579997 0.002350401 0.002068238 PC(21:1_20:5)+CH3COO 0.004041215 0.004333601 0.003695489 0.003888333 0.003708822 0.004328883 0.001021097 0.002073335 0.001878858 0.001268957 0.001535811 0.001037422 0.00211604 0.002528127 0.002438063 0.00228053 0.002308156 0.002271528 PC(5:0CHO_18:1)+CH3COO_1 0.001324893 0.000404208 0.001119693 0.001366581 0.000969139 0.000516617 0.004394865 0.003154956 0.002870661 0.003657237 0.0046011 0.003456727 0.001469269 0.001974515 0.002595219 0.002774824 0.001786381 0.002190213 PC(17:1_19:1)+CH3COO_2 0.048120938 0.036218929 0.030449694 0.049998251 0.046102975 0.040141306 0.036103131 0.034141204 0.033373001 0.024846097 0.016693452 0.025995329 0.04950968 0.04777159 0.041146324 0.038708098 0.044647416 0.042511003 PE(O-18:1_20:2)-H_2 0.003726809 0.003650676 0.0039977 0.003258491 0.00402529 0.003391812 0.001136474 0.002282999 0.002256358 0.002207885 0.002832087 0.00161413 0.00392402 0.004158136 0.004084022 0.002898129 0.003632645 0.002841336 PC(17:0_20:5)+HCOO 0.001170396 0.000827406 0.001162917 0.001068302 0.000955991 0.000942711 0.000285495 0.000598122 0.000614455 0.000182975 0.000351718 0.000231495 0.000824264 0.000759315 0.000870587 0.000740241 0.000612844 0.001029504 PC(14:1_18:1)+CH3COO 0.007741445 0.008113661 0.008631856 0.008831713 0.009175685 0.009511086 0.00358769 0.008555615 0.007412521 0.006666397 0.008472517 0.006672757 0.012235908 0.010218401 0.011554997 0.009125176 0.011058655 0.010568036 Cer(t22:0_17:0)-H 0.003145286 0.002885397 0.002386408 0.003178023 0.002758224 0.002721165 0.000248624 0.000732607 0.000922808 0.000471514 0.00073227 0.000500724 0.00107181 0.000983108 0.001242232 0.000967612 0.001122066 0.001097957 PC(19:1_20:4)-CH3_2 0.003135392 0.002813488 0.002294065 0.00297321 0.003029767 0.003208199 4.47E-05 0.000358358 3.20E-05 9.73E-05 0.000337573 7.19E-05 0.000641354 0.000522233 0.000550634 0.001204469 0.000668899 0.00060463 PE(O-18:1_15:0)-H 0.029711988 0.02910731 0.027326748 0.026822279 0.031339364 0.030730825 0.006008757 0.013073726 0.01314476 0.007688043 0.010464502 0.0074709 0.013735351 0.014925516 0.01975389 0.018973037 0.016797273 0.015912343 PE(15:1_20:5)-H 0.001901865 0.001823691 0.001569698 0.001595043 0.001760643 0.00178409 0.000670396 0.001428163 0.00110994 0.000751824 0.001043546 0.000620311 0.001309588 0.001417727 0.001845009 0.001811719 0.001777846 0.001698468 PE(17:0_18:1)-H_2 0.085371463 0.070987277 0.074470575 0.085417344 0.10857891 0.079711905 0.038039891 0.040108681 0.053796472 0.033081828 0.041652363 0.032820609 0.057987535 0.052276089 0.064119269 0.075810953 0.064175198 0.053339894 PE(17:0_18:1)-H_3 0.085371463 0.070987277 0.074470575 0.085417344 0.10857891 0.079711905 0.038039891 0.040108681 0.053796472 0.033081828 0.041652363 0.032820609 0.057987535 0.052276089 0.064119269 0.075810953 0.064175198 0.053339894 PC(14:1_20:5)+CH3COO_3 0.000648295 0.004691052 0.00132442 0.000507852 0.000945954 0.000946569 0.000283634 0.000709862 0.001122592 0.000567899 0.000838316 0.000317496 0.001441634 0.003467667 0.002167633 0.001941658 0.00163455 0.001866454 PE(17:0_20:5CHO)-H 0.000730504 0.000222235 0.000473397 0.000631224 0.000550573 0.000440763 0.000319556 0.000428222 0.000397652 0.000283965 0.000436057 0.000302777 0.000809854 0.00077993 0.000642717 0.000689474 0.000957056 0.000417207 PE(O-19:2_20:5)-H 0.002461745 0.002584057 0.002284427 0.002184718 0.002563702 0.002490374 0.000521195 0.001048536 0.001125362 0.000537624 0.000865146 0.000458724 0.001094234 0.001339271 0.001693562 0.001610316 0.001527563 0.001306112 PC(18:1_20:2)+CH3COO 0.024667533 0.026813736 0.024425222 0.022896285 0.020372331 0.025354931 0.00564527 0.013101222 0.010084666 0.009308219 0.011584076 0.007307927 0.019333704 0.024698805 0.020796432 0.013102412 0.015492043 0.017442719 PE(18:2_18:2)-H 0.0095008 0.008642665 0.007766079 0.007437159 0.009578198 0.008156451 0.000719949 0.003845687 0.002330704 0.001995585 0.003320862 0.001950675 0.004615828 0.004525905 0.005573102 0.003650389 0.005090751 0.004691327 PC(15:0_16:0)+CH3COO_2 0.000714609 0.000966158 0.000373327 0.000934042 0.0006125 0.000714849 0.000255491 0.000282792 0.000748777 0.000385311 0.000716922 0.000324429 0.000117394 8.29E-05 7.37E-07 2.43E-05 1.03E-07 3.37E-07 PE(20:0_20:5)-H 0.021132461 0.022017007 0.020023977 0.020762813 0.022334336 0.022851965 0.005704398 0.014702884 0.009702223 0.008430644 0.010805775 0.007469212 0.01402037 0.015342412 0.018153178 0.017046145 0.015829867 0.014480037 PE(14:0_16:1)-H 0.004660496 0.004680348 0.004146514 0.004636909 0.005124077 0.00473827 0.001371446 0.003083321 0.002517313 0.001827955 0.002540891 0.002038106 0.003781879 0.003066221 0.00417695 0.005132553 0.004077865 0.003375595 PE(18:3_18:3)-H 0.001556249 0.001442426 0.001671197 0.001466304 0.001713242 0.001527829 0.000118492 0.000585023 0.00053113 0.000482745 0.000491912 0.000238738 0.000765154 0.000613774 0.000908367 0.000909113 0.000935387 0.000745214 PE(17:0_18:1COOH)-H_4 0.001168915 0.000180099 0.001075784 0.001032047 0.000825286 0.000759035 0.0003044 0.000466875 0.000474673 0.000525057 0.000616573 0.000587689 0.001167467 0.000904152 0.000838817 0.000953651 0.000940986 0.000575144 PC(17:0_20:5)-CH3_2 0.002867609 0.001731401 0.001557921 0.00224825 0.001693224 0.002480435 0.000424666 0.000564525 0.000355913 0.000455608 0.000420543 0.000252551 0.000698125 0.000654454 0.000675889 0.000641044 0.00078985 0.000508547 PC(16:0_18:2)+CH3COO 0.034093773 0.035484513 0.03328516 0.033977142 0.032829133 0.035042123 0.027936253 0.025040437 0.023463053 0.017086939 0.021479663 0.018314492 0.036251488 0.03474657 0.029464 0.028834463 0.031657015 0.028692062 PC(18:1_20:4)+CH3COO_2 0.132244175 0.113108471 0.140540108 0.139276613 0.129260426 0.108436399 0.027903022 0.059066525 0.071155249 0.036811855 0.069970843 0.047295046 0.078788942 0.084969046 0.095276671 0.086372605 0.080474485 0.087602817 PC(19:1_18:2)+CH3COO_3 0.000612759 0.003416667 0.004265179 0.001361388 0.000953982 0.000647164 0.000470963 0.000637546 0.000502627 0.001175244 0.000514268 0.00034611 0.002774347 0.00259883 0.003315111 0.002171287 0.000605877 0.002797181 LPC(20:0)+CH3COO 0.00070039 0.000445814 0.000348083 0.000283742 0.000282558 0.00052337 7.05E-05 0.000119654 0.000107251 3.34E-05 3.19E-05 0.000298698 0.000295045 0.000196187 0.000237949 0.000199681 0.000128941 PC(14:1_18:3)+CH3COO 0.001393896 0.000832139 0.002012683 0.0017907 0.001734416 0.001770114 0.000917048 0.001605704 0.00138603 0.001097775 0.001858962 0.000799478 0.002521333 0.002328657 0.002209681 0.002058508 0.002062618 0.001746279 PC(18:1_10:2CHO)+CH3COO_2 0.003208801 0.00027769 0.001228957 0.00143088 0.000833708 0.000656362 0.001192197 0.001091441 0.001177695 0.001318238 0.001345029 0.000972935 0.002571466 0.001990798 0.001493421 0.001965343 0.001611732 0.001804033 PC(19:1_20:3)-CH3 0.001874931 0.00145281 0.001286611 0.001737575 0.00170492 0.002048897 0.000214861 0.000177413 7.79E-05 0.000262978 5.71E-05 0.000314496 0.000500317 0.000527163 0.000809468 0.000532779 0.000470675 PC(18:1_18:3)+CH3COO_3 0.051048214 0.04514499 0.057953181 0.050791412 0.052890812 0.046614673 0.010515432 0.03386598 0.024967282 0.017522022 0.029912692 0.017110894 0.037284351 0.045051785 0.040249806 0.035609455 0.03872559 0.037617949 PC(16:1_18:1)+CH3COO 0.046535739 0.047113365 0.046158501 0.0479268 0.044621947 0.053389252 0.024532027 0.037196357 0.039916941 0.031090995 0.039513179 0.028286726 0.053565677 0.05249898 0.054711285 0.039324001 0.045783601 0.047365322 PE(18:1_18:2)-H_2 0.137241019 0.129152197 0.139771768 0.13156293 0.144456011 0.13302541 0.019970638 0.069866756 0.055528871 0.046814445 0.062808115 0.040712937 0.084031674 0.078986819 0.091948498 0.082154261 0.088221716 0.073212057 PE(18:1_19:1)-H_2 0.026605138 0.030919179 0.031721169 0.033023275 0.033221254 0.033285734 0.00625301 0.01397303 0.013593003 0.00975525 0.014380724 0.010687198 0.018805169 0.017178249 0.017931859 0.022743179 0.019510781 0.015348361 PC(19:0_20:3)+CH3COO_1 0.00170226 0.000470769 0.0020124 0.000640578 0.001573389 0.000871321 0.000430146 0.000283964 0.000402898 0.000358759 0.000573986 0.000221562 0.001118409 0.000848139 0.001040125 0.001110062 0.001095056 0.000382811 PE(O-20:2_18:2)-H 0.005569713 0.005558037 0.006014487 0.004947129 0.005306402 0.005115238 0.000516462 0.002680214 0.001622933 0.001919922 0.001631003 0.001107167 0.002481393 0.004577737 0.00399148 0.003184301 0.003510872 0.002914001 PC(20:4COOH_20:5)+CH3COO_4 0.001429314 0.001412622 0.003053751 0.00258952 0.002581638 0.002119054 7.71E-05 0.000544468 0.000517324 0.000147601 0.000508469 4.69E-05 0.000695624 0.001154204 0.002014018 0.001975327 0.001023205 0.001189913 PE(17:0_20:4)-H_3 0.02942048 0.029536046 0.023125381 0.027004836 0.030693555 0.029180412 0.006155688 0.010970266 0.011539789 0.009053606 0.012817417 0.007596628 0.013001571 0.014854212 0.020654597 0.015813574 0.016183707 0.015509508 PC(18:1_22:1)+CH3COO 0.000893622 0.000637492 0.000757832 0.000794246 0.000834037 0.000882374 0.000137964 0.000211546 0.000282514 0.000260803 0.000489633 0.000162482 0.00059803 0.00075555 0.000536687 0.000489028 0.000468151 0.000471447 PE(O-17:1_15:0)-H 0.001826367 0.002076099 0.002006354 0.001962299 0.002030411 0.002324796 0.000381624 0.00069418 0.000920802 0.000432655 0.000510535 0.000503395 0.001264376 0.000771291 0.001031727 0.00119831 0.001267872 0.00091478 PE(21:0_18:1)-H 0.02030061 0.021126572 0.021007506 0.022667142 0.024869914 0.022598287 0.010777533 0.015616788 0.014928614 0.010820866 0.012645427 0.012068913 0.018202443 0.016599896 0.018057186 0.020662564 0.018662966 0.014737231 PC(18:1_22:3)+CH3COO 0.000887026 0.001035768 0.001062809 0.000751988 0.000892986 0.000775107 6.91E-05 0.000277069 0.000215226 0.000290026 0.000286451 0.000162094 0.000752337 0.000960501 0.000509184 0.000421624 0.000485622 0.000513365 PC(17:0_18:2)-CH3_1 0.004129399 0.003450277 0.002860478 0.004802822 0.004607222 0.005212373 6.58E-05 0.000629013 0.000256515 0.000554213 0.000366416 0.000472671 0.000969553 0.000799569 0.001210375 0.000810413 0.000677892 0.000791736 PI(18:0_20:4)-H_1 0.00108271 0.001017141 0.001136723 0.00121462 0.001379523 0.001172512 0.003951331 0.004533672 0.003524355 0.003861645 0.004706926 0.004351203 0.002368538 0.002495338 0.002451754 0.003864345 0.003265751 0.002798698 PE(19:0_20:5)-H_2 0.018973026 0.020994281 0.016729824 0.01728326 0.022581198 0.01957125 0.004514104 0.012455174 0.011153898 0.0073081 0.009904432 0.006245963 0.012474448 0.013628796 0.014974836 0.015305057 0.015579425 0.013804402 LPE(18:3)-H_2 0.004680138 0.002279583 0.003899309 0.00524622 0.003481147 0.003631181 0.001624477 0.002520505 0.003080611 0.002675342 0.003035981 0.002570108 0.004653073 0.004083016 0.005018577 0.003437622 0.004544503 0.003135238 PC(14:0_16:0)-CH3 0.004477781 0.004222593 0.004227811 0.004566378 0.004738186 0.004282626 0.00202819 0.002847325 0.002654977 0.001849283 0.002571849 0.00190787 0.003514035 0.002692649 0.004222151 0.004418338 0.003867429 0.003183437 PE(17:0_18:1COOH)-H_5 0.000657004 9.45E-05 0.000648495 0.000814543 0.000671222 0.000554158 0.000512591 0.000538466 0.000534216 0.000445725 0.000546394 0.000547289 0.000893348 0.000852391 0.000678568 0.000602947 0.000797628 0.000622887 PE(18:1_18:2COOH)-H_1 0.001528534 0.000792189 0.001602735 0.001601317 0.001284152 0.000913901 0.000645046 0.000712334 0.001047529 0.000873266 0.000849398 0.000978222 0.001664986 0.0011553 0.001111286 0.001999594 0.002042832 0.001508483 PS(18:0_20:5)-H_5 0.001054573 0.001281331 0.001601301 0.001512943 0.001694447 0.001357571 0.000275834 0.000592076 0.000484614 0.000779141 0.000494421 0.000830184 0.000742262 0.000938471 0.001209608 0.001145368 0.001014455 0.001197309 PE(22:0_20:4)-H_2 0.002903083 0.002861264 0.002716152 0.002968019 0.003345567 0.002689619 0.00088816 0.001685953 0.001281109 0.000921848 0.001509745 0.000843553 0.001725196 0.001782994 0.002702013 0.002628078 0.00197836 0.001965129 PC(19:0_20:3)+CH3COO_2 0.001911607 0.001217602 0.001427281 0.001997459 0.001219916 0.00185999 0.000430873 0.000517025 0.000524444 0.000301544 0.000512856 0.00056975 0.001188649 0.002226821 0.001212508 0.000749466 0.001156491 0.001416571 PC(22:0_18:2)+CH3COO 0.002719816 0.002797762 0.002370298 0.002587051 0.002892142 0.002665725 0.001084721 0.001258884 0.001396959 0.000818849 0.001199771 0.000718678 0.001807005 0.001973449 0.001533605 0.001572625 0.001636098 0.001377978 PE(17:1_19:1)-H_1 0.003275532 0.002865497 0.003023595 0.002999616 0.003191607 0.003267889 0.000991043 0.001010833 0.000758889 0.000638865 0.000908087 0.000752701 0.001277231 0.001119174 0.001632786 0.001415739 0.001371416 0.00099359 PE(18:1_18:3)-H_1 0.037404571 0.041408639 0.037841653 0.041179084 0.039909466 0.040875767 0.00561943 0.022883456 0.018344352 0.014653501 0.017511537 0.013180639 0.024511871 0.021847498 0.028581254 0.028006999 0.028430434 0.025901009 LBPA(16:0_18:1)-H 0.001668603 0.001538337 0.001253106 0.001531651 0.001780264 0.002518445 0.002502248 0.003920553 0.004812083 0.003764546 0.00645676 0.003605495 0.002053582 0.00209639 0.002189056 0.001400348 0.001764503 0.001696856 PC(17:1_20:4)+CH3COO_2 0.007180372 0.008615827 0.003319057 0.010013931 0.006338946 0.009429472 0.001560735 0.002680124 0.002069272 0.000824696 0.001918768 0.001412515 0.005658763 0.004126996 0.00199552 0.003640874 0.004872955 0.004217751 PE(21:0_18:2)-H 0.015653537 0.015971382 0.016886978 0.013842817 0.016637524 0.016671278 0.005709624 0.010195925 0.008550981 0.007563276 0.007690622 0.007556908 0.012467043 0.013694275 0.010393407 0.010310342 0.011983103 0.009763695 PC(17:0_18:3)+CH3COO_2 0.005398178 0.005885816 0.006316241 0.00665551 0.005410657 0.006035912 0.00224042 0.004717506 0.004001237 0.002744783 0.004345742 0.002610147 0.006071811 0.004820303 0.005738401 0.004859308 0.005176598 0.00563885 PC(19:1_18:2)+CH3COO_4 0.062897527 0.062761677 0.060139352 0.054343039 0.064605985 0.065692334 0.032150394 0.055659581 0.042131827 0.037977933 0.04215201 0.034352161 0.058899165 0.066321065 0.059978713 0.046793842 0.057297514 0.06161199 PE(15:0_18:3)-H_2 0.002623895 0.002314799 0.002085167 0.002637177 0.002502573 0.002798752 0.000118206 0.000641226 0.000619752 0.000428555 0.000535071 0.000482184 0.000884151 0.000757823 0.001066702 0.001184262 0.00139232 0.000747039 PC(15:0_17:0)-CH3_1 0.020368853 0.019960617 0.016233027 0.019692686 0.023934901 0.020596404 0.002324361 0.006666474 0.008603112 0.005161858 0.006802984 0.005186649 0.009148054 0.008534098 0.010519683 0.011326483 0.009985167 0.008947014 PC(18:1_18:4)+CH3COO_1 0.033693081 0.033636811 0.036653662 0.034792696 0.035039934 0.03592554 0.006442286 0.023328489 0.017896764 0.015939508 0.02076439 0.014246014 0.025250627 0.026125619 0.031702668 0.023949526 0.029112735 0.027757663 PC(18:1_18:4)+CH3COO_2 0.033693081 0.033636811 0.036653662 0.034792696 0.035039934 0.03592554 0.006442286 0.023328489 0.017896764 0.015939508 0.02076439 0.014246014 0.025250627 0.026125619 0.031702668 0.023949526 0.029112735 0.027757663 PE(18:0_20:4)-H_2 0.032351892 0.035956628 0.032047983 0.033775462 0.03831262 0.033277622 0.009075335 0.016908625 0.01494599 0.009743605 0.016480388 0.009247433 0.018406966 0.018536946 0.024092816 0.027887296 0.021611797 0.019146493 LPC(17:1)+HCOO 0.000691003 0.000636089 0.000387712 0.000525654 0.000463302 0.000644662 0.000329745 0.0002814 0.000396375 0.000266496 0.000404393 0.000254765 0.000481973 0.000517298 0.000557213 0.000806823 0.000616749 0.000432188 PC(18:1_19:1COOH)+HCOO_2 0.003926773 0.001300335 0.005701878 0.003246349 0.002829998 0.002719084 0.002280422 0.002949794 0.003645228 0.003828436 0.004975225 0.002714373 0.008815749 0.007188502 0.006640649 0.004074427 0.006945526 0.005477218 PE(18:1_17:2)-H 0.009326099 0.008657543 0.011755692 0.012015166 0.011711821 0.009615031 0.002147365 0.005933811 0.005319041 0.003291226 0.00418317 0.003841322 0.007502894 0.006860623 0.006208669 0.008025974 0.007621776 0.00536821 OAHFA(5:0_14:1)-H 0.000703531 0.003956827 0.004371501 0.003848682 0.003107246 0.001029114 0.005833029 0.007539684 0.007735261 0.005864848 0.006154121 0.005335614 0.004148203 0.00445044 0.005528304 0.004445184 0.004629181 0.004259172 PE(23:7_17:0COOH)-H 0.001130372 0.001389098 0.002141797 0.001499055 0.001896575 0.00147037 0.002607715 0.003494742 0.002911936 0.002648315 0.002901628 0.002286237 0.002373851 0.001801614 0.002015634 0.002080588 0.002152926 0.001929266 PC(18:1_20:1)+CH3COO 0.013887381 0.01406753 0.015182214 0.013178425 0.011754978 0.012853311 0.002775873 0.006197273 0.0060328 0.005084017 0.007254633 0.004247054 0.009543973 0.009976468 0.010066005 0.007058875 0.007244285 0.008287094 PC(21:0_20:4)+CH3COO 0.000564394 0.000611265 0.001101528 0.000604561 0.000597714 0.000728963 9.24E-05 0.000213469 0.00032607 6.51E-05 0.000322351 0.000115969 0.000565345 0.000832966 0.00043337 0.000952191 0.000469423 0.000404532 PE(27:0_18:2)-H 0.0010242 0.00104882 0.000674028 0.000775626 0.000922051 0.001121111 0.00024819 0.000680892 0.000519363 0.000584215 0.000595784 0.000442702 0.000603276 0.00091877 0.000907225 0.001076494 0.00091301 0.00080171 LPE(19:1)-H_2 0.018743721 0.014851005 0.011096888 0.015705232 0.020757555 0.017884791 0.009866263 0.015820035 0.013569599 0.010373157 0.014454042 0.010734529 0.016181485 0.015093869 0.018524774 0.017597109 0.020402923 0.017310397 PC(16:1_20:5)-CH3_3 0.000896784 0.0008274 0.000681416 0.000901427 0.000768866 0.00083219 3.74E-05 3.54E-05 0.000152669 7.59E-05 0.000211515 5.46E-05 0.000177566 0.000220987 0.000300273 0.000310013 0.000188938 0.000266435 PC(18:0CHO_20:5)-CH3 0.012900735 0.009149203 0.01758262 0.010922339 0.009318762 0.011243946 0.003043221 0.004842784 0.004026816 0.002902151 0.006038001 0.002981615 0.006781945 0.007032825 0.008935408 0.004971141 0.006620813 0.007030971 Cer(d14:0_28:0)-H 0.000604423 0.000528961 0.000463008 0.000517743 0.000395068 0.000560386 9.48E-05 2.88E-05 7.70E-07 3.67E-05 0.000158725 0.000279159 0.000214457 0.00030442 0.000130611 0.000166518 LPE(20:4)-H_2 0.007294922 0.003196756 0.005687761 0.007929238 0.00608429 0.006564416 0.002346727 0.002902974 0.004340271 0.002834394 0.0034901 0.002639964 0.004378148 0.004980827 0.005458193 0.006048055 0.005345373 0.003530913 LBPA(18:2_18:2)-H 0.000168551 1.57E-06 2.44E-05 0.000159338 6.34E-05 5.30E-05 0.000402756 0.002030133 0.001841987 0.001334802 0.001291477 0.000941477 7.08E-07 2.88E-08 3.22E-08 4.32E-09 PC(22:0COOH_19:1)-CH3 0.025621364 0.026515967 0.024521363 0.026433412 0.023977313 0.02804251 0.011739425 0.012908277 0.015507134 0.009244727 0.013482198 0.012429384 0.023169511 0.025432741 0.019913349 0.014761076 0.021498354 0.015855757 PC(20:4_20:5)-CH3_2 0.003639724 0.003158637 0.001941915 0.003199264 0.00286875 0.004219658 3.03E-05 0.000249022 0.000234253 0.000149193 0.000250593 6.75E-05 0.000290292 0.00038344 0.000488851 0.000749743 0.000518927 0.000378334 PE(26:0_18:2)-H 0.00239318 0.002743417 0.002000363 0.002246892 0.002619099 0.002358034 0.000619993 0.001122596 0.000964626 0.000711537 0.000972673 0.00066486 0.000978552 0.001307935 0.001587986 0.001615245 0.001441937 0.001209941 LPC(20:5)+HCOO_2 0.001148238 0.000963303 0.000632718 0.001060673 0.000770825 0.000975874 0.000127574 0.000428925 0.000275844 0.000172118 0.000420254 0.000186606 0.000467279 0.000668504 0.000801707 0.000391489 0.000727958 0.000545715 PE(O-17:1_18:1)-H_2 0.073892423 0.085576163 0.087567321 0.087430189 0.100243589 0.092025221 0.035286896 0.061539025 0.059846376 0.039923945 0.042750865 0.046873534 0.07423863 0.058730972 0.072194901 0.078310557 0.078526891 0.059715971 PC(19:1_20:5)+CH3COO_3 0.189598815 0.176522729 0.179789938 0.189991998 0.182573957 0.195766911 0.084460385 0.125960129 0.109358053 0.080237211 0.103302757 0.07421168 0.120487137 0.141007748 0.12963588 0.127509345 0.130402663 0.132343826 PE(19:1_20:2)-H_2 0.000372014 0.000372876 0.000399977 0.000639779 0.000555837 0.000393728 4.78E-05 4.68E-05 0.000162698 3.94E-07 1.17E-06 9.09E-07 9.00E-05 0.000206351 0.000179348 0.000145517 0.000255109 0.000206144 PC(5:0CHO_20:5)+CH3COO 0.002492615 0.000892779 0.003346306 0.002026984 0.002014622 0.002604592 0.000977282 0.00178083 0.002266927 0.001549736 0.002378174 0.001129705 0.002653149 0.003616192 0.002543826 0.0036819 0.003419224 0.002280049 PE(16:0_18:1COOH)-H 0.001655813 0.000686681 0.002727221 0.001834818 0.001587524 0.001300381 0.000308955 0.000657967 0.000617154 0.000548565 0.000819751 0.000331962 0.002598962 0.001044315 0.001298092 0.002000382 0.00142681 0.001088249 PC(19:1_20:5)+HCOO 0.002415496 0.002118658 0.00234978 0.003597152 0.002201319 0.002630367 0.001097644 0.00168339 0.001295966 0.000927157 0.001196771 0.001025085 0.001574181 0.001610857 0.001743099 0.001953873 0.001633675 0.001630838 PE(19:1_21:1)-H 0.001063731 0.000761269 0.000841907 0.000680095 0.000885059 0.000818072 0.000107013 0.000193559 0.0001606 9.01E-05 8.73E-05 0.000148433 0.000169315 0.000315971 0.000269235 0.000237093 0.000224952 0.000210321 PE(16:0_20:4)-H_2 0.018829773 0.019646291 0.016454014 0.021046665 0.021831972 0.020944346 0.003952574 0.00728747 0.006600059 0.004754018 0.007463853 0.004641203 0.008675471 0.007683471 0.010821585 0.014140174 0.010376425 0.009244577 PE(17:0_17:0)-H 0.019899081 0.019761522 0.015785589 0.01930749 0.023310789 0.021497889 0.00224157 0.006694217 0.008383325 0.005070324 0.006677476 0.0049993 0.008913117 0.008288431 0.010261598 0.010963698 0.00963141 0.008550293 PE(O-18:0_20:5)-H 0.046012555 0.0488747 0.044519625 0.045642642 0.049309569 0.049723409 0.013271658 0.029361412 0.023383995 0.016848308 0.026774002 0.014570144 0.028471978 0.02972717 0.035505725 0.035182845 0.033652961 0.032071342 PC(19:1_20:5)+CH3COO_4 0.028650772 0.035679046 0.023874494 0.03396898 0.024591692 0.018773878 0.007385255 0.012226837 0.011358161 0.008361093 0.008044139 0.006863541 0.012146899 0.021036057 0.011050024 0.016613169 0.020429338 0.018003065 PC(19:1_20:5)+CH3COO_5 0.028650772 0.035679046 0.023874494 0.03396898 0.024591692 0.035792549 0.007385255 0.012226837 0.011358161 0.003678401 0.008044139 0.006863541 0.012146899 0.021036057 0.011050024 0.016613169 0.020429338 0.018003065 Cer(d16:0_4:0)-H 0.001061457 0.000373958 0.000650709 0.000572347 0.000511207 0.000657107 0.000897881 0.000923085 0.001036002 0.000925231 0.000799887 0.000523037 0.000506553 0.000632997 0.000485303 0.000136182 0.000557297 0.000441929 PC(21:0_19:1)+CH3COO 0.00095366 0.00085745 0.000956648 0.001105969 0.001047558 0.000852369 0.000456468 0.000445516 0.000375517 0.000445754 0.00052515 0.000432499 0.00073847 0.000742094 0.000504486 0.000649948 0.000842695 0.000528127 PI(19:0_20:5)-H 0.000895335 0.000989379 0.001460936 0.001128399 0.001564232 0.001242203 0.001595998 0.002193359 0.001999587 0.00168206 0.001599122 0.001741509 0.001218714 0.00094734 0.000969408 0.001622427 0.001492503 0.000955474 PC(17:1_18:1COOH)+CH3COO_2 0.000990175 0.000249094 0.001311684 0.001119776 0.000919071 0.000746817 0.001291707 0.001225947 0.001383487 0.001636382 0.001847154 0.001391064 0.00348839 0.002749564 0.002562009 0.002110544 0.00247396 0.001637257 PC(O-14:0_18:1)+CH3COO 0.002374317 0.000704508 0.002172117 0.002609055 0.002595386 0.001853598 0.002974278 0.003070092 0.004612738 0.004025021 0.004540369 0.003829176 0.003090275 0.002346388 0.002249305 0.002921462 0.002543093 0.001557358 PC(15:0_19:2COOH)-CH3 0.000998909 0.001468077 0.001175669 0.001434499 0.001501561 0.001657446 0.000912959 0.000658093 0.00081047 0.000734139 0.001076727 0.000887976 0.002003758 0.001117388 0.001212725 0.001660272 0.001316467 0.002233773 PC(16:0_20:5)-CH3_2 0.000741041 0.000710835 0.000320373 0.001145543 0.000632051 0.00085745 2.66E-05 3.48E-05 0.000138887 6.36E-05 1.16E-06 2.49E-05 0.000145067 9.99E-05 0.00010186 0.000191676 0.000189421 0.00014974 PC(18:1_20:5CHO)+CH3COO_2 0.000410092 0.00010858 0.000566339 0.000531669 0.000322743 0.000340646 0.000151727 0.000599201 0.000447087 0.000324407 0.000390191 0.000376587 0.000722905 0.00072675 0.000602696 0.00054652 0.000668503 0.000566835 PC(17:1_18:1)+CH3COO_3 0.008320642 0.006975307 0.005229886 0.006799663 0.006569161 0.007662991 0.008562315 0.006497113 0.006353175 0.004908743 0.005510068 0.004979565 0.008613749 0.00841312 0.00787678 0.007971687 0.008353785 0.008530211 PE(19:1_20:5)-H_1 0.010528658 0.011193001 0.014978136 0.015694107 0.009400003 0.01138308 0.002005716 0.007256817 0.004486392 0.002466533 0.004002073 0.002652151 0.008704254 0.008351312 0.007934634 0.00861049 0.006472251 0.005095004 PC(19:1_20:1)+CH3COO_2 0.010589575 0.009912729 0.008828327 0.009739248 0.009013536 0.010664105 0.003430557 0.00595098 0.005607507 0.004408841 0.005869353 0.003747457 0.006407269 0.006993158 0.006989676 0.006204313 0.006272161 0.007202584 PC(18:0_20:0)+CH3COO 0.000666392 0.000761167 0.00068463 0.000747296 0.000688689 0.000791825 0.000125348 0.000441149 0.000260157 0.000150873 0.0002628 9.19E-05 0.00038909 0.000478425 0.000484676 0.000381458 0.000449952 0.000404778 PE(O-18:0_20:2)-H 0.038865557 0.040959697 0.038048072 0.03404264 0.039780738 0.036270769 0.018547132 0.025436014 0.021749765 0.019254574 0.023017279 0.018517478 0.025992092 0.030694426 0.027817975 0.027740845 0.026899079 0.022723836 PC(17:0_19:0)+CH3COO_2 0.000954309 0.00084856 0.000647482 0.000680553 0.000600069 0.001164188 0.000276059 0.000198338 0.000434798 0.000124405 0.000241429 0.000198194 0.000388801 0.000405275 0.000458966 0.0005823 0.000547334 0.000363404 PE(14:0_20:4)-H 0.007327315 0.00685798 0.00679202 0.006425365 0.007603112 0.007071387 0.000903355 0.003307473 0.002511539 0.001697126 0.001890032 0.001651755 0.003201186 0.002962467 0.004188487 0.005079245 0.004047385 0.003144977 Cer(t17:0_23:0)-H 0.001185845 0.00125423 0.000918828 0.001079259 0.001094967 0.001184133 0.000135858 0.000273616 0.000447168 0.000241388 0.000254903 0.000167434 0.000576917 0.000527244 0.000870612 0.000505925 0.000523717 0.000359039 PG(16:0_18:1)-H 0.002044767 0.002355066 0.002053234 0.002046801 0.002084449 0.002533832 0.002520125 0.003866379 0.004799478 0.003765604 0.007315148 0.003664764 0.001986252 0.001991675 0.002000437 0.001395184 0.001704319 0.001695541 PE(19:0_18:3)-H 0.002425679 0.003093494 0.002841077 0.002994858 0.002949864 0.002883863 0.000857535 0.001677444 0.001620679 0.000987687 0.001096033 0.001140265 0.002194638 0.001625796 0.001890129 0.002559862 0.001908639 0.001672614 PE(19:1_18:2)-H_1 0.033428779 0.031697811 0.029844622 0.033898426 0.037791312 0.02991743 0.010699641 0.020251366 0.017764543 0.016431243 0.017725983 0.019218937 0.022693484 0.023136302 0.021884821 0.028101019 0.022436984 0.021652295 PE(14:0_18:3)-H 0.001626099 0.001812013 0.001514704 0.001714068 0.001654469 0.00165 8.26E-05 0.000477598 0.000577651 0.000282032 0.000424331 0.000378636 0.000674059 0.000669039 0.000521083 0.000915624 0.000881357 0.000641897 PE(17:0_18:3)-H_2 0.026340014 0.029126474 0.025997404 0.028799628 0.030908574 0.029679259 0.004859611 0.015747261 0.012351759 0.010258898 0.012572606 0.008974729 0.015803538 0.01424185 0.018923237 0.020940485 0.019814847 0.016236047 PC(10:2CHO_20:5)+CH3COO 0.002031965 0.000616163 0.001817085 0.001460064 0.000745877 0.001797553 0.000303252 0.000506572 0.000577153 0.00041399 0.000643017 0.000359664 0.000801231 0.001790032 0.000828703 0.001202288 0.002150866 0.001100362 PE(19:0_20:3)-H 0.004258814 0.005181031 0.004069344 0.004706874 0.006332561 0.00467068 0.001992644 0.002668239 0.002909615 0.001963678 0.002348454 0.001869539 0.003159339 0.003567955 0.003575931 0.00414096 0.004233624 0.002370264 LPE(20:3)-H_1 0.010277075 0.003907042 0.00937004 0.011824622 0.009262856 0.008731126 0.004380349 0.004773651 0.007782611 0.005409963 0.007257591 0.004770827 0.008380852 0.00768871 0.008871009 0.009536269 0.008523683 0.006852829 PC(17:1_18:3)-CH3_2 0.001818869 0.001456279 0.001587104 0.001861563 0.00160835 0.001995704 0.000217199 1.21E-06 6.21E-05 0.000191023 7.25E-07 0.000259236 0.000399395 0.000633482 0.000504181 0.000286318 0.00028692 PE(18:1_20:5CHO)-H 0.001012294 0.000142718 0.000894932 0.000763388 0.000639093 0.000712926 0.000206952 0.000585504 0.000657062 0.000625198 0.000830812 0.000390543 0.001178269 0.000899873 0.001043551 0.001034888 0.001020372 0.000656647 Cer(d14:1_28:0)-H_2 0.000626353 0.000647796 0.000523612 0.000726749 0.000488614 0.000576353 3.72E-05 5.43E-05 0.000137754 3.79E-05 6.73E-07 3.28E-07 6.46E-05 0.00019811 0.00039256 0.000218994 0.000268713 0.000189857 PE(19:0_18:1)-H_1 0.019708133 0.015879069 0.023453488 0.023610597 0.024922308 0.02568228 0.009999573 0.01441784 0.013295881 0.010336546 0.01161813 0.011042454 0.01745042 0.015909796 0.014306958 0.017022208 0.018741856 0.012612532 PC(16:1_17:1)+CH3COO_1 0.029728404 0.029094779 0.030108779 0.029173715 0.032979788 0.030116732 0.001384149 0.036801609 0.034350166 0.031574687 0.033873866 0.032667431 0.053269629 0.051899191 0.047568629 0.043269669 0.048635778 0.049597303 PE(14:0_17:0)-H 0.001162963 0.001300927 0.001335393 0.001550029 0.001413084 0.001373598 0.000392404 0.000493198 0.000527164 0.000375425 0.000478158 0.000551488 0.000776894 0.000605808 0.000891275 0.001320652 0.001099561 0.000655794 PG(18:1_18:1)-H 0.009127995 0.007959988 0.008780552 0.008571414 0.010029239 0.012121994 0.005296492 0.011429864 0.012953287 0.009760014 0.018312693 0.009575107 0.004278276 0.00481979 0.005226298 0.005315939 0.004853747 0.004171 LBPA(18:2_18:3)-H 9.78E-05 5.65E-07 4.14E-05 4.03E-08 5.08E-07 0.000103325 0.000346109 0.000908002 0.000722903 0.00086512 0.000676421 0.000580423 2.72E-05 2.31E-10 PE(16:0_17:0)-H_1 0.028274808 0.02568716 0.025167326 0.028159797 0.031502873 0.02764192 0.007564939 0.013129795 0.014518294 0.008812404 0.013233008 0.008779667 0.0152684 0.013923455 0.017885971 0.021864355 0.017235628 0.015793379 PC(19:1COOH_18:2)+HCOO_2 0.003479281 0.000709063 0.002449102 0.002643073 0.002701553 0.001677532 0.002229585 0.001946803 0.002940981 0.002617056 0.002521424 0.001946828 0.003231044 0.006028563 0.005546352 0.002545239 0.00466868 0.004404136 PE(15:1_20:4)-H 0.001900609 0.001739811 0.001875505 0.001810616 0.002155644 0.002051886 0.000492358 0.001387877 0.000918778 0.000612847 0.001170733 0.000717605 0.001339266 0.001269236 0.0016124 0.001867275 0.001813783 0.001268067 PE(17:0_20:4)-H_4 0.012640553 0.014522182 0.012530664 0.013011932 0.018650225 0.015115013 0.004013708 0.00500033 0.006863873 0.003037701 0.004462037 0.003902287 0.006541047 0.005419876 0.007765951 0.008976217 0.007628718 0.006715531 PC(4:0CHO_19:1)+CH3COO 0.001237226 0.00019225 0.001880112 0.001053385 0.000703268 0.000570601 0.003006873 0.002045214 0.002663778 0.003485744 0.002440591 0.003150808 0.002486607 0.001390647 0.000928178 0.002044595 0.001511622 0.001812182 Cer(d17:1_23:0)-H 0.002685677 0.003177448 0.002645755 0.002617853 0.00224767 0.002278263 0.000714553 0.001235698 0.000847915 0.000241871 0.000697888 0.00054569 0.001333961 0.00214786 0.001572326 0.001331253 0.001210574 0.001092892 Cer(d17:1_21:0)-H 0.002651266 0.002992085 0.002368839 0.002550823 0.00245057 0.002097146 0.000285148 0.000691724 0.000942218 0.000228525 0.000610429 0.000267968 0.001244671 0.001298786 0.000765905 0.001154155 0.000855123 0.000913061 PE(16:0_20:3)-H 0.018347862 0.018084588 0.017810512 0.019803588 0.020154226 0.018917071 0.007567579 0.0128859 0.011326538 0.007192588 0.010910986 0.008047867 0.013461773 0.014065318 0.014647304 0.020847942 0.017586807 0.012172276 PC(21:3COOH_20:4)+HCOO_2 0.000418874 0.000719568 0.001310963 0.001767777 0.001355552 0.001110024 1.45E-06 0.0004306 0.000466793 5.10E-05 0.000573113 0.00018683 0.00126279 0.002241658 0.000911197 0.002179271 0.001209136 0.00045071 PI(18:1_19:1)-H 0.000153191 0.000266934 0.000408637 0.000290636 0.000461198 0.0001475 0.000983504 0.001149297 0.001247616 0.001471187 0.002280837 0.002153457 0.000624419 0.000551696 0.00064557 0.001082126 0.00073034 0.000606347 PI(19:1_20:4)-H 0.000556018 0.000536285 0.000718805 0.000635629 0.000820212 0.000649826 0.00184118 0.002024868 0.00159344 0.001704485 0.001831793 0.001514278 0.001036328 0.001024953 0.001050772 0.001827516 0.001267053 0.001156557 PE(15:0_16:2)-H 0.000949708 0.000945206 0.000873993 0.001085155 0.001161959 0.001026384 2.67E-05 0.000345442 0.000410626 0.000130751 0.000390056 0.000262514 0.000570254 0.000351631 0.000691615 0.000791701 0.000699859 0.00044675 PA(21:5_20:5)-H 0.008274081 0.039195487 0.004225692 0.008058809 0.025895377 0.015572162 0.001056459 0.00231512 0.002747403 0.00029744 0.00077615 0.000974887 0.005429567 0.005342863 0.015811087 0.006257408 0.004491654 0.008784297 PE(15:0_15:0)-H 0.004819254 0.00499244 0.004920268 0.00542604 0.006199095 0.005562555 0.00061874 0.001595775 0.002436855 0.00122816 0.001487532 0.00177996 0.002549579 0.002237973 0.003081386 0.004411117 0.00298888 0.002476204 PC(13:0_15:0)-CH3 0.005113655 0.0049976 0.004830018 0.005729675 0.006198803 0.005531049 0.000584034 0.001601028 0.002473418 0.001221869 0.001480209 0.001730114 0.002641885 0.002218648 0.003129516 0.004403459 0.002914953 0.002456101 PE(20:0_20:4)-H 0.008929851 0.008660077 0.00758414 0.008819627 0.009089048 0.008190019 0.002211757 0.004483877 0.004021699 0.002398208 0.00516039 0.002622317 0.005241496 0.004829821 0.006580979 0.007376371 0.005556769 0.00510503 PE(17:0_21:0)-H 0.000928184 0.001017766 0.000951919 0.001054078 0.001222332 0.001046348 0.000297979 0.000457905 0.000661029 0.000304188 0.000437862 0.000292696 0.000661266 0.000646298 0.000628164 0.000830466 0.000640144 0.000542051 PE(O-18:1_18:1)-H_1 0.832842336 0.806438822 0.820609103 0.783413431 0.931266482 0.855402989 0.328783356 0.645705567 0.560292075 0.463469947 0.598172825 0.420697708 0.646893692 0.642611217 0.784983871 0.796112059 0.71332172 0.642999065 PI(20:5_20:5)-H 0.000444736 0.000471305 0.000422856 0.000547594 0.000561897 0.000535854 4.59E-05 0.000133041 0.000186447 9.52E-05 0.000151629 0.000138193 0.000200143 0.000187521 0.000237058 0.000296148 0.000213259 0.000178946 PC(17:1_17:2)+CH3COO_1 0.008479644 0.008263525 0.009106269 0.009870722 0.009063803 0.009839894 0.008972414 0.009830961 0.008949922 0.00788896 0.011236885 0.009295108 0.009782241 0.01126694 0.011915472 0.011468428 0.012352068 0.011679126 PC(17:0_18:2)+CH3COO_1 0.053214953 0.054482788 0.047935413 0.044192485 0.050383614 0.056183324 0.012597055 0.026353935 0.02213793 0.024325304 0.02818875 0.021693318 0.03706361 0.051109695 0.035790146 0.025418054 0.046727829 0.032848001 PC(17:1_17:1)+HCOO 0.000965704 0.000848188 0.000993416 0.000985231 0.000951792 0.000837226 5.83E-07 0.000907506 0.001093429 0.000849789 0.000950901 0.000771241 0.00133481 0.00121155 0.001393249 0.001417581 0.001311618 0.001309708 PC(16:0_17:0)+CH3COO_2 0.001025776 0.001300183 0.000509657 0.001061047 0.001169501 0.001051763 0.000258017 0.000267085 0.000744233 0.0004087 0.000682572 0.000320972 5.88E-05 0.000213506 0.000182537 6.92E-05 0.000154518 7.71E-05 LBPA(18:1_18:4)-H 6.89E-05 3.11E-05 7.67E-05 7.26E-10 2.92E-09 0.0001027 0.000562273 0.001543668 0.001201318 0.000987836 0.001097721 0.000869836 2.72E-05 2.31E-10 PC(19:0_18:3)+CH3COO 0.001125541 0.000706346 0.001870031 0.001798795 0.001257648 0.001115171 0.00033077 0.000991553 0.0008584 0.000561011 0.000863133 0.000311 0.001239768 0.001553056 0.001286769 0.000775341 0.001098325 0.001324122 Cer(t17:1_24:1)-H_2 0.001444678 0.000897769 0.000881303 0.001871372 0.001486054 0.001240233 0.000386412 0.000201434 0.000399277 0.000259691 0.000302418 0.000222019 0.000581318 0.000528681 0.000491467 0.000581887 0.000410034 0.00031764 PC(19:1_20:5)-CH3_2 0.001898952 0.001289345 0.001400615 0.002110768 0.001637933 0.001893839 8.61E-07 0.000252122 0.000292658 0.00022507 0.000280369 0.000220247 0.000428495 0.0005084 0.000433698 0.000301416 0.000327015 0.000395971 PC(19:1_20:5)-CH3_3 0.001898952 0.001289345 0.001400615 0.002110768 0.001637933 0.001893839 8.61E-07 0.000252122 0.000292658 0.00022507 0.000280369 0.000220247 0.000428495 0.0005084 0.000433698 0.000301416 0.000327015 0.000395971 PE(28:0_8:0CHO)-H 0.002904886 0.000565066 0.002315913 0.002711007 0.002413576 0.001980136 0.001324898 0.001349745 0.002195673 0.00189483 0.00235797 0.001543492 0.002789816 0.002652634 0.002554082 0.002481422 0.002369472 0.002101246 PE(18:3_20:5)-H_2 0.003458383 0.002823163 0.002623133 0.002135422 0.002711251 0.002464431 0.000303371 0.001425959 0.000821387 0.000519971 0.000930384 0.000565643 0.00126243 0.001259839 0.001466428 0.001247031 0.002134407 0.001747361 PC(17:0_20:0)+CH3COO 0.001314757 0.001620776 0.001014651 0.001189069 0.001395426 0.001159969 0.000237292 0.000466883 0.000724995 0.000239902 0.000453243 0.000165602 0.000392048 0.00100008 0.000904601 0.000925121 0.000741359 0.001062698 PC(15:0_18:3)+CH3COO_3 0.002387386 0.002665778 0.003047432 0.002626807 0.00259104 0.002996911 0.001778696 0.003144193 0.002199047 0.0025375 0.002274406 0.002008782 0.003461584 0.003220531 0.003348016 0.002985362 0.004707649 0.003012739 PE(23:7_19:1COOH)-H 0.001879324 0.002252142 0.003377075 0.001835942 0.002426205 0.00200817 0.002602609 0.006475159 0.005600209 0.00441997 0.004846722 0.003887925 0.002979948 0.002508274 0.002567394 0.002630145 0.002820753 0.002760022 PE(18:1_10:2CHO)-H 0.001285306 0.000349676 0.001312036 0.001327997 0.001295528 0.000915934 0.000545482 0.000576893 0.000804309 0.000558851 0.000981133 0.000427987 0.001023159 0.001863288 0.001087285 0.001096579 0.002090329 0.001098487 PC(16:0_18:3)+CH3COO_2 0.004718676 0.005106733 0.005130434 0.004642778 0.004997271 0.005055152 0.001340211 0.002914135 0.002392381 0.001956288 0.00274027 0.001276231 0.004181742 0.003180138 0.003894933 0.002794466 0.003736632 0.002701573 PE(16:0_17:0)-H_2 0.002779444 0.002767218 0.003213476 0.003445029 0.003499281 0.003047074 0.001341781 0.001572309 0.001651984 0.001005435 0.001364449 0.001297495 0.00242006 0.001615814 0.00225587 0.003141463 0.002241569 0.001659295 PC(16:1_18:2)+CH3COO_2 0.030783996 0.001106203 0.030324445 0.028306856 0.028513001 0.029606254 0.011378644 0.001051218 0.019788812 0.000750579 0.000859995 0.000739479 0.001257148 0.036132153 0.037214414 0.026353213 0.032749317 0.033984665 LBPA(18:2_20:4)-H 0.000151903 0.000201058 5.27E-08 0.000109724 0.000113127 0.000103343 0.000559132 0.001505824 0.001009853 0.001009046 0.001241926 0.000893531 7.08E-05 4.85E-05 LPE(18:2)-H_1 0.03520681 0.013421533 0.025689188 0.032640835 0.025965868 0.026233866 0.015960188 0.017732186 0.02272089 0.018749939 0.022099751 0.016430655 0.026663662 0.025277866 0.026643141 0.02204898 0.026540287 0.020146647 Cer(t17:0_22:2)-H 0.001460473 0.00139475 0.001334619 0.001258494 0.001239402 0.001547297 4.83E-05 0.000388867 0.000326769 0.000229428 0.000370085 0.000129068 0.000512373 0.000781146 0.000659763 0.000428546 0.000408169 0.000425981 PC(8:1COOH_18:2)+CH3COO 0.000312419 0.000105993 0.001155654 0.00065379 0.000443548 0.000257166 0.001034649 0.000544272 0.001202381 0.001150456 0.001036962 0.000893418 0.001447989 0.001900401 0.001369676 0.001603709 0.001200375 0.001265138 PE(O-20:1_18:2)-H 0.004502386 0.00428055 0.004707052 0.003888354 0.004161634 0.00420916 0.000974304 0.002899772 0.002276115 0.002058798 0.002429737 0.001577306 0.003171552 0.003184179 0.003705373 0.00280964 0.002777864 0.002918713 PE(O-19:1_19:1)-H_1 0.006221874 0.006194487 0.00460535 0.00600797 0.007129233 0.006780538 0.011130702 0.008430437 0.008491041 0.006517351 0.007662606 0.006591254 0.00500852 0.004081865 0.005879348 0.007193017 0.00415836 0.005391353 PE(O-18:1_20:1)-H 0.025120863 0.0260766 0.024767299 0.023454733 0.027109958 0.026576286 0.00776915 0.014309411 0.013823066 0.008471999 0.013681519 0.008621104 0.014585392 0.015198764 0.017370963 0.017709762 0.015893422 0.014317191 LPC(17:0)+CH3COO_2 0.013346211 0.014326056 0.008487784 0.011802201 0.010973851 0.012959992 0.003543514 0.005570918 0.006053852 0.004156713 0.004612048 0.003825554 0.006147027 0.007563739 0.008936769 0.004933813 0.006771422 0.00737782 PC(5:0CHO_19:1)+CH3COO 0.002830683 0.000846661 0.003564068 0.002029582 0.002064618 0.002338658 0.011236377 0.005418943 0.00826896 0.006491734 0.009728422 0.008234171 0.006362666 0.00572841 0.003935722 0.005093899 0.005150021 0.003859849 PC(17:2_19:2COOH)+CH3COO 0.002307507 0.000486448 0.002276485 0.002563892 0.001946263 0.002241672 0.001530218 0.002029706 0.0024194 0.002381117 0.00230398 0.001864536 0.002624842 0.005310715 0.003592163 0.002466651 0.003493678 0.004322824 PC(19:1COOH_18:3)+HCOO 0.002686984 0.000456866 0.002982312 0.002430455 0.001984784 0.002260764 0.00103843 0.002497581 0.002327856 0.002380675 0.002621595 0.00111883 0.004074388 0.005373888 0.003574475 0.002747647 0.003193023 0.002966949 PE(23:7_18:0COOH)-H 0.002108711 0.002981845 0.003629444 0.002360236 0.003240707 0.002359195 0.003040331 0.005276777 0.004589533 0.004089405 0.004416529 0.004034589 0.002784081 0.003009686 0.002982003 0.003572989 0.003415539 0.003120984 PE(18:0_18:2COOH)-H 0.001041233 0.000485132 0.002737705 0.001069533 0.00074785 0.002125215 0.000903415 0.001360368 0.001100357 0.000862264 0.001123651 0.000933114 0.000846785 0.002263794 0.002995428 0.00205746 0.002043544 0.001980906 PC(14:0_20:5)-CH3 0.001217201 0.001036143 0.000827587 0.001307514 0.001116888 0.001362504 2.56E-10 3.63E-05 4.78E-08 0.000208563 0.000125345 0.000200936 0.00038646 0.000185984 0.000175639 LPC(P-15:2)+CH3COO_1 0.000719602 0.000218609 0.000412995 0.000858916 0.000859777 0.000606672 0.001099504 0.000614608 0.000912223 0.000584563 0.000754703 0.000582934 0.000567699 0.000361341 0.000488683 0.000512835 0.000385325 0.000382955 PC(16:0_19:1COOH)-CH3 0.003387971 0.002625465 0.004006563 0.003543849 0.003209514 0.002486818 0.000194234 0.00255659 0.001323389 0.000686261 0.001717212 0.000939132 0.002841224 0.002300096 0.00265389 0.001858958 0.002920043 0.002342041 LBPA(18:0_17:1)-H_1 0.001337734 0.001511324 0.001192917 0.001139267 0.001775432 0.002234929 0.001471879 0.00232186 0.002216792 0.001705507 0.00133222 0.001916436 0.001098245 0.000828591 0.000811714 0.001237225 0.0016798 0.001165917 PC(9:1COOH_19:1)+HCOO 0.000721392 9.82E-05 0.001332874 0.000880563 0.000472257 0.000202155 0.004109445 0.002108308 0.003767729 0.00322245 0.003098864 0.00285176 0.002316043 0.002277392 0.001896989 0.002146806 0.002474798 0.001171328 PE(18:1_22:3COOH)-H 0.003106891 0.004282942 0.005678 0.003799326 0.004646977 0.003407859 0.004542003 0.008833693 0.007819237 0.006858146 0.008050702 0.00684237 0.006020977 0.004626387 0.004915061 0.004685686 0.005035638 0.004912757 PE(15:1_18:3)-H 0.001817466 0.001382613 0.001320655 0.00290332 0.001416136 0.002994526 0.000234043 0.000998244 0.000450626 0.000486778 0.000793851 0.000348915 0.00100903 0.000887571 0.001294842 0.001989039 0.001521098 0.000843695 LPC(15:0)+CH3COO_2 0.015943457 0.000646147 0.01034965 0.015503229 0.000282456 0.016137467 0.0011025 0.000605613 0.000813674 0.000484873 0.001209167 0.000656558 0.0014876 0.0104736 0.011755056 0.000765898 0.010584771 0.009532027 PC(18:1_19:2COOH)-CH3 0.003206059 0.001851289 0.00283452 0.002780854 0.002721937 0.002453586 0.001227026 0.001582592 0.001199482 0.001454101 0.001930192 0.001021099 0.002303781 0.002373823 0.002752358 0.001207098 0.002553161 0.002275103 PC(17:0_20:1)+CH3COO 0.004509973 0.006883667 0.004111892 0.006319599 0.004309063 0.006375211 0.000524125 0.002381271 0.002015679 0.001761181 0.002048982 0.001169228 0.004501408 0.003357498 0.002840729 0.002561541 0.002399207 0.002595953 PC(8:1COOH_19:1)+CH3COO 0.00072193 0.000100042 0.001108259 0.000880391 0.000458641 0.000478356 0.004107387 0.001713224 0.003998184 0.003103204 0.003919357 0.002850368 0.002065918 0.002080418 0.001848043 0.001993929 0.002417117 0.001057287 PC(17:0_18:2)+CH3COO_2 0.036834779 0.037294251 0.047935413 0.044192485 0.033490557 0.053378169 0.012597055 0.026353935 0.02213793 0.024325304 0.02818875 0.014497436 0.03706361 0.051109695 0.035790146 0.025418054 0.031194427 0.032848001 PC(15:0_17:1)+CH3COO_2 0.001064528 0.001273246 0.001455555 0.001430759 0.001101421 0.001353055 0.001709382 0.000953935 0.0011173 0.000856832 0.001010484 0.000869713 0.002555814 0.001398433 0.002200176 0.001514849 0.001855123 0.001467149 PC(17:1_18:1CHO)+CH3COO_1 0.001227517 0.001147538 0.001117822 0.001206265 0.00122257 0.001328903 0.001257573 0.000894262 0.001082633 0.001012548 0.001305117 0.001090503 0.001544624 0.001388541 0.001301848 0.001461428 0.001206743 0.001287217 PE(O-18:1_17:0)-H 0.020113025 0.021949831 0.017406406 0.017469679 0.021878646 0.021084296 0.004339355 0.009347562 0.01094251 0.005997554 0.00838308 0.005242887 0.009269277 0.010508194 0.012610793 0.011834761 0.011328901 0.010883443 PE(22:0_18:1)-H 0.019010312 0.018453817 0.018323936 0.019157174 0.020738993 0.019567968 0.007097611 0.013239927 0.011742249 0.009381115 0.0126628 0.008262145 0.013745032 0.013737516 0.014852711 0.018585946 0.015288741 0.012202868 LPC(19:0)+CH3COO_1 0.000558029 0.000648671 0.000361239 0.000698292 0.000505391 0.000543947 8.14E-05 0.000226524 0.000278771 0.000126029 0.000131797 0.000141914 0.000242304 0.000309814 0.000301235 0.000325358 0.00026915 0.000209504 PC(18:0_18:3)+CH3COO_2 0.005406211 0.005328796 0.005758185 0.004613057 0.00485369 0.004965994 0.001713515 0.003777731 0.003659348 0.001991943 0.003005951 0.002852875 0.00433963 0.003969453 0.004182936 0.00350173 0.0043313 0.003782063 PE(15:0_18:1)-H_1 0.00526383 0.005863542 0.004417478 0.020752203 0.003213322 0.019437968 0.00635678 0.005812961 0.008208786 0.003375345 0.005590048 0.003948146 0.003491176 0.002991265 0.002959492 0.003159571 0.004042448 0.002342479 PC(20:5_20:5)-CH3_2 0.000212476 0.000311074 0.000172327 0.000730575 0.000364934 0.000395981 6.64E-08 0.000129765 0.000157177 5.66E-05 0.000170701 1.28E-08 0.000307963 0.000294634 0.000225306 0.000321484 6.53E-05 0.000433706 PE(16:0_17:0)-H_3 0.002151984 0.002853059 0.001201743 0.00227901 0.002601102 0.002389641 0.00029298 0.000951532 0.001894329 0.000881885 0.001926263 0.0008044 0.0002666 0.00022007 0.000273762 0.000307992 0.000298063 0.000295535 PC(19:1_20:5)-CH3_4 0.001898952 0.000877767 0.001443703 0.002110768 0.001637933 0.001893839 4.86E-09 0.000249409 0.000291751 0.000195277 0.000278129 0.000218835 0.000362397 0.000478589 0.000464629 0.000296099 0.000286012 0.000393247 PE(O-17:1_17:1)-H 0.00557865 0.005300076 0.006010393 0.006595006 0.006518613 0.006059669 0.004057802 0.004803912 0.00371347 0.002637881 0.003264245 0.003322053 0.004786326 0.004273329 0.004668437 0.00639934 0.005606876 0.004560862 PE(15:0_16:0)-H_2 0.000979697 0.001306482 0.000467475 0.001186657 0.001127846 0.001258664 9.47E-08 0.000374509 0.00077075 0.000233989 0.000528255 0.000310825 3.73E-09 2.39E-05 4.19E-05 4.68E-05 5.19E-05 2.09E-05 PC(17:1_19:1COOH)+HCOO_2 0.000968724 0.000251313 0.00129218 0.000892926 0.00095458 0.000827513 0.001170978 0.001212205 0.001387624 0.001494473 0.001824055 0.001437323 0.003633963 0.002060948 0.002208213 0.002230562 0.002515964 0.001553549 PC(17:0_18:1)-CH3_2 0.008971669 0.003851322 0.005645311 0.00845465 0.007514076 0.006365991 0.016420036 0.011986404 0.008263433 0.013566686 0.021169813 0.01241301 0.009287932 0.008979 0.009545531 0.00433781 0.008196746 0.005529597 PC(18:1_9:2CHO)+CH3COO_1 0.002456095 0.000717769 0.003127952 0.002919156 0.00211115 0.002133209 0.002362744 0.002577204 0.003211724 0.002235524 0.003390328 0.002009675 0.004502315 0.004725335 0.004070155 0.00234443 0.005190398 0.003715209 PE(O-16:1_18:1)-H 0.008183859 0.007011383 0.007592853 0.007739994 0.007419616 0.007531911 0.002421752 0.005048527 0.004435922 0.004009418 0.004067537 0.003474558 0.005258893 0.005258446 0.00401549 0.006084882 0.006986396 0.006405901 PI(18:2_20:5)-H 0.000678781 0.000600314 0.00073946 0.00069207 0.000624639 0.000581321 9.23E-05 0.000343737 0.000255331 4.43E-05 0.000301943 9.39E-05 0.000272355 0.000301169 0.000497657 0.000480344 0.000453885 0.000344875 LPE(14:0)-H 0.003706446 0.003062153 0.003066853 0.003428985 0.003239732 0.003353413 0.000579741 0.001123402 0.000998398 0.000585358 0.001231033 0.000981081 0.001379492 0.001172528 0.002047009 0.002809356 0.002179136 0.001252485 PC(17:1_17:1)-CH3_1 0.003085502 0.003069764 0.002927468 0.003020909 0.003236053 0.003091988 0.001149361 0.001110155 0.000928212 0.000605819 0.000951779 0.000753858 0.001263799 0.001100956 0.001488263 0.001510274 0.00130225 0.001017589 PE(19:0_18:2)-H 0.009862829 0.014190434 0.007969783 0.183172221 0.016839083 0.178329648 0.001616407 0.002467068 0.137344651 0.113416838 0.002842711 0.114904623 0.141669054 0.127858172 0.156911187 0.201119602 0.151363876 0.132418035 PE(19:1_20:3)-H_2 0.015968255 0.016382862 0.013230647 0.015842497 0.016824554 0.016952296 0.006521835 0.010372497 0.008953188 0.00650432 0.010743164 0.006271455 0.010302156 0.010278854 0.01221955 0.016541882 0.012808157 0.010928573 PC(8:0CHO_18:1)+CH3COO 0.00119922 0.00021692 0.001811023 0.000802129 0.000623937 0.000597431 0.003563306 0.001784031 0.003532493 0.003032575 0.004131664 0.003109387 0.002787825 0.00220025 0.001963912 0.002009766 0.001988043 0.00157935 PE(19:1_20:4)-H_1 0.001701603 0.002149574 0.001823924 0.002034505 0.002146011 0.00231404 0.000341604 0.000549104 0.000541354 0.000283829 0.000612062 0.000404044 0.000575048 0.000841943 0.000887612 0.001031184 0.000607981 0.000554456 PC(18:1_19:1)+CH3COO_1 0.216457241 0.201581158 0.18964871 0.200924458 0.192036408 0.212647433 0.136964107 0.185356835 0.172294599 0.158462134 0.178074635 0.134757711 0.186160108 0.206527299 0.191300593 0.179809897 0.184142908 0.19140326 PE(15:0_21:0)-H 0.002189584 0.002265757 0.002146122 0.00268618 0.002695938 0.00266383 0.000766521 0.001221355 0.001422233 0.00091352 0.000991904 0.000870271 0.001453162 0.001260501 0.001338608 0.001867365 0.00159416 0.001229649 PC(18:1_20:1COOH)-CH3 0.001505538 0.000854919 0.001461673 0.001100815 0.001300642 0.001014468 0.002600478 0.002133974 0.001689161 0.001756978 0.002586377 0.001588667 0.00160515 0.001421048 0.001664061 0.000969607 0.001449362 0.00142798 PC(15:0_16:2)+CH3COO 0.005383887 0.003591738 0.003897634 0.00492533 0.004229831 0.00436728 0.001114464 0.001748674 0.001988228 0.001638463 0.002139763 0.00145892 0.005532222 0.00322736 0.004439756 0.0009034 0.004229942 0.003668871 PC(20:2_20:4)+CH3COO_2 0.002552233 0.003471221 0.003277673 0.000499122 0.001814932 0.000503873 0.000357543 0.000676619 0.000320139 0.00061413 0.000650907 0.000888802 0.000959529 0.001208457 0.000916112 0.002521955 0.001618262 0.001083862 PE(17:2_18:2)-H 0.000915052 0.001475191 0.000828223 0.001199677 0.002134336 0.00116747 0.000122859 0.00036191 0.000588635 0.000290369 0.000118069 0.000181003 0.000523259 0.000429442 0.000560456 0.000611047 0.000579682 0.000417759 PC(17:1_18:1)-CH3_1 0.001341586 0.001341938 0.003311092 0.002356461 0.00151051 0.001339785 0.000193761 0.000694287 0.000300402 0.000469165 0.000414947 0.000290917 0.000846855 0.000619477 0.000636121 0.000862734 0.000540347 0.000543592 PE(24:0_18:1)-H 0.00268687 0.002570593 0.002602314 0.002301304 0.003217903 0.002867937 0.000698751 0.001209051 0.00087413 0.000887172 0.001142502 0.000658877 0.001021543 0.00157012 0.001411378 0.002204046 0.00141465 0.001237799 Cer(d17:1_16:0)-H 0.000889993 0.000754347 0.000700578 0.000830701 0.000747389 0.000776024 0.00016989 0.000362973 0.000302442 0.000252333 0.000414796 0.000106961 0.000434804 0.000490295 0.000534424 0.000300067 0.000457047 0.000425297 PC(18:1_18:1)-CH3_2 0.007631781 0.005944749 0.004940928 0.005699962 0.006541863 0.006825113 0.005297617 0.004042069 0.002360492 0.004299327 0.005669973 0.003893052 0.002892386 0.00274866 0.003329233 0.001662579 0.003135707 0.001873774 PE(18:1_18:1)-H_1 0.004294952 0.001596041 0.004137065 0.004593686 0.004280389 0.003313045 0.004893289 0.003999712 0.005945919 0.005080211 0.006496286 0.004904525 0.00489208 0.00364114 0.004011316 0.004132551 0.003763634 0.003001497 PE(18:1_18:1)-H_2 0.22841251 0.251475349 0.249620682 0.227367275 0.278310724 0.225848612 0.051191286 0.140127503 0.149418856 0.106327932 0.163006122 0.10731907 0.169412846 0.157169895 0.192923727 0.187213981 0.171352061 0.155027299 LPE(15:0)-H 0.007604201 0.006396769 0.005737346 0.008072154 0.008469649 0.006897179 0.000972332 0.003033895 0.002286177 0.00193233 0.003267435 0.002420647 0.004004298 0.002683935 0.004851075 0.004309216 0.003780442 0.002828678 PC(19:1_10:2CHO)+CH3COO_1 0.001163237 0.000307076 0.001292211 0.000935358 0.000914696 0.000864094 0.000931209 0.00069089 0.001227825 0.000928033 0.001120829 0.001064274 0.001293394 0.001202712 0.00126033 0.001496233 0.001438077 0.001049264 PC(17:2_20:5)+CH3COO_3 0.002378004 0.0248379 0.002769932 0.001665969 0.001498701 0.003310804 0.002403639 0.010724656 0.009118607 0.001728119 0.000555983 0.005920254 0.001857835 0.014703641 0.015951531 0.016288877 0.017650504 0.015628583 PE(15:0_18:1)-H_2 0.037558822 0.034772326 0.032874747 0.036141477 0.043414761 0.038443174 0.005763341 0.016129031 0.01900287 0.012151552 0.018172971 0.01215344 0.018907426 0.017386137 0.022745342 0.025751425 0.022695136 0.018233213 PC(4:0CHO_18:1)+CH3COO 0.000920709 0.000212938 0.001415554 0.001188769 0.001152474 0.000670342 0.002602196 0.001536998 0.001984702 0.00199665 0.00287148 0.001797753 0.001529742 0.001772828 0.001451224 0.001038197 0.00170238 0.001076585 LPE(15:1)-H 0.001102667 0.001045531 0.000754699 0.001312682 0.001379216 0.001495792 0.000508509 0.000811549 0.000767489 0.000505972 0.000829325 0.000548315 0.00081946 0.000785736 0.001386846 0.001120516 0.001106784 0.000803274 PE(17:0_17:1)-H_2 0.165709246 0.152216357 0.153318249 0.162744807 0.180130384 0.163906776 0.064540253 0.109333832 0.106736661 0.080732755 0.104706636 0.077672887 0.113131252 0.100242828 0.124419539 0.145390761 0.132997089 0.107212356 PC(20:5_20:5)-CH3_3 0.000344527 0.000311074 0.000173031 0.000678636 0.00017173 0.00024875 4.91E-09 0.000129236 8.84E-05 5.56E-05 0.00016846 1.28E-08 0.000306009 0.000294714 0.000224873 0.000151891 6.54E-05 0.000203468 PC(19:1_10:2CHO)+CH3COO_2 0.000854071 0.000149383 0.000851582 0.001305523 0.000616213 0.000682511 0.000467005 0.000565124 0.000782319 0.000721087 0.000734775 0.000484953 0.00153585 0.000934945 0.000721654 0.001000337 0.001021098 0.000793092 PE(18:1_18:1COOH)-H_2 0.002079186 0.000515141 0.002736914 0.002030264 0.002759158 0.002042702 0.001320013 0.001525896 0.000929769 0.001731841 0.002107201 0.000756863 0.001749778 0.002302071 0.00237212 0.002137404 0.002199641 0.001694993 PE(14:0_17:1)-H_1 0.012000009 0.010810293 0.011838639 0.012685665 0.013452463 0.01195968 0.00365807 0.007601761 0.006962136 0.005129504 0.007314364 0.005789231 0.008519733 0.006817418 0.009539307 0.012143579 0.010567555 0.006989695 PC(7:1CHO_18:1)+CH3COO_1 0.000555692 0.000186595 0.001557545 0.000797783 0.000471607 0.000566244 0.002436808 0.001939999 0.003900381 0.00181289 0.003044998 0.002043 0.002023719 0.001351197 0.001994132 0.000973585 0.000759817 0.001330793 PE(O-19:0_20:5)-H_2 0.002361733 0.002150426 0.001601578 0.002670582 0.003059297 0.002227404 0.00099947 0.001904151 0.001530435 0.001128752 0.002136807 0.000983766 0.002041533 0.001959816 0.002188715 0.002514194 0.001889022 0.001923677 PC(17:1_18:1)-CH3_2 0.021969917 0.016501745 0.015060369 0.017442501 0.017363366 0.019218283 0.005916588 0.000724181 0.004090189 0.005956915 0.00740326 0.00471998 0.007680573 0.007536185 0.009682824 0.007755872 0.007063157 0.006748774 PE(16:0_18:0)-H 0.00371839 0.003791618 0.004055918 0.003797028 0.004227703 0.004041701 0.002200454 0.002428033 0.002587078 0.002194298 0.002763729 0.001934578 0.003079315 0.00244348 0.003568018 0.004324187 0.003539414 0.00253263 PE(O-18:2_18:1)-H_1 0.03630043 0.037482054 0.035413031 0.032621979 0.043135608 0.034316498 0.008103143 0.031532549 0.024971416 0.019860861 0.030115347 0.016996928 0.031483344 0.029844033 0.037636373 0.034068996 0.031736755 0.031030026 PC(17:1_17:1)+CH3COO_2 0.002293093 0.001116915 0.002130119 0.001704519 0.001731072 0.001677307 0.003701202 0.002982661 0.002273092 0.002524587 0.003715306 0.002249171 0.002027212 0.002082907 0.002415415 0.001433162 0.002279695 0.00201499 PC(17:1_19:1COOH)-CH3_1 0.002527081 0.001502746 0.002336488 0.002238019 0.002266211 0.002210433 0.003971044 0.003209113 0.002408195 0.002897973 0.004350776 0.002210157 0.002182538 0.002065297 0.002481417 0.001926983 0.002302505 0.002077519 PC(18:1_20:5)-CH3_1 0.001538392 0.000875244 0.001148445 0.001383159 0.001267042 0.000486344 4.18E-09 0.000371112 0.000216213 0.000242444 0.000331803 4.77E-05 0.000310137 0.000575809 0.000722553 0.00037989 0.000294978 0.00046177 PC(17:0_20:1COOH)-CH3 0.002197867 0.001049393 0.002043329 0.001652177 0.001651974 0.001564296 0.00364688 0.003006224 0.002317991 0.002500584 0.003707425 0.002266793 0.002046207 0.002108635 0.002566139 0.001449332 0.002219711 0.001976505 PE(17:0_18:0)-H 0.013454056 0.013255013 0.013429655 0.013879244 0.01571614 0.015109556 0.003928528 0.006579839 0.007163071 0.004929485 0.007485033 0.004891455 0.006994359 0.00671471 0.009401643 0.011400642 0.008547361 0.007465594 PE(O-19:1_18:1)-H_1 0.077898751 0.092757488 0.09973756 0.086678909 0.109312143 0.096866631 0.037289968 0.059814771 0.06013495 0.038362845 0.03810044 0.039110777 0.063136477 0.056871773 0.054711002 0.062926564 0.068645281 0.053024334 PE(O-18:1_16:0)-H 0.002545493 0.002560023 0.002708664 0.0031834 0.003606681 0.002859795 0.001835722 0.002255132 0.00197073 0.001487877 0.002373331 0.001412633 0.002204108 0.002076332 0.002697371 0.002608089 0.002672233 0.002282081 PE(19:1_20:3)-H_3 0.000703415 0.000991259 0.001023181 0.00121604 0.000890348 0.001017118 0.000105154 0.000434659 0.000499174 0.000272121 0.000338689 0.0003267 0.000708233 0.000610691 0.000400695 0.000696518 0.000560669 0.000358883 PC(17:1_20:4)+CH3COO_3 0.00633207 0.007277123 0.010898631 0.007814336 0.008855119 0.007428862 0.002941331 0.004186167 0.006165091 0.002349653 0.002882217 0.003210943 0.006021833 0.004716018 0.00476516 0.005847904 0.005903868 0.004786329 PC(8:0CHO_19:1)+CH3COO 0.000758643 7.97E-05 0.000670174 0.000519361 0.000443196 0.000505553 0.002078276 0.000989061 0.001642048 0.00147172 0.002003691 0.001820166 0.001317226 0.001482268 0.000969846 0.001102097 0.001105256 0.001016156 LPC(19:1)+CH3COO 0.030928914 0.026898783 0.019152244 0.026908282 0.024797629 0.030883009 0.015325327 0.021331257 0.015120446 0.013502921 0.019575645 0.0140875 0.018602926 0.019793836 0.022320773 0.021376237 0.02150456 0.019068252 PE(O-18:1_17:1)-H_2 0.0710725 0.07130605 0.064797136 0.06723451 0.081205834 0.073453777 0.05522256 0.064161377 0.054594496 0.044710722 0.058199374 0.04293986 0.059257176 0.058590346 0.07218087 0.081784167 0.067960993 0.061409689 PE(4:1CHO_20:5)-H 0.001213579 0.000952119 0.001360703 0.00146656 0.001232926 0.001307338 0.000298766 0.000849172 0.000868289 0.000491141 0.000851967 0.000465545 0.000915788 0.000918974 0.00128992 0.000814143 0.001183682 0.000829712 PC(18:1_13:2CHO)+HCOO 0.000828743 0.000136068 0.001167487 0.001140674 0.001062985 0.000689413 0.000999117 0.001023551 0.001168461 0.001062476 0.00123902 0.000842897 0.001032137 0.001621808 0.001517331 0.001736316 0.001879324 0.001071359 PE(14:0_17:1)-H_2 0.001141249 0.002029315 0.001668958 0.001399672 0.001004131 0.001324627 0.00078737 0.000508938 0.000527044 0.000360452 0.000508455 0.000716512 0.00103687 0.000619831 0.000627471 0.000838997 0.001096565 0.000881038 PG(18:3_20:5)-H 0.000477604 0.000489981 0.000313765 0.000390522 0.000487725 0.000457782 0.001831968 0.004971688 0.003604734 0.001903308 0.003626372 0.001995275 4.94E-05 2.83E-05 PC(17:1_18:1)+CH3COO_4 0.00067274 0.000474581 0.000637946 0.00049113 0.000611597 0.000529592 0.001289295 0.000946648 0.000863159 0.000640947 0.00084952 0.000865159 0.000695055 0.000660116 0.000745817 0.000505595 0.000754125 0.000430583 PC(15:0_16:1)+CH3COO_2 0.000913814 0.002116858 0.000697432 0.001039251 0.001066228 0.000705229 0.001519763 0.000783848 0.000788933 0.00082497 0.001065729 0.001459279 0.001518673 0.001367101 0.001299218 0.001732596 0.001710728 0.00137004 PE(18:1_18:4)-H_1 0.006426143 0.006389167 0.006654196 0.006555424 0.007519289 0.006486833 0.000997176 0.004485963 0.003612754 0.002617369 0.003488861 0.002078901 0.003964022 0.00396958 0.004927254 0.004573739 0.004582209 0.003908579 PC(18:1_20:4)-CH3_3 0.000533167 0.000467125 0.0003467 0.00062052 0.000379583 0.000725605 2.60E-09 0.000125416 7.59E-05 7.89E-05 8.30E-05 3.39E-05 9.14E-05 0.000320373 0.000299493 0.000139309 8.29E-05 0.000190314 PG(17:0_18:1)-H 0.001636185 0.001402028 0.001751913 0.002101291 0.002035093 0.001938791 0.001390472 0.001828313 0.001721102 0.001280569 0.001460133 0.001490431 0.001319962 0.00105005 0.001162755 0.001419719 0.00141256 0.000936608 PC(17:0_20:5)+CH3COO_3 0.022875044 0.023948205 0.021593694 0.022422894 0.020705435 0.022691908 0.023467158 0.012634265 0.005619368 0.006980286 0.010664219 0.00639998 0.019544045 0.02106628 0.020711526 0.019056284 0.016813552 0.014803832 PC(17:1_20:5)-CH3_3 0.001100138 0.001187306 0.000534764 0.001146891 0.000876776 0.001460171 5.55E-05 0.00019232 9.51E-05 6.50E-05 8.60E-05 9.45E-05 0.000227226 0.00021425 0.000228252 0.000318764 0.00016307 PC(16:0_17:1)+CH3COO_1 0.013163376 0.013170407 0.012595724 0.013625208 0.011878809 0.014184176 0.01890158 0.010826787 0.010608235 0.007681128 0.009574551 0.007648511 0.014720789 0.01535703 0.015288038 0.015939358 0.015842205 0.015213473 PC(15:0_17:1)+CH3COO_3 0.004881615 0.005594551 0.005012339 0.006009269 0.006417806 0.005263303 0.003136869 0.003045441 0.003509664 0.002642211 0.002552442 0.00359792 0.005018869 0.003768388 0.003411819 0.00358646 0.003837796 0.00355488 PC(19:1_19:4)+CH3COO_1 0.003056089 0.003378465 0.004161965 0.006175807 0.004036289 0.00268939 0.00044019 0.003309201 0.001245553 0.000506764 0.00130393 0.001431412 0.002227157 0.002289384 0.002686682 0.003050053 0.003223696 0.002059347 PE(16:0_17:1)-H_1 0.042271316 0.041937147 0.042776051 0.04527056 0.053264491 0.048413464 0.027304949 0.038938902 0.034261137 0.027783769 0.039372805 0.02977163 0.040047273 0.03283379 0.046727365 0.053105283 0.044615471 0.037642382 LPE(18:2)-H_2 0.008768071 0.005659257 0.006292063 0.007767876 0.009792797 0.007272372 0.00325197 0.005527793 0.005345626 0.004010038 0.004669144 0.00455789 0.005613563 0.005274741 0.006483692 0.005484364 0.006391474 0.004867672 PE(O-18:1_18:2)-H_2 0.284735285 0.28589558 0.004635919 0.000352737 0.000431143 0.000508005 0.0003076 0.00034239 0.001375743 0.097265228 0.001663291 0.001801887 0.003026564 0.002481701 0.219424455 0.18947679 0.200267165 0.182505588 PE(18:1_18:3)-H_2 0.010547297 0.010771891 0.01194353 0.010867558 0.01226293 0.011461358 0.00161076 0.006115962 0.005808488 0.004187215 0.005317154 0.003524225 0.006489951 0.005892691 0.007145011 0.006451281 0.006467971 0.005490546 PE(17:2_2:0)-H 0.003768452 0.001359068 0.002645707 0.003540036 0.00297451 0.003386646 0.0013905 0.001473612 0.002368083 0.001629446 0.00187249 0.001328695 0.002526942 0.002373223 0.002214228 0.001854829 0.002253693 0.001865576 PE(O-18:0_20:4)-H_2 0.017396756 0.017291887 0.014530905 0.017032287 0.01863066 0.017508975 0.005842868 0.010178844 0.0090232 0.005825165 0.010829653 0.005091432 0.009332279 0.010227338 0.012665153 0.013560502 0.010972733 0.009417582 PE(24:2_18:1)-H 0.000347737 0.000550256 0.000541323 0.000345598 0.000393518 0.000482732 0.000368597 0.000679053 0.000588431 0.00049028 0.000523683 0.000450139 0.000898064 0.000720406 0.000885641 0.000480309 0.000566622 0.000927296 LPE(20:3)-H_2 0.002430208 0.001642337 0.001650279 0.002107997 0.002556139 0.002091802 0.000669749 0.001552018 0.001578925 0.00108742 0.00151549 0.001018429 0.001783529 0.001486034 0.001949651 0.002338102 0.002351439 0.001216925 PE(20:1_20:4)-H 0.001726158 0.00202029 0.0020923 0.00185652 0.002216705 0.001902932 0.00018446 0.000762013 0.000748039 0.000535061 0.000868863 0.000416914 0.000768733 0.000805838 0.001030317 0.001129463 0.000832218 0.000803147 LBPA(16:0_17:1)-H 0.001089308 0.001284342 0.000860518 0.001428349 0.001507626 0.003354925 0.000893283 0.001501939 0.001092338 0.001195007 0.001624992 0.001167211 0.002071442 0.001668627 0.002074151 0.001207074 0.001496875 0.001651314 PE(17:1_18:2)-H 0.032794169 0.029283948 0.028643593 0.031955228 0.033611116 0.030861942 0.007305024 0.021105755 0.017890365 0.014861863 0.017809795 0.012214769 0.020039231 0.019467513 0.021104934 0.022669911 0.02298968 0.017821085 PC(18:1CHO_20:5)+CH3COO_4 0.000605886 0.00010307 0.001009324 0.000473826 0.000634768 0.000465596 5.22E-05 0.00049385 0.000274141 7.89E-05 0.000189489 0.000167498 0.000265604 0.000534269 0.000373079 0.000291783 0.000552093 0.00050966 PE(20:0_20:2)-H 0.001493667 0.00162088 0.001379477 0.001295794 0.001551041 0.001347988 0.000661002 0.000819918 0.000954152 0.000478368 0.000807363 0.000576249 0.000653037 0.00095357 0.001213061 0.00119806 0.001233428 0.000864946 PE(22:2COOH_20:5)-H 0.003221861 0.004223532 0.005406346 0.003620911 0.004920435 0.003707103 0.005141881 0.007752289 0.006858404 0.005861206 0.006802101 0.005439626 0.005641996 0.005176752 0.005358603 0.005395892 0.003681095 0.005079286 PC(18:1_19:1)+CH3COO_2 0.004890491 0.005091134 0.005129093 0.006967946 0.00659995 0.00685951 0.007087885 0.006053853 0.004713851 0.003784483 0.004233653 0.004554099 0.009227213 0.007937914 0.00577489 0.005514287 0.006693743 0.006804285 PE(16:0_16:2)-H 0.002794633 0.00247979 0.002584932 0.002772312 0.003405208 0.003063961 0.000806393 0.002011235 0.001627937 0.001306956 0.001673146 0.001176153 0.002267259 0.001304781 0.002618904 0.002819024 0.001930896 0.001924881 PC(15:0_18:1)+CH3COO 0.004007334 0.007989641 0.005405472 0.009006096 0.008823511 0.007278907 0.00339596 0.005494709 0.004219753 0.002826691 0.004963408 0.003267732 0.007387554 0.004963797 0.004984383 0.004221555 0.006290936 0.005796169 PE(19:1_20:5)-H_2 0.027659932 0.029691331 0.023355185 0.025097683 0.031291125 0.02837077 0.00852532 0.019784696 0.015897969 0.010661361 0.013124071 0.010122262 0.015125789 0.015917545 0.020076448 0.020033355 0.020655784 0.016299687 PG(18:0_18:1)-H 0.078274248 0.061279805 0.068401346 0.079723232 0.087637608 0.082103732 0.033728127 0.044228734 0.042704674 0.037338949 0.049008582 0.032796054 0.044622705 0.045470852 0.054439834 0.065413294 0.053056393 0.042429621 PE(22:2COOH_20:3)-H 0.001139569 0.00184612 0.001828174 0.001395076 0.001659364 0.001349214 0.001484046 0.001739077 0.001535029 0.00142123 0.001911169 0.001314827 0.001762579 0.001696545 0.002022209 0.001945614 0.001883138 0.001686194 PE(18:0_18:3)-H_2 0.008015174 0.007878449 0.008592761 0.00793385 0.009357899 0.007831379 0.00165733 0.005136009 0.00481624 0.003276508 0.004897003 0.003162007 0.004642722 0.005088388 0.006100072 0.00624888 0.005862394 0.004533896 PE(17:0_20:0)-H 0.002934062 0.003018307 0.002756459 0.002900754 0.00330253 0.002804561 0.000725435 0.001689161 0.001676957 0.0012279 0.001636103 0.001046273 0.001649171 0.001688017 0.001970305 0.002500103 0.001896025 0.00152751 PC(18:1_19:1)+CH3COO_3 0.025885997 0.019341222 0.043090284 0.028446699 0.02511751 0.015185486 0.012128031 0.022799988 0.017212637 0.008900957 0.010523213 0.012409581 0.033225556 0.04252152 0.029330183 0.019958657 0.015408971 0.015816943 OAHFA(2:0_23:0)-H 0.006316419 0.007309483 0.00461334 0.005739075 0.004836297 0.00609531 0.001357459 0.002941518 0.001529025 0.001477687 0.001602072 0.001397079 0.002134633 0.002216795 0.00295825 0.002802722 0.002398609 0.002059194 LBPA(17:0_18:1)-H_2 0.001679165 0.001419131 0.001586127 0.002103715 0.002042617 0.001939574 0.001412007 0.001851037 0.001825086 0.001222248 0.001509243 0.001460236 0.001317778 0.001052129 0.00108037 0.001484775 0.001427983 0.00093663 PC(6:0COOH_19:1)-CH3 0.000443481 0.000247979 0.000938816 0.000950529 0.000642587 0.00050493 0.003664853 0.001177074 0.00291265 0.002416008 0.002951048 0.002694703 0.002175769 0.001854099 0.001275107 0.001973986 0.00166604 0.001621162 PC(18:3_20:5)+HCOO_2 0.00155503 0.000953462 0.000784417 0.000483043 0.001050303 0.000997896 6.50E-05 0.000643271 0.000229133 0.000103496 0.000277279 0.000272824 0.000352872 0.00105077 0.000524597 0.001374117 0.000350232 0.001941719 PE(O-18:0_16:0)-H 0.002576328 0.002899701 0.002966227 0.003443441 0.003722828 0.003121416 0.002018822 0.002610515 0.004814178 0.002290135 0.003392927 0.002199035 0.001860051 0.001959277 0.001429552 0.002099934 0.001991104 0.001486218 PE(19:0_18:1)-H_2 0.024127317 0.005536366 0.02410419 0.00732662 0.006184779 0.026288865 0.011875498 0.015048829 0.015494078 0.009991294 0.012850606 0.012960466 0.017459036 0.014107465 0.015926617 0.019773956 0.017560665 0.012729163 PC(7:1CHO_19:1)+CH3COO 0.00023172 3.72E-05 0.000439419 0.000444605 0.00045226 0.000249106 0.001852508 0.001031079 0.001633639 0.001293218 0.002704958 0.001407072 0.001682783 0.000964007 0.000755225 0.000787255 0.000896742 0.000789052 PC(17:1_17:1)-CH3_2 0.001168678 0.000678308 0.000599088 0.000969964 0.001009405 0.001158686 0.002644113 0.00167072 0.000953327 0.00181108 0.002124473 0.001470155 0.000820111 0.001319405 0.001606672 0.000516072 0.00146789 0.000542061 PC(16:0_17:1)-CH3 0.102400609 0.089767049 0.092856914 0.104320622 0.111530603 0.103900297 0.058881502 0.075895762 0.070529958 0.05690388 0.077731287 0.056226079 0.075581665 0.066662379 0.087841829 0.105355712 0.086529624 0.073289076 PE(26:0_18:1)-H 0.003609937 0.00308839 0.002730592 0.003370318 0.003734361 0.00345797 0.001494594 0.002090155 0.00186792 0.001361451 0.002156814 0.001542773 0.001867342 0.002100178 0.0028032 0.003120959 0.002732906 0.00173491 PE(18:0_17:1)-H 0.101501819 0.098000551 0.09402256 0.10296471 0.109758405 0.09983352 0.05898672 0.073555661 0.070047146 0.056823702 0.07867839 0.054754288 0.074897205 0.067905093 0.086026404 0.108411311 0.087479449 0.071957115 PC(17:1_20:5)+CH3COO_4 0.038715552 0.045682703 0.020865799 0.049542079 0.036524254 0.048112079 0.001174243 0.024438752 0.002153342 0.001491179 0.010979343 0.001692987 0.036222285 0.004266138 0.028495885 0.026985138 0.008657108 0.029905119 PC(19:0COOH_17:1)-H 0.002227387 0.001052291 0.002052943 0.001629337 0.001774716 0.001571184 0.003748284 0.003090176 0.001807876 0.002616967 0.003605954 0.002342921 0.002066767 0.002060316 0.002501103 0.001456075 0.002308187 0.001990475 PC(17:1_19:1)+CH3COO_3 0.001510453 0.00113107 0.001729524 0.001516679 0.001255974 0.000908452 0.000591916 0.001166041 0.001250871 0.000908364 0.001322259 0.000909707 0.001972847 0.001787283 0.00117411 0.000898388 0.001877887 0.001398274 PE(18:0CHO_18:1)-H_1 0.001832032 0.000318654 0.001286138 0.001699045 0.001414814 0.001250456 0.000845144 0.000665509 0.000985508 0.001451722 0.000874971 0.000680445 0.001533093 0.001584738 0.001271704 0.001258871 0.001312449 0.000828666 PC(13:0CHO_20:5)+CH3COO 0.000238102 0.000683243 0.000121493 0.000169437 4.87E-05 0.000109497 7.67E-05 0.000303688 1.30E-06 0.000194573 0.000209322 0.000112693 0.000405449 0.000138115 0.000213485 0.000350834 0.000373769 0.000277113 PE(17:0_17:1)-H_3 0.028170356 0.028682069 0.03157791 0.034400927 0.038557483 0.033292411 0.019785108 0.022154616 0.023268182 0.016333101 0.019721776 0.01972673 0.026779146 0.019000165 0.024604502 0.033444668 0.029514528 0.021208625 PI(18:0_20:5)-H_1 0.038653148 0.043578899 0.049488505 0.03909271 0.055257871 0.043692739 0.04875203 0.073315506 0.065194401 0.054819017 0.075080246 0.056201638 0.041743601 0.043199298 0.046220672 0.064749419 0.053704314 0.044437075 LPE(16:0)-H_1 0.002909818 0.002612208 0.001611661 0.002519255 0.001467513 0.001910361 0.000826732 0.001056907 0.001336507 0.001008654 0.002094092 0.00079037 0.001681533 0.00161128 0.002300153 0.002073793 0.002397898 0.001036338 PC(18:1_18:1CHO)+CH3COO_1 0.001013412 0.000896488 0.001376396 0.001198211 0.000965821 0.001030129 0.000962939 0.00078434 0.001110577 0.001061124 0.001240677 0.00097121 0.001480033 0.001361701 0.001293468 0.000989275 0.001203967 0.001123227 PC(18:2_20:5)+CH3COO_2 0.001689705 0.00182596 0.001471271 0.001722614 0.001699343 0.001816512 0.00041157 0.001243248 0.000674144 0.000322043 0.000776796 0.000844455 0.000827128 0.001062504 0.001070556 0.001092173 0.001036095 0.001149056 PI(19:1_20:5)-H_2 0.000623759 0.000529666 0.000896076 0.000613398 0.000933188 0.000694621 0.000685873 0.001108826 0.001224859 0.000705636 0.000829682 0.000621514 0.000517837 0.000351283 0.000339014 0.000893713 0.000717113 0.000526837 PC(19:1_19:1)+CH3COO_3 0.034371544 0.031769799 0.028529233 0.030820748 0.031368436 0.034362907 0.052093429 0.045379118 0.043231969 0.03523801 0.040595976 0.03177112 0.033293165 0.03750782 0.033766497 0.031025919 0.035400552 0.035013374 PE(25:2_18:1COOH)-H 0.00135558 0.001964331 0.001909649 0.00160412 0.002181693 0.001765847 0.002088218 0.002279421 0.002314595 0.002085508 0.002443166 0.002044708 0.001545625 0.001613352 0.001918077 0.002220667 0.002190587 0.00196275 PC(19:1_19:4)+CH3COO_2 0.002235624 0.00302511 0.002642604 0.004823346 0.002940122 0.002601275 0.002908299 0.001618082 0.002845952 0.001807986 0.001949528 0.002268335 0.00239731 0.002936662 0.002346221 0.002962262 0.003721692 0.003169799 PC(18:0CHO_15:0)-CH3 0.001407911 0.000887924 0.001421299 0.001017318 0.001060067 0.001180743 0.000491522 0.000899857 0.000535843 0.000591918 0.000840552 0.000320234 0.000853818 0.000802529 0.001261456 0.0006185 0.000901812 0.000907293 PE(19:1_19:2)-H 0.001472366 0.001581873 0.001758572 0.001819923 0.001509176 0.001758113 0.000355819 0.000822295 0.001361539 0.000638743 0.000775947 0.000563471 0.001213616 0.001088182 0.001139757 0.00133079 0.001266929 0.000707415 PE(19:1_20:4)-H_2 0.014527677 0.01410296 0.012349535 0.01519333 0.015871937 0.013288684 0.004859375 0.009108943 0.007566368 0.005285132 0.008225927 0.005075515 0.00768703 0.007620969 0.009041697 0.012910626 0.00969861 0.008059467 PC(15:1_16:2)+CH3COO_2 0.000896867 0.00060839 0.000921691 0.00105027 0.00102442 0.000847045 0.000477817 0.000851864 0.001070216 0.001259599 0.000938585 0.000578307 0.001362756 0.001007276 0.001234088 0.001083541 0.001182215 0.001063995 PC(19:0_18:1)+CH3COO 0.0056528 0.006689609 0.008789263 0.006724621 0.005136353 0.007421795 0.001869521 0.003966376 0.004349636 0.002821739 0.002424373 0.002736916 0.005251658 0.0068105 0.003798982 0.003849916 0.004090076 0.00318714 PC(19:1_19:1)+CH3COO_4 0.034371544 0.031769799 0.028529233 0.030820748 0.031368436 0.034362907 0.052093429 0.045379118 0.043231969 0.03523801 0.040595976 0.031330145 0.033293165 0.03750782 0.033766497 0.031025919 0.035400552 0.035013374 PE(17:0_16:1)-H_1 0.022094971 0.023637802 0.016600646 0.022118528 0.024322924 0.023729138 0.003196791 0.008327897 0.007872224 0.006711652 0.008730856 0.006033391 0.008734606 0.006983719 0.010513089 0.010237333 0.009254452 0.008274843 PC(O-18:0_20:5)+CH3COO 0.005938168 0.0072014 0.0056639 0.005764473 0.005327667 0.006543243 0.001275298 0.003258493 0.00253662 0.001503945 0.002412823 0.001262368 0.002653974 0.003256459 0.003053584 0.002454915 0.002541519 0.003023018 Cer(d14:1_30:0)-H 0.00034141 0.000201956 0.000229073 0.0002506 0.000242414 0.000242025 8.26E-05 5.95E-10 3.07E-05 6.37E-05 8.04E-05 0.000145276 0.000260424 0.000259845 0.000198496 9.69E-10 9.02E-05 PC(19:1_18:2)+CH3COO_5 0.0034166 0.004053095 0.003386345 0.003491888 0.003488872 0.003832664 0.00177433 0.003339768 0.003189405 0.002270765 0.002592041 0.002101561 0.003646329 0.003941757 0.002791164 0.002565511 0.003237805 0.003412427 PE(16:0_18:2COOH)-H 0.000839259 0.000104599 0.000590939 0.000764888 0.000661021 0.000766198 0.000557589 0.00051572 0.000827714 0.000695126 0.000785731 0.00053914 0.00102963 0.000909549 0.000721447 0.001029307 0.000914045 0.000554169 LPE(17:0)-H_1 0.039768091 0.036398403 0.028480889 0.03888962 0.046861857 0.039850459 0.008927791 0.022221832 0.020014998 0.013912963 0.019342169 0.01476783 0.019910778 0.016987063 0.026609787 0.02672016 0.02166905 0.020683976 PC(16:0_20:5)+CH3COO_3 0.020281206 0.02849318 0.01134972 0.028490718 0.021506845 0.024401795 0.002548481 0.006972685 0.009875131 0.004271683 0.008255271 0.003777935 0.003606193 0.003864356 0.004015021 0.002710144 0.002743271 0.003223072 OAHFA(2:0_25:0)-H 0.003358992 0.003603345 0.002883342 0.003391272 0.003269239 0.004348454 0.001478576 0.00261925 0.003121088 0.001723974 0.001823737 0.0016226 0.002158174 0.00337935 0.003026546 0.002440004 0.002918843 0.00265615 PC(17:1_18:1CHO)+CH3COO_2 0.00043362 2.31E-05 0.000586717 0.000435732 0.000185978 0.000357027 0.000783962 0.000632435 0.001057478 0.000899372 0.000889287 0.000867339 0.001526707 0.00152207 0.001130971 0.001114556 0.001013314 0.000686312 LBPA(16:0_16:1)-H 0.001212981 0.002141698 0.001666656 0.000922715 0.001011342 0.001998975 0.001288586 0.000417073 0.00206334 0.00030953 0.001418322 0.001114338 0.000586154 0.00046208 0.000605641 0.000581539 0.000465784 0.000418118 LPC(20:5)+CH3COO_1 0.013450634 0.045391891 0.011887999 0.017483465 0.012487793 0.044325126 0.011473339 0.013536537 0.006590911 0.005532128 0.006555134 0.012691868 0.011797176 0.039594625 0.03859758 0.014168414 0.014880633 0.01108637 PE(20:0CHO_18:2)-H 0.011469262 0.007613081 0.011058581 0.008336965 0.008489129 0.008911177 0.005810025 0.009205766 0.005724518 0.005958988 0.009206841 0.005267338 0.009401431 0.0100089 0.011372932 0.005636255 0.009044407 0.009474455 LPC(20:4)+CH3COO_3 0.017478082 0.016271561 0.010179283 0.01654603 0.002848998 0.005719981 0.003701147 0.006127229 0.004863159 0.003077272 0.000816561 0.003823044 0.009486781 0.003023032 0.001021426 0.014423899 0.012168442 0.011784525 PC(18:1_20:4)+CH3COO_3 0.003667144 0.006376353 0.045013662 0.045664028 0.043620596 0.047153977 0.002006511 0.035219162 0.03061397 0.001905611 0.001384052 0.002188669 0.057602024 0.004244421 0.059774656 0.004043536 0.053892814 0.058905668 PC(18:1_19:1)+HCOO 0.0029353 0.002184485 0.002256959 0.002723578 0.002699918 0.002607371 0.00192806 0.00236606 0.002059244 0.001894427 0.002238726 0.001665687 0.002200504 0.002843636 0.002323978 0.002449954 0.002074394 0.002184947 LPE(18:1)-H_1 0.000973724 0.000258174 0.000806646 0.001022756 0.001076202 0.000655735 0.000860847 0.000819032 0.001244596 0.001143818 0.001055413 0.001075717 0.001055836 0.00059068 0.000931413 0.000848318 0.000874313 0.000721849 PG(16:0_17:1)-H 0.001083431 0.001242865 0.000818464 0.001440676 0.001505854 0.003345926 0.000905415 0.001512644 0.001578302 0.001164022 0.00165619 0.001174566 0.002090346 0.001824739 0.002010903 0.001217362 0.001452968 0.001649419 PC(18:3_18:3)+CH3COO 0.006115465 0.00782649 0.006523601 0.004747253 0.005201452 0.00497539 0.002719693 0.002637061 0.001252867 0.001502856 0.00132391 0.0061942 0.005006515 0.003827978 0.004741021 0.004340413 0.003573875 0.00400874 PI(17:0_20:5)-H 0.000788047 0.000857441 0.001115506 0.000978264 0.001422105 0.000857478 0.001142085 0.00190536 0.001599097 0.00137522 0.001629413 0.001325862 0.001060474 0.000860076 0.000951693 0.001637558 0.001402558 0.001032216 PS(17:1_18:1)-H 0.002608091 0.001750438 0.002455494 0.002032172 0.00237972 0.002168301 0.002825937 0.00299087 0.002462055 0.002565595 0.004405688 0.002513354 0.002582139 0.002259682 0.002771278 0.001780341 0.002144353 0.002142626 PE(O-19:1_20:3)-H_2 0.005484911 0.005537005 0.0048598 0.006066566 0.006514648 0.006139338 0.002568552 0.003526154 0.002888605 0.001983304 0.00376953 0.002172382 0.002842467 0.003519492 0.003229327 0.00494762 0.003732668 0.003696803 PC(20:3_20:4)+CH3COO_2 0.052022977 0.019923323 0.048139306 0.016323286 0.017810656 0.050093828 0.000637348 0.001367929 0.001868658 0.002297845 0.000862185 0.004222098 0.000905515 0.005894272 0.005910114 0.02320015 0.030006232 0.004775676 PC(7:0CHO_19:1)+CH3COO 0.000556245 5.80E-05 0.000601185 0.000764792 0.000272912 0.000219104 0.001876207 0.000885255 0.001204097 0.000943819 0.001575445 0.001253165 0.00113375 0.001078472 0.000717819 0.001046056 0.000999697 0.000570345 PC(12:1_18:1)+CH3COO 0.0028457 0.00184155 0.002678415 0.002336141 0.001881092 0.002232297 0.000515897 0.001169919 0.001127769 0.00077546 0.001605754 0.000705972 0.001434265 0.001330679 0.001549627 0.000961335 0.001796765 0.001244241 PE(O-18:0_19:1)-H 0.053395945 0.05957148 0.064458009 0.061663215 0.068690045 0.055626908 0.031211924 0.041549119 0.045619977 0.027664296 0.0331748 0.033271049 0.04612845 0.039810219 0.040006724 0.04798327 0.044667325 0.03505103 PC(20:5_21:6)+HCOO 0.000761411 0.000990614 0.00031107 0.000672893 0.000551216 0.000896356 3.12E-10 8.91E-05 2.89E-10 3.06E-05 4.29E-10 4.89E-08 3.98E-05 0.000111806 7.86E-05 0.000140899 0.000159525 PE(18:3_17:1)-H 0.005389531 0.004189346 0.004855496 0.004239298 0.005208447 0.005427668 0.001582712 0.003404318 0.003012973 0.002118674 0.002847631 0.001944389 0.003087736 0.002763511 0.003281162 0.003927805 0.00369604 0.002520003 PE(15:0_16:1)-H 0.007151956 0.007408495 0.006092784 0.007951387 0.008194812 0.007770388 0.000798771 0.003302234 0.003719052 0.00196049 0.003202788 0.002723668 0.003425446 0.002949642 0.003695237 0.004988266 0.004113435 0.003011958 PC(18:1_18:1)+CH3COO 0.000594499 0.000393875 0.000593221 0.000531229 0.000493214 0.000511089 0.001299383 0.000912703 0.000671478 0.000649968 0.001258953 0.000726238 0.000637392 0.000718485 0.000769218 0.000459415 0.000778509 0.000602625 PC(17:1_19:1)+CH3COO_4 0.00119453 0.00107919 0.001729524 0.001516679 0.001255974 0.000928258 0.000591916 0.001166041 0.001361664 0.000908364 0.001322259 0.000909707 0.001270786 0.001336152 0.00117411 0.001146298 0.001870993 0.001398274 PC(19:0_20:4)+CH3COO 0.001748938 0.001822781 0.002651866 0.001797609 0.00183106 0.002124265 0.000395008 0.001528596 0.000821901 0.000387435 0.001575357 0.000525391 0.001209094 0.001430982 0.001900571 0.001745087 0.000997612 0.001148892 PE(17:1_20:5)-H 0.000778018 0.001268809 0.000446942 0.000874961 0.000746459 0.001169547 3.02E-05 0.000128803 2.04E-06 3.61E-05 3.64E-05 6.45E-05 0.000228343 2.77E-05 0.000223036 0.000117422 9.80E-05 6.08E-05 PE(18:0_10:2COOH)-H 0.000810221 0.000247145 0.000845005 0.000680528 0.000647042 0.000537612 0.000562888 0.00048229 0.000735524 0.00061688 0.000653027 0.000394988 0.000591822 0.00110212 0.001210885 0.000682503 0.001339066 0.000422696 PC(17:1_18:2COOH)+CH3COO_1 0.003485408 0.00099886 0.005044279 0.003967662 0.002875293 0.002543635 0.006944309 0.004912142 0.006831146 0.003987263 0.006909728 0.0055331 0.009720442 0.008968646 0.006214714 0.006341306 0.007329263 0.00612459 PE(23:2_19:1COOH)-H 0.001627109 0.002409387 0.001754109 0.001992575 0.002768672 0.001911332 0.001826765 0.003002755 0.002880033 0.00257446 0.003290725 0.002326305 0.002112126 0.001768384 0.002420725 0.002596059 0.002047291 0.002077604 PE(19:0_18:1)-H_3 0.013728279 0.013487639 0.014292073 0.015738468 0.015978112 0.017414119 0.003144599 0.008203116 0.010901586 0.007177133 0.010784921 0.005918812 0.010529215 0.010259827 0.012310296 0.009886818 0.011844838 0.007606225 PC(18:3_18:4)+CH3COO_2 0.005044122 0.001348496 0.003961748 0.004910795 0.005172636 0.005505863 0.000668265 0.001215533 0.001319266 0.001717639 0.000906155 0.00079245 0.001013902 0.013714441 0.002954464 0.014308287 0.002714266 0.001650419 PC(17:1_17:2)+CH3COO_2 0.011719798 0.001689369 0.015350695 0.014593879 0.002407767 0.014633172 0.002894746 0.002491196 0.00292398 0.00311413 0.002999247 0.003262408 0.002430688 0.006098415 0.001565017 0.006000193 0.015183173 0.014254756 PE(15:0_17:1)-H_1 0.063957974 0.037562171 0.06008897 0.045123623 0.043060876 0.042412701 0.008513874 0.038997684 0.025561669 0.015648223 0.019554344 0.021465309 0.042856548 0.036578544 0.026116078 0.042264446 0.030034938 0.018716662 PE(18:1_18:1)-H_3 0.001940121 0.000917574 0.001157941 0.001598114 0.00158625 0.0016909 0.002126265 0.001615046 0.001156798 0.00143917 0.001734986 0.001698447 0.001684505 0.001162855 0.001333802 0.000757215 0.001586138 0.001044885 PE(16:1_20:5)-H 0.003784691 0.003654398 0.003831233 0.003561204 0.003722026 0.00406488 0.000613044 0.002648484 0.001920571 0.001636686 0.001985614 0.001070901 0.002313879 0.002000729 0.002643786 0.002722686 0.002080962 0.001840267 PC(18:3_18:4)+CH3COO_3 0.005043515 0.001315596 0.003959949 0.004910352 0.00517208 0.005504042 0.000668252 0.002452375 0.001308829 0.001716072 0.000905881 0.000723447 0.001012632 0.013713386 0.002954464 0.014306946 0.002713731 0.00164965 PC(17:1_18:1)+CH3COO_5 0.00067928 0.00132063 0.000700076 0.000524535 0.001081484 0.00071223 0.000175903 0.000581905 0.000588444 0.000463264 0.000684208 0.000603059 0.000574721 0.000714841 0.002066072 0.000803968 0.001001218 0.000627813 PC(16:2_18:4)+CH3COO 0.00103509 0.000853533 0.002106808 0.001010119 0.001424662 0.000906838 0.000116027 0.000931491 0.000622652 0.000343222 0.000575654 0.000238759 0.001043932 0.000482556 0.000683971 0.000681007 0.000635637 0.000968008 PC(15:0_17:0)-CH3_2 0.008616686 0.007554035 0.008949745 0.010231191 0.010315958 0.010382001 0.002481891 0.004067537 0.005020183 0.0027094 0.0036361 0.003171548 0.004794138 0.003586491 0.004128934 0.006005894 0.004713138 0.003720837 PE(18:1_19:1)-H_3 0.160229547 0.143781441 0.149693367 0.165487628 0.159721043 0.163276343 0.082437344 0.139102393 0.130404652 0.111444992 0.145571568 0.102212904 0.132139523 0.121124884 0.14666753 0.179239731 0.146828953 0.128913264 PC(19:1_19:1)+CH3COO_5 0.00027007 0.000222411 0.000304968 0.000359996 0.000235068 0.000289848 0.000402726 0.000568251 0.000263355 0.000265892 0.000298315 0.000514284 0.000256887 0.000290926 0.000318476 0.000237406 0.000333915 0.000253559 PC(17:0_19:3COOH)-CH3 0.001378491 0.000834595 0.001439179 0.001145116 0.001163168 0.001167842 0.00075816 0.000988836 0.000849005 0.000779854 0.00133002 0.000629918 0.001099863 0.001265316 0.001430283 0.000765198 0.001101813 0.001146917 PC(14:0_17:1)+CH3COO_2 0.002019762 0.001146999 0.00130042 0.002213809 0.001066228 0.001490644 0.002191535 0.001744284 0.001781843 0.001594833 0.000808261 0.001393188 0.003014157 0.002783548 0.001676854 0.002989949 0.001632282 0.00137004 PE(O-19:1_18:1)-H_2 0.009302855 0.010310334 0.007144324 0.007973659 0.011436884 0.009614957 0.002255694 0.005701961 0.008319405 0.005578178 0.00710663 0.003952741 0.006480695 0.007577181 0.007576162 0.0063483 0.007807067 0.007111446 PC(18:1_20:5)-CH3_2 0.001601485 0.001189276 0.001148445 0.001383159 0.001267042 0.001279002 4.18E-09 0.000370648 0.000215508 0.00029066 0.000450667 4.72E-05 0.000308521 0.000353547 0.000515915 0.000368397 0.000261223 0.00046177 PE(18:1_20:1)-H 0.020374967 0.020676086 0.022302266 0.018371911 0.021643704 0.019802627 0.003401263 0.009878084 0.010923034 0.006938549 0.012051172 0.006816111 0.01219771 0.009305659 0.013337995 0.012101346 0.009670889 0.009494213 PC(17:1_10:2CHO)+CH3COO 0.00155877 0.000643521 0.003127952 0.002003678 0.001288485 0.002133209 0.002362744 0.001332563 0.001510606 0.002235524 0.003390328 0.002001265 0.002925443 0.004725335 0.002308375 0.003021209 0.003146188 0.001984753 PE(19:1_18:2)-H_2 0.004924862 0.007672767 0.006425106 0.007373145 0.006425035 0.005739886 0.001096883 0.001968496 0.004699526 0.001642936 0.000580222 0.001890495 0.002490233 0.003148437 0.002431488 0.003493739 0.004952746 0.002871335 PE(18:0CHO_18:1)-H_2 0.004165507 0.001214357 0.001860574 0.002571604 0.001991239 0.002235165 0.002063272 0.002113737 0.00165238 0.002163992 0.003460517 0.002433111 0.001974942 0.001810742 0.002539515 0.000926602 0.001814981 0.001018482 PE(O-18:1_18:1)-H_2 0.014805298 0.016580712 0.01925642 0.015545207 0.019566055 0.020401864 0.013509655 0.014178191 0.01367959 0.011171891 0.011325779 0.017092301 0.015594624 0.01539719 0.013636748 0.018589189 0.016702576 0.013614288 PC(18:0CHO_18:2)-CH3 0.011419284 0.007954815 0.011132652 0.008864468 0.009157693 0.009673888 0.005996654 0.009695934 0.006662664 0.006338941 0.009944294 0.005398574 0.008872884 0.010043896 0.012649894 0.005589001 0.009817507 0.010241381 PC(17:1_20:5)-CH3_4 0.001100138 0.001187306 0.000534764 0.001146891 0.000876776 0.001460171 5.54E-05 0.000123395 3.61E-05 1.20E-06 3.94E-05 3.86E-05 2.80E-05 0.000106818 0.000228252 0.000175037 0.000163123 PE(18:1_19:3)-H 0.001579915 0.001772053 0.002017014 0.00228209 0.002600272 0.002073243 0.000337347 0.001234349 0.001593079 0.000572719 0.000700051 0.000556706 0.001458844 0.000960887 0.00108196 0.001557245 0.001359229 0.000920927 PE(16:0_16:1)-H 0.065842234 0.023630853 0.017643984 0.021288084 0.02584459 0.021595479 0.009048087 0.013947002 0.015184746 0.012000877 0.017011291 0.009107439 0.012669555 0.010951087 0.021674063 0.016079778 0.02022767 0.017045413 PC(18:4_20:5)-CH3 0.000991152 0.001078629 0.000669994 0.00066842 0.000865428 0.001134788 1.92E-05 5.44E-05 8.62E-10 5.08E-05 6.83E-05 2.84E-05 4.39E-05 5.87E-05 7.37E-05 0.000127521 PE(7:1CHO_18:1)-H 0.00077523 0.000117122 0.0004724 0.00074494 0.000429888 0.000414743 0.001338298 0.001072911 0.001914865 0.001414063 0.002142872 0.001837413 0.001227465 0.001465818 0.001351419 0.001120471 0.001636892 0.000829157 LPE(18:0)-H_1 0.003714819 0.003615735 0.002956233 0.003666926 0.004783206 0.003768575 0.001444568 0.003661186 0.002595174 0.001922988 0.003183375 0.002231506 0.002939246 0.00232384 0.003470648 0.003569642 0.003600846 0.003133084 PE(17:1_20:4)-H 0.013890038 0.012469895 0.010981781 0.013393725 0.014391729 0.013163718 0.003894345 0.008410136 0.006609653 0.00506316 0.007609177 0.005066292 0.00666629 0.006178212 0.008210141 0.009617961 0.007895328 0.006973027 LPC(20:5)+CH3COO_2 0.03410121 0.045391891 0.018838273 0.026085535 0.027538564 0.060110833 0.011473339 0.017123363 0.01565983 0.010904877 0.01012368 0.012691868 0.033934826 0.000997539 0.044575667 0.022583591 0.019229209 0.019111792 PE(22:0_19:1)-H 0.003366012 0.003214888 0.002999987 0.003488 0.00385302 0.003294098 0.002345994 0.002648996 0.002102134 0.001834814 0.002234806 0.001637115 0.001889024 0.002605057 0.002612768 0.003375143 0.00282126 0.002122075 PE(17:0_18:2COOH)-H_1 0.001406273 0.000128206 0.001293187 0.001279793 0.000807477 0.000880822 0.000641966 0.000813064 0.000970585 0.000931281 0.000778039 0.000844281 0.001636234 0.000823217 0.001026207 0.000951768 0.001043214 0.000825097 PE(18:1_18:1CHO)-H 0.001531242 0.000855694 0.00131459 0.001578435 0.001418781 0.001378851 0.000613099 0.000800382 0.001021514 0.001024969 0.001147323 0.000731595 0.001489754 0.001052668 0.00125118 0.0010939 0.001056201 0.000726665 PE(18:0_20:1)-H 0.001058364 0.040458785 0.001261909 0.041264168 0.048623251 0.040735141 0.017618684 0.000502604 0.000388529 0.000356125 0.000412933 0.000469755 0.029807224 0.027134385 0.00053309 0.038415306 0.000472544 0.000458231 PE(22:1CHO_18:1)-H 0.002007916 0.001018838 0.002114754 0.001802246 0.001745036 0.001421783 0.00159611 0.001685601 0.00122491 0.001495327 0.002315504 0.00135016 0.002114626 0.002285037 0.002303251 0.001263239 0.002011357 0.00189884 PC(O-18:0_19:1)+CH3COO 0.000543812 0.000430473 0.000393111 0.000239883 0.000281377 0.000663233 0.000441873 0.000573442 0.000458564 0.000178004 0.000423913 0.000246521 0.000199203 0.000397533 0.000263383 0.000268791 0.000321303 0.000200457 PE(18:0_18:2)-H_2 0.000554605 0.00081119 0.000985106 0.000281088 0.001009487 0.000959807 0.000521666 0.000787953 0.000747696 0.000568236 0.00082736 0.000602625 0.000747086 0.000703656 0.000693386 0.000891558 0.000881274 0.000764008 PC(14:0_17:1)+CH3COO_3 0.001103795 0.001146999 0.000601652 0.001172549 0.001312821 0.000783987 0.002131395 0.000890817 0.000936511 0.00071454 0.001387855 0.001393188 0.001399903 0.001413947 0.001676854 0.001254592 0.002272549 0.002081588 PC(17:1_19:2COOH)+CH3COO 0.002000571 0.000726229 0.003526408 0.002265282 0.001670921 0.001425493 0.003449588 0.003445537 0.004246217 0.004476052 0.004561314 0.003706003 0.005113488 0.006792061 0.006006221 0.003056281 0.00359704 0.0053798 PC(19:1_20:2)+CH3COO_2 0.000829846 0.000789617 0.001305463 0.000720729 0.000706789 0.001045987 0.000451994 0.000504041 0.00036982 0.000309619 0.000389312 0.000206622 0.000514744 0.000478421 0.000486806 0.000539506 0.000417082 0.000321862 LPC(20:1)+CH3COO 0.002286359 0.002354766 0.001703384 0.002044943 0.001696372 0.002277467 0.000292769 0.000906712 0.000884337 0.000557914 0.001355156 0.000624508 0.001018384 0.001204702 0.001405738 0.000842978 0.000989871 0.000856443 PC(17:2_18:3)+CH3COO_2 0.002018615 0.001783098 0.002172574 0.007300187 0.002016619 0.006566017 0.00115204 0.003601886 0.002940352 0.001483913 0.001356737 0.001937971 0.002569434 0.007306284 0.001352645 0.0071694 0.003757051 0.001654899 PE(16:1_17:1)-H_1 0.012414192 0.014582819 0.01528587 0.015904624 0.017857291 0.01748316 0.000498011 0.01416373 0.012344964 0.009178815 0.014408058 0.010553397 0.013426523 0.010729062 0.014660814 0.016206345 0.015028722 0.013031001 PC(18:1_18:1)-CH3_3 0.002685396 0.001702656 0.00228237 0.002260854 0.002796709 0.002899311 0.001508248 0.001788829 0.000787265 0.001464919 0.002604054 0.001062813 0.002355707 0.002374099 0.002399817 0.001415747 0.002043845 0.001648693 PE(O-18:1_16:1)-H 0.011473593 0.011296388 0.01215123 0.010888594 0.015556766 0.011845584 0.006979045 0.013543523 0.011618404 0.008681497 0.012177732 0.007166505 0.012033907 0.009594555 0.015778296 0.015412283 0.011952837 0.010422143 PC(17:1_18:2)+CH3COO_2 0.009706757 0.008924924 0.002250241 0.01011294 0.009689144 0.002936357 0.00269855 0.003309033 0.002167202 0.003153945 0.002223252 0.002247728 0.00179169 0.009010484 0.002957124 0.003595294 0.009604889 0.002641301 PE(O-18:1_20:5)-H_2 0.007433731 0.243785481 0.207066052 0.008764807 0.233936687 0.004760347 0.000855407 0.077564924 0.002267118 0.000589727 0.001621681 0.000940114 0.101408506 0.002564404 0.140367191 0.005488723 0.00261444 0.113252049 PE(16:1_18:2)-H 0.008160768 0.007416759 0.007810474 0.007401506 0.008122968 0.007962674 0.001136276 0.005760899 0.004623351 0.003708888 0.005673701 0.00346093 0.005386764 0.003977672 0.005692123 0.006098781 0.005799655 0.004858466 PC(O-18:0_18:2)+CH3COO 0.003389152 0.004301289 0.002230587 0.002951945 0.001812683 0.002915556 0.000836225 0.002179863 2.04E-07 0.000819474 0.000607438 0.000308988 0.001040928 0.001886903 0.00138111 0.001035016 0.001340903 0.001271177 PE(17:1_18:1)-H_1 0.091540602 0.078323686 0.091907227 0.086295383 0.101501587 0.087254449 0.036694437 0.065702169 0.069762743 0.055129013 0.07531329 0.058756462 0.066663129 0.06057845 0.080470735 0.078323233 0.074817701 0.063097474 PE(18:1_18:1COOH)-H_3 0.001000718 0.000242872 0.000866444 0.001077996 0.00084919 0.000628449 0.00060904 0.00065799 0.00096311 0.000772622 0.000752283 0.000730264 0.001240537 0.000792118 0.001030342 0.000856875 0.000788142 0.000693954 PE(22:3COOH_18:2)-H 0.002035033 0.002631787 0.00324893 0.001500396 0.003154916 0.001291227 0.001773299 0.004393239 0.003962955 0.002913598 0.003833976 0.003258191 0.003029358 0.002474831 0.002604206 0.002897705 0.002933158 0.002410856 PE(18:0_20:5)-H_2 0.253389266 0.262357775 0.233145941 0.238461347 0.014105462 0.243306224 0.070227968 0.137660579 0.110674797 0.083403247 0.11441179 0.072335143 0.152167143 0.007076996 0.193533732 0.187618297 0.17834109 0.162279724 PE(18:1_19:1)-H_4 0.000123354 0.023163026 0.004346576 0.025004586 0.027738948 0.023569404 0.004303121 0.160119903 0.013587706 0.003485406 0.156363532 0.003692774 0.004357344 0.00245492 0.003579342 0.005460068 0.017427611 0.003518287 PE(21:1_18:2)-H 0.00166258 0.000931034 0.00208628 0.001682913 0.001492722 0.010790223 0.000443722 0.000731098 0.000829404 0.000640152 0.000851513 0.000358138 0.001482092 0.000874652 0.000631531 0.007334447 0.000681341 0.002937294 PC(17:1_17:1)+CH3COO_3 0.000653548 0.000580637 0.000648428 0.00078259 0.001002258 0.00042784 0.000399675 0.000812919 0.000630411 0.000705091 0.000837379 0.000118629 0.00087521 0.00019244 0.001248141 0.000543566 0.001329058 0.001757669 PC(17:1_19:1)-CH3 0.002236223 0.00129357 0.00120307 0.001376011 0.001713444 0.002023131 0.000596407 0.000529861 0.000366311 0.000572394 0.000316811 0.000500159 0.000530679 0.000627679 0.000485494 0.000585941 0.000620104 0.000517358 PE(16:0_7:1CHO)-H 0.000419044 6.95E-05 0.000722555 0.000547923 0.000439536 0.000342282 0.001303041 0.000937738 0.001552063 0.001233957 0.0019304 0.001160943 0.00137162 0.00099591 0.000994551 0.0012983 0.000996811 0.000990415 PC(17:2_18:3)+CH3COO_3 0.002018615 0.001783098 0.002172574 0.001775577 0.002016619 0.001985317 0.00115204 0.003601886 0.002940352 0.001483913 0.001356737 0.001444406 0.002569434 0.007306284 0.001352645 0.0071694 0.002791127 0.001654899 PC(14:0_19:1COOH)-CH3 0.002693243 0.001878053 0.00277964 0.002446638 0.001860868 0.002135038 0.000518475 0.001298556 0.00126244 0.000806223 0.001921395 0.00072773 0.001511001 0.001484078 0.00174708 0.000962224 0.001787357 0.001263367 PE(17:0_19:1COOH)-H 0.003130499 0.000345065 0.002225467 0.002258328 0.002158581 0.00209446 0.000689378 0.001436906 0.002089182 0.001575052 0.00239002 0.0016372 0.002186672 0.002026978 0.002090758 0.001996704 0.00250579 0.001496277 PC(18:1_19:1COOH)-CH3 0.000900446 0.000631904 0.001014089 0.000777517 0.001006345 0.00070032 0.000426278 0.000744865 0.00065435 0.00052734 0.000464584 0.000503843 0.000832898 0.000715656 0.000876438 0.000399969 0.00059315 0.000683747 PC(18:0_20:5)+CH3COO_3 0.001213565 0.001612822 0.001286169 0.001278903 0.001040129 0.042712477 0.000683051 0.001057031 0.000955177 0.000935487 0.000535098 0.000595036 0.001081214 0.001589227 0.001273607 0.000904406 0.001213076 0.00038378 PE(25:2_19:2COOH)-H 0.001252138 0.001662787 0.00143756 0.001092163 0.001518146 0.001207222 0.000474934 0.00127426 0.000915335 0.000801602 0.001090363 0.000833047 0.00106175 0.001105518 0.001073727 0.001051023 0.001089654 0.001004962 LPE(17:0)-H_2 0.005956581 0.004306468 0.004923471 0.007513178 0.006598839 0.006030726 0.002644065 0.004440702 0.004177077 0.003023898 0.002840501 0.003794851 0.005324234 0.003369002 0.004168817 0.004149273 0.004210472 0.003427842 PE(O-20:1_18:1)-H 0.012534504 0.012854147 0.014487318 0.013144551 0.015525572 0.011559604 0.003664422 0.010902009 0.010850383 0.009854939 0.012205634 0.008025385 0.011083771 0.011762009 0.013249869 0.011643561 0.011161136 0.008810989 CL(18:2_18:2_20:3_20:4)-H 0.001055478 0.001117443 0.001293317 0.001026582 0.001787266 0.001158743 0.000607595 0.001188029 0.001170878 0.001065109 0.001111097 0.00100896 0.000824029 0.000730217 0.001004679 0.001031882 0.000845732 0.000838359 PI(18:0_20:5)-H_2 0.001618519 0.002188146 0.002787474 0.001121892 0.001644859 0.000124095 0.003640366 0.004506937 0.005288932 0.002085958 0.00205332 0.004020679 0.002475246 0.001643772 0.050451346 0.003451527 0.058609826 0.00113074 PC(8:1COOH_20:5)+CH3COO 0.000974614 0.000224372 0.001677093 0.001059033 0.000946008 0.000685532 0.001804738 0.000948234 0.001549579 0.001114843 0.001531986 0.000753396 0.00171072 0.003043005 0.001310584 0.001207386 0.001871628 0.001350545 PI(18:1_20:5)-H_1 9.43E-05 0.000158629 0.000326209 0.0001356 0.000409751 0.000228441 0.000441077 0.000778853 0.000282497 0.001158288 0.000823658 0.000684605 0.000409718 0.000482446 0.000559545 0.000619567 0.000615996 0.000348648 PE(17:0_4:1CHO)-H_1 0.000675773 0.001189165 0.0006647 0.000698728 0.001347265 0.000914103 0.000502048 0.00089939 0.001070019 0.000294918 0.000709653 0.000733184 0.000392053 0.000237707 0.000518425 0.000560048 0.000635856 0.000731557 PE(17:0_18:2COOH)-H_2 0.001771586 0.000277746 0.002109675 0.001941741 0.001437061 0.001238008 0.000796926 0.000870449 0.002069323 0.001251303 0.001643519 0.001181046 0.002176855 0.001490903 0.00147021 0.001589346 0.00174153 0.001314039 PC(15:0_18:4)+CH3COO 0.00620445 0.006274975 0.005975216 0.009002677 0.007198272 0.006774337 0.004118083 0.005900461 0.005055714 0.002625612 0.003946294 0.003125587 0.009832616 0.003420213 0.001782546 0.004866986 0.008162063 0.008590521 PE(16:0_18:3)-H_2 0.003699468 0.003445225 0.004042801 0.005019177 0.00352947 0.004213209 0.001084369 0.003025279 0.002269648 0.001823985 0.002323475 0.002280753 0.002674605 0.002553232 0.001940645 0.003919366 0.003137099 0.001967612 PE(20:1_18:2)-H 0.006652359 0.006188084 0.007224099 0.00669981 0.007313486 0.006734204 0.000920449 0.002372337 0.002226598 0.00214175 0.002523749 0.001756826 0.002835536 0.002452168 0.012485128 0.00282122 0.002805982 0.00239075 PE(24:2_19:1COOH)-H 0.001764761 0.002135156 0.002057499 0.001833378 0.002397873 0.001680729 0.001276572 0.001875343 0.001838676 0.001496684 0.001733816 0.001546922 0.002015011 0.001555308 0.001867545 0.002170094 0.001991219 0.001419232 PC(7:0CHO_18:1)+CH3COO 0.001998926 0.000177156 0.00202403 0.001772442 0.001276492 0.000936897 0.004638451 0.001784695 0.003930517 0.002298031 0.004270576 0.002868975 0.002828187 0.003237503 0.00245792 0.002603895 0.002410347 0.002179619 LPE(20:2)-H_1 0.004630429 0.001922771 0.00445437 0.004811309 0.004309766 0.003875929 0.002992281 0.002442492 0.00331867 0.002910352 0.003071956 0.002552778 0.003476574 0.003067553 0.00440008 0.002761305 0.003423049 0.002585837 PC(16:0_18:1)-CH3 0.003624728 0.002389481 0.002790797 0.003339134 0.003476402 0.003509023 0.002533589 0.001927553 0.00135971 0.001577761 0.002168941 0.001464976 0.001880677 0.001426628 0.001410395 0.001611589 0.001760718 0.001284309 PE(21:1CHO_18:1)-H 0.002744615 0.001379414 0.002143657 0.002282106 0.002219104 0.002155472 0.002996025 0.002667358 0.001793776 0.002150339 0.003134299 0.002000315 0.002373501 0.002354638 0.002472239 0.001263304 0.002100491 0.001862069 PC(15:0_17:1)+CH3COO_4 0.003186442 0.007027435 0.002696746 0.004709964 0.005840201 0.004978657 7.21E-05 0.000121656 0.000134052 5.39E-05 6.57E-05 7.70E-05 0.00014877 0.000162051 4.68E-05 6.96E-05 0.000183325 0.000115568 PE(18:1_18:2COOH)-H_2 0.001399163 0.000397763 0.001400779 0.001333605 0.001104306 0.000929311 0.000563193 0.000939923 0.001252577 0.001000783 0.001184635 0.001036414 0.001854685 0.001327871 0.001098462 0.00091181 0.001235855 0.000913304 PC(O-18:0_20:4)+CH3COO 0.001145098 0.001248159 0.001090407 0.001136841 0.000892212 0.001052782 0.000231089 0.000534686 0.000549282 0.00033226 0.00034353 0.00022665 0.000451221 0.000509679 0.000474585 0.000359096 0.000382996 0.000551189 PC(17:1_20:4COOH)+CH3COO_4 0.00036285 0.000247519 0.000314651 0.000187093 0.000490036 0.000428725 0.000182508 0.000428803 0.000262696 0.000122202 9.03E-07 0.000158362 0.000314336 0.004204722 0.000396766 0.0004588 0.000374362 0.000393056 PE(17:0_17:2)-H 0.030657181 0.03147853 0.033851003 0.032361359 0.006772637 0.032665118 0.001527125 0.003095393 0.023603528 0.002582853 0.024888677 0.002525709 0.001910877 0.002967478 0.003377642 0.004426118 0.005413622 0.004048113 LPE(18:1)-H_2 0.057095469 0.03673974 0.047940592 0.052542189 0.054359716 0.054088687 0.022021185 0.036783245 0.042630502 0.03133119 0.060317371 0.0328893 0.053226805 0.045000202 0.048188464 0.044065131 0.043344224 0.036590574 PC(18:1_11:2COOH)+CH3COO 0.000475455 0.000145338 0.000878546 0.000602035 0.000289243 0.000262916 0.00137814 0.000819063 0.002595141 0.001512524 0.002686299 0.001333325 0.00175989 0.001275968 0.001028525 0.00107527 0.001494638 0.00118327 LPE(16:0)-H_2 0.022607922 0.019399937 0.018143448 0.023941429 0.025114516 0.021734663 0.009579482 0.015328777 0.014905182 0.010309371 0.015275151 0.010754494 0.013202339 0.010328189 0.019698686 0.016562318 0.015665067 0.013878482 PE(20:0_18:1)-H 0.037568414 0.035949278 0.037873694 0.039260422 0.040651145 0.036284303 0.016572337 0.029157024 0.03104981 0.02552982 0.033737535 0.022790456 0.028528725 0.02609429 0.033763654 0.036752086 0.030954547 0.026224192 PE(25:2_19:1COOH)-H 0.001700574 0.002119613 0.002052805 0.001602164 0.002031955 0.001629038 0.000900713 0.001785067 0.001473237 0.001280733 0.001663869 0.001159829 0.001402591 0.001267187 0.00191053 0.001907157 0.001643984 0.001446397 PE(18:2_18:3)-H 0.003004188 0.00268013 0.001810251 0.00239783 0.002272037 0.002817836 9.73E-05 0.001366676 0.000445645 0.000412831 0.001029798 0.00084439 0.000885728 0.000951372 0.001258627 0.000898791 0.000999342 0.000734994 PC(O-19:1_18:1)+CH3COO 0.005106699 0.004666354 0.004575041 0.004553629 0.003873146 0.004810613 0.003963562 0.005622243 0.004814172 0.004030182 0.005009758 0.003390598 0.003977651 0.005155044 0.003892182 0.003080648 0.003891253 0.00353368 PC(5:0CHO_18:2)+CH3COO 0.001098493 0.000342912 0.001527722 0.001421066 0.000649383 0.001099857 0.002340086 0.001249883 0.001625006 0.001567343 0.002387532 0.001808861 0.002070734 0.003506311 0.00221357 0.002307542 0.001667699 0.001693993 PC(18:1_18:2CHO)+CH3COO_1 0.001041748 0.000340682 0.001768212 0.001096696 0.000836293 0.000894265 0.00084806 0.001097816 0.001454836 0.001301759 0.001498629 0.000952612 0.001937405 0.00156567 0.001370841 0.000958244 0.001442883 0.00118822 PC(19:1_18:2)+CH3COO_6 0.006063255 0.006318814 0.009562806 0.008413396 0.007657752 0.006995869 0.003297404 0.003097697 0.004815751 0.002424419 0.005027642 0.002256332 0.008847993 0.009391013 0.00309381 0.001566608 0.001881846 0.007652426 PC(18:1CHO_18:2)+CH3COO 0.000720524 0.000683141 0.000914119 0.000743934 0.000804198 0.00075316 0.000763961 0.000471451 0.000383837 0.000430368 0.000576343 0.000706019 0.000704406 0.001068147 0.000573822 0.000735385 0.000633115 0.000421486 PE(18:1_18:2COOH)-H_3 0.000993076 0.000255026 0.000502991 0.000399695 0.000536902 0.000341492 0.000565553 0.000341133 0.000557081 0.000683576 0.000480176 0.00054356 0.000625136 0.000536344 0.000575077 0.000505179 0.001382157 0.000597221 PC(19:1_20:4)+CH3COO_6 0.000292412 0.002234078 0.001643232 0.000590847 0.002120356 0.001903732 0.001917639 0.000859842 0.000354904 0.001418096 0.00165344 0.0006632 0.002536773 0.000353241 0.002236656 0.038146724 0.003797271 0.002962703 PC(18:0COOH_18:1)+CH3COO 0.001111701 8.03E-05 0.001572874 0.000995868 0.000755447 0.000484721 0.00086922 0.000673073 0.001899541 0.001586825 0.002366608 0.001476524 0.002976642 0.002156404 0.002046417 0.001839921 0.001355609 0.001144766 PI(16:0_20:5)-H 0.001443692 0.001303181 0.001836589 0.001346363 0.002054549 0.001457125 0.002690698 0.003255845 0.002823423 0.002280295 0.002998349 0.002224833 0.002079372 0.002039349 0.002432011 0.00298903 0.002858561 0.00220842 PE(4:0CHO_18:0)-H 0.000433885 0.000352773 0.000576147 0.000555139 0.000473155 0.00050285 0.000964719 0.000392143 0.0010667 0.000520211 0.000901662 0.000814734 0.000531522 0.000790404 0.000637795 0.000744771 0.00056777 0.000557247 PC(17:1_19:1)+CH3COO_5 0.082767048 0.067634573 0.060354826 0.063975137 0.06280359 0.069327597 0.093506078 0.08011082 0.07426637 0.073497732 0.073576877 0.058075974 0.080274096 0.082718876 0.081591485 0.080487032 0.080324396 0.080718741 PC(16:0COOH_17:0)-CH3 0.000756692 0.000424751 0.00097022 0.000944329 0.000668833 0.000558854 0.000468505 0.000417554 0.000326516 0.000426189 0.000965433 0.000429381 0.000746929 0.000701268 0.000831993 0.000370095 0.000618 0.00057116 PE(20:0_4:1CHO)-H 0.00035707 0.000469117 0.000387204 0.000322545 0.000343069 0.000510195 0.00011453 0.000464339 0.000374225 0.000206713 0.000402188 0.00019644 0.000239346 0.000126799 0.000271914 0.000221915 0.000255599 0.000222195 LPE(17:0)-H_3 0.015379739 0.014525618 0.013820832 0.019260374 0.015285438 0.018116236 0.008848181 0.011317887 0.01204943 0.006203143 0.007886447 0.006993714 0.009887906 0.008072287 0.012422527 0.012326705 0.01129448 0.008041917 PC(O-19:1_20:5)+CH3COO 0.002165369 0.002344302 0.001878122 0.001846634 0.001696657 0.00225524 0.000808677 0.001467346 0.001315369 0.000668023 0.001024779 0.000638933 0.001104557 0.00129947 0.001211488 0.00093055 0.001175965 0.001230342 PC(16:1_17:1)-CH3 0.004693629 0.003661095 0.004816461 0.005447345 0.004951251 0.004634179 0.004364674 0.00400236 0.003397491 0.002987523 0.00367278 0.005381861 0.004286234 0.002653317 0.003678547 0.004387846 0.003217477 0.00216296 PE(O-19:2_18:1)-H 0.02350167 0.026449018 0.022116956 0.023086622 0.027412691 0.02591925 0.01479809 0.02307305 0.021396408 0.01649645 0.020491475 0.015426756 0.017661718 0.019320735 0.021566411 0.02249968 0.022150016 0.019523838 PE(18:1_18:1)-H_4 0.011481592 0.016119941 0.016528517 0.012426675 0.014960973 0.012080492 0.007962054 0.012273191 0.008954638 0.007849302 0.006908087 0.009505408 0.012246434 0.006798227 0.01036654 0.01723559 0.010676178 0.007704921 PC(17:1_19:2COOH)+HCOO_1 0.001752104 0.000678359 0.00241152 0.001910129 0.001441381 0.001253089 0.003714978 0.002063185 0.003487373 0.003439921 0.003028387 0.002877729 0.004801948 0.004030682 0.00327463 0.002910737 0.003305479 0.002920932 PC(21:0_18:2)+CH3COO_2 0.001839324 0.00205516 0.002340756 0.001957698 0.000899887 0.000967533 0.000772944 0.000625279 0.000800038 0.000619813 0.000567812 0.002773184 0.001408895 0.002463222 0.001525781 0.000815014 0.001623421 0.001157378 PC(18:1_22:5)+CH3COO 0.001603779 0.001652645 0.001788399 0.001066409 0.001302415 0.001238642 0.000664892 0.000673878 0.000759601 0.000453171 0.000934953 0.000509372 0.000821751 0.000746911 0.000800285 0.000705074 0.000673937 0.000752621 Cer(t17:1_22:1)-H 0.00143666 0.000745858 0.000935058 0.001784016 0.001511668 0.001484143 0.000774185 0.000506396 0.000925151 0.00058622 0.000777 0.000560213 0.001033697 0.000898017 0.000794054 0.000831499 0.000617523 0.000596964 PC(17:1_18:2CHO)+CH3COO_1 0.000739847 0.000163271 0.000671004 0.000909846 0.000366433 0.000332121 0.0010045 0.000620765 0.000948808 0.001156156 0.001099773 0.001014077 0.001840433 0.001167683 0.000928534 0.001033294 0.001362804 0.000708726 LBPA(18:0_17:1)-H_2 0.00125962 0.001375131 0.001100984 0.001480506 0.001498105 0.002234767 0.000875979 0.00232186 0.001582265 0.001710866 0.001300586 0.001916436 0.001927049 0.001468704 0.001373336 0.001237225 0.000851647 0.001167591 PE(27:0_18:1)-H 0.000986145 0.000973383 0.000740225 0.001067656 0.001323986 0.001103929 0.000464469 0.000781434 0.001006076 0.000664866 0.001302438 0.000669528 0.000629106 0.001151924 0.001116127 0.001431891 0.000683221 0.001017004 PC(18:1_18:2CHO)+CH3COO_2 0.000750357 0.000403026 0.001245877 0.000675492 0.000470473 0.000476721 0.001033447 0.000741969 0.000604299 0.000789416 0.000363611 0.000949118 0.000544459 0.001303758 0.000375886 0.000378076 0.000361859 0.000339033 PE(17:1_17:1)-H 0.048981726 0.044656936 0.044771079 0.048826855 0.055310738 0.04671217 0.024518221 0.042235037 0.038037607 0.031206328 0.039693839 0.03111406 0.035468182 0.030856124 0.03943266 0.048810716 0.042672255 0.033846878 PE(20:4_20:5)-H_3 0.01733337 0.018462162 0.014846943 0.000440398 0.016467669 0.017540592 5.01E-05 0.000207055 1.77E-06 4.26E-05 0.000154064 4.36E-05 4.64E-05 0.000243981 0.000205074 0.0102346 0.000205136 0.000222969 PC(17:1_18:1)+CH3COO_6 0.021858155 0.026311682 0.011533013 0.027811401 0.021538402 0.027765074 0.000405665 0.000592242 0.000657938 0.000638485 0.000571253 0.00080221 0.000835483 0.000832849 0.000781133 0.000434543 0.000693286 0.000612713 LPC(15:0)+CH3COO_3 0.001361257 0.000821484 0.000621123 0.001253208 0.00054362 0.001507759 0.002927986 0.000408482 0.000355021 0.00015096 0.00598646 0.000354668 0.000800288 0.000651302 0.000804472 0.000648683 0.000680603 0.000535346 PE(18:0_20:4)-H_3 0.0009481 0.00093179 0.001092275 0.001040035 0.000998115 0.001147484 0.00047241 0.00066108 0.00067707 0.000368889 0.000694508 0.000341421 0.00056514 0.000945783 0.000750956 0.000939492 0.000149928 0.000732408 PE(21:2COOH_18:1)-H 0.002345658 0.003483243 0.004295684 0.003677512 0.004013216 0.003177592 0.002707045 0.005217081 0.005735686 0.004279235 0.004477617 0.004177072 0.004040056 0.00396943 0.003776799 0.004199772 0.003963079 0.003975814 LPE(19:0)-H_1 0.0042662 0.004722365 0.004183621 0.005143174 0.005405073 0.004592676 0.001791004 0.003095116 0.002787562 0.001677885 0.002153559 0.002547715 0.002945784 0.002137875 0.002215645 0.003346312 0.003109864 0.002258937 PC(20:0_18:3)+CH3COO 0.000961925 0.001494204 0.000799787 0.00099832 0.000972292 0.000949994 0.000635336 0.000847162 0.000693437 0.000402478 0.000314647 0.000730407 0.000590655 0.001385981 0.000616197 0.000722619 0.000582815 0.000663638 PE(15:0_18:3)-H_3 0.011213247 0.010747592 0.010318027 0.011025174 0.012265612 0.010524221 0.000730281 0.00452843 0.003894343 0.002659272 0.003476483 0.002712995 0.006116775 0.002266445 0.003535793 0.00755615 0.00278742 0.002259333 PE(16:1_17:1)-H_2 0.000671766 0.000757086 0.000348234 0.000721351 0.000648776 0.000853823 0.002134286 4.34E-05 4.71E-05 1.55E-06 8.30E-07 5.99E-07 5.95E-07 8.18E-07 4.32E-07 1.73E-06 4.77E-05 1.44E-06 PC(16:1_17:1)+CH3COO_2 0.001015113 0.001498298 0.000493349 0.001439461 0.00146056 0.001679768 0.01229167 3.92E-05 0.000106105 8.22E-05 0.000183269 5.42E-05 0.000154963 3.96E-07 8.88E-05 2.81E-05 4.54E-07 5.06E-05 PE(16:0_17:1)-H_2 0.000696337 0.00121424 0.00016155 0.001238124 0.000971331 0.001115783 9.28E-07 8.69E-05 1.76E-06 7.77E-07 4.80E-07 1.14E-06 6.71E-07 3.70E-07 1.30E-06 1.00E-06 8.23E-07 2.97E-07 PC(18:0_22:5CHO)-CH3 0.001209396 0.001778852 0.001737895 0.001391959 0.001764447 0.001276998 0.001383231 0.0021167 0.001626457 0.001712283 0.001868379 0.001534264 0.001803962 0.001949467 0.001764384 0.001865247 0.001823099 0.00171192 PE(16:0_17:2)-H 0.001243619 0.000983298 0.001161867 0.001683022 0.001585149 0.001335882 4.88E-07 0.001003781 0.000848582 0.000766398 0.000602014 0.000595873 0.000895412 0.000427341 0.000646882 0.001231361 0.001091945 0.000666866 PC(15:0_18:1)+HCOO 0.005766198 0.006953508 0.002719124 0.007870164 0.006189715 0.007716481 7.21E-05 0.000121118 0.000166637 5.38E-05 6.70E-05 7.92E-05 0.000147973 0.000162378 4.77E-05 7.06E-05 0.0001827 0.000116241 LPE(18:0)-H_2 0.041201888 0.037129617 0.031081476 0.04006959 0.045557866 0.039904938 0.01671153 0.029577692 0.027153929 0.019792412 0.030328578 0.021208622 0.024881935 0.021147187 0.033031546 0.031123584 0.028144836 0.023936479 PC(18:0_17:1)+CH3COO_2 0.022055488 0.000413237 0.000349085 0.000291772 0.000314431 0.000384719 0.008213536 0.000178293 8.38E-05 4.88E-05 0.000413156 3.29E-05 0.000143831 0.000101979 0.000265576 0.00029161 8.31E-05 0.000213287 PC(17:1_18:2)+CH3COO_3 0.002141487 0.002779042 0.006234583 0.005193313 0.000474005 0.002936357 0.001021541 0.003050479 0.002849619 0.000827018 0.003263305 0.001212565 0.00179169 0.003328084 0.00658008 0.002891737 0.000805292 0.002278317 PC(17:1_19:1)+HCOO_1 0.000944751 0.000833173 0.000978198 0.000880626 0.000934887 0.000768164 0.001146824 0.001137894 0.001026661 0.000870824 0.000866881 0.000661358 0.00098007 0.001053769 0.001100337 0.00105775 0.001073077 0.000919052 PE(17:0_20:5)-H_3 0.195737255 0.211049379 0.001659105 0.1850786 0.202015322 0.200641782 0.000193688 0.088009853 0.077476069 0.050440264 0.000608409 0.044710733 0.001695506 0.001481146 0.001705503 0.001201754 0.002391681 0.113910508 PC(19:1_19:1)+CH3COO_6 0.025887432 0.002519308 0.009000497 0.002583274 0.02305075 0.028233601 0.008994975 0.005475238 0.003925944 0.004190273 0.004066761 0.00089117 0.005764007 0.007532849 0.003896033 0.006472579 0.004454124 0.006410319 PC(14:0_18:1COOH)-CH3 0.003389403 0.002467284 0.003499733 0.002864779 0.003017619 0.003013867 0.001914936 0.002249658 0.002274965 0.001424625 0.003378577 0.001679185 0.00309054 0.003012063 0.002072556 0.001452368 0.002783033 0.00270515 PC(18:1_18:1CHO)+CH3COO_2 0.000244622 4.48E-07 0.000635758 0.000250034 0.000120289 0.000179615 0.000478508 0.000593104 0.001135505 0.001018015 0.000911178 0.000882307 0.00154942 0.00133733 0.000837235 0.00062478 0.00110268 0.000635125 PC(18:3_20:5)+CH3COO_3 0.000392357 0.000225347 0.000388323 0.167332752 0.000920212 0.000480381 0.000184209 0.000149719 0.05323108 0.000325692 0.000116982 0.000119568 0.000391425 0.000571689 0.000922166 0.000724006 0.000798298 0.000125212 PC(17:1_19:1)+HCOO_2 0.000944751 0.000833173 0.000954275 0.000880626 0.000934887 0.000768164 0.001166138 0.001103088 0.001022572 0.000832528 0.000846234 0.000662163 0.001023832 0.001053769 0.001017635 0.00105775 0.001056493 0.000891475 PE(O-18:2_18:1)-H_2 0.002623517 0.0029936 0.003186955 0.002820261 0.003476159 0.003250506 0.074430296 0.002099471 0.001644224 0.00130746 0.001420846 0.001074882 0.002075118 0.002102715 0.002565275 0.002458916 0.002475272 0.00171963 PC(18:1_19:1)-CH3_1 0.00068019 0.00042423 0.000592493 0.000712662 0.000758296 0.00057845 0.000526564 0.000891264 0.000683083 0.000686632 0.000989614 0.000571768 0.000959449 0.001191549 0.000894913 0.000842373 0.000594507 0.000549281 PC(O-18:1_18:1)+CH3COO_2 0.001112824 0.001141834 0.001160279 0.000990793 0.000953758 0.000954318 0.00041101 0.000754233 0.001054378 0.000759599 0.001144573 0.000719276 0.000988022 0.001098964 0.000986174 0.000689235 0.000918293 0.000832575 PE(16:0_20:0)-H 0.001438431 0.001183207 0.00114321 0.001093142 0.00142453 0.001328946 0.000611511 0.000939876 0.000959142 0.000606945 0.000721686 0.000637364 0.000833197 0.00060722 0.000858929 0.001088601 0.00079897 0.000792788 PE(O-17:0_18:1)-H_1 0.048095353 0.046215818 0.059976714 0.064054674 0.057234287 0.060062263 0.045074333 0.060699717 0.064028559 0.043292744 0.050235699 0.052893735 0.065336683 0.046711345 0.054969614 0.067337351 0.062281005 0.047094877 LPE(16:1)-H 0.001237733 0.000990249 0.001075256 0.001327211 0.001324639 0.001385505 0.000526869 0.001357143 0.001249818 0.000982997 0.001466554 0.001014348 0.001090316 0.001141838 0.001512523 0.001292168 0.001305684 0.001086972 PC(17:1_18:2)+CH3COO_4 0.006752873 0.008354227 0.003647586 0.007200704 0.005758792 0.008670956 0.000113033 0.000270272 0.000363265 0.000161517 0.000209676 0.000255276 0.000282337 0.000314097 0.000290991 0.000184364 0.000236993 0.000282306 PE(22:0_17:1)-H 0.019728034 0.019870325 0.019257382 0.019419971 0.026271762 0.020346455 0.015807204 0.01787721 0.016160038 0.011915795 0.017998169 0.013887745 0.015219325 0.015024425 0.017816621 0.021661771 0.017397907 0.014356808 PC(17:1_18:1)+CH3COO_7 0.007153634 0.00093263 0.001338278 0.002023135 0.001337671 0.001175693 0.000697753 0.00102821 0.0069676 0.000262772 0.000608246 0.000784769 0.000857176 0.008317212 0.004652678 0.001905394 0.001588176 0.001395486 PC(17:1_18:1)+CH3COO_8 0.007153634 0.00093263 0.001338278 0.002023135 0.001337671 0.001175693 0.000697753 0.00102821 0.0069676 0.000262772 0.000608246 0.000784769 0.000857176 0.008317212 0.004652678 0.001905394 0.001588176 0.001395486 PE(18:1_22:1CHO)-H 0.001237836 0.000595165 0.001202455 0.000887803 0.000965263 0.000813452 0.000486056 0.001083796 0.000727233 0.000829122 0.001622629 0.000692132 0.001162162 0.001331828 0.001334665 0.000660229 0.000927105 0.001057124 LPC(18:3)+CH3COO 0.005808345 0.006965927 0.00325083 0.005000513 0.003490789 0.005698033 0.00277196 0.005840281 0.004336248 0.003551394 0.002057778 0.00399871 0.003675038 0.009075806 0.010642449 0.002742733 0.001049738 0.004021731 PE(18:1_21:2COOH)-H 0.002821869 0.003345227 0.004112625 0.002641002 0.002852947 0.00307339 0.003482282 0.004121236 0.004409208 0.003207849 0.003338355 0.003749997 0.003926081 0.003091411 0.002790676 0.00391786 0.003953113 0.003122193 PC(15:1_20:5)+CH3COO_5 0.001145006 0.001266948 0.00169914 0.00105478 0.000963085 0.001696889 0.004312465 0.001085198 0.000569246 0.003514679 0.005064475 0.003070828 0.001499011 0.015276386 0.000786047 0.000803197 0.014403089 0.000682171 PC(15:0_20:5)+CH3COO 0.000549137 0.00040108 0.008546552 0.000295226 0.009297887 0.000617688 0.000486296 0.000472593 0.000942772 0.000368593 0.000439256 0.000317484 0.000514267 0.000719817 0.000127519 0.000310501 0.000249304 0.006358303 PC(O-19:1_18:2)+CH3COO 0.001503781 0.001165283 0.001343389 0.001234793 0.001403524 0.001460165 0.000795508 0.001365505 0.001177953 0.000877251 0.00078103 0.000656377 0.000817423 0.001078153 0.00086001 0.000663093 0.000776605 0.000813532 PC(18:1_20:4)+CH3COO_4 0.003667144 0.006652805 0.136515171 0.160183369 0.005625862 0.132411576 0.002493656 0.001365134 0.002893288 0.047181339 0.001384052 0.042046351 0.001670452 0.006687183 0.001903 0.103055521 0.001530397 0.10003502 LPE(22:0)-H_1 9.72E-05 2.58E-05 1.56E-06 8.89E-05 7.25E-05 6.50E-05 1.46E-06 5.08E-07 1.86E-06 5.51E-07 3.59E-05 3.31E-05 4.14E-07 2.34E-05 5.76E-05 6.23E-05 4.07E-07 4.19E-07 PC(17:1_18:1COOH)+CH3COO_3 0.000483201 4.48E-05 0.00090149 0.000604688 0.00034416 0.000426976 0.002206506 0.000973773 0.001018608 0.001183496 0.000968874 0.001198377 0.000984925 0.001468224 0.001027557 0.001000507 0.001159098 0.000812927 PC(16:1_20:4)+CH3COO 0.01932837 0.056305762 0.003975854 0.02253058 0.004654647 0.022158597 0.004767991 0.02785042 0.003410005 0.001578451 0.011462547 0.005250661 0.030843936 0.006036462 0.031447514 0.005599337 0.005430862 0.00834251 PC(17:0CHO_18:2)-CH3 0.004154699 0.001126999 0.00191989 0.002086997 0.001865757 0.002099361 0.002559477 0.001883376 0.001018888 0.001918283 0.00303176 0.00172165 0.002285734 0.001812688 0.002289276 0.000680119 0.002044868 0.001001583 PC(16:1_18:1COOH)-CH3 0.001494979 0.001203381 0.001743601 0.001450907 0.001197727 0.000987095 0.000527123 0.000644391 0.001221004 0.000562506 0.001744951 0.000839105 0.001154096 0.00117818 0.001417585 0.000797126 0.001014871 0.001037828 PC(19:1_20:5)+CH3COO_6 0.00812753 0.018101541 0.007122267 0.008628244 0.014034139 0.010588674 0.005510329 0.009303343 0.007293633 0.088478296 0.006652051 0.00477617 0.007585259 0.010354879 0.009991225 0.007365588 0.008741242 0.010305617 PC(19:1_20:5)+CH3COO_7 0.00812753 0.018101541 0.007122267 0.008628244 0.014034139 0.010588674 0.005510329 0.009303343 0.007293633 0.088478296 0.006652051 0.00477617 0.007585259 0.010354879 0.009991225 0.007365588 0.008741242 0.010305617 PC(7:1CHO_18:1)+CH3COO_2 0.000659039 0.000268988 0.001196722 0.00071927 0.000525782 0.000300061 0.001734023 0.000830131 0.001927913 0.001802258 0.002191713 0.001665864 0.002238374 0.001646416 0.001202832 0.00122648 0.00137712 0.001222821 PE(18:0CHO_18:1)-H_3 0.002513979 0.000455643 0.002337103 0.002281854 0.002093546 0.001726389 0.001198831 0.0015784 0.002232264 0.002489949 0.002524691 0.001440951 0.002531765 0.002165771 0.002311775 0.001952438 0.002315055 0.001530603 PE(18:1_18:2COOH)-H_4 0.002364823 0.000315816 0.002239588 0.001251583 0.001022686 0.001628297 0.000728082 0.000861205 0.001781403 0.001210669 0.001349438 0.001084253 0.001166603 0.001371243 0.002213706 0.001291547 0.001165199 0.000938609 PE(18:2_21:2COOH)-H 0.002703103 0.003772825 0.004781806 0.003279096 0.004385785 0.002733903 0.001710978 0.004848306 0.004071451 0.003670543 0.003755523 0.003418232 0.004222644 0.003616311 0.003936627 0.003757779 0.004337398 0.003678134 PE(18:2_20:3)-H 0.005388221 0.003616239 0.002790541 0.003708117 0.004520792 0.003366808 0.000357479 0.001094826 0.01370661 0.00085031 0.001783391 0.009108746 0.001970801 0.002784113 0.002560275 0.003304257 0.003058984 0.002513587 PC(17:0CHO_20:5)-CH3 0.004629267 0.001966466 0.002280475 0.003115732 0.002458296 0.002767311 0.003927549 0.00341473 0.001864518 0.002950366 0.004331669 0.002456423 0.003046748 0.003214855 0.00359538 0.001545152 0.002902157 0.002414837 LPC(21:1)+CH3COO 0.000715325 0.000623447 0.000538355 0.000720324 0.000512879 0.000799865 0.000283343 0.000366822 0.000418377 0.00041503 0.000451687 0.000510862 0.000257315 0.000285688 0.000481032 0.000452629 0.000380584 0.00036569 PC(16:0_17:1)+CH3COO_2 0.003843287 0.009271602 0.004932358 0.006427505 0.008291235 0.007532848 0.003201764 0.004798964 0.002939584 0.001440573 0.005519845 0.003196139 0.005166694 0.004294315 0.002968312 0.003506477 0.005081649 0.003346058 PC(O-18:0_18:1)+CH3COO 0.010995211 0.007329991 0.00775104 0.007287206 0.009043178 0.007594932 0.00334764 0.00678911 0.006111548 0.004671494 0.006369001 0.003958415 0.005717884 0.006996437 0.006243699 0.004529125 0.00498217 0.005928446 PC(18:3_20:5)+CH3COO_4 0.070787528 0.075170176 0.064087071 0.066199684 0.069941159 0.078897408 0.005450873 0.093847289 0.016570867 0.009257116 0.016239642 0.009332115 0.034020587 0.034672429 0.043863217 0.030499816 0.034406673 0.036771012 PE(17:0_4:1CHO)-H_2 0.000398269 0.000903255 0.000383 0.000722546 0.000948587 0.0006465 0.000267485 0.000510064 0.000498686 0.00043888 0.000811006 0.000216259 0.000267239 0.00024599 0.0003016 0.000398288 0.00064005 0.000420855 PC(16:0_18:1)+CH3COO_2 0.0084687 0.011423981 0.008081957 0.011200783 0.010253291 0.00730646 0.002887491 0.005743115 0.008691659 0.005136857 0.008861984 0.004137879 0.007387102 0.008080088 0.006378076 0.005843726 0.006224224 0.006217409 PE(15:1_17:1)-H 0.002803876 0.002437613 0.002082122 0.002649473 0.003281563 0.002589214 0.001525786 0.003297232 0.002941077 0.002303482 0.002695199 0.002211442 0.002461816 0.002091984 0.002822209 0.003484341 0.003147932 0.002430716 PC(18:2_19:2)+CH3COO 0.001124909 0.00132884 0.002199202 0.001602805 0.001509733 1.79E-05 2.28E-06 0.000407853 0.000653872 0.000385166 0.000449059 0.000360419 5.54E-06 0.000451058 3.32E-06 0.000367035 3.44E-06 0.004916622 PC(19:1COOH_18:2)+HCOO_3 0.002023213 0.000709063 0.003882616 0.002320803 0.001611477 0.001182615 0.003469584 0.003397496 0.004077425 0.004515745 0.004452973 0.003634562 0.005160787 0.005473594 0.00453399 0.003086256 0.003633957 0.003564627 LPC(20:4)+CH3COO_4 0.006764328 0.001348278 0.004453322 0.001510796 0.000994822 0.008826875 0.000316799 0.000170689 0.000377674 0.00049825 0.002543968 0.000409171 0.000927132 0.003869882 0.000651732 0.000656249 0.001063068 1.91E-06 LPE(19:0)-H_2 0.002991678 0.003144503 0.002195397 0.002980615 0.003737819 0.003212454 0.000811872 0.002109475 0.002519808 0.001234061 0.002297645 0.001428219 0.001904669 0.001506467 0.002544316 0.002134569 0.002032908 0.0016256 PC(17:1_19:2COOH)+HCOO_2 0.001752104 0.000678359 0.00241152 0.001910129 0.001441381 0.001253089 0.003714978 0.002063185 0.004273353 0.003439921 0.003028387 0.002877729 0.004801948 0.004030682 0.00327463 0.002910737 0.003305479 0.002920932 PE(15:0_17:1)-H_2 0.003068291 0.003258015 0.001216753 0.003547628 0.003027187 0.004927546 4.16E-09 3.31E-07 6.61E-05 1.28E-06 8.81E-07 0.000139839 2.75E-05 5.83E-07 8.98E-07 6.88E-05 5.00E-07 4.28E-07 PC(17:1_20:5)-CH3_5 0.003509812 0.00192907 0.002687614 0.00231514 0.002125868 0.00294631 0.001644141 0.001883161 0.000943481 0.001507406 0.002424944 0.001507024 0.002159796 0.002031719 0.002460574 0.001067611 0.001971872 0.001423595 PE(18:1_21:1)-H 0.00777608 0.007168432 0.007698688 0.007931251 0.009298003 0.007024424 0.00333143 0.005208946 0.005033526 0.004209951 0.005043226 0.003528017 0.003942319 0.004162792 0.005214263 0.006498398 0.004707766 0.00398289 PC(17:1_18:1)-CH3_3 0.000987596 0.001119348 0.001039618 0.00118405 0.001620983 0.001552195 0.000440367 0.000992476 0.000160664 0.001234517 0.000326142 0.001062362 0.000440231 0.000747059 0.000370128 0.000656794 0.000788112 0.000415826 PE(20:0_18:2)-H 0.055276472 0.05267416 0.047606664 0.048449056 0.058304534 0.054479795 0.034026576 0.045804238 0.039270901 0.034662563 0.040830717 0.028781315 0.033704777 0.033640104 0.041088901 0.046657259 0.044749614 0.036936585 PE(19:1_19:1)-H_2 0.058087562 0.05267416 0.047606664 0.048449056 0.058304534 0.054479795 0.034026576 0.045804238 0.039270901 0.034662563 0.040830717 0.028781315 0.033704777 0.033640104 0.041088901 0.046657259 0.044749614 0.036936585 PC(17:1_18:2COOH)+CH3COO_2 0.000435757 0.000305446 0.001091262 0.000859319 0.000984054 0.000635626 0.003478098 0.001840117 0.002653271 0.002371987 0.003292321 0.002306043 0.004377073 0.002994662 0.001320112 0.001177412 0.001333197 0.002489751 PE(4:1CHO_19:1)-H 0.000680179 0.000924077 0.000397304 0.00051521 0.000842698 0.000561458 0.000369871 0.000827845 0.000604311 0.000381164 0.000701316 0.000494508 0.000669489 0.000540811 0.000504305 0.000489799 0.00085396 0.000686205 PC(17:1_20:5)+HCOO_2 0.001097986 0.001258942 0.000903753 0.001252984 0.001312345 0.001248129 0.00074393 0.00149251 0.002064304 0.000946524 0.000388044 0.001225579 0.00186382 0.00038285 0.000776457 0.002397035 0.000603904 0.002514138 PC(20:4_20:4)+CH3COO_3 0.001755151 0.015499105 0.160061918 0.016059848 0.000690993 0.015294521 0.025241169 0.000174412 0.000172793 0.000203328 0.000216002 0.00016835 0.000410771 0.009499106 0.010615308 0.011908043 0.000963966 0.009945912 OAHFA(2:0_24:0)-H_2 0.112727575 0.00120558 0.000704386 0.115372575 0.00103469 0.001183781 0.008489314 0.000102078 0.000316603 0.014475685 0.000363078 0.000236068 0.00031224 0.00058963 0.056312134 0.00056754 0.000736411 0.000395606 PC(16:1_17:1)+CH3COO_3 0.001262423 0.000954064 0.003189269 0.000868004 0.001432849 0.000938905 0.000389167 0.001138177 0.002225933 0.002661901 0.001152425 0.000546909 0.002878247 0.001321255 0.001468888 0.001220692 0.001968179 0.000903412 PC(16:1_17:1)+CH3COO_4 0.001262423 0.000954064 0.003189269 0.000868004 0.001432849 0.000938905 0.000389167 0.001138177 0.002225933 0.002661901 0.001152425 0.000546909 0.002878247 0.001321255 0.001468888 0.001220692 0.001968179 0.000903412 PC(5:0CHO_17:1)+CH3COO 0.001350069 0.000508206 0.002172831 0.001461969 0.00121294 0.001559392 0.004945896 0.002325215 0.003679073 0.003393566 0.004733956 0.003679981 0.003931156 0.004011288 0.002904354 0.004089634 0.003691365 0.002479564 PC(16:0_18:1COOH)-CH3 0.01090899 0.006942756 0.009422889 0.009549162 0.009133252 0.008920817 0.006582206 0.007884545 0.007018546 0.006371539 0.011005344 0.006128276 0.008410774 0.007870375 0.009900118 0.005615627 0.008408166 0.008012093 PC(17:1_18:2CHO)+CH3COO_2 0.000936672 0.000545181 0.000512143 0.000864025 0.000485495 0.000884101 0.000917488 0.000489317 0.001086034 0.000544701 0.000847827 0.000652606 0.000933379 0.000696318 0.000528844 0.000394916 0.000881659 0.000668537 PS(18:2_20:2)-H 0.002596242 0.003809269 0.004759302 0.003309135 0.004423317 0.002881821 0.001690627 0.004810322 0.004252182 0.003644308 0.003730158 0.003464347 0.004273499 0.003613959 0.003924905 0.003796836 0.003829754 0.003657926 PC(O-17:0_18:1)+CH3COO 0.001722146 0.001881255 0.001667516 0.001859109 0.001654986 0.001960313 0.000771797 0.001305764 0.001263999 0.000754796 0.000801017 0.000765812 0.001185289 0.001038933 0.001066311 0.000909144 0.001017559 0.000849285 PC(18:1_18:1COOH)+CH3COO_1 0.000562408 5.03E-05 0.000485499 0.000628793 0.000342363 0.000313433 0.000652636 0.000785071 0.001192552 0.001099512 0.001228643 0.001054474 0.001039158 0.001070974 0.001064966 0.000612176 0.000788725 0.001040903 LPE(18:1)-H_3 0.014687528 0.010642376 0.027229503 0.029107747 0.022737924 0.146194562 0.014360028 0.009683267 0.013725497 0.011681346 0.02839326 0.012213327 0.027143319 0.010220414 0.023185375 0.013907122 0.013321645 0.014531197 PC(16:1_20:5)+CH3COO 0.026776751 0.015240154 0.029043075 0.032585529 0.027308625 0.028228621 0.009205353 0.015177671 0.030922414 0.015010943 0.037732628 0.01215615 0.013885939 0.014228339 0.039363404 0.011197756 0.02779499 0.035480713 LPE(21:0)-H 0.002993982 0.003054909 0.003342735 0.003463012 0.004116114 0.003301588 0.001766775 0.002993287 0.002804428 0.002109375 0.002669633 0.002739339 0.002573896 0.002190281 0.002767022 0.002929901 0.003152659 0.00221375 PE(O-19:2_18:2)-H_2 0.004090441 0.004380068 0.00378608 0.003609953 0.004527536 0.003737582 0.001430094 0.003137879 0.002119678 0.001913551 0.002180163 0.001464608 0.0018188 0.001903836 0.002455407 0.002009088 0.002522069 0.002319652 PC(17:1_19:1COOH)-CH3_2 0.000813564 0.000521319 0.001194889 0.00078813 0.000680716 0.000702078 0.000957851 0.00108083 0.000841077 0.000859046 0.000805592 0.000564439 0.001187301 0.000693116 0.001117546 0.000505546 0.001020333 0.000924579 PE(23:2_19:2COOH)-H 0.001992334 0.002284024 0.002578969 0.002139701 0.002768854 0.0020494 0.002700472 0.003438814 0.003458775 0.000495653 0.003072094 0.002740058 0.0024208 0.002075798 0.002390269 0.00256955 0.002918363 0.002334177 PE(16:1_18:1)-H 0.027898286 0.029009609 0.031281942 0.029459902 0.026084706 0.02917022 0.005603524 0.016980202 0.020440093 0.013429584 0.023277865 0.013131217 0.020658949 0.012742329 0.022862949 0.015759384 0.015134562 0.013503321 PC(20:1_20:5)+CH3COO_2 0.00209586 0.002693686 0.002438066 0.002482944 0.002438918 0.002513747 0.001430716 0.001869706 0.001781518 0.000719371 0.001438264 0.001435506 0.001713375 0.001297785 0.001339031 0.001240534 0.001779613 0.001805925 PC(17:1_18:1COOH)-CH3 0.004910538 0.003424741 0.006135589 0.004575585 0.009396265 0.004535155 0.004647225 0.00593912 0.008868781 0.005630586 0.007977484 0.00423939 0.005447364 0.006114399 0.010196404 0.003679617 0.004472151 0.00435659 PC(18:1_18:1)-CH3_4 0.00060541 0.000620483 0.000502674 0.000490766 0.000299038 0.000304479 0.000122957 0.000482085 0.000421226 0.000293704 0.000782829 0.000186431 0.000559336 0.000335945 0.000256497 0.00013778 0.000760311 0.000566255 PE(17:0_16:1)-H_2 0.016717942 0.01758212 0.012617355 0.013971886 0.021555829 0.019537958 0.009342419 0.014412445 0.009308817 0.00756512 0.007857424 0.012229602 0.012052005 0.007682852 0.010263045 0.013245119 0.011854376 0.008863615 LPC(P-15:2)+CH3COO_2 0.00079414 0.000270901 0.000684856 0.000765629 0.0005827 0.000544009 0.000225974 0.000614608 0.000388391 0.000303711 0.000353224 0.000244959 0.000377088 0.000290316 0.000395362 0.00028545 0.000498269 0.00010054 PC(18:1CHO_18:2)-CH3 0.001425831 0.00053988 0.001194492 0.001038872 0.000914106 0.000808288 0.001000852 0.001021396 0.000520241 0.000945522 0.001362648 0.001090733 0.000932273 0.001061677 0.001193984 0.000735613 0.000945099 0.000768268 PC(16:1_17:1)+CH3COO_5 0.0336566 0.002303515 0.00240585 0.002139168 0.003285444 0.001709406 0.00099755 0.002622733 0.001574808 0.00234001 0.002011241 0.032060196 0.001511822 0.002278659 0.003008688 0.001433353 0.052997757 0.002959543 PE(O-18:1_19:1)-H 0.029989973 0.029868311 0.02768813 0.028325422 0.033944735 0.029954945 0.032904548 0.035862564 0.023126494 0.022729869 0.02456095 0.024075423 0.022594355 0.022716809 0.030668802 0.031179281 0.026705777 0.022921583 PE(7:0CHO_17:0)-H 0.00123578 0.000144644 0.000910142 0.001577176 0.000968814 0.000818449 0.001111792 0.000544867 0.001262653 0.000723685 0.001321119 0.000667893 0.001342294 0.000998466 0.000885501 0.001044894 0.000996633 0.000722932 LPC(16:0)+CH3COO_2 0.001569988 0.001580927 0.000480936 0.0009624 0.001073631 0.001400867 0.000299475 0.000587417 0.000782008 0.000386251 0.000657776 0.000290818 0.000372147 0.000477616 0.000603567 0.000385243 0.000513687 0.000450313 PE(17:1_19:1)-H_2 0.048597974 0.04240865 0.041937418 0.048853019 0.057870177 0.04705182 0.041478307 0.054399541 0.042307682 0.040466183 0.049893532 0.042772628 0.037412697 0.039014318 0.040294255 0.060328046 0.048011666 0.036644409 PE(18:1_18:4)-H_2 0.000824192 0.001025743 0.000673432 0.001399424 0.000952639 0.000803114 8.58E-05 0.000414335 0.000334293 0.000641326 0.000309107 0.001005603 0.000248543 0.00043225 0.000599619 0.000875784 0.000468461 0.000502557 PI(17:1_20:5)-H 0.0001988 0.000207725 0.000391917 0.000323749 0.000348724 0.000301297 0.00021392 0.000438432 0.000324407 0.000263014 0.000457072 0.000283697 0.00026857 0.000231595 0.000298586 0.00047387 0.000285553 0.000309545 LPE(22:0)-H_2 0.002085634 0.002054061 0.00220456 0.002357736 0.002612582 0.00208776 0.001332337 0.002464019 0.002080152 0.001922885 0.002668912 0.002041834 0.001690645 0.00196309 0.002108929 0.002374819 0.002237127 0.001671269 LPE(20:0)-H 0.007199555 0.006251598 0.005269113 0.006417841 0.007777531 0.006864192 0.002616414 0.005900116 0.005299161 0.004664203 0.006174415 0.004638393 0.004355448 0.003653164 0.005273086 0.005438653 0.005053018 0.004295208 PE(O-17:0_18:1)-H_2 0.000760437 0.000421726 0.000827727 0.000904144 0.000517644 0.000592139 0.000124856 0.001760298 0.001428994 0.000726456 0.001384596 0.001316876 0.000737634 0.001658337 0.00160822 0.000908528 0.00138878 0.00103293 PC(18:1_18:1)-CH3_5 0.000823429 0.00063016 0.000576823 0.000549606 0.000326279 0.000573192 0.000465648 0.00056867 0.000608185 0.000392847 0.001116981 0.000380477 0.000519233 0.001085912 0.000860305 0.000333646 0.000565167 0.000494881 PC(17:0CHO_18:1)-CH3 0.002957561 0.002111116 0.003508932 0.002854741 0.003170074 0.002767233 0.004779038 0.00388606 0.00338233 0.002950993 0.003699363 0.003215925 0.004512886 0.003400238 0.003504935 0.0024741 0.003827164 0.003427274 PE(18:0_18:2CHO)-H 0.001315338 6.82E-05 0.001132447 0.000843503 0.00074387 0.00067707 0.001138225 0.000510431 0.000815416 0.001126987 0.000980604 0.000853944 0.001245569 0.000723716 0.000661393 0.00102782 0.000854102 0.000641486 LPE(20:2)-H_2 0.000303366 0.001994893 0.000337718 0.000819832 0.000174383 0.000390732 0.003066142 0.002521182 0.000151829 0.000407195 0.003331583 0.002656378 0.000339993 0.000501098 0.000467436 0.002892153 0.003635109 0.002694341 PE(17:0_17:1)-H_4 0.0062579 0.007568054 0.002556153 0.008984793 0.008226398 0.008533909 0.00018405 0.000233766 0.000150998 0.003830607 3.26E-05 0.000172325 0.000373259 0.000120551 0.000230427 0.002164398 0.000278847 0.000104579 PE(17:0_19:1)-H 0.007337385 0.004341592 0.010160436 0.00982278 0.006794761 0.007719962 0.001688132 0.002933021 0.006601355 0.002356255 0.005392522 0.002464427 0.006376482 0.002975486 0.005495235 0.003214655 0.002913418 0.0024243 PC(10:1CHO_19:1)+CH3COO 0.000622497 2.84E-05 0.000350679 0.000376653 0.000754557 0.00051897 0.000953018 0.000420413 0.000837487 0.000604815 0.001026739 0.000780592 0.001550337 0.000720165 0.000567627 0.000730844 0.0007596 0.000615122 PC(6:0COOH_18:1)-CH3 0.00110198 0.000301733 0.001581386 0.001367207 0.000757583 0.000837204 0.001710676 0.001109548 0.002698258 0.001957305 0.002691455 0.001843208 0.002460651 0.002425348 0.002097912 0.00220084 0.001737761 0.001610975 PE(22:2COOH_20:4)-H 0.000688391 0.000784005 0.000798215 0.000628729 0.000906931 0.000598012 0.001086727 0.001503068 0.00123076 0.001085617 0.001185467 0.001071809 0.001283503 0.000951568 0.001252625 0.001341899 0.00129126 0.001200333 PC(16:0_20:1COOH)-CH3 0.00130949 0.000439043 0.001269889 0.00078545 0.001043943 0.000730717 1.16E-08 0.001230047 0.000852207 0.000436131 0.000795102 0.00046267 0.000700876 0.000643047 0.000680831 0.000458937 0.000487011 0.000487116 CL(18:2_18:2_20:4_20:4)-H 0.001596862 0.001820434 0.001627841 0.001513447 0.002139159 0.00180187 0.000688878 0.001787864 0.001314892 0.001200471 0.001478218 0.00084834 0.000817504 0.001158165 0.001369867 0.001331322 0.001242894 0.001090913 PE(O-19:1_15:0)-H 0.00617413 0.005782954 0.00495225 0.005963626 0.006045424 0.008227092 0.001455262 0.00240648 0.003576574 0.002927765 0.003172899 0.002480439 0.003148537 0.002017724 0.003246934 0.002439632 0.002694439 0.003068309 PE(7:0CHO_18:0)-H 0.001081332 0.000134832 0.000963374 0.001501206 0.000886411 0.000719742 0.001005298 0.000764802 0.001165569 0.000986168 0.001117697 0.000941649 0.001200849 0.001142933 0.000869839 0.001125418 0.000960004 0.000818894 PE(18:0_19:1)-H 0.048513501 0.038678712 0.041916663 0.04738974 0.048197618 0.04588668 0.04256792 0.042043399 0.042990255 0.033343837 0.049234156 0.037210528 0.037546376 0.033102435 0.03816651 0.051244936 0.045578239 0.036416996 PE(15:0_17:1)-H_3 0.00281731 0.003010874 0.002103698 0.003342269 0.003423595 0.003105716 0.000180327 0.000857657 0.001381809 0.000625217 0.001238453 0.000819269 0.000980754 0.000629274 0.000862334 0.00120641 0.000916419 0.000797391 PE(18:1_20:5)-H 0.222848829 0.003611307 0.003386385 0.002708446 0.00452342 0.003498745 0.001026614 0.001828829 0.108058988 0.081948811 0.002313604 0.001266358 0.135577828 0.002482963 0.004238084 0.003805919 0.00415362 0.003963782 PC(17:0_17:1)+CH3COO_2 0.00525034 0.004480961 0.002159957 0.006629236 0.003573112 0.007892841 0.002332811 0.000502229 0.000517231 0.004551278 0.000249551 0.000373182 0.001030689 0.002918006 0.000693114 0.002539627 0.001810808 0.000660402 PC(18:1_18:2CHO)+CH3COO_3 0.000334701 8.08E-05 0.000358191 0.000278352 0.000181287 0.000128215 0.000236237 0.000498426 0.000620314 0.000755557 0.00079902 0.000802475 0.000884334 0.0006837 0.000554104 0.000470091 0.000550228 0.000720516 PE(16:1_16:1)-H 0.002097248 0.002807945 0.002744747 0.00259501 0.002934992 0.002381505 0.000518927 0.002043829 0.002165515 0.001499232 0.002022752 0.001435874 0.001696783 0.001134953 0.001577476 0.001908123 0.001761538 0.001218829 PC(17:0_18:2)-CH3_2 0.004129399 0.003450277 0.002860478 0.004802822 0.004607222 0.004290685 2.38E-06 0.00510394 0.00020342 0.000388941 0.000366416 0.000297231 0.000969553 0.000799569 0.001210375 0.000810413 0.000677892 0.000791736 OAHFA(2:0_18:0)-H 0.031509558 0.022587628 0.03187168 0.02558072 0.025550285 0.024838294 0.037143739 0.036767357 0.04928839 0.04371013 0.03438355 0.03851704 0.032568987 0.03987811 0.060198839 0.037528875 0.032341544 0.030583177 PC(17:1_18:2COOH)+CH3COO_3 0.001609533 0.000686362 0.002311003 0.001887308 0.001532852 0.001159202 0.006944309 0.001977531 0.00281377 0.004065932 0.004699318 0.003845588 0.006420708 0.005790686 0.002927836 0.002704191 0.00356694 0.004152865 PC(17:0_17:1)+CH3COO_3 0.007429038 0.00270589 0.003827368 0.007113448 0.012249531 0.00585903 0.002307865 0.003724884 0.00911498 0.001026657 0.009121855 0.001117507 0.004973074 0.004278319 0.004348113 0.003976884 0.006763251 0.004145648 PE(22:2COOH_18:2)-H 0.00289535 0.003982912 0.004103402 0.003038892 0.004120683 0.003415702 0.003298161 0.004895203 0.004199258 0.00356566 0.003935761 0.003467416 0.004155498 0.003717676 0.0037596 0.003820696 0.004040183 0.003555732 PC(17:1_17:1)+CH3COO_4 0.00103608 0.000989755 0.000194499 0.001397021 0.000923226 0.001303106 2.00E-09 3.70E-09 3.65E-09 3.09E-09 5.99E-09 9.75E-09 7.98E-09 3.26E-09 3.45E-09 6.25E-09 2.52E-09 3.02E-09 PE(O-19:1_19:1)-H_2 0.002436006 0.002874416 0.002741544 0.002894227 0.004088081 0.003069489 0.003102131 0.002462558 0.002434002 0.001916296 0.001308161 0.001712327 0.002355903 0.001844826 0.001978526 0.002743256 0.002417327 0.001919136 PI(18:0_20:4)-H_2 2.25E-05 5.54E-05 0.000101261 4.88E-05 0.000137738 5.27E-05 0.004277507 0.000272504 0.000249135 0.000261304 0.000134899 0.00028502 9.66E-05 0.000174828 0.000110566 0.004020243 7.95E-05 0.000141892 PC(18:1_9:2CHO)+CH3COO_2 0.000842287 0.00030342 0.002386196 0.000834983 0.000766397 0.001736026 0.001935662 0.001142129 0.001605703 0.000872378 0.002585191 0.002009675 0.001413709 0.002205887 0.001610558 0.001153868 0.001875222 0.001624212 LPC(19:0)+CH3COO_2 0.000790676 0.000793339 0.000584075 0.00078407 0.000851742 0.000784909 0.000211707 0.000331912 0.000457224 0.000259834 0.000360344 0.00031131 0.000393004 0.000353873 0.00034415 0.000247043 0.000298048 0.000258925 PC(17:1_18:1COOH)+CH3COO_4 0.000377318 3.68E-07 0.000637771 0.000472902 0.000246433 0.000418082 0.001343083 0.000569331 0.001497661 0.000992152 0.00106531 0.001203901 0.001573437 0.00112444 0.000928834 0.000935843 0.00136236 0.000892662 PC(18:1_19:1COOH)+HCOO_3 0.000150594 1.61E-06 0.000669116 0.000122163 0.000308932 0.000207924 0.000246261 0.000758093 0.000841338 6.64E-07 4.39E-05 0.000282766 0.000358896 0.000244636 0.00057486 0.000430777 0.000540814 0.00015629 PC(18:1_19:1)-CH3_2 0.001918876 0.001547148 0.001545012 0.003344344 0.00198117 0.002539626 0.000668963 0.000806886 0.000798185 0.001066555 0.001109676 0.000561789 0.00142521 0.000740664 0.000560806 0.000957175 0.000787448 0.000412369 PC(5:0CHO_18:1)+CH3COO_2 0.000780624 0.00023685 0.000806634 0.000624668 0.000569777 0.000455246 0.001553405 0.001801608 0.002724542 0.001678231 0.002696629 0.003279859 0.001604404 0.006342472 0.001987132 0.001083894 0.002088152 0.001268305 PC(5:0CHO_18:1)+CH3COO_3 0.003407473 0.00147344 0.005626647 0.004066868 0.00231345 0.003095279 0.007501498 0.005279702 0.008499423 0.007348115 0.009549297 0.006879769 0.006191784 0.008412861 0.006943856 0.010540486 0.006477397 0.005923128 PE(16:1_2:0)-H 0.004624274 0.000213532 0.001677764 0.004547354 0.002408272 0.002796776 0.00293405 0.000923088 0.003352526 0.002645866 0.004204995 0.002718972 0.00450338 0.002716957 0.003361304 0.002354357 0.002730618 0.001457838 PE(18:0_18:1)-H 0.024169723 0.023087387 0.021975029 0.024309225 0.028672099 0.023361883 0.021967861 0.022296983 0.024965203 0.019956117 0.015467248 0.018823878 0.023684491 0.017891042 0.014805706 0.028079009 0.023080352 0.017303742 PC(18:0COOH_18:1)-CH3 0.00638812 0.004745729 0.006559062 0.005478825 0.00589543 0.005517185 0.001703993 0.007692496 0.006555722 0.006426099 0.010222967 0.005599041 0.006982352 0.006394014 0.00798911 0.004616011 0.006729573 0.006166404 PE(17:1_18:1)-H_2 0.00305432 0.004015197 0.003717665 0.003363577 0.005899754 0.074744751 0.004271919 0.003614486 0.005104691 0.003019001 0.003146509 0.00295687 0.00406086 0.002082686 0.004823578 0.005180399 0.003619243 0.002648728 PI(18:1_20:5)-H_2 0.018568786 0.018604888 0.026424077 0.020307508 0.027196674 0.01999533 0.011308043 0.024156233 0.021525118 0.017751891 0.026844147 0.016915322 0.015959305 0.01758323 0.020323089 0.026044674 0.020239071 0.017156188 PC(16:0_20:5)+CH3COO_4 0.01932837 0.026272667 0.012656997 0.02253058 0.020970396 0.01981449 0.003048212 0.005915062 0.009631904 0.0054134 0.009489248 0.004424844 0.006410848 0.009083263 0.002820545 0.006837071 0.008866286 0.003223072 PC(17:1_18:2COOH)+CH3COO_4 0.001609533 0.000686362 0.002311003 0.001887308 0.001532852 0.001159202 0.006944309 0.001977531 0.00281377 0.003987263 0.004699318 0.0055331 0.006420708 0.005790686 0.002927836 0.002704191 0.00356694 0.004152865 PC(19:1_9:2CHO)+CH3COO 0.00109839 8.65E-05 0.001259454 0.001192451 0.000932901 0.000584274 0.001652323 0.001497209 0.001710448 0.001396797 0.001511227 0.001279657 0.00141864 0.002014465 0.001237754 0.001431019 0.001740898 0.001258212 LPE(20:2)-H_3 0.001422657 0.000957544 0.001105557 0.001350432 0.001598246 0.001033206 0.001078226 0.000701032 0.000584745 0.000607444 0.000917038 0.000516235 0.000610666 0.000775379 0.000960798 0.000733002 0.000629526 0.000725056 LPE(20:1)-H 0.002887462 0.002463424 0.002035389 0.002627946 0.002768346 0.002584115 0.000521726 0.001482165 0.001342889 0.001180504 0.001419882 0.00118033 0.001282686 0.000895652 0.001485911 0.001249715 0.001227169 0.001032516 PC(18:1_18:1COOH)+CH3COO_2 0.000741084 3.96E-05 0.000615848 0.000458621 0.00053665 0.00021449 0.001114555 0.00079961 0.001261673 0.001028188 0.001396452 0.00113447 0.001389691 0.001586504 0.000991779 0.000679106 0.001323298 0.000729532 PE(18:0_20:3)-H_2 0.000647856 0.001570909 0.003550275 0.001708594 0.046319029 0.001955511 0.015550457 0.022580101 0.00088891 0.000840182 0.000633859 0.000745848 0.000986365 0.00088106 0.037588512 0.001265965 0.00131421 0.00022207 PC(18:0_22:6CHO)-CH3 0.000583751 0.000886358 0.001108542 0.000571059 0.000929743 0.000630506 0.000456949 0.000649358 0.000583089 0.000538257 0.000718509 0.000470148 0.000689585 0.000452872 0.000542154 0.000544481 0.000528904 0.000652951 LPE(18:1)-H_4 0.155268484 0.048177167 0.12433797 0.157628652 0.135652766 0.131114092 0.088544508 0.101513317 0.167401046 0.124634165 0.155345215 0.122881322 0.148867552 0.124788377 0.132522021 0.122737715 0.124977381 0.105355271 PE(18:0CHO_18:1)-H_4 0.001389688 0.000110368 0.001066606 0.001408502 0.00119234 0.001045618 0.000655107 0.000826654 0.001223639 0.001044057 0.001434696 0.000853183 0.001046882 0.001273598 0.001253484 0.001049682 0.000948109 0.000468125 CL(20:3_20:3_20:4_20:4)-2H 0.004784882 0.005739446 0.004484241 0.005006955 0.006485257 0.005171438 0.003354021 0.003311236 0.003284553 0.002109342 0.003170902 0.002114426 0.003324019 0.003358719 0.003966348 0.004994313 0.003643306 0.004018723 CL(20:3_20:3_20:3_20:4)-2H 0.001743787 0.001818946 0.001110478 0.001671371 0.002307437 0.001797329 0.002266754 0.001808162 0.001646931 0.001392029 0.002101149 0.001183157 0.001965986 0.002108272 0.002529271 0.002662628 0.002333952 0.0020065 CL(20:4_20:4_20:4_20:4)-2H_1 0.005490624 0.005631069 0.005016165 0.004699502 0.005408522 0.005422368 0.001478693 0.001978789 0.002834436 0.001733214 0.002577667 0.001329994 0.002685617 0.002193231 0.002744851 0.00279047 0.002555165 0.002354492 CL(20:3_20:4_20:4_20:4)-2H 0.006857174 0.007598858 0.006360635 0.008662206 0.008727224 0.007220131 0.003232682 0.004277337 0.004164746 0.002642904 0.003932518 0.002484073 0.003829237 0.003857839 0.004947153 0.006000652 0.003301946 0.004153952 CL(20:4_20:4_20:4_20:4)-2H_2 0.001349373 0.001894335 0.001447148 0.001462898 0.001745584 0.00203962 0.000752506 0.000633055 0.000773511 0.001060654 0.001552606 0.000502376 0.001578598 0.000777397 0.001248516 0.001189328 0.001161193 0.000947509 CL(18:2_20:4_20:4_20:4)-2H 0.00225584 0.002947448 0.00235817 0.002700185 0.003259204 0.003050269 0.001233536 0.001895455 0.001498327 0.001284532 0.002291031 0.001192312 0.001568771 0.001498126 0.002384179 0.002247491 0.001767283 0.001870198 CL(18:2_20:3_20:4_20:4)-2H 0.003215155 0.00291401 0.002990667 0.002839818 0.004009653 0.002577804 0.001633094 0.002567077 0.002252382 0.00209671 0.002401396 0.001681857 0.002247871 0.002004221 0.002422501 0.002505914 0.002333154 0.0018968 CL(18:2_20:3_20:3_20:4)-2H 0.001497667 0.001616628 0.0014411 0.001727165 0.002003513 0.001434066 0.001153699 0.001627395 0.001731326 0.001233596 0.001757599 0.001312695 0.001346521 0.001500926 0.001658635 0.00182313 0.00172573 0.001094617 MS_METABOLITE_DATA_END #METABOLITES METABOLITES_START metabolite_name LipidMapID LipidGroup Charge CalcMz BaseRt Class SubClass AdductIon Pubchem CID KEGG_ID REFMET_ID IonFormula MolStructure LBPA(17:1_18:3)-H_1 LBPA(17:1_18:3)-H LBPA(35:4)-H -1 755.4868615 7.478251418 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H72 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC LBPA(15:0_17:0)-H LBPA(15:0_17:0)-H LBPA(32:0)-H -1 721.5025115 9.745571922 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C38 H74 O10 P1 CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCC LBPA(17:1_18:3)-H_2 LBPA(17:1_18:3)-H LBPA(35:4)-H -1 755.4868615 7.741380735 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H72 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC LBPA(17:1_20:3)-H LBPA(17:1_20:3)-H LBPA(37:4)-H -1 783.5181615 9.206410623 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C43 H76 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCC=CC=CC=CC LBPA(15:0_16:0)-H LBPA(15:0_16:0)-H LBPA(31:0)-H -1 707.4868615 8.794362383 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C37 H72 O10 P1 CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC PG(17:1_18:3)-H PG(17:1_18:3)-H PG(35:4)-H -1 755.4868615 7.739953397 PG diacyl M-H RM0089984 C41 H72 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCC(CO)O PG(16:0_20:5)-H PG(16:0_20:5)-H PG(36:5)-H -1 767.4868615 7.7566365 PG diacyl M-H RM0008060 C42 H72 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PG(15:0_20:5)-H PG(15:0_20:5)-H PG(35:5)-H -1 753.4712115 6.690725297 PG diacyl M-H RM0009202 C41 H70 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O LBPA(16:1_17:1)-H LBPA(16:1_17:1)-H LBPA(33:2)-H -1 731.4868615 8.244846214 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C39 H72 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCC=CC PC(14:0_15:1)+CH3COO PC(14:0_15:1)+CH3COO PC(29:1)+CH3COO -1 748.5134105 7.801625295 PC diacyl M+CH3COO RM0010626 C39 H75 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(19:1_19:1)-H LBPA(19:1_19:1)-H LBPA(38:2)-H -1 801.5651115 14.01395227 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C44 H82 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCC=CC LBPA(17:1_17:1)-H LBPA(17:1_17:1)-H LBPA(34:2)-H -1 745.5025115 9.487305389 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C40 H74 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCC=CC PC(15:0_17:0)+CH3COO PC(15:0_17:0)+CH3COO PC(32:0)+CH3COO -1 792.5760105 12.16444888 PC diacyl M+CH3COO RM0171217 C42 H83 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:1_20:3)+CH3COO PC(O-18:1_20:3)+CH3COO PC(O-38:4)+CH3COO -1 854.6280455 15.35975078 PC alkyl-acyl M+CH3COO RM0017289 C48 H89 N1 O9 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:1_18:4)+CH3COO PC(15:1_18:4)+CH3COO PC(33:5)+CH3COO -1 796.5134105 6.488213505 PC diacyl M+CH3COO RM0000475 C43 H75 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(17:1_18:1)-H PG(17:1_18:1)-H PG(35:2)-H -1 759.5181615 10.14463988 PG diacyl M-H RM0007600 C41 H76 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O LBPA(18:1_19:1)-H LBPA(18:1_19:1)-H LBPA(37:2)-H -1 787.5494615 12.43742598 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C43 H80 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCC=CC PC(18:0_20:3)+CH3COO PC(18:0_20:3)+CH3COO PC(38:3)+CH3COO -1 870.6229605 14.48374803 PC diacyl M+CH3COO RM0170562 C48 H89 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(17:1_18:1)-H LBPA(17:1_18:1)-H LBPA(35:2)-H -1 759.5181615 10.1734822 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H76 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC LPC(14:0)+CH3COO LPC(14:0)+CH3COO LPC(14:0)+CH3COO -1 526.3150455 2.004361486 LPC monoacyl M+CH3COO 460604 C04230 RM0135070 C24 H49 N1 O9 P1 CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_19:1)-H_1 PE(18:1_19:1)-H PE(37:2)-H -1 756.5548805 15.0534601 PE diacyl M-H RM0097460 C42 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_20:3COOH)+CH3COO PC(17:1_20:3COOH)+CH3COO PC(37:4COOH)+CH3COO -1 884.5658405 5.422387091 PC carboxylic M+CH3COO - - - C47 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_16:1)+CH3COO PC(14:0_16:1)+CH3COO PC(30:1)+CH3COO -1 762.5290605 8.494000415 PC diacyl M+CH3COO RM0090012 C40 H77 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:3)+CH3COO PC(17:1_20:3)+CH3COO PC(37:4)+CH3COO -1 854.5916605 11.23012359 PC diacyl M+CH3COO RM0104000 C47 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(19:1_20:4)-H_1 LBPA(19:1_20:4)-H LBPA(39:5)-H -1 809.5338115 10.44567564 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C45 H78 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC=CC PC(14:0_20:5)+CH3COO PC(14:0_20:5)+CH3COO PC(34:5)+CH3COO -1 810.5290605 7.749317396 PC diacyl M+CH3COO RM0171040 C44 H77 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(12:0_20:5)+CH3COO_1 PC(12:0_20:5)+CH3COO PC(32:5)+CH3COO -1 782.4977605 6.100894193 PC diacyl M+CH3COO RM0090075 C42 H73 N1 O10 P1 CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:3_20:3)+CH3COO PC(20:3_20:3)+CH3COO PC(40:6)+CH3COO -1 892.6073105 10.85371438 PC diacyl M+CH3COO RM0000942 C50 H87 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:4COOH)+CH3COO_1 PC(17:1_20:4COOH)+CH3COO PC(37:5COOH)+CH3COO -1 882.5501905 5.188894646 PC carboxylic M+CH3COO - - - C47 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_20:4)+CH3COO_1 PC(14:0_20:4)+CH3COO PC(34:4)+CH3COO -1 812.5447105 8.675638438 PC diacyl M+CH3COO RM0000558 C44 H79 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(20:4)+CH3COO_1 LPC(20:4)+CH3COO LPC(20:4)+CH3COO -1 602.3463455 2.41264551 LPC monoacyl M+CH3COO RM0048636 C30 H53 N1 O9 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C Cer(t18:1_24:0)-H_1 Cer(t18:1_24:0)-H Cer(t42:1)-H -1 664.6249325 18.50579481 Cer phytoceramides M-H RM0030583 C42 H82 N1 O4 CCCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(14:0_15:0)+CH3COO PC(14:0_15:0)+CH3COO PC(29:0)+CH3COO -1 750.5290605 8.968584916 PC diacyl M+CH3COO RM0090055 C39 H77 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_18:3)+CH3COO_1 PC(18:0_18:3)+CH3COO PC(36:3)+CH3COO -1 842.5916605 12.56271735 PC diacyl M+CH3COO RM0000424 C46 H85 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:3_20:4)+CH3COO_1 PC(20:3_20:4)+CH3COO PC(40:7)+CH3COO -1 890.5916605 9.356832024 PC diacyl M+CH3COO RM0000550 C50 H85 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_20:5)+CH3COO_1 PC(20:4_20:5)+CH3COO PC(40:9)+CH3COO -1 886.5603605 7.665219069 PC diacyl M+CH3COO RM0171159 C50 H81 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:0_24:0)-H Cer(d17:0_24:0)-H Cer(d41:0)-H -1 636.6300175 19.07126204 Cer acylsphinganines M-H 134731836 RM0122384 C41 H82 N1 O3 CCCCCCCCCCCCCCC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(15:1_20:4)+CH3COO PC(15:1_20:4)+CH3COO PC(35:5)+CH3COO -1 824.5447105 8.045217881 PC diacyl M+CH3COO RM0171240 C45 H79 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:2)-CH3_1 PC(17:1_18:2)-CH3 PC(35:3)-CH3 -1 754.5392305 10.76255667 PC diacyl M-CH3 RM0025431 C42 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(16:0_18:2)-H LBPA(16:0_18:2)-H LBPA(34:2)-H -1 745.5025115 9.241842302 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188194 C40 H74 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCC=CC=CC Cer(t17:0_23:1)-H_1 Cer(t17:0_23:1)-H Cer(t40:1)-H -1 636.5936325 17.77967361 Cer phytoceramides M-H RM0184866 C40 H78 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCC=CC)O Cer(t18:1_24:0)-H_2 Cer(t18:1_24:0)-H Cer(t42:1)-H -1 664.6249325 18.33279076 Cer phytoceramides M-H RM0030583 C42 H82 N1 O4 CCCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(20:4_20:4)+CH3COO_1 PC(20:4_20:4)+CH3COO PC(40:8)+CH3COO -1 888.5760105 8.922701881 PC diacyl M+CH3COO RM0136719 C50 H83 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(20:3)+CH3COO LPC(20:3)+CH3COO LPC(20:3)+CH3COO -1 604.3619955 2.865597781 LPC monoacyl M+CH3COO RM0134469 C30 H55 N1 O9 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(15:1_20:5)+CH3COO_1 PC(15:1_20:5)+CH3COO PC(35:6)+CH3COO -1 822.5290605 6.937168914 PC diacyl M+CH3COO RM0171229 C45 H77 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4COOH_20:5)+CH3COO_1 PC(20:4COOH_20:5)+CH3COO PC(40:9COOH)+CH3COO -1 916.5345405 4.198733196 PC carboxylic M+CH3COO - - - C50 H79 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_20:4)+CH3COO PC(17:0_20:4)+CH3COO PC(37:4)+CH3COO -1 854.5916605 12.21155103 PC diacyl M+CH3COO RM0024950 C47 H85 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(18:1_20:4)-H_1 PG(18:1_20:4)-H PG(38:5)-H -1 795.5181615 9.021915853 PG diacyl M-H RM0030872 C44 H76 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PC(14:0_17:1)+CH3COO_1 PC(14:0_17:1)+CH3COO PC(31:1)+CH3COO -1 776.5447105 9.8255685 PC diacyl M+CH3COO RM0097915 C41 H79 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(13:0_20:5)+CH3COO PC(13:0_20:5)+CH3COO PC(33:5)+CH3COO -1 796.5134105 6.410961279 PC diacyl M+CH3COO RM0001066 C43 H75 N1 O10 P1 CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d12:1_16:0_21:3)+HCOO_1 Cer(d12:1_16:0_21:3)+HCOO Cer(d49:4)+HCOO -1 800.6773625 18.98698537 Cer acylceramides M+HCOO - - - C50 H90 N1 O6 CCCCCCCC=CC(C(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC)NC(=O)CCCCCCCCCCCCCCC)O PC(18:2_21:3COOH)+HCOO_1 PC(18:2_21:3COOH)+HCOO PC(39:5COOH)+HCOO -1 896.5658405 5.030012556 PC carboxylic M+HCOO - - - C48 H83 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(20:3_21:4COOH)+HCOO PC(20:3_21:4COOH)+HCOO PC(41:7COOH)+HCOO -1 920.5658405 4.959410539 PC carboxylic M+HCOO - - - C50 H83 N1 O12 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_18:3)+CH3COO_1 PC(15:0_18:3)+CH3COO PC(33:3)+CH3COO -1 800.5447105 8.604865551 PC diacyl M+CH3COO RM0010922 C43 H79 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C OAHFA(2:0_24:0)-H_1 OAHFA(2:0_24:0)-H OAHFA(26:0)-H -1 425.3636335 7.240578886 OAHFA Fatty ethers M-H - - - C26 H49 O4 CC(=O)OCCCCCCCCCCCCCCCCCCCCCCCC(=O)O PC(15:1_20:5)+CH3COO_2 PC(15:1_20:5)+CH3COO PC(35:6)+CH3COO -1 822.5290605 7.084170055 PC diacyl M+CH3COO RM0171229 C45 H77 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_20:4)+CH3COO_1 PC(18:0_20:4)+CH3COO PC(38:4)+CH3COO -1 868.6073105 12.81594751 PC diacyl M+CH3COO RM0134946 C48 H87 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_18:3)+CH3COO_1 PC(14:0_18:3)+CH3COO PC(32:3)+CH3COO -1 786.5290605 7.921535621 PC diacyl M+CH3COO RM0036655 C42 H77 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:3COOH)+CH3COO PC(18:1_20:3COOH)+CH3COO PC(38:4COOH)+CH3COO -1 898.5814905 5.778266895 PC carboxylic M+CH3COO - - - C48 H85 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_18:4)+CH3COO PC(14:0_18:4)+CH3COO PC(32:4)+CH3COO -1 784.5134105 6.821092253 PC diacyl M+CH3COO RM0025104 C42 H75 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d14:1_28:0)-H_1 Cer(d14:1_28:0)-H Cer(d42:1)-H -1 648.6300175 19.15797123 Cer acylsphingosines M-H 145714679 RM0030212 C42 H82 N1 O3 CCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCCCCCC)O PC(19:1COOH_20:5)+HCOO PC(19:1COOH_20:5)+HCOO PC(39:6COOH)+HCOO -1 894.5501905 4.489009144 PC carboxylic M+HCOO - - - C48 H81 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:4COOH)-H_1 PE(17:0_20:4COOH)-H PE(37:4COOH)-H -1 782.4977605 6.11238688 PE carboxylic M-H - - - C42 H73 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)(O)OCCN Cer(t17:0_24:1)-H_1 Cer(t17:0_24:1)-H Cer(t41:1)-H -1 650.6092825 18.10995766 Cer phytoceramides M-H RM0013477 C41 H80 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC=CC)O Cer(d17:1_24:0)-H_1 Cer(d17:1_24:0)-H Cer(d41:1)-H -1 634.6143675 18.58395588 Cer acylsphingosines M-H 71581116 RM0030140 C41 H80 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(15:0_16:0)+CH3COO_1 PC(15:0_16:0)+CH3COO PC(31:0)+CH3COO -1 778.5603605 11.28146845 PC diacyl M+CH3COO RM0134942 C41 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PG(17:1_17:1)-H PG(17:1_17:1)-H PG(34:2)-H -1 745.5025115 9.460814401 PG diacyl M-H RM0010528 C40 H74 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O PC(16:0_20:3)+CH3COO PC(16:0_20:3)+CH3COO PC(36:3)+CH3COO -1 842.5916605 11.93329337 PC diacyl M+CH3COO RM0014008 C46 H85 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:5)-CH3_1 PC(18:2_20:5)-CH3 PC(38:7)-CH3 -1 788.5235805 7.987400035 PC diacyl M-CH3 RM0171080 C45 H75 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:0_20:3)+CH3COO PC(20:0_20:3)+CH3COO PC(40:3)+CH3COO -1 898.6542605 16.22423039 PC diacyl M+CH3COO RM0097913 C50 H93 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t19:0_24:0)-H Cer(t19:0_24:0)-H Cer(t43:0)-H -1 680.6562325 19.22422949 Cer phytoceramides M-H 145715045 RM0001831 C43 H86 N1 O4 CCCCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(18:1COOH_20:5)+CH3COO PC(18:1COOH_20:5)+CH3COO PC(38:6COOH)+CH3COO -1 894.5501905 4.504567103 PC carboxylic M+CH3COO - - - C48 H81 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:0_26:1)-H_1 Cer(t17:0_26:1)-H Cer(t43:1)-H -1 678.6405825 18.99463656 Cer phytoceramides M-H RM0048174 C43 H84 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC=CC)O PC(15:0_15:0)+CH3COO PC(15:0_15:0)+CH3COO PC(30:0)+CH3COO -1 764.5447105 9.702721692 PC diacyl M+CH3COO 24778654 RM0135044 C40 H79 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_20:4COOH)+CH3COO_1 PC(15:0_20:4COOH)+CH3COO PC(35:4COOH)+CH3COO -1 856.5345405 4.810347739 PC carboxylic M+CH3COO - - - C45 H79 N1 O12 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C LBPA(18:1_20:3)-H LBPA(18:1_20:3)-H LBPA(38:4)-H -1 797.5338115 9.866832909 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188247 C44 H78 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCC=CC=CC=CC LBPA(17:1_19:1)-H LBPA(17:1_19:1)-H LBPA(36:2)-H -1 773.5338115 11.67211383 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C42 H78 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCC=CC PC(17:0_18:3)+CH3COO_1 PC(17:0_18:3)+CH3COO PC(35:3)+CH3COO -1 828.5760105 11.09701107 PC diacyl M+CH3COO RM0025609 C45 H83 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:1_15:1)+CH3COO PC(15:1_15:1)+CH3COO PC(30:2)+CH3COO -1 760.5134105 7.489118133 PC diacyl M+CH3COO RM0010936 C40 H75 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:1_20:4)-H_1 PE(O-19:1_20:4)-H PE(O-39:5)-H -1 764.5599655 15.6683891 PE alkyl-acyl M-H RM0182190 C44 H79 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:2_18:2)-CH3 PC(18:2_18:2)-CH3 PC(36:4)-CH3 -1 766.5392305 9.640485156 PC diacyl M-CH3 RM0134908 C43 H77 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:0_20:4)+CH3COO_1 PC(20:0_20:4)+CH3COO PC(40:4)+CH3COO -1 896.6386105 15.60054185 PC diacyl M+CH3COO RM0000901 C50 H91 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:0_20:4)+CH3COO_2 PC(20:0_20:4)+CH3COO PC(40:4)+CH3COO -1 896.6386105 15.16487874 PC diacyl M+CH3COO RM0000901 C50 H91 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_18:3)+CH3COO_1 PC(16:0_18:3)+CH3COO PC(34:3)+CH3COO -1 814.5603605 10.04938581 PC diacyl M+CH3COO RM0000422 C44 H81 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_20:4)+CH3COO_2 PC(18:0_20:4)+CH3COO PC(38:4)+CH3COO -1 868.6073105 13.46867876 PC diacyl M+CH3COO RM0134946 C48 H87 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t16:0_22:1)-H Cer(t16:0_22:1)-H Cer(t38:1)-H -1 608.5623325 16.81294021 Cer phytoceramides M-H RM0171489 C38 H74 N1 O4 CCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCC=CC)O Cer(t17:0_23:1)-H_2 Cer(t17:0_23:1)-H Cer(t40:1)-H -1 636.5936325 17.57393474 Cer phytoceramides M-H RM0184866 C40 H78 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCC=CC)O PC(18:2_20:4COOH)+CH3COO_1 PC(18:2_20:4COOH)+CH3COO PC(38:6COOH)+CH3COO -1 894.5501905 5.651283206 PC carboxylic M+CH3COO - - - C48 H81 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C Cer(t18:1_26:0)-H Cer(t18:1_26:0)-H Cer(t44:1)-H -1 692.6562325 19.37622529 Cer phytoceramides M-H RM0161776 C44 H86 N1 O4 CCCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCCCC)O PC(16:0_20:4)+CH3COO_1 PC(16:0_20:4)+CH3COO PC(36:4)+CH3COO -1 840.5760105 10.33743315 PC diacyl M+CH3COO RM0134944 C46 H83 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_20:4)+CH3COO_2 PC(16:0_20:4)+CH3COO PC(36:4)+CH3COO -1 840.5760105 10.92956226 PC diacyl M+CH3COO RM0134944 C46 H83 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(20:4_20:5)-H_1 PG(20:4_20:5)-H PG(40:9)-H -1 815.4868615 6.377263167 PG diacyl M-H RM0012201 C46 H72 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PC(20:4_20:5)+CH3COO_2 PC(20:4_20:5)+CH3COO PC(40:9)+CH3COO -1 886.5603605 7.306709228 PC diacyl M+CH3COO RM0171159 C50 H81 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(15:0)+CH3COO_1 LPC(15:0)+CH3COO LPC(15:0)+CH3COO -1 540.3306955 2.38592607 LPC monoacyl M+CH3COO RM0017309 C25 H51 N1 O9 P1 CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C Cer(t16:0_24:1)-H Cer(t16:0_24:1)-H Cer(t40:1)-H -1 636.5936325 17.96534057 Cer phytoceramides M-H RM0171499 C40 H78 N1 O4 CCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC=CC)O PC(21:3COOH_20:4)+HCOO_1 PC(21:3COOH_20:4)+HCOO PC(41:7COOH)+HCOO -1 920.5658405 5.033477131 PC carboxylic M+HCOO - - - C50 H83 N1 O12 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:1_20:5)+CH3COO_1 PC(O-18:1_20:5)+CH3COO PC(O-38:6)+CH3COO -1 850.5967455 12.94650998 PC alkyl-acyl M+CH3COO RM0051852 C48 H85 N1 O9 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:1_20:5)+CH3COO_2 PC(O-18:1_20:5)+CH3COO PC(O-38:6)+CH3COO -1 850.5967455 12.95932228 PC alkyl-acyl M+CH3COO RM0051852 C48 H85 N1 O9 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d12:0_16:0_16:0)+HCOO_1 Cer(d12:0_16:0_16:0)+HCOO Cer(d44:0)+HCOO -1 738.6617125 18.99352413 Cer acylceramides M+HCOO - - - C45 H88 N1 O6 CCCCCCCCCC(C(COC(=O)CCCCCCCCCCCCCCC)NC(=O)CCCCCCCCCCCCCCC)O PC(20:4_20:4COOH)+CH3COO PC(20:4_20:4COOH)+CH3COO PC(40:8COOH)+CH3COO -1 918.5501905 4.508733488 PC carboxylic M+CH3COO - - - C50 H81 N1 O12 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C Cer(t18:1_24:0)+HCOO Cer(t18:1_24:0)+HCOO Cer(t42:1)+HCOO -1 710.6304125 18.73427778 Cer phytoceramides M+HCOO RM0030583 C43 H84 N1 O6 CCCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(17:0_18:0)+CH3COO_1 PC(17:0_18:0)+CH3COO PC(35:0)+CH3COO -1 834.6229605 15.86657573 PC diacyl M+CH3COO RM0097697 C45 H89 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4)-CH3_1 PC(18:1_20:4)-CH3 PC(38:5)-CH3 -1 792.5548805 10.98663525 PC diacyl M-CH3 RM0134948 C45 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(17:1)-H_1 LPE(17:1)-H LPE(17:1)-H -1 464.2782655 3.017179564 LPE monoacyl M-H RM0007291 C22 H43 N1 O7 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN LBPA(17:1_20:5)-H LBPA(17:1_20:5)-H LBPA(37:6)-H -1 779.4868615 7.098409927 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C43 H72 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCC=CC=CC=CC=CC=CC PC(17:2_20:3)+CH3COO PC(17:2_20:3)+CH3COO PC(37:5)+CH3COO -1 852.5760105 9.235514613 PC diacyl M+CH3COO RM0171259 C47 H83 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:1_24:0)+HCOO Cer(d17:1_24:0)+HCOO Cer(d41:1)+HCOO -1 680.6198475 18.75716308 Cer acylsphingosines M+HCOO 71581116 RM0030140 C42 H82 N1 O5 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O LBPA(20:4_20:5)-H_1 LBPA(20:4_20:5)-H LBPA(40:9)-H -1 815.4868615 6.393323394 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188371 C46 H72 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC=CC PC(18:1_20:4)+CH3COO_1 PC(18:1_20:4)+CH3COO PC(38:5)+CH3COO -1 866.5916605 10.98663525 PC diacyl M+CH3COO RM0134948 C48 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_20:5)+CH3COO_1 PC(18:0_20:5)+CH3COO PC(38:5)+CH3COO -1 866.5916605 11.86441951 PC diacyl M+CH3COO RM0025394 C48 H85 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_20:5)+CH3COO_1 PC(16:0_20:5)+CH3COO PC(36:5)+CH3COO -1 838.5603605 9.632717234 PC diacyl M+CH3COO RM0171098 C46 H81 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(22:0_20:5)+CH3COO PC(22:0_20:5)+CH3COO PC(42:5)+CH3COO -1 922.6542605 16.14583994 PC diacyl M+CH3COO RM0011101 C52 H93 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(22:0_18:1)+CH3COO PC(22:0_18:1)+CH3COO PC(40:1)+CH3COO -1 902.6855605 17.97147607 PC diacyl M+CH3COO RM0000034 C50 H97 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1)+HCOO PC(17:1_18:1)+HCOO PC(35:2)+HCOO -1 816.5760105 12.37056314 PC diacyl M+HCOO RM0000418 C44 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:3)+CH3COO_1 PC(17:1_18:3)+CH3COO PC(35:4)+CH3COO -1 826.5603605 9.411412046 PC diacyl M+CH3COO RM0097695 C45 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_20:4)+CH3COO_2 PC(14:0_20:4)+CH3COO PC(34:4)+CH3COO -1 812.5447105 8.182748369 PC diacyl M+CH3COO RM0000558 C44 H79 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(21:0_20:5)+CH3COO PC(21:0_20:5)+CH3COO PC(41:5)+CH3COO -1 908.6386105 15.36174608 PC diacyl M+CH3COO RM0000197 C51 H91 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:5_20:5)+CH3COO PC(20:5_20:5)+CH3COO PC(40:10)+CH3COO -1 884.5447105 6.613268337 PC diacyl M+CH3COO RM0134892 C50 H79 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d12:1_16:0_21:3)+HCOO_2 Cer(d12:1_16:0_21:3)+HCOO Cer(d49:4)+HCOO -1 800.6773625 19.14619085 Cer acylceramides M+HCOO - - - C50 H90 N1 O6 CCCCCCCC=CC(C(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC)NC(=O)CCCCCCCCCCCCCCC)O PC(20:4_20:5)+HCOO_1 PC(20:4_20:5)+HCOO PC(40:9)+HCOO -1 872.5447105 7.665219069 PC diacyl M+HCOO RM0171159 C49 H79 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:5_20:5)+HCOO_1 PC(20:5_20:5)+HCOO PC(40:10)+HCOO -1 870.5290605 6.613268337 PC diacyl M+HCOO RM0134892 C49 H77 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:4_20:5)+CH3COO_1 PC(19:4_20:5)+CH3COO PC(39:9)+CH3COO -1 872.5447105 6.895613912 PC diacyl M+CH3COO - - - C49 H79 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_20:3)+CH3COO PC(18:3_20:3)+CH3COO PC(38:6)+CH3COO -1 864.5760105 8.959368078 PC diacyl M+CH3COO RM0000029 C48 H83 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1CHO_20:5)+CH3COO_1 PC(18:1CHO_20:5)+CH3COO PC(38:6CHO)+CH3COO -1 878.5552755 5.163358433 PC aldehyde M+CH3COO - - - C48 H81 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_20:4COOH)+CH3COO_2 PC(15:0_20:4COOH)+CH3COO PC(35:4COOH)+CH3COO -1 856.5345405 5.639699317 PC carboxylic M+CH3COO - - - C45 H79 N1 O12 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1CHO_20:5)+CH3COO_2 PC(18:1CHO_20:5)+CH3COO PC(38:6CHO)+CH3COO -1 878.5552755 5.075068387 PC aldehyde M+CH3COO - - - C48 H81 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:0_22:1)-H_1 Cer(t17:0_22:1)-H Cer(t39:1)-H -1 622.5779825 17.00250312 Cer phytoceramides M-H RM0124848 C39 H76 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCC=CC)O PC(20:4_21:4COOH)+HCOO_1 PC(20:4_21:4COOH)+HCOO PC(41:8COOH)+HCOO -1 918.5501905 5.234539424 PC carboxylic M+HCOO - - - C50 H81 N1 O12 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PG(19:1_20:5)-H PG(19:1_20:5)-H PG(39:6)-H -1 807.5181615 9.106063994 PG diacyl M-H - - - C45 H76 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PC(17:0_18:4)+CH3COO PC(17:0_18:4)+CH3COO PC(35:4)+CH3COO -1 826.5603605 9.764020024 PC diacyl M+CH3COO RM0097661 C45 H81 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:0_22:0)-H Cer(d17:0_22:0)-H Cer(d39:0)-H -1 608.5987175 18.16324023 Cer acylsphinganines M-H 134743225 RM0012635 C39 H78 N1 O3 CCCCCCCCCCCCCCC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC)O PC(19:1_20:5)+CH3COO_1 PC(19:1_20:5)+CH3COO PC(39:6)+CH3COO -1 878.5916605 10.57155179 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_20:4COOH)+CH3COO PC(16:0_20:4COOH)+CH3COO PC(36:4COOH)+CH3COO -1 870.5501905 5.437793849 PC carboxylic M+CH3COO - - - C46 H81 N1 O12 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_20:4)-H_1 PE(O-18:1_20:4)-H PE(O-38:5)-H -1 750.5443155 15.19461825 PE alkyl-acyl M-H RM0008857 C43 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(O-19:1_20:5)-H_1 PE(O-19:1_20:5)-H PE(O-39:6)-H -1 762.5443155 14.91205607 PE alkyl-acyl M-H - - - C44 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(20:2_20:4)+CH3COO_1 PC(20:2_20:4)+CH3COO PC(40:6)+CH3COO -1 892.6073105 11.46804324 PC diacyl M+CH3COO RM0011314 C50 H87 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_21:3COOH)+HCOO_2 PC(18:2_21:3COOH)+HCOO PC(39:5COOH)+HCOO -1 896.5658405 4.963126592 PC carboxylic M+HCOO - - - C48 H83 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(20:0_20:5)+CH3COO PC(20:0_20:5)+CH3COO PC(40:5)+CH3COO -1 894.6229605 14.39412488 PC diacyl M+CH3COO RM0001103 C50 H89 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(18:2_20:5)-H LBPA(18:2_20:5)-H LBPA(38:7)-H -1 791.4868615 6.668662736 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188365 C44 H72 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCC=CC=CC=CC=CC=CC PE(22:3COOH_17:1)-H PE(22:3COOH_17:1)-H PE(39:4COOH)-H -1 810.5290605 13.12580026 PE carboxylic M-H - - - C44 H77 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)(O)OCCN PC(14:0_18:3)+CH3COO_2 PC(14:0_18:3)+CH3COO PC(32:3)+CH3COO -1 786.5290605 7.665113852 PC diacyl M+CH3COO RM0036655 C42 H77 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-20:2_20:4)-H PE(O-20:2_20:4)-H PE(O-40:6)-H -1 776.5599655 15.12960853 PE alkyl-acyl M-H RM0054835 C45 H79 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:1_20:5)+CH3COO_1 PC(18:1_20:5)+CH3COO PC(38:6)+CH3COO -1 864.5760105 9.833384019 PC diacyl M+CH3COO RM0000028 C48 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_20:5)+CH3COO_1 PC(18:3_20:5)+CH3COO PC(38:8)+CH3COO -1 860.5447105 7.050619814 PC diacyl M+CH3COO RM0024946 C48 H79 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:0_21:0)-H Cer(d17:0_21:0)-H Cer(d38:0)-H -1 594.5830675 17.64090747 Cer acylsphinganines M-H 134741107 RM0124689 C38 H76 N1 O3 CCCCCCCCCCCCCCC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCC)O PC(19:1_20:3)+CH3COO_1 PC(19:1_20:3)+CH3COO PC(39:4)+CH3COO -1 882.6229605 13.73609064 PC diacyl M+CH3COO RM0181476 C49 H89 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:0_20:4)-H PE(O-19:0_20:4)-H PE(O-39:4)-H -1 766.5756155 16.05603971 PE alkyl-acyl M-H RM0182184 C44 H81 N1 O7 P1 CCCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:0_19:0)+CH3COO PC(18:0_19:0)+CH3COO PC(37:0)+CH3COO -1 862.6542605 17.44572687 PC diacyl M+CH3COO RM0171079 C47 H93 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(20:4_20:5)-H_2 LBPA(20:4_20:5)-H LBPA(40:9)-H -1 815.4868615 6.125947972 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188371 C46 H72 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC=CC Cer(t17:0_26:1)-H_2 Cer(t17:0_26:1)-H Cer(t43:1)-H -1 678.6405825 19.14521588 Cer phytoceramides M-H RM0048174 C43 H84 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC=CC)O PC(15:0_20:4)+CH3COO PC(15:0_20:4)+CH3COO PC(35:4)+CH3COO -1 826.5603605 8.895695479 PC diacyl M+CH3COO RM0098329 C45 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(17:1_20:4)-H LBPA(17:1_20:4)-H LBPA(37:5)-H -1 781.5025115 7.974335881 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C43 H74 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC=CC PC(18:1_18:2COOH)+CH3COO_1 PC(18:1_18:2COOH)+CH3COO PC(36:3COOH)+CH3COO -1 872.5658405 5.729156981 PC carboxylic M+CH3COO - - - C46 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(20:4_20:5)-H_1 PE(20:4_20:5)-H PE(40:9)-H -1 784.4922805 8.168584327 PE diacyl M-H RM0043955 C45 H71 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:0_18:0)+CH3COO_2 PC(17:0_18:0)+CH3COO PC(35:0)+CH3COO -1 834.6229605 16.14553503 PC diacyl M+CH3COO RM0097697 C45 H89 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:3_20:5)+HCOO PC(20:3_20:5)+HCOO PC(40:8)+HCOO -1 874.5603605 8.499522482 PC diacyl M+HCOO RM0000188 C49 H81 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:1_17:1)+CH3COO PC(15:1_17:1)+CH3COO PC(32:2)+CH3COO -1 788.5447105 9.340504634 PC diacyl M+CH3COO RM0001078 C42 H79 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_20:5)+HCOO_2 PC(20:4_20:5)+HCOO PC(40:9)+HCOO -1 872.5447105 7.306709228 PC diacyl M+HCOO RM0171159 C49 H79 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(17:1)+CH3COO LPC(17:1)+CH3COO LPC(17:1)+CH3COO -1 566.3463455 2.857293811 LPC monoacyl M+CH3COO RM0134477 C27 H53 N1 O9 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PG(20:5_20:5)-H PG(20:5_20:5)-H PG(40:10)-H -1 813.4712115 5.594525585 PG diacyl M-H RM0030938 C46 H70 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O Cer(d12:1_16:0_16:0)+HCOO Cer(d12:1_16:0_16:0)+HCOO Cer(d44:1)+HCOO -1 736.6460625 18.17283249 Cer acylceramides M+HCOO - - - C45 H86 N1 O6 CCCCCCCC=CC(C(COC(=O)CCCCCCCCCCCCCCC)NC(=O)CCCCCCCCCCCCCCC)O PC(14:0_18:2)+CH3COO PC(14:0_18:2)+CH3COO PC(32:2)+CH3COO -1 788.5447105 8.968157484 PC diacyl M+CH3COO RM0000621 C42 H79 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:1_18:2)+CH3COO PC(O-18:1_18:2)+CH3COO PC(O-36:3)+CH3COO -1 828.6123955 14.88869019 PC alkyl-acyl M+CH3COO RM0017288 C46 H87 N1 O9 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_18:3)+CH3COO_2 PC(15:0_18:3)+CH3COO PC(33:3)+CH3COO -1 800.5447105 8.31030465 PC diacyl M+CH3COO RM0010922 C43 H79 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(18:1_18:2)-H LBPA(18:1_18:2)-H LBPA(36:3)-H -1 771.5181615 9.301376929 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188242 C42 H76 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC PC(17:1_18:3)+CH3COO_2 PC(17:1_18:3)+CH3COO PC(35:4)+CH3COO -1 826.5603605 9.118417185 PC diacyl M+CH3COO RM0097695 C45 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:1_24:0)-H_2 Cer(d17:1_24:0)-H Cer(d41:1)-H -1 634.6143675 18.75716308 Cer acylsphingosines M-H 71581116 RM0030140 C41 H80 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(18:1_20:3)-CH3 PC(18:1_20:3)-CH3 PC(38:4)-CH3 -1 794.5705305 12.45397461 PC diacyl M-CH3 RM0171082 C45 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:1_20:4)-H_2 PE(O-19:1_20:4)-H PE(O-39:5)-H -1 764.5599655 15.26739457 PE alkyl-acyl M-H RM0182190 C44 H79 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN LPC(16:0)+CH3COO_1 LPC(16:0)+CH3COO LPC(16:0)+CH3COO -1 554.3463455 3.12360562 LPC monoacyl M+CH3COO RM0134475 C26 H53 N1 O9 P1 CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_20:4COOH)-H PE(16:0_20:4COOH)-H PE(36:4COOH)-H -1 768.4821105 5.671172277 PE carboxylic M-H - - - C41 H71 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)(O)OCCN PC(18:3_20:4)+CH3COO PC(18:3_20:4)+CH3COO PC(38:7)+CH3COO -1 862.5603605 7.557563441 PC diacyl M+CH3COO RM0171097 C48 H81 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:4)+CH3COO_1 PC(19:1_20:4)+CH3COO PC(39:5)+CH3COO -1 880.6073105 11.9314747 PC diacyl M+CH3COO RM0000618 C49 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_18:0)+CH3COO PC(15:0_18:0)+CH3COO PC(33:0)+CH3COO -1 806.5916605 13.90804191 PC diacyl M+CH3COO RM0171221 C43 H85 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C LPC(17:2)+CH3COO_1 LPC(17:2)+CH3COO LPC(17:2)+CH3COO -1 564.3306955 2.023195019 LPC monoacyl M+CH3COO RM0134495 C27 H51 N1 O9 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C LPC(17:2)+CH3COO_2 LPC(17:2)+CH3COO LPC(17:2)+CH3COO -1 564.3306955 2.04859532 LPC monoacyl M+CH3COO RM0134495 C27 H51 N1 O9 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(19:3_20:3)+CH3COO PC(19:3_20:3)+CH3COO PC(39:6)+CH3COO -1 878.5916605 9.845396446 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_18:1COOH)-H_1 PE(17:0_18:1COOH)-H PE(35:1COOH)-H -1 760.5134105 6.857371175 PE carboxylic M-H - - - C40 H75 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PE(17:0_18:1COOH)-H_2 PE(17:0_18:1COOH)-H PE(35:1COOH)-H -1 760.5134105 6.885621362 PE carboxylic M-H - - - C40 H75 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN Cer(d12:0_16:0_16:0)+HCOO_2 Cer(d12:0_16:0_16:0)+HCOO Cer(d44:0)+HCOO -1 738.6617125 19.14715886 Cer acylceramides M+HCOO - - - C45 H88 N1 O6 CCCCCCCCCC(C(COC(=O)CCCCCCCCCCCCCCC)NC(=O)CCCCCCCCCCCCCCC)O PC(15:0_17:1)+CH3COO_1 PC(15:0_17:1)+CH3COO PC(32:1)+CH3COO -1 790.5603605 10.59067496 PC diacyl M+CH3COO RM0036654 C42 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1)+CH3COO_1 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 13.14760719 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_20:3)+CH3COO PC(15:0_20:3)+CH3COO PC(35:3)+CH3COO -1 828.5760105 10.44313243 PC diacyl M+CH3COO RM0024925 C45 H83 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(17:1_18:2)-H LBPA(17:1_18:2)-H LBPA(35:3)-H -1 757.5025115 8.685778312 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H74 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCC=CC=CC LPC(17:0)+CH3COO_1 LPC(17:0)+CH3COO LPC(17:0)+CH3COO -1 568.3619955 3.333034085 LPC monoacyl M+CH3COO RM0134474 C27 H55 N1 O9 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(18:4_20:5)+CH3COO PC(18:4_20:5)+CH3COO PC(38:9)+CH3COO -1 858.5290605 6.086982809 PC diacyl M+CH3COO RM0011025 C48 H77 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:5_20:5)+HCOO_2 PC(20:5_20:5)+HCOO PC(40:10)+HCOO -1 870.5290605 5.987099727 PC diacyl M+HCOO RM0134892 C49 H77 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_20:4COOH)-H PE(18:0_20:4COOH)-H PE(38:4COOH)-H -1 796.5134105 7.083759327 PE carboxylic M-H - - - C43 H75 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)(O)OCCN PC(19:1_20:5)+CH3COO_2 PC(19:1_20:5)+CH3COO PC(39:6)+CH3COO -1 878.5916605 10.39756375 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_18:3)+CH3COO PC(19:1_18:3)+CH3COO PC(37:4)+CH3COO -1 854.5916605 11.75100079 PC diacyl M+CH3COO RM0171078 C47 H85 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(17:1_20:5)-H PG(17:1_20:5)-H PG(37:6)-H -1 779.4868615 7.298059728 PG diacyl M-H RM0010576 C43 H72 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PC(15:0_17:1)-CH3 PC(15:0_17:1)-CH3 PC(32:1)-CH3 -1 716.5235805 10.59067496 PC diacyl M-CH3 RM0036654 C39 H75 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4COOH)+CH3COO PC(18:1_20:4COOH)+CH3COO PC(38:5COOH)+CH3COO -1 896.5658405 5.507335466 PC carboxylic M+CH3COO - - - C48 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(23:0_20:5)-H PE(23:0_20:5)-H PE(43:5)-H -1 834.6018305 17.10635795 PE diacyl M-H RM0001211 C48 H85 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(19:3_20:4)+CH3COO PC(19:3_20:4)+CH3COO PC(39:7)+CH3COO -1 876.5760105 8.425559029 PC diacyl M+CH3COO - - - C49 H83 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4CHO)+CH3COO_1 PC(18:1_20:4CHO)+CH3COO PC(38:5CHO)+CH3COO -1 880.5709255 6.215600503 PC aldehyde M+CH3COO - - - C48 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PG(20:4_20:5)-H_2 PG(20:4_20:5)-H PG(40:9)-H -1 815.4868615 6.096730284 PG diacyl M-H RM0012201 C46 H72 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O Cer(t17:0_24:1)-H_2 Cer(t17:0_24:1)-H Cer(t41:1)-H -1 650.6092825 18.28803512 Cer phytoceramides M-H RM0013477 C41 H80 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC=CC)O PC(18:1_13:3CHO)+CH3COO PC(18:1_13:3CHO)+CH3COO PC(31:4CHO)+CH3COO -1 784.4770255 4.079059963 PC aldehyde M+CH3COO - - - C41 H71 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(18:4_20:5)+HCOO_1 PC(18:4_20:5)+HCOO PC(38:9)+HCOO -1 844.5134105 6.348339035 PC diacyl M+HCOO RM0011025 C47 H75 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(18:0)+CH3COO_1 LPC(18:0)+CH3COO LPC(18:0)+CH3COO -1 582.3776455 3.840836074 LPC monoacyl M+CH3COO RM0106163 C28 H57 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:4COOH)+CH3COO_2 PC(18:2_20:4COOH)+CH3COO PC(38:6COOH)+CH3COO -1 894.5501905 4.746064589 PC carboxylic M+CH3COO - - - C48 H81 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:3)+CH3COO PC(18:2_20:3)+CH3COO PC(38:5)+CH3COO -1 866.5916605 10.26965027 PC diacyl M+CH3COO RM0025205 C48 H85 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_20:5)-CH3_1 PC(20:4_20:5)-CH3 PC(40:9)-CH3 -1 812.5235805 7.665219069 PC diacyl M-CH3 RM0171159 C47 H75 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:2_20:5)+CH3COO PC(19:2_20:5)+CH3COO PC(39:7)+CH3COO -1 876.5760105 8.976429999 PC diacyl M+CH3COO - - - C49 H83 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:1_20:3)+CH3COO PC(20:1_20:3)+CH3COO PC(40:4)+CH3COO -1 896.6386105 14.43747673 PC diacyl M+CH3COO RM0000109 C50 H91 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_16:1)+CH3COO_1 PC(15:0_16:1)+CH3COO PC(31:1)+CH3COO -1 776.5447105 9.215419745 PC diacyl M+CH3COO RM0024964 C41 H79 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(20:2_20:4)-H PE(20:2_20:4)-H PE(40:6)-H -1 790.5392305 11.55943997 PE diacyl M-H RM0044368 C45 H77 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(18:4_20:5)+HCOO_2 PC(18:4_20:5)+HCOO PC(38:9)+HCOO -1 844.5134105 5.775342352 PC diacyl M+HCOO RM0011025 C47 H75 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_20:2COOH)-H PE(18:1_20:2COOH)-H PE(38:3COOH)-H -1 798.5290605 13.9532376 PE carboxylic M-H - - - C43 H77 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(17:2_20:4)+CH3COO PC(17:2_20:4)+CH3COO PC(37:6)+CH3COO -1 850.5603605 7.915811225 PC diacyl M+CH3COO RM0010941 C47 H81 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(18:1)+CH3COO_1 LPC(18:1)+CH3COO LPC(18:1)+CH3COO -1 580.3619955 3.047037499 LPC monoacyl M+CH3COO RM0042845 C28 H55 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4CHO_20:5)+CH3COO_1 PC(20:4CHO_20:5)+CH3COO PC(40:9CHO)+CH3COO -1 900.5396255 4.600798949 PC aldehyde M+CH3COO - - - C50 H79 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PG(17:0_20:5)-H PG(17:0_20:5)-H PG(37:5)-H -1 781.5025115 8.385083963 PG diacyl M-H RM0010529 C43 H74 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PC(20:5_21:5CHO)+HCOO PC(20:5_21:5CHO)+HCOO PC(41:10CHO)+HCOO -1 898.5239755 4.180709804 PC aldehyde M+HCOO - - - C50 H77 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCC=CC=CC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(17:1COOH_18:2)-CH3 PC(17:1COOH_18:2)-CH3 PC(35:3COOH)-CH3 -1 784.5134105 12.52856558 PC carboxylic M-CH3 - - - C42 H75 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PI(18:0_18:2)-H PI(18:0_18:2)-H PI(36:2)-H -1 861.5498565 10.95940717 PI diacyl M-H RM0106274 C45 H82 O13 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(O-17:1_20:5)-H PE(O-17:1_20:5)-H PE(O-37:6)-H -1 734.5130155 12.51142244 PE alkyl-acyl M-H RM0054616 C42 H73 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN LPC(18:2)+CH3COO_1 LPC(18:2)+CH3COO LPC(18:2)+CH3COO -1 578.3463455 2.508747524 LPC monoacyl M+CH3COO RM0048598 C28 H53 N1 O9 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PG(18:2_20:5)-H PG(18:2_20:5)-H PG(38:7)-H -1 791.4868615 6.671922775 PG diacyl M-H RM0008009 C44 H72 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PC(14:0_18:0)+CH3COO PC(14:0_18:0)+CH3COO PC(32:0)+CH3COO -1 792.5760105 13.01746074 PC diacyl M+CH3COO RM0090021 C42 H83 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_20:3)+CH3COO_1 PC(17:0_20:3)+CH3COO PC(37:3)+CH3COO -1 856.6073105 12.78924488 PC diacyl M+CH3COO RM0011279 C47 H87 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:1_20:3)-H_1 PE(O-19:1_20:3)-H PE(O-39:4)-H -1 766.5756155 16.32013918 PE alkyl-acyl M-H - - - C44 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(22:4COOH_20:5)-CH3 PC(22:4COOH_20:5)-CH3 PC(42:9COOH)-CH3 -1 870.5290605 5.978502389 PC carboxylic M-CH3 - - - C49 H77 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_20:3)+CH3COO_2 PC(17:0_20:3)+CH3COO PC(37:3)+CH3COO -1 856.6073105 12.90175298 PC diacyl M+CH3COO RM0011279 C47 H87 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:1_18:1)+CH3COO_1 PC(O-18:1_18:1)+CH3COO PC(O-36:2)+CH3COO -1 830.6280455 16.12202956 PC alkyl-acyl M+CH3COO RM0017287 C46 H89 N1 O9 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1COOH)+HCOO_1 PC(17:1_19:1COOH)+HCOO PC(36:2COOH)+HCOO -1 860.5658405 5.973778726 PC carboxylic M+HCOO - - - C45 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4COOH_20:5)+CH3COO_2 PC(20:4COOH_20:5)+CH3COO PC(40:9COOH)+CH3COO -1 916.5345405 4.682750848 PC carboxylic M+CH3COO - - - C50 H79 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:2_20:5)+CH3COO_1 PC(17:2_20:5)+CH3COO PC(37:7)+CH3COO -1 848.5447105 7.422887049 PC diacyl M+CH3COO RM0171030 C47 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:0_20:1)-H Cer(t17:0_20:1)-H Cer(t37:1)-H -1 594.5466825 15.82793818 Cer phytoceramides M-H RM0060536 C37 H72 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCC=CC)O PC(16:0_17:0)+CH3COO_1 PC(16:0_17:0)+CH3COO PC(33:0)+CH3COO -1 806.5916605 14.30739183 PC diacyl M+CH3COO RM0000552 C43 H85 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(21:1_20:3)+CH3COO PC(21:1_20:3)+CH3COO PC(41:4)+CH3COO -1 910.6542605 15.71521165 PC diacyl M+CH3COO RM0181583 C51 H93 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(15:1)+CH3COO LPC(15:1)+CH3COO LPC(15:1)+CH3COO -1 538.3150455 1.856569696 LPC monoacyl M+CH3COO RM0048635 C25 H49 N1 O9 P1 CC=CCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_18:1)+CH3COO_1 PC(17:0_18:1)+CH3COO PC(35:1)+CH3COO -1 832.6073105 14.36779677 PC diacyl M+CH3COO RM0090135 C45 H87 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(21:0_20:5)-H PE(21:0_20:5)-H PE(41:5)-H -1 806.5705305 15.79226095 PE diacyl M-H RM0001422 C46 H81 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:0_20:5)+CH3COO_1 PC(17:0_20:5)+CH3COO PC(37:5)+CH3COO -1 852.5760105 10.23295367 PC diacyl M+CH3COO RM0001077 C47 H83 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(14:0_18:2)-H PE(14:0_18:2)-H PE(32:2)-H -1 686.4766305 9.585094188 PE diacyl M-H RM0044115 C37 H69 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(17:0_17:1)-H_1 PE(17:0_17:1)-H PE(34:1)-H -1 716.5235805 13.63242318 PE diacyl M-H RM0103851 C39 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(20:1_20:5)+CH3COO_1 PC(20:1_20:5)+CH3COO PC(40:6)+CH3COO -1 892.6073105 11.78329817 PC diacyl M+CH3COO RM0000886 C50 H87 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_18:2)-H PE(15:0_18:2)-H PE(33:2)-H -1 700.4922805 10.87729398 PE diacyl M-H RM0102628 C38 H71 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(20:4_20:5)-H_2 PE(20:4_20:5)-H PE(40:9)-H -1 784.4922805 7.795414842 PE diacyl M-H RM0043955 C45 H71 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_20:4)-CH3_1 PC(19:1_20:4)-CH3 PC(39:5)-CH3 -1 806.5705305 13.15939724 PC diacyl M-CH3 RM0000618 C46 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_21:4COOH)+HCOO_2 PC(20:4_21:4COOH)+HCOO PC(41:8COOH)+HCOO -1 918.5501905 4.504775441 PC carboxylic M+HCOO - - - C50 H81 N1 O12 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(20:1_20:4)+CH3COO_1 PC(20:1_20:4)+CH3COO PC(40:5)+CH3COO -1 894.6229605 13.47693567 PC diacyl M+CH3COO RM0000107 C50 H89 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(13:1_20:5)+CH3COO PC(13:1_20:5)+CH3COO PC(33:6)+CH3COO -1 794.4977605 5.73346994 PC diacyl M+CH3COO RM0181048 C43 H73 N1 O10 P1 CC=CCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_18:0)+HCOO PC(17:0_18:0)+HCOO PC(35:0)+HCOO -1 820.6073105 15.00664587 PC diacyl M+HCOO RM0097697 C44 H87 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:3)-CH3_1 PC(17:1_18:3)-CH3 PC(35:4)-CH3 -1 752.5235805 9.411412046 PC diacyl M-CH3 RM0097695 C42 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:4)+CH3COO PC(18:2_20:4)+CH3COO PC(38:6)+CH3COO -1 864.5760105 8.70428683 PC diacyl M+CH3COO RM0171068 C48 H83 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_18:1COOH)-H PE(18:0_18:1COOH)-H PE(36:1COOH)-H -1 774.5290605 7.725226919 PE carboxylic M-H - - - C41 H77 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(18:2_18:3)+CH3COO PC(18:2_18:3)+CH3COO PC(36:5)+CH3COO -1 838.5603605 8.273852298 PC diacyl M+CH3COO RM0171045 C46 H81 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:4)+CH3COO_2 PC(19:1_20:4)+CH3COO PC(39:5)+CH3COO -1 880.6073105 12.06421439 PC diacyl M+CH3COO RM0000618 C49 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d12:1_17:0_21:3)+HCOO Cer(d12:1_17:0_21:3)+HCOO Cer(d50:4)+HCOO -1 814.6930125 19.3706872 Cer acylceramides M+HCOO - - - C51 H92 N1 O6 CCCCCCCC=CC(C(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC)NC(=O)CCCCCCCCCCCCCCCC)O PC(18:1_20:4CHO)+CH3COO_2 PC(18:1_20:4CHO)+CH3COO PC(38:5CHO)+CH3COO -1 880.5709255 5.499421844 PC aldehyde M+CH3COO - - - C48 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(20:0_19:1)+CH3COO PC(20:0_19:1)+CH3COO PC(39:1)+CH3COO -1 888.6699105 17.63130497 PC diacyl M+CH3COO - - - C49 H95 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_20:5)-CH3 PC(18:3_20:5)-CH3 PC(38:8)-CH3 -1 786.5079305 7.050619814 PC diacyl M-CH3 RM0024946 C45 H73 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(18:0)+CH3COO_2 LPC(18:0)+CH3COO LPC(18:0)+CH3COO -1 582.3776455 3.997495461 LPC monoacyl M+CH3COO RM0106163 C28 H57 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(21:0_18:1)+CH3COO PC(21:0_18:1)+CH3COO PC(39:1)+CH3COO -1 888.6699105 17.43173776 PC diacyl M+CH3COO RM0000032 C49 H95 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_18:2)+CH3COO_1 PC(19:1_18:2)+CH3COO PC(37:3)+CH3COO -1 856.6073105 12.539204 PC diacyl M+CH3COO RM0104145 C47 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_18:0)+CH3COO PC(16:0_18:0)+CH3COO PC(34:0)+CH3COO -1 820.6073105 15.31789593 PC diacyl M+CH3COO RM0000437 C44 H87 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_20:4COOH)-H PE(18:1_20:4COOH)-H PE(38:5COOH)-H -1 794.4977605 5.740824046 PE carboxylic M-H - - - C43 H73 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)(O)OCCN PC(17:0_17:0)+CH3COO_1 PC(17:0_17:0)+CH3COO PC(34:0)+CH3COO -1 820.6073105 14.64591036 PC diacyl M+CH3COO 24778784 RM0135052 C44 H87 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:4)-H_1 PE(17:0_20:4)-H PE(37:4)-H -1 752.5235805 12.52903608 PE diacyl M-H RM0008623 C42 H75 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(14:1_18:2)+CH3COO PC(14:1_18:2)+CH3COO PC(32:3)+CH3COO -1 786.5290605 7.428795344 PC diacyl M+CH3COO RM0041666 C42 H77 N1 O10 P1 CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_18:4)+CH3COO_1 PC(18:3_18:4)+CH3COO PC(36:7)+CH3COO -1 834.5290605 6.459319053 PC diacyl M+CH3COO RM0010988 C46 H77 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_18:1COOH)-H_3 PE(17:0_18:1COOH)-H PE(35:1COOH)-H -1 760.5134105 7.065373505 PE carboxylic M-H - - - C40 H75 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(15:0_20:5)-CH3_1 PC(15:0_20:5)-CH3 PC(35:5)-CH3 -1 750.5079305 8.193972152 PC diacyl M-CH3 RM0036657 C42 H73 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(20:3_20:5)-H PE(20:3_20:5)-H PE(40:8)-H -1 786.5079305 9.074125099 PE diacyl M-H RM0134792 C45 H73 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(18:4_18:4)+CH3COO PC(18:4_18:4)+CH3COO PC(36:8)+CH3COO -1 832.5134105 5.657757808 PC diacyl M+CH3COO RM0037598 C46 H75 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:4COOH)+CH3COO_3 PC(18:2_20:4COOH)+CH3COO PC(38:6COOH)+CH3COO -1 894.5501905 4.799003445 PC carboxylic M+CH3COO - - - C48 H81 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:1)+HCOO PC(18:1_18:1)+HCOO PC(36:2)+HCOO -1 830.5916605 13.51091019 PC diacyl M+HCOO RM0090053 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:3)-H PE(17:0_20:3)-H PE(37:3)-H -1 754.5392305 13.5895527 PE diacyl M-H RM0098912 C42 H77 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(O-18:1_20:5)-H_1 PE(O-18:1_20:5)-H PE(O-38:6)-H -1 748.5286655 13.78151192 PE alkyl-acyl M-H RM0008821 C43 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:1_18:1COOH)+CH3COO_1 PC(17:1_18:1COOH)+CH3COO PC(35:2COOH)+CH3COO -1 860.5658405 5.58718561 PC carboxylic M+CH3COO - - - C45 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(O-17:1_20:4)-H_1 PE(O-17:1_20:4)-H PE(O-37:5)-H -1 736.5286655 13.56457744 PE alkyl-acyl M-H RM0054615 C42 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(O-19:1_18:3)-H PE(O-19:1_18:3)-H PE(O-37:4)-H -1 738.5443155 14.97949042 PE alkyl-acyl M-H - - - C42 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_18:2)+CH3COO_2 PC(19:1_18:2)+CH3COO PC(37:3)+CH3COO -1 856.6073105 12.54633724 PC diacyl M+CH3COO RM0104145 C47 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PS(18:0_20:5)-H_1 PS(18:0_20:5)-H PS(38:5)-H -1 808.5134105 10.30433409 PS diacyl M-H RM0091477 C44 H75 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(C(=O)O)N PC(20:3CHO_20:5)+CH3COO_1 PC(20:3CHO_20:5)+CH3COO PC(40:8CHO)+CH3COO -1 902.5552755 5.15707436 PC aldehyde M+CH3COO - - - C50 H81 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(20:3CHO_20:5)+CH3COO_2 PC(20:3CHO_20:5)+CH3COO PC(40:8CHO)+CH3COO -1 902.5552755 5.23811313 PC aldehyde M+CH3COO - - - C50 H81 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPC(18:4)+CH3COO_1 LPC(18:4)+CH3COO LPC(18:4)+CH3COO -1 574.3150455 1.512920284 LPC monoacyl M+CH3COO RM0017488 C28 H49 N1 O9 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C LPC(18:4)+CH3COO_2 LPC(18:4)+CH3COO LPC(18:4)+CH3COO -1 574.3150455 1.484417885 LPC monoacyl M+CH3COO RM0017488 C28 H49 N1 O9 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:5)+HCOO_1 PC(17:1_20:5)+HCOO PC(37:6)+HCOO -1 836.5447105 8.863639925 PC diacyl M+HCOO RM0104001 C46 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:2)-H_1 PE(18:1_18:2)-H PE(36:3)-H -1 740.5235805 12.52781459 PE diacyl M-H RM0011593 C41 H75 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_20:4COOH)+CH3COO_2 PC(17:1_20:4COOH)+CH3COO PC(37:5COOH)+CH3COO -1 882.5501905 5.250534697 PC carboxylic M+CH3COO - - - C47 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:4COOH)+CH3COO_3 PC(17:1_20:4COOH)+CH3COO PC(37:5COOH)+CH3COO -1 882.5501905 5.325666131 PC carboxylic M+CH3COO - - - C47 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:1_24:1)-H_1 Cer(t17:1_24:1)-H Cer(t41:2)-H -1 648.5936325 17.34208446 Cer phytoceramides M-H RM0184896 C41 H78 N1 O4 CCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC=CC)O PC(20:4CHO_20:5)+CH3COO_2 PC(20:4CHO_20:5)+CH3COO PC(40:9CHO)+CH3COO -1 900.5396255 4.931555153 PC aldehyde M+CH3COO - - - C50 H79 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_20:5)-CH3_2 PC(15:0_20:5)-CH3 PC(35:5)-CH3 -1 750.5079305 8.103701486 PC diacyl M-CH3 RM0036657 C42 H73 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(17:1_18:2)-H PG(17:1_18:2)-H PG(35:3)-H -1 757.5025115 8.669774989 PG diacyl M-H RM0089983 C41 H74 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCC(CO)O PC(17:1_18:2)+CH3COO_1 PC(17:1_18:2)+CH3COO PC(35:3)+CH3COO -1 828.5760105 10.76255667 PC diacyl M+CH3COO RM0025431 C45 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:1_22:0)-H Cer(d17:1_22:0)-H Cer(d39:1)-H -1 606.5830675 17.77955843 Cer acylsphingosines M-H 134752283 RM0029808 C39 H76 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC)O PC(20:5_20:3)+CH3COO PC(20:5_20:3)+CH3COO PC(40:8)+CH3COO -1 888.5760105 8.484237114 PC diacyl M+CH3COO RM0000188 C50 H83 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(19:1_20:4)-H_2 LBPA(19:1_20:4)-H LBPA(39:5)-H -1 809.5338115 9.90438775 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C45 H78 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC=CC PC(20:3_20:5)+CH3COO PC(20:3_20:5)+CH3COO PC(40:8)+CH3COO -1 888.5760105 8.499522482 PC diacyl M+CH3COO RM0000188 C50 H83 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(20:4)+CH3COO_2 LPC(20:4)+CH3COO LPC(20:4)+CH3COO -1 602.3463455 2.228211568 LPC monoacyl M+CH3COO RM0048636 C30 H53 N1 O9 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_18:1)+CH3COO_1 PC(16:0_18:1)+CH3COO PC(34:1)+CH3COO -1 818.5916605 13.10571457 PC diacyl M+CH3COO RM0090134 C44 H85 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:0_21:1)-H Cer(t17:0_21:1)-H Cer(t38:1)-H -1 608.5623325 16.57682448 Cer phytoceramides M-H - - - C38 H74 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCC=CC)O PC(19:1_19:1)+CH3COO_1 PC(19:1_19:1)+CH3COO PC(38:2)+CH3COO -1 872.6386105 15.09569705 PC diacyl M+CH3COO RM0001025 C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_20:5)-CH3_1 PC(16:0_20:5)-CH3 PC(36:5)-CH3 -1 764.5235805 9.409359806 PC diacyl M-CH3 RM0171098 C43 H75 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:5)+HCOO PC(18:2_20:5)+HCOO PC(38:7)+HCOO -1 848.5447105 7.987400035 PC diacyl M+HCOO RM0171080 C47 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(20:5_20:5)-H_1 PE(20:5_20:5)-H PE(40:10)-H -1 782.4766305 7.019260605 PE diacyl M-H RM0001732 C45 H69 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN OAHFA(2:0_26:0)-H OAHFA(2:0_26:0)-H OAHFA(28:0)-H -1 453.3949335 9.260024651 OAHFA Fatty ethers M-H - - - C28 H53 O4 CC(=O)OCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O PE(18:3_20:5)-H_1 PE(18:3_20:5)-H PE(38:8)-H -1 758.4766305 7.513742475 PE diacyl M-H RM0001147 C43 H69 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:0COOH_16:1)-CH3 PC(17:0COOH_16:1)-CH3 PC(33:1COOH)-CH3 -1 760.5134105 10.22682245 PC carboxylic M-CH3 - - - C40 H75 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:0_23:0)-H Cer(d17:0_23:0)-H Cer(d40:0)-H -1 622.6143675 18.64513021 Cer acylsphinganines M-H 134768082 RM0123274 C40 H80 N1 O3 CCCCCCCCCCCCCCC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCC)O LBPA(17:0_18:1)-H_1 LBPA(17:0_18:1)-H LBPA(35:1)-H -1 761.5338115 11.55020547 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H78 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC PC(18:1CHO_20:4)+CH3COO PC(18:1CHO_20:4)+CH3COO PC(38:5CHO)+CH3COO -1 880.5709255 5.779808545 PC aldehyde M+CH3COO - - - C48 H83 N1 O11 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4CHO)+CH3COO_3 PC(18:1_20:4CHO)+CH3COO PC(38:5CHO)+CH3COO -1 880.5709255 5.831280914 PC aldehyde M+CH3COO - - - C48 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_18:1COOH)+CH3COO PC(15:0_18:1COOH)+CH3COO PC(33:1COOH)+CH3COO -1 834.5501905 5.177890156 PC carboxylic M+CH3COO - - - C43 H81 N1 O12 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4CHO_20:5)+CH3COO_3 PC(20:4CHO_20:5)+CH3COO PC(40:9CHO)+CH3COO -1 900.5396255 4.862380904 PC aldehyde M+CH3COO - - - C50 H79 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(O-20:2_20:5)-H PE(O-20:2_20:5)-H PE(O-40:7)-H -1 774.5443155 13.76415331 PE alkyl-acyl M-H RM0054836 C45 H77 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_22:0)-H PE(17:0_22:0)-H PE(39:0)-H -1 788.6174805 18.46784694 PE diacyl M-H RM0001918 C44 H87 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(16:0_20:5)+CH3COO_2 PC(16:0_20:5)+CH3COO PC(36:5)+CH3COO -1 838.5603605 9.409359806 PC diacyl M+CH3COO RM0171098 C46 H81 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_21:4COOH)+HCOO PC(17:1_21:4COOH)+HCOO PC(38:5COOH)+HCOO -1 882.5501905 5.637736944 PC carboxylic M+HCOO - - - C47 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:5)+CH3COO_1 PC(17:1_20:5)+CH3COO PC(37:6)+CH3COO -1 850.5603605 8.590837967 PC diacyl M+CH3COO RM0104001 C47 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(16:1_18:1)-H LBPA(16:1_18:1)-H LBPA(34:2)-H -1 745.5025115 8.885171801 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188210 C40 H74 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC PE(17:1_21:3COOH)-H PE(17:1_21:3COOH)-H PE(38:4COOH)-H -1 796.5134105 12.30247869 PE carboxylic M-H - - - C43 H75 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)(O)OCCN PE(O-18:1_18:3)-H_1 PE(O-18:1_18:3)-H PE(O-36:4)-H -1 724.5286655 14.48508085 PE alkyl-acyl M-H RM0054647 C41 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_18:2)-H PE(17:0_18:2)-H PE(35:2)-H -1 728.5235805 12.87615128 PE diacyl M-H RM0134811 C40 H75 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(O-19:2_18:2)-H_1 PE(O-19:2_18:2)-H PE(O-37:4)-H -1 738.5443155 14.05510609 PE alkyl-acyl M-H - - - C42 H77 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(18:2_20:4)-H PE(18:2_20:4)-H PE(38:6)-H -1 762.5079305 9.409982619 PE diacyl M-H RM0001467 C43 H73 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:3_20:4COOH)+CH3COO PC(18:3_20:4COOH)+CH3COO PC(38:7COOH)+CH3COO -1 892.5345405 4.332824754 PC carboxylic M+CH3COO - - - C48 H79 N1 O12 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(12:0_18:2)+CH3COO PC(12:0_18:2)+CH3COO PC(30:2)+CH3COO -1 760.5134105 7.085771918 PC diacyl M+CH3COO RM0000639 C40 H75 N1 O10 P1 CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_18:2)-H_1 PE(18:0_18:2)-H PE(36:2)-H -1 742.5392305 14.52605556 PE diacyl M-H RM0001471 C41 H77 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(18:1_19:2COOH)+HCOO PC(18:1_19:2COOH)+HCOO PC(37:3COOH)+HCOO -1 872.5658405 5.971257532 PC carboxylic M+HCOO - - - C46 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PI(18:0_18:1)-H PI(18:0_18:1)-H PI(36:1)-H -1 863.5655065 12.60315748 PI diacyl M-H RM0134535 C45 H84 O13 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(21:0_20:3)-H PE(21:0_20:3)-H PE(41:3)-H -1 810.6018305 17.17506276 PE diacyl M-H RM0001433 C46 H85 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(17:0_10:2CHO)-H PE(17:0_10:2CHO)-H PE(27:2CHO)-H -1 630.3776455 4.009497683 PE aldehyde M-H - - - C32 H57 N1 O9 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)(O)OCCN PE(16:0_20:4)-H_1 PE(16:0_20:4)-H PE(36:4)-H -1 738.5079305 11.65255922 PE diacyl M-H RM0134803 C41 H73 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:0_18:0)+CH3COO PC(18:0_18:0)+CH3COO PC(36:0)+CH3COO -1 848.6386105 16.84404305 PC diacyl M+CH3COO 94190 RM0135036 C46 H91 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_20:4)-H_1 PE(18:0_20:4)-H PE(38:4)-H -1 766.5392305 14.21458402 PE diacyl M-H RM0134782 C43 H77 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:0_19:1)+CH3COO PC(19:0_19:1)+CH3COO PC(38:1)+CH3COO -1 874.6542605 17.07818556 PC diacyl M+CH3COO RM0181458 C48 H93 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(14:1_20:5)+CH3COO_1 PC(14:1_20:5)+CH3COO PC(34:6)+CH3COO -1 808.5134105 6.217905602 PC diacyl M+CH3COO RM0025111 C44 H75 N1 O10 P1 CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_18:4)+CH3COO PC(18:2_18:4)+CH3COO PC(36:6)+CH3COO -1 836.5447105 7.357014071 PC diacyl M+CH3COO RM0025204 C46 H79 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(20:5)-H LPE(20:5)-H LPE(20:5)-H -1 498.2626155 1.824202577 LPE monoacyl M-H RM0134462 C25 H41 N1 O7 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(O-17:1_20:3)-H PE(O-17:1_20:3)-H PE(O-37:4)-H -1 738.5443155 14.55636111 PE alkyl-acyl M-H RM0098266 C42 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PG(16:1_18:1)-H PG(16:1_18:1)-H PG(34:2)-H -1 745.5025115 8.851666841 PG diacyl M-H RM0134575 C40 H74 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O LBPA(18:1_20:4)-H LBPA(18:1_20:4)-H LBPA(38:5)-H -1 795.5181615 8.553873372 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188248 C44 H76 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC=CC PC(17:1_17:1)+CH3COO_1 PC(17:1_17:1)+CH3COO PC(34:2)+CH3COO -1 816.5760105 11.58118474 PC diacyl M+CH3COO RM0103999 C44 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4COOH_20:5)+CH3COO_3 PC(20:4COOH_20:5)+CH3COO PC(40:9COOH)+CH3COO -1 916.5345405 4.853514615 PC carboxylic M+CH3COO - - - C50 H79 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_18:3)+CH3COO PC(16:1_18:3)+CH3COO PC(34:4)+CH3COO -1 812.5447105 7.846818941 PC diacyl M+CH3COO RM0099476 C44 H79 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_20:2)-H_1 PE(O-18:1_20:2)-H PE(O-38:3)-H -1 754.5756155 16.44952654 PE alkyl-acyl M-H RM0054655 C43 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN LBPA(16:1_20:5)-H LBPA(16:1_20:5)-H LBPA(36:6)-H -1 765.4712115 6.351784217 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188362 C42 H70 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCC=CC=CC=CC=CC=CC PE(17:0_20:5)-H_1 PE(17:0_20:5)-H PE(37:5)-H -1 750.5079305 11.30748092 PE diacyl M-H RM0028171 C42 H73 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:1_18:3)+CH3COO_1 PC(18:1_18:3)+CH3COO PC(36:4)+CH3COO -1 840.5760105 10.11871135 PC diacyl M+CH3COO RM0025434 C46 H83 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(18:2)+CH3COO_2 LPC(18:2)+CH3COO LPC(18:2)+CH3COO -1 578.3463455 2.605243217 LPC monoacyl M+CH3COO RM0048598 C28 H53 N1 O9 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C LBPA(17:0_20:5)-H LBPA(17:0_20:5)-H LBPA(37:5)-H -1 781.5025115 8.385172306 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C43 H74 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCC=CC=CC=CC=CC=CC PC(17:0_20:5)+CH3COO_2 PC(17:0_20:5)+CH3COO PC(37:5)+CH3COO -1 852.5760105 10.61565675 PC diacyl M+CH3COO RM0001077 C47 H83 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_18:2)+CH3COO_1 PC(16:1_18:2)+CH3COO PC(34:3)+CH3COO -1 814.5603605 9.183381924 PC diacyl M+CH3COO RM0098371 C44 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:2_18:2)+CH3COO PC(17:2_18:2)+CH3COO PC(35:4)+CH3COO -1 826.5603605 8.685107317 PC diacyl M+CH3COO RM0091729 C45 H81 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:2_20:5)+CH3COO PC(16:2_20:5)+CH3COO PC(36:7)+CH3COO -1 834.5290605 6.691663208 PC diacyl M+CH3COO - - - C46 H77 N1 O10 P1 CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:5)+CH3COO_2 PC(17:1_20:5)+CH3COO PC(37:6)+CH3COO -1 850.5603605 8.863639925 PC diacyl M+CH3COO RM0104001 C47 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:1_17:0)-H Cer(d17:1_17:0)-H Cer(d34:1)-H -1 536.5048175 13.06781881 Cer acylsphingosines M-H 134771264 RM0124694 C34 H66 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCC)O PC(18:3_20:5)+HCOO_1 PC(18:3_20:5)+HCOO PC(38:8)+HCOO -1 846.5290605 7.050619814 PC diacyl M+HCOO RM0024946 C47 H77 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_20:5)-CH3_1 PC(16:1_20:5)-CH3 PC(36:6)-CH3 -1 762.5079305 7.571447042 PC diacyl M-CH3 RM0103865 C43 H73 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:5)-H_2 PE(17:0_20:5)-H PE(37:5)-H -1 750.5079305 10.90645603 PE diacyl M-H RM0028171 C42 H73 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(20:3_20:4)-H PE(20:3_20:4)-H PE(40:7)-H -1 788.5235805 10.00702567 PE diacyl M-H RM0044409 C45 H75 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(17:1_20:5)+CH3COO_3 PC(17:1_20:5)+CH3COO PC(37:6)+CH3COO -1 850.5603605 8.72554516 PC diacyl M+CH3COO RM0104001 C47 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:3_20:4)-H PE(18:3_20:4)-H PE(38:7)-H -1 760.4922805 8.01954014 PE diacyl M-H RM0002103 C43 H71 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(15:0_18:2)+CH3COO PC(15:0_18:2)+CH3COO PC(33:2)+CH3COO -1 802.5603605 9.380249631 PC diacyl M+CH3COO RM0011315 C43 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:0_20:4)-H PE(19:0_20:4)-H PE(39:4)-H -1 780.5548805 15.22409626 PE diacyl M-H RM0098905 C44 H79 N1 O8 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:1_20:5)-CH3_1 PC(17:1_20:5)-CH3 PC(37:6)-CH3 -1 776.5235805 8.863639925 PC diacyl M-CH3 RM0104001 C44 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_21:6)-CH3 PC(17:1_21:6)-CH3 PC(38:7)-CH3 -1 788.5235805 10.23877711 PC diacyl M-CH3 - - - C45 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCC=CC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:1_22:0)+HCOO Cer(d17:1_22:0)+HCOO Cer(d39:1)+HCOO -1 652.5885475 17.77955843 Cer acylsphingosines M+HCOO 134752283 RM0029808 C40 H78 N1 O5 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC)O PC(22:0_18:3)+CH3COO PC(22:0_18:3)+CH3COO PC(40:3)+CH3COO -1 898.6542605 16.5735215 PC diacyl M+CH3COO RM0103406 C50 H93 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(14:0_15:0)-H PE(14:0_15:0)-H PE(29:0)-H -1 648.4609805 9.592837982 PE diacyl M-H RM0104544 C34 H67 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:2_18:3)+CH3COO_1 PC(17:2_18:3)+CH3COO PC(35:5)+CH3COO -1 824.5447105 7.698573907 PC diacyl M+CH3COO RM0171256 C45 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:1_20:5)-H_2 PE(O-19:1_20:5)-H PE(O-39:6)-H -1 762.5443155 14.56907112 PE alkyl-acyl M-H - - - C44 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_20:4)+CH3COO_3 PC(19:1_20:4)+CH3COO PC(39:5)+CH3COO -1 880.6073105 13.15939724 PC diacyl M+CH3COO RM0000618 C49 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:5_20:5)-CH3_1 PC(20:5_20:5)-CH3 PC(40:10)-CH3 -1 810.5079305 6.613268337 PC diacyl M-CH3 RM0134892 C47 H73 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_20:4)-H_2 PE(O-18:1_20:4)-H PE(O-38:5)-H -1 750.5443155 14.72508322 PE alkyl-acyl M-H RM0008857 C43 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(20:4_20:4)-H PE(20:4_20:4)-H PE(40:8)-H -1 786.5079305 8.590876719 PE diacyl M-H RM0044346 C45 H73 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:0_18:1)+CH3COO_2 PC(17:0_18:1)+CH3COO PC(35:1)+CH3COO -1 832.6073105 13.98282918 PC diacyl M+CH3COO RM0090135 C45 H87 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(19:1)-H_1 LPE(19:1)-H LPE(19:1)-H -1 492.3095655 3.770328306 LPE monoacyl M-H RM0097955 C24 H47 N1 O7 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(20:3CHO_20:5)+CH3COO_3 PC(20:3CHO_20:5)+CH3COO PC(40:8CHO)+CH3COO -1 902.5552755 5.299888966 PC aldehyde M+CH3COO - - - C50 H81 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_20:3)-H PE(O-18:1_20:3)-H PE(O-38:4)-H -1 752.5599655 15.51802886 PE alkyl-acyl M-H RM0054656 C43 H79 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(20:2_20:3)+CH3COO PC(20:2_20:3)+CH3COO PC(40:5)+CH3COO -1 894.6229605 12.47815641 PC diacyl M+CH3COO RM0042606 C50 H89 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:5_22:5)+CH3COO PC(20:5_22:5)+CH3COO PC(42:10)+CH3COO -1 912.5760105 7.819128564 PC diacyl M+CH3COO RM0000194 C52 H83 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:1)+CH3COO_1 PC(19:1_20:1)+CH3COO PC(39:2)+CH3COO -1 886.6542605 16.05885957 PC diacyl M+CH3COO RM0181475 C49 H93 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_20:5)-H_1 PE(18:0_20:5)-H PE(38:5)-H -1 764.5235805 12.58554482 PE diacyl M-H RM0043840 C43 H75 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:2_21:4COOH)+HCOO PC(18:2_21:4COOH)+HCOO PC(39:6COOH)+HCOO -1 894.5501905 4.760487644 PC carboxylic M+HCOO - - - C48 H81 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_20:2)-H PE(18:1_20:2)-H PE(38:3)-H -1 768.5548805 14.3304399 PE diacyl M-H RM0099140 C43 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN LBPA(18:1_18:3)-H LBPA(18:1_18:3)-H LBPA(36:4)-H -1 769.5025115 8.312466094 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188243 C42 H74 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC PC(18:1_20:3)+CH3COO PC(18:1_20:3)+CH3COO PC(38:4)+CH3COO -1 868.6073105 12.45397461 PC diacyl M+CH3COO RM0171082 C48 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-17:1_20:4)-H_2 PE(O-17:1_20:4)-H PE(O-37:5)-H -1 736.5286655 14.17454391 PE alkyl-acyl M-H RM0054615 C42 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_20:4)+CH3COO_4 PC(19:1_20:4)+CH3COO PC(39:5)+CH3COO -1 880.6073105 12.96867125 PC diacyl M+CH3COO RM0000618 C49 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(22:0_20:4)-H_1 PE(22:0_20:4)-H PE(42:4)-H -1 822.6018305 17.5893119 PE diacyl M-H RM0001230 C47 H85 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(20:2_20:5)-H PE(20:2_20:5)-H PE(40:7)-H -1 788.5235805 10.61672708 PE diacyl M-H RM0044389 C45 H75 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PG(18:1_18:3)-H PG(18:1_18:3)-H PG(36:4)-H -1 769.5025115 8.308746693 PG diacyl M-H RM0011357 C42 H74 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O PC(20:4_20:4)+CH3COO_2 PC(20:4_20:4)+CH3COO PC(40:8)+CH3COO -1 888.5760105 8.04471602 PC diacyl M+CH3COO RM0136719 C50 H83 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_20:5)+CH3COO_2 PC(18:3_20:5)+CH3COO PC(38:8)+CH3COO -1 860.5447105 7.199011808 PC diacyl M+CH3COO RM0024946 C48 H79 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1)+CH3COO_2 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 12.37056314 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:5)+CH3COO_2 PC(18:1_20:5)+CH3COO PC(38:6)+CH3COO -1 864.5760105 9.413968582 PC diacyl M+CH3COO RM0000028 C48 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_20:5)+CH3COO_2 PC(18:0_20:5)+CH3COO PC(38:5)+CH3COO -1 866.5916605 11.67690934 PC diacyl M+CH3COO RM0025394 C48 H85 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_21:4COOH)+HCOO_3 PC(20:4_21:4COOH)+HCOO PC(41:8COOH)+HCOO -1 918.5501905 4.604995166 PC carboxylic M+HCOO - - - C50 H81 N1 O12 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4CHO_20:5)+CH3COO_4 PC(20:4CHO_20:5)+CH3COO PC(40:9CHO)+CH3COO -1 900.5396255 4.188837394 PC aldehyde M+CH3COO - - - C50 H79 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(22:0_20:5)-H PE(22:0_20:5)-H PE(42:5)-H -1 820.5861805 16.48961984 PE diacyl M-H RM0001591 C47 H83 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN LBPA(19:1_18:2)-H LBPA(19:1_18:2)-H LBPA(37:3)-H -1 785.5338115 10.75006578 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C43 H78 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCC=CC PE(19:0_20:5)-H_1 PE(19:0_20:5)-H PE(39:5)-H -1 778.5392305 13.90260603 PE diacyl M-H RM0003074 C44 H77 N1 O8 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(21:0_20:4)-H PE(21:0_20:4)-H PE(41:4)-H -1 808.5861805 16.3772896 PE diacyl M-H RM0001231 C46 H83 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:1_20:4)+CH3COO_1 PC(17:1_20:4)+CH3COO PC(37:5)+CH3COO -1 852.5760105 9.720531598 PC diacyl M+CH3COO RM0001068 C47 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:1)-CH3_1 PC(18:1_18:1)-CH3 PC(36:2)-CH3 -1 770.5705305 13.63653944 PC diacyl M-CH3 RM0090053 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(22:2CHO_20:4)-H PE(22:2CHO_20:4)-H PE(42:6CHO)-H -1 832.5497955 15.18042893 PE aldehyde M-H - - - C47 H79 N1 O9 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC=CC(=O))COP(=O)(O)OCCN PE(18:0_20:3)-H_1 PE(18:0_20:3)-H PE(38:3)-H -1 768.5548805 15.05400628 PE diacyl M-H RM0001660 C43 H79 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(21:4COOH_20:5)-CH3 PC(21:4COOH_20:5)-CH3 PC(41:9COOH)-CH3 -1 856.5134105 5.503202906 PC carboxylic M-CH3 - - - C48 H75 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(O-20:3_18:1)-H PE(O-20:3_18:1)-H PE(O-38:4)-H -1 752.5599655 14.95372346 PE alkyl-acyl M-H RM0182209 C43 H79 N1 O7 P1 CC=CC=CC=CCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_19:3)+CH3COO PC(18:1_19:3)+CH3COO PC(37:4)+CH3COO -1 854.5916605 10.88775577 PC diacyl M+CH3COO RM0181365 C47 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_19:1)+CH3COO_2 PC(19:1_19:1)+CH3COO PC(38:2)+CH3COO -1 872.6386105 15.61989605 PC diacyl M+CH3COO RM0001025 C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_17:1)+CH3COO_1 PC(18:0_17:1)+CH3COO PC(35:1)+CH3COO -1 832.6073105 14.75597243 PC diacyl M+CH3COO RM0001080 C45 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:1_16:2)+CH3COO_1 PC(15:1_16:2)+CH3COO PC(31:3)+CH3COO -1 772.5134105 6.807896746 PC diacyl M+CH3COO - - - C41 H75 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_20:5)-H PE(16:0_20:5)-H PE(36:5)-H -1 736.4922805 10.09215184 PE diacyl M-H RM0044209 C41 H71 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_20:4)-H_2 PE(17:0_20:4)-H PE(37:4)-H -1 752.5235805 12.97578447 PE diacyl M-H RM0008623 C42 H75 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(15:0_17:0)-H PE(15:0_17:0)-H PE(32:0)-H -1 690.5079305 12.91863856 PE diacyl M-H RM0001328 C37 H73 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(23:0_18:1)-H PE(23:0_18:1)-H PE(41:1)-H -1 814.6331305 18.61436623 PE diacyl M-H RM0002043 C46 H89 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PS(18:0_20:5)-H_2 PS(18:0_20:5)-H PS(38:5)-H -1 808.5134105 10.09821239 PS diacyl M-H RM0091477 C44 H75 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(C(=O)O)N PC(20:1_20:4)+CH3COO_2 PC(20:1_20:4)+CH3COO PC(40:5)+CH3COO -1 894.6229605 12.81569823 PC diacyl M+CH3COO RM0000107 C50 H89 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_18:1)+CH3COO PC(18:0_18:1)+CH3COO PC(36:1)+CH3COO -1 846.6229605 15.35270092 PC diacyl M+CH3COO RM0171088 C46 H89 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:5)+CH3COO_1 PC(18:2_20:5)+CH3COO PC(38:7)+CH3COO -1 862.5603605 7.987400035 PC diacyl M+CH3COO RM0171080 C48 H81 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d14:0_4:0)-H Cer(d14:0_4:0)-H Cer(d18:0)-H -1 314.2700675 3.226959605 Cer acylsphinganines M-H - - - C18 H36 N1 O3 CCCCCCCCCCCC(C(CO)NC(=O)CCC)O PC(19:1_20:4COOH)+CH3COO PC(19:1_20:4COOH)+CH3COO PC(39:5COOH)+CH3COO -1 910.5814905 6.313585364 PC carboxylic M+CH3COO - - - C49 H85 N1 O12 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_18:3)-H_1 PE(17:0_18:3)-H PE(35:3)-H -1 726.5079305 11.97414663 PE diacyl M-H RM0003078 C40 H73 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN Cer(t17:0_24:0)-H Cer(t17:0_24:0)-H Cer(t41:0)-H -1 652.6249325 18.22087688 Cer phytoceramides M-H 145715001 RM0009193 C41 H82 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PC(18:1_20:4CHO)+CH3COO_4 PC(18:1_20:4CHO)+CH3COO PC(38:5CHO)+CH3COO -1 880.5709255 6.783182363 PC aldehyde M+CH3COO - - - C48 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPC(18:1)+HCOO LPC(18:1)+HCOO LPC(18:1)+HCOO -1 566.3463455 3.282650914 LPC monoacyl M+HCOO RM0042845 C27 H53 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C LPC(16:2)+CH3COO LPC(16:2)+CH3COO LPC(16:2)+CH3COO -1 550.3150455 1.67103479 LPC monoacyl M+CH3COO RM0027571 C26 H49 N1 O9 P1 CC=CC=CCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_18:2)+HCOO PC(19:1_18:2)+HCOO PC(37:3)+HCOO -1 842.5916605 13.04895932 PC diacyl M+HCOO RM0104145 C46 H85 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(14:1_20:5)+CH3COO_2 PC(14:1_20:5)+CH3COO PC(34:6)+CH3COO -1 808.5134105 6.38303442 PC diacyl M+CH3COO RM0025111 C44 H75 N1 O10 P1 CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:4)-CH3 PC(17:1_20:4)-CH3 PC(37:5)-CH3 -1 778.5392305 9.843392512 PC diacyl M-CH3 RM0001068 C44 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:4)-CH3 PC(18:2_20:4)-CH3 PC(38:6)-CH3 -1 790.5392305 9.187124314 PC diacyl M-CH3 RM0171068 C45 H77 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(21:3COOH_20:5)+HCOO PC(21:3COOH_20:5)+HCOO PC(41:8COOH)+HCOO -1 918.5501905 5.041973355 PC carboxylic M+HCOO - - - C50 H81 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:5)-CH3_2 PC(17:1_20:5)-CH3 PC(37:6)-CH3 -1 776.5235805 8.504413835 PC diacyl M-CH3 RM0104001 C44 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_10:2CHO)-H PE(18:0_10:2CHO)-H PE(28:2CHO)-H -1 644.3932955 4.505413977 PE aldehyde M-H - - - C33 H59 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)(O)OCCN LPE(20:4)-H_1 LPE(20:4)-H LPE(20:4)-H -1 500.2782655 2.372753984 LPE monoacyl M-H RM0097815 C25 H43 N1 O7 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(CO)COP(=O)(O)OCCN PC(19:0_20:5)+CH3COO PC(19:0_20:5)+CH3COO PC(39:5)+CH3COO -1 880.6073105 13.60144519 PC diacyl M+CH3COO RM0000056 C49 H87 N1 O10 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(18:1_20:4)-H_2 PG(18:1_20:4)-H PG(38:5)-H -1 795.5181615 8.563089801 PG diacyl M-H RM0030872 C44 H76 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PE(O-18:1_18:2)-H_1 PE(O-18:1_18:2)-H PE(O-36:3)-H -1 726.5443155 15.47226228 PE alkyl-acyl M-H RM0054646 C41 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(18:1CHO_20:5)+CH3COO_3 PC(18:1CHO_20:5)+CH3COO PC(38:6CHO)+CH3COO -1 878.5552755 5.242438116 PC aldehyde M+CH3COO - - - C48 H81 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:0_20:5)-H_1 PE(O-19:0_20:5)-H PE(O-39:5)-H -1 764.5599655 14.92772782 PE alkyl-acyl M-H - - - C44 H79 N1 O7 P1 CCCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(15:1_20:5)+CH3COO_3 PC(15:1_20:5)+CH3COO PC(35:6)+CH3COO -1 822.5290605 6.836901891 PC diacyl M+CH3COO RM0171229 C45 H77 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4)-CH3_2 PC(18:1_20:4)-CH3 PC(38:5)-CH3 -1 792.5548805 10.43153208 PC diacyl M-CH3 RM0134948 C45 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1)+CH3COO_1 PC(17:1_19:1)+CH3COO PC(36:2)+CH3COO -1 844.6073105 14.02583957 PC diacyl M+CH3COO RM0181295 C46 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-16:0_18:1)-H PE(O-16:0_18:1)-H PE(O-34:1)-H -1 702.5443155 15.26735791 PE alkyl-acyl M-H RM0097957 C39 H77 N1 O7 P1 CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(19:1_19:1)-CH3 PC(19:1_19:1)-CH3 PC(38:2)-CH3 -1 798.6018305 15.90894397 PC diacyl M-CH3 RM0001025 C45 H85 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:1_24:0)-H Cer(t17:1_24:0)-H Cer(t41:1)-H -1 650.6092825 18.47960589 Cer phytoceramides M-H RM0161721 C41 H80 N1 O4 CCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)O PI(18:0_19:4)-H PI(18:0_19:4)-H PI(37:4)-H -1 871.5342065 9.603217391 PI diacyl M-H - - - C46 H80 O13 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(15:1_20:5)+CH3COO_4 PC(15:1_20:5)+CH3COO PC(35:6)+CH3COO -1 822.5290605 6.740377099 PC diacyl M+CH3COO RM0171229 C45 H77 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PS(18:0_20:5)-H_3 PS(18:0_20:5)-H PS(38:5)-H -1 808.5134105 10.15457052 PS diacyl M-H RM0091477 C44 H75 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(C(=O)O)N PC(20:1_20:2)+CH3COO PC(20:1_20:2)+CH3COO PC(40:3)+CH3COO -1 898.6542605 15.59476903 PC diacyl M+CH3COO RM0000100 C50 H93 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_14:0)-H PE(O-18:1_14:0)-H PE(O-32:1)-H -1 674.5130155 14.94281853 PE alkyl-acyl M-H RM0008806 C37 H73 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC)COP(=O)(O)OCCN PE(18:4_20:5)-H PE(18:4_20:5)-H PE(38:9)-H -1 756.4609805 6.460767193 PE diacyl M-H RM0001425 C43 H67 N1 O8 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PI(18:1_18:2)-H PI(18:1_18:2)-H PI(36:3)-H -1 859.5342065 8.791840466 PI diacyl M-H RM0057155 C45 H80 O13 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(18:2_20:5)-H_1 PE(18:2_20:5)-H PE(38:7)-H -1 760.4922805 8.642334726 PE diacyl M-H RM0001939 C43 H71 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_20:3)+CH3COO_2 PC(19:1_20:3)+CH3COO PC(39:4)+CH3COO -1 882.6229605 13.04432589 PC diacyl M+CH3COO RM0181476 C49 H89 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(17:1)-H_2 LPE(17:1)-H LPE(17:1)-H -1 464.2782655 2.79835642 LPE monoacyl M-H RM0007291 C22 H43 N1 O7 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(22:0_18:2)-H PE(22:0_18:2)-H PE(40:2)-H -1 798.6018305 17.4865344 PE diacyl M-H RM0002045 C45 H85 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(O-18:0_20:4)-H_1 PE(O-18:0_20:4)-H PE(O-38:4)-H -1 752.5599655 15.15114846 PE alkyl-acyl M-H RM0017815 C43 H79 N1 O7 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(O-18:2_20:5)-H PE(O-18:2_20:5)-H PE(O-38:7)-H -1 746.5130155 11.2810783 PE alkyl-acyl M-H RM0054698 C43 H73 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN LPC(20:2)+CH3COO LPC(20:2)+CH3COO LPC(20:2)+CH3COO -1 606.3776455 3.518435095 LPC monoacyl M+CH3COO RM0104271 C30 H57 N1 O9 P1 CC=CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_18:3)-H_1 PE(18:0_18:3)-H PE(36:3)-H -1 740.5235805 13.32711907 PE diacyl M-H RM0001967 C41 H75 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(19:4_20:5)+CH3COO_2 PC(19:4_20:5)+CH3COO PC(39:9)+CH3COO -1 872.5447105 6.562934189 PC diacyl M+CH3COO - - - C49 H79 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_18:3)-H_1 PE(16:0_18:3)-H PE(34:3)-H -1 712.4922805 10.72849336 PE diacyl M-H RM0001916 C39 H71 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(18:1_18:3)+CH3COO_2 PC(18:1_18:3)+CH3COO PC(36:4)+CH3COO -1 840.5760105 10.51972264 PC diacyl M+CH3COO RM0025434 C46 H83 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_18:2)-H PE(16:0_18:2)-H PE(34:2)-H -1 714.5079305 12.02569779 PE diacyl M-H RM0011470 C39 H73 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(22:0_20:3)-H PE(22:0_20:3)-H PE(42:3)-H -1 824.6174805 17.7273436 PE diacyl M-H RM0028544 C47 H87 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN Cer(t17:0_22:1)-H_2 Cer(t17:0_22:1)-H Cer(t39:1)-H -1 622.5779825 17.22964843 Cer phytoceramides M-H RM0124848 C39 H76 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCC=CC)O PC(15:1_16:1)+CH3COO PC(15:1_16:1)+CH3COO PC(31:2)+CH3COO -1 774.5290605 8.078579148 PC diacyl M+CH3COO RM0025584 C41 H77 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:0_18:1)+CH3COO PC(20:0_18:1)+CH3COO PC(38:1)+CH3COO -1 874.6542605 16.84396254 PC diacyl M+CH3COO RM0171035 C48 H93 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(22:2COOH_18:1)-H PE(22:2COOH_18:1)-H PE(40:3COOH)-H -1 826.5603605 15.82245081 PE carboxylic M-H - - - C45 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PE(O-19:1_18:2)-H PE(O-19:1_18:2)-H PE(O-37:3)-H -1 740.5599655 14.84099502 PE alkyl-acyl M-H RM0182189 C42 H79 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN Cer(d17:1_26:0)-H Cer(d17:1_26:0)-H Cer(d43:1)-H -1 662.6456675 19.53404348 Cer acylsphingosines M-H 134777854 RM0030120 C43 H84 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCCCC)O PE(15:0_18:3)-H_1 PE(15:0_18:3)-H PE(33:3)-H -1 698.4766305 9.157986835 PE diacyl M-H RM0024692 C38 H69 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(16:1_18:4)+CH3COO PC(16:1_18:4)+CH3COO PC(34:5)+CH3COO -1 810.5290605 7.223649581 PC diacyl M+CH3COO RM0025587 C44 H77 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(23:0_18:2)-H PE(23:0_18:2)-H PE(41:2)-H -1 812.6174805 17.8503347 PE diacyl M-H RM0102657 C46 H87 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:1_20:4CHO)+CH3COO PC(17:1_20:4CHO)+CH3COO PC(37:5CHO)+CH3COO -1 866.5552755 5.825330084 PC aldehyde M+CH3COO - - - C47 H81 N1 O11 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPE(18:3)-H_1 LPE(18:3)-H LPE(18:3)-H -1 474.2626155 1.974125894 LPE monoacyl M-H RM0134465 C23 H41 N1 O7 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(15:0_20:5)-H PE(15:0_20:5)-H PE(35:5)-H -1 722.4766305 8.625759745 PE diacyl M-H RM0001867 C40 H69 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:2_20:5)-CH3_2 PC(18:2_20:5)-CH3 PC(38:7)-CH3 -1 788.5235805 7.717974423 PC diacyl M-CH3 RM0171080 C45 H75 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:2COOH)+CH3COO_2 PC(18:1_18:2COOH)+CH3COO PC(36:3COOH)+CH3COO -1 872.5658405 5.107179008 PC carboxylic M+CH3COO - - - C46 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_17:0)+CH3COO_2 PC(17:0_17:0)+CH3COO PC(34:0)+CH3COO -1 820.6073105 14.99621247 PC diacyl M+CH3COO 24778784 RM0135052 C44 H87 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(12:0_20:5)+CH3COO_2 PC(12:0_20:5)+CH3COO PC(32:5)+CH3COO -1 782.4977605 5.913681831 PC diacyl M+CH3COO RM0090075 C42 H73 N1 O10 P1 CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PI(19:1_20:5)-H_1 PI(19:1_20:5)-H PI(39:6)-H -1 895.5342065 8.639696146 PI diacyl M-H - - - C48 H80 O13 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(15:0_16:0)-H_1 PE(15:0_16:0)-H PE(31:0)-H -1 676.4922805 12.03329029 PE diacyl M-H RM0001869 C36 H71 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(15:0_20:5)+HCOO PC(15:0_20:5)+HCOO PC(35:5)+HCOO -1 810.5290605 8.103701486 PC diacyl M+HCOO RM0036657 C44 H77 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(9:2CHO_20:5)+CH3COO PC(9:2CHO_20:5)+CH3COO PC(29:7CHO)+CH3COO -1 750.3987755 2.258080882 PC aldehyde M+CH3COO - - - C39 H61 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_10:2CHO)+CH3COO_1 PC(18:1_10:2CHO)+CH3COO PC(28:3CHO)+CH3COO -1 744.4457255 3.72875943 PC aldehyde M+CH3COO - - - C38 H67 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:4)+CH3COO_5 PC(19:1_20:4)+CH3COO PC(39:5)+CH3COO -1 880.6073105 12.51841467 PC diacyl M+CH3COO RM0000618 C49 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(21:0_18:3)-H PE(21:0_18:3)-H PE(39:3)-H -1 782.5705305 16.55052214 PE diacyl M-H RM0002097 C44 H81 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(19:1COOH_18:2)+HCOO_1 PC(19:1COOH_18:2)+HCOO PC(37:3COOH)+HCOO -1 872.5658405 5.642260674 PC carboxylic M+HCOO - - - C46 H83 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:5)-CH3_1 PC(19:1_20:5)-CH3 PC(39:6)-CH3 -1 804.5548805 11.10224553 PC diacyl M-CH3 - - - C46 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_20:3)-H PE(18:1_20:3)-H PE(38:4)-H -1 766.5392305 12.75119454 PE diacyl M-H RM0001990 C43 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(18:2CHO_20:5)+CH3COO PC(18:2CHO_20:5)+CH3COO PC(38:7CHO)+CH3COO -1 876.5396255 4.799462461 PC aldehyde M+CH3COO - - - C48 H79 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_19:2)+CH3COO PC(19:1_19:2)+CH3COO PC(38:3)+CH3COO -1 870.6229605 14.17493378 PC diacyl M+CH3COO - - - C48 H89 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(15:0_17:1)-H PG(15:0_17:1)-H PG(32:1)-H -1 719.4868615 8.690890274 PG diacyl M-H RM0008724 C38 H72 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O PE(15:0_20:4)-H PE(15:0_20:4)-H PE(35:4)-H -1 724.4922805 9.490428862 PE diacyl M-H RM0001861 C40 H71 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(16:1_20:5)-CH3_2 PC(16:1_20:5)-CH3 PC(36:6)-CH3 -1 762.5079305 7.639862902 PC diacyl M-CH3 RM0103865 C43 H73 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4CHO_20:4)+CH3COO PC(20:4CHO_20:4)+CH3COO PC(40:8CHO)+CH3COO -1 902.5552755 5.387184997 PC aldehyde M+CH3COO - - - C50 H81 N1 O11 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPC(20:5)+HCOO_1 LPC(20:5)+HCOO LPC(20:5)+HCOO -1 586.3150455 1.777552159 LPC monoacyl M+HCOO RM0106165 C29 H49 N1 O9 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_20:4)-CH3 PC(15:0_20:4)-CH3 PC(35:4)-CH3 -1 752.5235805 8.895695479 PC diacyl M-CH3 RM0098329 C42 H75 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:2_20:5)+CH3COO PC(20:2_20:5)+CH3COO PC(40:7)+CH3COO -1 890.5916605 9.914219766 PC diacyl M+CH3COO RM0000885 C50 H85 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_18:1)-CH3_1 PC(17:0_18:1)-CH3 PC(35:1)-CH3 -1 758.5705305 13.86975775 PC diacyl M-CH3 RM0090135 C42 H81 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_18:4)-H PE(O-18:1_18:4)-H PE(O-36:5)-H -1 722.5130155 12.86140328 PE alkyl-acyl M-H RM0098273 C41 H73 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(O-17:1_18:1)-H_1 PE(O-17:1_18:1)-H PE(O-35:2)-H -1 714.5443155 15.08084984 PE alkyl-acyl M-H RM0054614 C40 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN LPC(18:2)+CH3COO_3 LPC(18:2)+CH3COO LPC(18:2)+CH3COO -1 578.3463455 2.323675296 LPC monoacyl M+CH3COO RM0048598 C28 H53 N1 O9 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_21:4COOH)+HCOO_4 PC(20:4_21:4COOH)+HCOO PC(41:8COOH)+HCOO -1 918.5501905 4.445836695 PC carboxylic M+HCOO - - - C50 H81 N1 O12 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C LPC(16:1)+CH3COO LPC(16:1)+CH3COO LPC(16:1)+CH3COO -1 552.3306955 2.218173137 LPC monoacyl M+CH3COO RM0048603 C26 H51 N1 O9 P1 CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(15:1_18:3)+CH3COO PC(15:1_18:3)+CH3COO PC(33:4)+CH3COO -1 798.5290605 7.544301325 PC diacyl M+CH3COO RM0171234 C43 H77 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_19:0)+CH3COO_1 PC(17:0_19:0)+CH3COO PC(36:0)+CH3COO -1 848.6386105 16.31389947 PC diacyl M+CH3COO RM0097696 C46 H91 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PS(18:0_20:5)-H_4 PS(18:0_20:5)-H PS(38:5)-H -1 808.5134105 10.51124184 PS diacyl M-H RM0091477 C44 H75 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(C(=O)O)N PE(18:2_20:5)-H_2 PE(18:2_20:5)-H PE(38:7)-H -1 760.4922805 8.291170838 PE diacyl M-H RM0001939 C43 H71 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(20:5_20:5)-H_2 PE(20:5_20:5)-H PE(40:10)-H -1 782.4766305 7.186020108 PE diacyl M-H RM0001732 C45 H69 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:0_20:5)-CH3 PC(18:0_20:5)-CH3 PC(38:5)-CH3 -1 792.5548805 11.86441951 PC diacyl M-CH3 RM0025394 C45 H79 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_21:4COOH)+HCOO PC(18:1_21:4COOH)+HCOO PC(39:5COOH)+HCOO -1 896.5658405 4.860375664 PC carboxylic M+HCOO - - - C48 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:0_20:3)+CH3COO PC(O-18:0_20:3)+CH3COO PC(O-38:3)+CH3COO -1 856.6436955 15.69101121 PC alkyl-acyl M+CH3COO RM0107156 C48 H91 N1 O9 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_20:3)-H_1 PE(19:1_20:3)-H PE(39:4)-H -1 780.5548805 11.64931752 PE diacyl M-H - - - C44 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(O-18:1_17:1)-H_1 PE(O-18:1_17:1)-H PE(O-35:2)-H -1 714.5443155 15.18497892 PE alkyl-acyl M-H RM0008813 C40 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PI(18:1_18:1)-H PI(18:1_18:1)-H PI(36:2)-H -1 861.5498565 10.3193683 PI diacyl M-H RM0056674 C45 H82 O13 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(17:1_22:4COOH)-H PC(17:1_22:4COOH)-H PC(39:5COOH)-H -1 850.5603605 8.587382547 PC carboxylic M-H - - - C47 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:1COOH)-H_1 PE(18:1_18:1COOH)-H PE(36:2COOH)-H -1 772.5134105 6.249980245 PE carboxylic M-H - - - C41 H75 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(O-19:0_18:1)+HCOO PC(O-19:0_18:1)+HCOO PC(O-37:1)+HCOO -1 832.6436955 15.30371091 PC alkyl-acyl M+HCOO RM0180522 C46 H91 N1 O9 P1 CCCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_18:3)-H_2 PE(O-18:1_18:3)-H PE(O-36:4)-H -1 724.5286655 14.18403889 PE alkyl-acyl M-H RM0054647 C41 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(18:0_19:1)+CH3COO PC(18:0_19:1)+CH3COO PC(37:1)+CH3COO -1 860.6386105 16.39582824 PC diacyl M+CH3COO RM0104143 C47 H91 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_18:4)-H PE(16:0_18:4)-H PE(34:4)-H -1 710.4766305 9.232157402 PE diacyl M-H RM0001914 C39 H69 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(19:1_20:1)-H PE(19:1_20:1)-H PE(39:2)-H -1 784.5861805 16.5019353 PE diacyl M-H RM0182781 C44 H83 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_19:1COOH)+HCOO_1 PC(18:1_19:1COOH)+HCOO PC(37:2COOH)+HCOO -1 874.5814905 6.850730308 PC carboxylic M+HCOO - - - C46 H85 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_17:1)+CH3COO_1 PC(17:0_17:1)+CH3COO PC(34:1)+CH3COO -1 818.5916605 13.62381216 PC diacyl M+CH3COO RM0025585 C44 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:2_20:5)+CH3COO_2 PC(17:2_20:5)+CH3COO PC(37:7)+CH3COO -1 848.5447105 7.206135019 PC diacyl M+CH3COO RM0171030 C47 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_19:1)-H_1 PE(19:1_19:1)-H PE(38:2)-H -1 770.5705305 16.05777938 PE diacyl M-H RM0182777 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_18:2)-CH3_2 PC(17:1_18:2)-CH3 PC(35:3)-CH3 -1 754.5392305 11.76053057 PC diacyl M-CH3 RM0025431 C42 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_18:2)+CH3COO PC(18:2_18:2)+CH3COO PC(36:4)+CH3COO -1 840.5760105 9.640485156 PC diacyl M+CH3COO RM0134908 C46 H83 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(21:0_18:2)+CH3COO_1 PC(21:0_18:2)+CH3COO PC(39:2)+CH3COO -1 886.6542605 16.621953 PC diacyl M+CH3COO RM0000027 C49 H93 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C LPC(18:1)+CH3COO_2 LPC(18:1)+CH3COO LPC(18:1)+CH3COO -1 580.3619955 3.282650914 LPC monoacyl M+CH3COO RM0042845 C28 H55 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4CHO_20:5)+CH3COO_5 PC(20:4CHO_20:5)+CH3COO PC(40:9CHO)+CH3COO -1 900.5396255 4.79542385 PC aldehyde M+CH3COO - - - C50 H79 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:2)+CH3COO_1 PC(19:1_20:2)+CH3COO PC(39:3)+CH3COO -1 884.6386105 15.09596727 PC diacyl M+CH3COO - - - C49 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(21:1_20:4)+CH3COO PC(21:1_20:4)+CH3COO PC(41:5)+CH3COO -1 908.6386105 14.50654228 PC diacyl M+CH3COO RM0181600 C51 H91 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:4COOH)-H_2 PE(17:0_20:4COOH)-H PE(37:4COOH)-H -1 782.4977605 6.310595921 PE carboxylic M-H - - - C42 H73 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)(O)OCCN PC(18:1_20:5)+HCOO PC(18:1_20:5)+HCOO PC(38:6)+HCOO -1 850.5603605 9.296392579 PC diacyl M+HCOO RM0000028 C47 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_20:2)-H_1 PE(19:1_20:2)-H PE(39:3)-H -1 782.5705305 15.90989568 PE diacyl M-H - - - C44 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(17:0_18:1)-H_1 PE(17:0_18:1)-H PE(35:1)-H -1 730.5392305 14.6368439 PE diacyl M-H RM0028162 C40 H77 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(O-17:1_18:2)-H PE(O-17:1_18:2)-H PE(O-35:3)-H -1 712.5286655 14.51588794 PE alkyl-acyl M-H RM0098264 C40 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(18:1_18:2)+CH3COO PC(18:1_18:2)+CH3COO PC(36:3)+CH3COO -1 842.5916605 11.36045486 PC diacyl M+CH3COO RM0000423 C46 H85 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_20:5)-CH3_1 PC(17:0_20:5)-CH3 PC(37:5)-CH3 -1 778.5392305 10.37216591 PC diacyl M-CH3 RM0001077 C44 H77 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(25:0_18:2)-H PE(25:0_18:2)-H PE(43:2)-H -1 840.6487805 18.82609467 PE diacyl M-H RM0001975 C48 H91 N1 O8 P1 CCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(18:1_20:5CHO)+CH3COO_1 PC(18:1_20:5CHO)+CH3COO PC(38:6CHO)+CH3COO -1 878.5552755 5.503875658 PC aldehyde M+CH3COO - - - C48 H81 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(21:1_20:5)+CH3COO PC(21:1_20:5)+CH3COO PC(41:6)+CH3COO -1 906.6229605 13.63270893 PC diacyl M+CH3COO - - - C51 H89 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(5:0CHO_18:1)+CH3COO_1 PC(5:0CHO_18:1)+CH3COO PC(23:1CHO)+CH3COO -1 678.3987755 3.674230723 PC aldehyde M+CH3COO - - - C33 H61 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1)+CH3COO_2 PC(17:1_19:1)+CH3COO PC(36:2)+CH3COO -1 844.6073105 13.95788605 PC diacyl M+CH3COO RM0181295 C46 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_20:2)-H_2 PE(O-18:1_20:2)-H PE(O-38:3)-H -1 754.5756155 15.24644388 PE alkyl-acyl M-H RM0054655 C43 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(17:0_20:5)+HCOO PC(17:0_20:5)+HCOO PC(37:5)+HCOO -1 838.5603605 9.98497011 PC diacyl M+HCOO RM0001077 C46 H81 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(14:1_18:1)+CH3COO PC(14:1_18:1)+CH3COO PC(32:2)+CH3COO -1 788.5447105 8.719238468 PC diacyl M+CH3COO RM0025106 C42 H79 N1 O10 P1 CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t22:0_17:0)-H Cer(t22:0_17:0)-H Cer(t39:0)-H -1 624.5936325 17.70319625 Cer phytoceramides M-H 145715117 RM0124895 C39 H78 N1 O4 CCCCCCCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCC)O PC(19:1_20:4)-CH3_2 PC(19:1_20:4)-CH3 PC(39:5)-CH3 -1 806.5705305 12.51841467 PC diacyl M-CH3 RM0000618 C46 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_15:0)-H PE(O-18:1_15:0)-H PE(O-33:1)-H -1 688.5286655 15.55239375 PE alkyl-acyl M-H RM0134788 C38 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(15:1_20:5)-H PE(15:1_20:5)-H PE(35:6)-H -1 720.4609805 7.538733835 PE diacyl M-H RM0001874 C40 H67 N1 O8 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_18:1)-H_2 PE(17:0_18:1)-H PE(35:1)-H -1 730.5392305 14.96968829 PE diacyl M-H RM0028162 C40 H77 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(17:0_18:1)-H_3 PE(17:0_18:1)-H PE(35:1)-H -1 730.5392305 15.01621005 PE diacyl M-H RM0028162 C40 H77 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(14:1_20:5)+CH3COO_3 PC(14:1_20:5)+CH3COO PC(34:6)+CH3COO -1 808.5134105 6.078769985 PC diacyl M+CH3COO RM0025111 C44 H75 N1 O10 P1 CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:5CHO)-H PE(17:0_20:5CHO)-H PE(37:5CHO)-H -1 764.4871955 6.139076126 PE aldehyde M-H - - - C42 H71 N1 O9 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC(=O))COP(=O)(O)OCCN PE(O-19:2_20:5)-H PE(O-19:2_20:5)-H PE(O-39:7)-H -1 760.5286655 13.002148 PE alkyl-acyl M-H - - - C44 H75 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:1_20:2)+CH3COO PC(18:1_20:2)+CH3COO PC(38:3)+CH3COO -1 870.6229605 13.6657303 PC diacyl M+CH3COO RM0000033 C48 H89 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:2_18:2)-H PE(18:2_18:2)-H PE(36:4)-H -1 738.5079305 10.30905854 PE diacyl M-H RM0008639 C41 H73 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(15:0_16:0)+CH3COO_2 PC(15:0_16:0)+CH3COO PC(31:0)+CH3COO -1 778.5603605 10.87615358 PC diacyl M+CH3COO RM0134942 C41 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(20:0_20:5)-H PE(20:0_20:5)-H PE(40:5)-H -1 792.5548805 14.95263459 PE diacyl M-H RM0098906 C45 H79 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(14:0_16:1)-H PE(14:0_16:1)-H PE(30:1)-H -1 660.4609805 9.073089806 PE diacyl M-H RM0001324 C35 H67 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:3_18:3)-H PE(18:3_18:3)-H PE(36:6)-H -1 734.4766305 7.46906857 PE diacyl M-H RM0104550 C41 H69 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_18:1COOH)-H_4 PE(17:0_18:1COOH)-H PE(35:1COOH)-H -1 760.5134105 6.682167618 PE carboxylic M-H - - - C40 H75 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(17:0_20:5)-CH3_2 PC(17:0_20:5)-CH3 PC(37:5)-CH3 -1 778.5392305 10.73474392 PC diacyl M-CH3 RM0001077 C44 H77 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_18:2)+CH3COO PC(16:0_18:2)+CH3COO PC(34:2)+CH3COO -1 816.5760105 11.25129064 PC diacyl M+CH3COO RM0104110 C44 H83 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4)+CH3COO_2 PC(18:1_20:4)+CH3COO PC(38:5)+CH3COO -1 866.5916605 10.43153208 PC diacyl M+CH3COO RM0134948 C48 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_18:2)+CH3COO_3 PC(19:1_18:2)+CH3COO PC(37:3)+CH3COO -1 856.6073105 13.72427048 PC diacyl M+CH3COO RM0104145 C47 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(20:0)+CH3COO LPC(20:0)+CH3COO LPC(20:0)+CH3COO -1 610.4089455 4.935475272 LPC monoacyl M+CH3COO RM0134472 C30 H61 N1 O9 P1 CCCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(14:1_18:3)+CH3COO PC(14:1_18:3)+CH3COO PC(32:4)+CH3COO -1 784.5134105 6.464009756 PC diacyl M+CH3COO RM0171153 C42 H75 N1 O10 P1 CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_10:2CHO)+CH3COO_2 PC(18:1_10:2CHO)+CH3COO PC(28:3CHO)+CH3COO -1 744.4457255 3.598239543 PC aldehyde M+CH3COO - - - C38 H67 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:3)-CH3 PC(19:1_20:3)-CH3 PC(39:4)-CH3 -1 808.5861805 13.73609064 PC diacyl M-CH3 RM0181476 C46 H83 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:3)+CH3COO_3 PC(18:1_18:3)+CH3COO PC(36:4)+CH3COO -1 840.5760105 9.799211162 PC diacyl M+CH3COO RM0025434 C46 H83 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_18:1)+CH3COO PC(16:1_18:1)+CH3COO PC(34:2)+CH3COO -1 816.5760105 10.81836745 PC diacyl M+CH3COO RM0134945 C44 H83 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:2)-H_2 PE(18:1_18:2)-H PE(36:3)-H -1 740.5235805 12.09411895 PE diacyl M-H RM0011593 C41 H75 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_19:1)-H_2 PE(18:1_19:1)-H PE(37:2)-H -1 756.5548805 14.93888924 PE diacyl M-H RM0097460 C42 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(19:0_20:3)+CH3COO_1 PC(19:0_20:3)+CH3COO PC(39:3)+CH3COO -1 884.6386105 15.50926421 PC diacyl M+CH3COO RM0000061 C49 H91 N1 O10 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-20:2_18:2)-H PE(O-20:2_18:2)-H PE(O-38:4)-H -1 752.5599655 15.03421995 PE alkyl-acyl M-H RM0024501 C43 H79 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(20:4COOH_20:5)+CH3COO_4 PC(20:4COOH_20:5)+CH3COO PC(40:9COOH)+CH3COO -1 916.5345405 4.444571929 PC carboxylic M+CH3COO - - - C50 H79 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:4)-H_3 PE(17:0_20:4)-H PE(37:4)-H -1 752.5235805 11.90408392 PE diacyl M-H RM0008623 C42 H75 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:1_22:1)+CH3COO PC(18:1_22:1)+CH3COO PC(40:2)+CH3COO -1 900.6699105 16.72637171 PC diacyl M+CH3COO RM0010612 C50 H95 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-17:1_15:0)-H PE(O-17:1_15:0)-H PE(O-32:1)-H -1 674.5130155 14.60469462 PE alkyl-acyl M-H RM0054605 C37 H73 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(21:0_18:1)-H PE(21:0_18:1)-H PE(39:1)-H -1 786.6018305 17.70986947 PE diacyl M-H RM0043797 C44 H85 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(18:1_22:3)+CH3COO PC(18:1_22:3)+CH3COO PC(40:4)+CH3COO -1 896.6386105 14.14156682 PC diacyl M+CH3COO RM0000617 C50 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_18:2)-CH3_1 PC(17:0_18:2)-CH3 PC(35:2)-CH3 -1 756.5548805 12.08409961 PC diacyl M-CH3 RM0000392 C42 H79 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PI(18:0_20:4)-H_1 PI(18:0_20:4)-H PI(38:4)-H -1 885.5498565 10.67890125 PI diacyl M-H RM0134537 C47 H82 O13 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(19:0_20:5)-H_2 PE(19:0_20:5)-H PE(39:5)-H -1 778.5392305 13.46876693 PE diacyl M-H RM0003074 C44 H77 N1 O8 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN LPE(18:3)-H_2 LPE(18:3)-H LPE(18:3)-H -1 474.2626155 1.90085372 LPE monoacyl M-H RM0134465 C23 H41 N1 O7 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(14:0_16:0)-CH3 PC(14:0_16:0)-CH3 PC(30:0)-CH3 -1 690.5079305 13.80855247 PC diacyl M-CH3 RM0098405 C37 H73 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_18:1COOH)-H_5 PE(17:0_18:1COOH)-H PE(35:1COOH)-H -1 760.5134105 5.471198496 PE carboxylic M-H - - - C40 H75 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PE(18:1_18:2COOH)-H_1 PE(18:1_18:2COOH)-H PE(36:3COOH)-H -1 770.4977605 6.002670592 PE carboxylic M-H - - - C41 H73 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PS(18:0_20:5)-H_5 PS(18:0_20:5)-H PS(38:5)-H -1 808.5134105 10.72582065 PS diacyl M-H RM0091477 C44 H75 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(C(=O)O)N PE(22:0_20:4)-H_2 PE(22:0_20:4)-H PE(42:4)-H -1 822.6018305 17.29667838 PE diacyl M-H RM0001230 C47 H85 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(19:0_20:3)+CH3COO_2 PC(19:0_20:3)+CH3COO PC(39:3)+CH3COO -1 884.6386105 15.42202431 PC diacyl M+CH3COO RM0000061 C49 H91 N1 O10 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(22:0_18:2)+CH3COO PC(22:0_18:2)+CH3COO PC(40:2)+CH3COO -1 900.6699105 17.20195186 PC diacyl M+CH3COO RM0000037 C50 H95 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:1_19:1)-H_1 PE(17:1_19:1)-H PE(36:2)-H -1 742.5392305 11.68301157 PE diacyl M-H RM0098138 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_18:3)-H_1 PE(18:1_18:3)-H PE(36:4)-H -1 738.5079305 10.79721627 PE diacyl M-H RM0001279 C41 H73 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN LBPA(16:0_18:1)-H LBPA(16:0_18:1)-H LBPA(34:1)-H -1 747.5181615 10.78037887 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188193 C40 H76 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC PC(17:1_20:4)+CH3COO_2 PC(17:1_20:4)+CH3COO PC(37:5)+CH3COO -1 852.5760105 9.074007774 PC diacyl M+CH3COO RM0001068 C47 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(21:0_18:2)-H PE(21:0_18:2)-H PE(39:2)-H -1 784.5861805 16.9094346 PE diacyl M-H RM0041559 C44 H83 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:0_18:3)+CH3COO_2 PC(17:0_18:3)+CH3COO PC(35:3)+CH3COO -1 828.5760105 11.42472226 PC diacyl M+CH3COO RM0025609 C45 H83 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_18:2)+CH3COO_4 PC(19:1_18:2)+CH3COO PC(37:3)+CH3COO -1 856.6073105 13.12128544 PC diacyl M+CH3COO RM0104145 C47 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_18:3)-H_2 PE(15:0_18:3)-H PE(33:3)-H -1 698.4766305 8.849771164 PE diacyl M-H RM0024692 C38 H69 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(15:0_17:0)-CH3_1 PC(15:0_17:0)-CH3 PC(32:0)-CH3 -1 718.5392305 15.21619771 PC diacyl M-CH3 RM0171217 C39 H77 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:4)+CH3COO_1 PC(18:1_18:4)+CH3COO PC(36:5)+CH3COO -1 838.5603605 8.701585076 PC diacyl M+CH3COO RM0000624 C46 H81 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:4)+CH3COO_2 PC(18:1_18:4)+CH3COO PC(36:5)+CH3COO -1 838.5603605 8.724523345 PC diacyl M+CH3COO RM0000624 C46 H81 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_20:4)-H_2 PE(18:0_20:4)-H PE(38:4)-H -1 766.5392305 13.6239434 PE diacyl M-H RM0134782 C43 H77 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN LPC(17:1)+HCOO LPC(17:1)+HCOO LPC(17:1)+HCOO -1 552.3306955 2.857293811 LPC monoacyl M+HCOO RM0134477 C26 H51 N1 O9 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_19:1COOH)+HCOO_2 PC(18:1_19:1COOH)+HCOO PC(37:2COOH)+HCOO -1 874.5814905 6.459916425 PC carboxylic M+HCOO - - - C46 H85 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_17:2)-H PE(18:1_17:2)-H PE(35:3)-H -1 726.5079305 10.92659746 PE diacyl M-H RM0019400 C40 H73 N1 O8 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN OAHFA(5:0_14:1)-H OAHFA(5:0_14:1)-H OAHFA(19:1)-H -1 325.2384335 1.123071408 OAHFA Fatty ethers M-H - - - C19 H33 O4 CCCCC(=O)OCCCCCCCCCCC=CCC(=O)O PE(23:7_17:0COOH)-H PE(23:7_17:0COOH)-H PE(40:7COOH)-H -1 818.4977605 10.06123244 PE carboxylic M-H - - - C45 H73 N1 O10 P1 CC=CC=CC=CC=CC=CC=CC=CCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(=O)O)COP(=O)(O)OCCN PC(18:1_20:1)+CH3COO PC(18:1_20:1)+CH3COO PC(38:2)+CH3COO -1 872.6386105 15.28040031 PC diacyl M+CH3COO RM0134947 C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(21:0_20:4)+CH3COO PC(21:0_20:4)+CH3COO PC(41:4)+CH3COO -1 910.6542605 15.97496581 PC diacyl M+CH3COO RM0103465 C51 H93 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(27:0_18:2)-H PE(27:0_18:2)-H PE(45:2)-H -1 868.6800805 19.42416832 PE diacyl M-H RM0098976 C50 H95 N1 O8 P1 CCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN LPE(19:1)-H_2 LPE(19:1)-H LPE(19:1)-H -1 492.3095655 3.907512459 LPE monoacyl M-H RM0097955 C24 H47 N1 O7 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(16:1_20:5)-CH3_3 PC(16:1_20:5)-CH3 PC(36:6)-CH3 -1 762.5079305 7.290293877 PC diacyl M-CH3 RM0103865 C43 H73 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0CHO_20:5)-CH3 PC(18:0CHO_20:5)-CH3 PC(38:5CHO)-CH3 -1 806.5341455 11.05943579 PC aldehyde M-CH3 - - - C45 H77 N1 O9 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C Cer(d14:0_28:0)-H Cer(d14:0_28:0)-H Cer(d42:0)-H -1 650.6456675 19.4700505 Cer acylsphinganines M-H 145714665 RM0048524 C42 H84 N1 O3 CCCCCCCCCCCC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCCCCCC)O LPE(20:4)-H_2 LPE(20:4)-H LPE(20:4)-H -1 500.2782655 2.189066348 LPE monoacyl M-H RM0097815 C25 H43 N1 O7 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(CO)COP(=O)(O)OCCN LBPA(18:2_18:2)-H LBPA(18:2_18:2)-H LBPA(36:4)-H -1 769.5025115 7.924714391 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188256 C42 H74 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCC=CC=CC PC(22:0COOH_19:1)-CH3 PC(22:0COOH_19:1)-CH3 PC(41:1COOH)-CH3 -1 872.6386105 15.62623702 PC carboxylic M-CH3 - - - C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_20:5)-CH3_2 PC(20:4_20:5)-CH3 PC(40:9)-CH3 -1 812.5235805 7.306709228 PC diacyl M-CH3 RM0171159 C47 H75 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(26:0_18:2)-H PE(26:0_18:2)-H PE(44:2)-H -1 854.6644305 19.21017463 PE diacyl M-H RM0102660 C49 H93 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN LPC(20:5)+HCOO_2 LPC(20:5)+HCOO LPC(20:5)+HCOO -1 586.3150455 1.857818376 LPC monoacyl M+HCOO RM0106165 C29 H49 N1 O9 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(O-17:1_18:1)-H_2 PE(O-17:1_18:1)-H PE(O-35:2)-H -1 714.5443155 15.37596749 PE alkyl-acyl M-H RM0054614 C40 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(19:1_20:5)+CH3COO_3 PC(19:1_20:5)+CH3COO PC(39:6)+CH3COO -1 878.5916605 11.10224553 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_20:2)-H_2 PE(19:1_20:2)-H PE(39:3)-H -1 782.5705305 15.77505934 PE diacyl M-H - - - C44 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(5:0CHO_20:5)+CH3COO PC(5:0CHO_20:5)+CH3COO PC(25:5CHO)+CH3COO -1 698.3674755 1.877097504 PC aldehyde M+CH3COO - - - C35 H57 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_18:1COOH)-H PE(16:0_18:1COOH)-H PE(34:1COOH)-H -1 746.4977605 6.182007418 PE carboxylic M-H - - - C39 H73 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(19:1_20:5)+HCOO PC(19:1_20:5)+HCOO PC(39:6)+HCOO -1 864.5760105 11.10224553 PC diacyl M+HCOO - - - C48 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_21:1)-H PE(19:1_21:1)-H PE(40:2)-H -1 798.6018305 15.90559779 PE diacyl M-H - - - C45 H85 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(16:0_20:4)-H_2 PE(16:0_20:4)-H PE(36:4)-H -1 738.5079305 10.99803602 PE diacyl M-H RM0134803 C41 H73 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_17:0)-H PE(17:0_17:0)-H PE(34:0)-H -1 718.5392305 15.20619981 PE diacyl M-H 46891875 RM0135078 C39 H77 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(O-18:0_20:5)-H PE(O-18:0_20:5)-H PE(O-38:5)-H -1 750.5443155 14.26485562 PE alkyl-acyl M-H RM0098021 C43 H77 N1 O7 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_20:5)+CH3COO_4 PC(19:1_20:5)+CH3COO PC(39:6)+CH3COO -1 878.5916605 10.64591253 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:5)+CH3COO_5 PC(19:1_20:5)+CH3COO PC(39:6)+CH3COO -1 878.5916605 10.66210495 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d16:0_4:0)-H Cer(d16:0_4:0)-H Cer(d20:0)-H -1 342.3013675 4.076517588 Cer acylsphinganines M-H - - - C20 H40 N1 O3 CCCCCCCCCCCCCC(C(CO)NC(=O)CCC)O PC(21:0_19:1)+CH3COO PC(21:0_19:1)+CH3COO PC(40:1)+CH3COO -1 902.6855605 18.14266584 PC diacyl M+CH3COO - - - C50 H97 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PI(19:0_20:5)-H PI(19:0_20:5)-H PI(39:5)-H -1 897.5498565 10.31115102 PI diacyl M-H RM0056703 C48 H82 O13 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(17:1_18:1COOH)+CH3COO_2 PC(17:1_18:1COOH)+CH3COO PC(35:2COOH)+CH3COO -1 860.5658405 5.929749924 PC carboxylic M+CH3COO - - - C45 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(O-14:0_18:1)+CH3COO PC(O-14:0_18:1)+CH3COO PC(O-32:1)+CH3COO -1 776.5810955 13.48433486 PC alkyl-acyl M+CH3COO RM0104357 C42 H83 N1 O9 P1 CCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_19:2COOH)-CH3 PC(15:0_19:2COOH)-CH3 PC(34:2COOH)-CH3 -1 772.5134105 6.938474631 PC carboxylic M-CH3 - - - C41 H75 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_20:5)-CH3_2 PC(16:0_20:5)-CH3 PC(36:5)-CH3 -1 764.5235805 9.008396898 PC diacyl M-CH3 RM0171098 C43 H75 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:5CHO)+CH3COO_2 PC(18:1_20:5CHO)+CH3COO PC(38:6CHO)+CH3COO -1 878.5552755 6.769211165 PC aldehyde M+CH3COO - - - C48 H81 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1)+CH3COO_3 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 12.84023873 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_20:5)-H_1 PE(19:1_20:5)-H PE(39:6)-H -1 776.5235805 11.32204283 PE diacyl M-H - - - C44 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_20:1)+CH3COO_2 PC(19:1_20:1)+CH3COO PC(39:2)+CH3COO -1 886.6542605 16.35833619 PC diacyl M+CH3COO RM0181475 C49 H93 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_20:0)+CH3COO PC(18:0_20:0)+CH3COO PC(38:0)+CH3COO -1 876.6699105 17.97973316 PC diacyl M+CH3COO RM0001041 C48 H95 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:0_20:2)-H PE(O-18:0_20:2)-H PE(O-38:2)-H -1 756.5912655 16.72270158 PE alkyl-acyl M-H RM0017814 C43 H83 N1 O7 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(17:0_19:0)+CH3COO_2 PC(17:0_19:0)+CH3COO PC(36:0)+CH3COO -1 848.6386105 16.59692614 PC diacyl M+CH3COO RM0097696 C46 H91 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(14:0_20:4)-H PE(14:0_20:4)-H PE(34:4)-H -1 710.4766305 8.718227578 PE diacyl M-H RM0001780 C39 H69 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN Cer(t17:0_23:0)-H Cer(t17:0_23:0)-H Cer(t40:0)-H -1 638.6092825 18.22660201 Cer phytoceramides M-H 145715000 RM0013472 C40 H80 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCC)O PG(16:0_18:1)-H PG(16:0_18:1)-H PG(34:1)-H -1 747.5181615 10.75489118 PG diacyl M-H RM0097814 C40 H76 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O PE(19:0_18:3)-H PE(19:0_18:3)-H PE(37:3)-H -1 754.5392305 14.5214805 PE diacyl M-H RM0024801 C42 H77 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(19:1_18:2)-H_1 PE(19:1_18:2)-H PE(37:3)-H -1 754.5392305 13.83744703 PE diacyl M-H RM0044057 C42 H77 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(14:0_18:3)-H PE(14:0_18:3)-H PE(32:3)-H -1 684.4609805 8.186479692 PE diacyl M-H RM0001783 C37 H67 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_18:3)-H_2 PE(17:0_18:3)-H PE(35:3)-H -1 726.5079305 11.55963116 PE diacyl M-H RM0003078 C40 H73 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(10:2CHO_20:5)+CH3COO PC(10:2CHO_20:5)+CH3COO PC(30:7CHO)+CH3COO -1 764.4144255 2.376060067 PC aldehyde M+CH3COO - - - C40 H63 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(19:0_20:3)-H PE(19:0_20:3)-H PE(39:3)-H -1 782.5705305 16.22406537 PE diacyl M-H RM0002118 C44 H81 N1 O8 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN LPE(20:3)-H_1 LPE(20:3)-H LPE(20:3)-H -1 502.2939155 2.815958492 LPE monoacyl M-H RM0012621 C25 H45 N1 O7 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(17:1_18:3)-CH3_2 PC(17:1_18:3)-CH3 PC(35:4)-CH3 -1 752.5235805 9.118417185 PC diacyl M-CH3 RM0097695 C42 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_20:5CHO)-H PE(18:1_20:5CHO)-H PE(38:6CHO)-H -1 776.4871955 5.779384536 PE aldehyde M-H - - - C43 H71 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC(=O))COP(=O)(O)OCCN Cer(d14:1_28:0)-H_2 Cer(d14:1_28:0)-H Cer(d42:1)-H -1 648.6300175 19.00255831 Cer acylsphingosines M-H 145714679 RM0030212 C42 H82 N1 O3 CCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCCCCCC)O PE(19:0_18:1)-H_1 PE(19:0_18:1)-H PE(37:1)-H -1 758.5705305 16.51933934 PE diacyl M-H RM0103853 C42 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(16:1_17:1)+CH3COO_1 PC(16:1_17:1)+CH3COO PC(33:2)+CH3COO -1 802.5603605 9.715174981 PC diacyl M+CH3COO RM0025143 C43 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(14:0_17:0)-H PE(14:0_17:0)-H PE(31:0)-H -1 676.4922805 12.48459515 PE diacyl M-H RM0001313 C36 H71 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PG(18:1_18:1)-H PG(18:1_18:1)-H PG(36:2)-H -1 773.5338115 10.85459746 PG diacyl M-H RM0134564 C42 H78 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O LBPA(18:2_18:3)-H LBPA(18:2_18:3)-H LBPA(36:5)-H -1 767.4868615 7.060709767 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188257 C42 H72 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCC=CC=CC PE(16:0_17:0)-H_1 PE(16:0_17:0)-H PE(33:0)-H -1 704.5235805 14.56443016 PE diacyl M-H RM0001908 C38 H75 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(19:1COOH_18:2)+HCOO_2 PC(19:1COOH_18:2)+HCOO PC(37:3COOH)+HCOO -1 872.5658405 5.801917149 PC carboxylic M+HCOO - - - C46 H83 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(15:1_20:4)-H PE(15:1_20:4)-H PE(35:5)-H -1 722.4766305 8.290973297 PE diacyl M-H RM0097580 C40 H69 N1 O8 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(17:0_20:4)-H_4 PE(17:0_20:4)-H PE(37:4)-H -1 752.5235805 12.31470922 PE diacyl M-H RM0008623 C42 H75 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(4:0CHO_19:1)+CH3COO PC(4:0CHO_19:1)+CH3COO PC(23:1CHO)+CH3COO -1 678.3987755 3.76454911 PC aldehyde M+CH3COO - - - C33 H61 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C Cer(d17:1_23:0)-H Cer(d17:1_23:0)-H Cer(d40:1)-H -1 620.5987175 18.28276107 Cer acylsphingosines M-H 134733542 RM0041297 C40 H78 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCC)O Cer(d17:1_21:0)-H Cer(d17:1_21:0)-H Cer(d38:1)-H -1 592.5674175 17.18605584 Cer acylsphingosines M-H 134727713 RM0029795 C38 H74 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCC)O PE(16:0_20:3)-H PE(16:0_20:3)-H PE(36:3)-H -1 740.5235805 12.70602148 PE diacyl M-H RM0134802 C41 H75 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(21:3COOH_20:4)+HCOO_2 PC(21:3COOH_20:4)+HCOO PC(41:7COOH)+HCOO -1 920.5658405 4.859012718 PC carboxylic M+HCOO - - - C50 H83 N1 O12 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PI(18:1_19:1)-H PI(18:1_19:1)-H PI(37:2)-H -1 875.5655065 11.77334324 PI diacyl M-H RM0058859 C46 H84 O13 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PI(19:1_20:4)-H PI(19:1_20:4)-H PI(39:5)-H -1 897.5498565 9.928844523 PI diacyl M-H RM0162494 C48 H82 O13 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(15:0_16:2)-H PE(15:0_16:2)-H PE(31:2)-H -1 672.4609805 8.377269657 PE diacyl M-H - - - C36 H67 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PA(21:5_20:5)-H PA(21:5_20:5)-H PA(41:10)-H -1 753.4500815 5.99556607 PA diacyl M-H - - - C44 H66 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)O PE(15:0_15:0)-H PE(15:0_15:0)-H PE(30:0)-H -1 662.4766305 10.35630201 PE diacyl M-H 9546807 RM0135076 C35 H69 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(13:0_15:0)-CH3 PC(13:0_15:0)-CH3 PC(28:0)-CH3 -1 662.4766305 10.36667175 PC diacyl M-CH3 RM0000631 C35 H69 N1 O8 P1 CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(20:0_20:4)-H PE(20:0_20:4)-H PE(40:4)-H -1 794.5705305 15.63496504 PE diacyl M-H RM0011711 C45 H81 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(17:0_21:0)-H PE(17:0_21:0)-H PE(38:0)-H -1 774.6018305 18.01171804 PE diacyl M-H RM0001917 C43 H85 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(O-18:1_18:1)-H_1 PE(O-18:1_18:1)-H PE(O-36:2)-H -1 728.5599655 16.59459879 PE alkyl-acyl M-H RM0134800 C41 H79 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PI(20:5_20:5)-H PI(20:5_20:5)-H PI(40:10)-H -1 901.4872565 5.328631507 PI diacyl M-H RM0013710 C49 H74 O13 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(17:1_17:2)+CH3COO_1 PC(17:1_17:2)+CH3COO PC(34:3)+CH3COO -1 814.5603605 9.551996764 PC diacyl M+CH3COO RM0041846 C44 H81 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_18:2)+CH3COO_1 PC(17:0_18:2)+CH3COO PC(35:2)+CH3COO -1 830.5916605 12.08409961 PC diacyl M+CH3COO RM0000392 C45 H85 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_17:1)+HCOO PC(17:1_17:1)+HCOO PC(34:2)+HCOO -1 802.5603605 11.58118474 PC diacyl M+HCOO RM0103999 C43 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_17:0)+CH3COO_2 PC(16:0_17:0)+CH3COO PC(33:0)+CH3COO -1 806.5916605 13.46877336 PC diacyl M+CH3COO RM0000552 C43 H85 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(18:1_18:4)-H LBPA(18:1_18:4)-H LBPA(36:5)-H -1 767.4868615 7.20832179 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C42 H72 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC PC(19:0_18:3)+CH3COO PC(19:0_18:3)+CH3COO PC(37:3)+CH3COO -1 856.6073105 13.91940167 PC diacyl M+CH3COO RM0000041 C47 H87 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:1_24:1)-H_2 Cer(t17:1_24:1)-H Cer(t41:2)-H -1 648.5936325 18.85427645 Cer phytoceramides M-H RM0184896 C41 H78 N1 O4 CCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCC=CC)O PC(19:1_20:5)-CH3_2 PC(19:1_20:5)-CH3 PC(39:6)-CH3 -1 804.5548805 10.64591253 PC diacyl M-CH3 - - - C46 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:5)-CH3_3 PC(19:1_20:5)-CH3 PC(39:6)-CH3 -1 804.5548805 10.66210495 PC diacyl M-CH3 - - - C46 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(28:0_8:0CHO)-H PE(28:0_8:0CHO)-H PE(36:0CHO)-H -1 760.5497955 8.921920958 PE aldehyde M-H - - - C41 H79 N1 O9 P1 CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC(=O))COP(=O)(O)OCCN PE(18:3_20:5)-H_2 PE(18:3_20:5)-H PE(38:8)-H -1 758.4766305 7.316362945 PE diacyl M-H RM0001147 C43 H69 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:0_20:0)+CH3COO PC(17:0_20:0)+CH3COO PC(37:0)+CH3COO -1 862.6542605 17.22887816 PC diacyl M+CH3COO RM0010712 C47 H93 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_18:3)+CH3COO_3 PC(15:0_18:3)+CH3COO PC(33:3)+CH3COO -1 800.5447105 8.905552883 PC diacyl M+CH3COO RM0010922 C43 H79 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(23:7_19:1COOH)-H PE(23:7_19:1COOH)-H PE(42:8COOH)-H -1 844.5134105 10.17791141 PE carboxylic M-H - - - C47 H75 N1 O10 P1 CC=CC=CC=CC=CC=CC=CC=CCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PE(18:1_10:2CHO)-H PE(18:1_10:2CHO)-H PE(28:3CHO)-H -1 642.3776455 3.836038215 PE aldehyde M-H - - - C33 H57 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)(O)OCCN PC(16:0_18:3)+CH3COO_2 PC(16:0_18:3)+CH3COO PC(34:3)+CH3COO -1 814.5603605 9.733775685 PC diacyl M+CH3COO RM0000422 C44 H81 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_17:0)-H_2 PE(16:0_17:0)-H PE(33:0)-H -1 704.5235805 14.90799468 PE diacyl M-H RM0001908 C38 H75 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(16:1_18:2)+CH3COO_2 PC(16:1_18:2)+CH3COO PC(34:3)+CH3COO -1 814.5603605 9.390845157 PC diacyl M+CH3COO RM0098371 C44 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LBPA(18:2_20:4)-H LBPA(18:2_20:4)-H LBPA(38:6)-H -1 793.5025115 7.259837495 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188262 C44 H74 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCC=CC=CC=CC=CC LPE(18:2)-H_1 LPE(18:2)-H LPE(18:2)-H -1 476.2782655 2.4590779 LPE monoacyl M-H RM0048672 C23 H43 N1 O7 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN Cer(t17:0_22:2)-H Cer(t17:0_22:2)-H Cer(t39:2)-H -1 620.5623325 16.05749716 Cer phytoceramides M-H RM0124849 C39 H74 N1 O4 CCCCCCCCCCCCCC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCC=CC=CC)O PC(8:1COOH_18:2)+CH3COO PC(8:1COOH_18:2)+CH3COO PC(26:3COOH)+CH3COO -1 732.4093405 2.456076278 PC carboxylic M+CH3COO - - - C36 H63 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(O-20:1_18:2)-H PE(O-20:1_18:2)-H PE(O-38:3)-H -1 754.5756155 15.35029454 PE alkyl-acyl M-H RM0054757 C43 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(O-19:1_19:1)-H_1 PE(O-19:1_19:1)-H PE(O-38:2)-H -1 756.5912655 16.92465473 PE alkyl-acyl M-H - - - C43 H83 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(O-18:1_20:1)-H PE(O-18:1_20:1)-H PE(O-38:2)-H -1 756.5912655 17.43026897 PE alkyl-acyl M-H RM0024409 C43 H83 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN LPC(17:0)+CH3COO_2 LPC(17:0)+CH3COO LPC(17:0)+CH3COO -1 568.3619955 3.522069464 LPC monoacyl M+CH3COO RM0134474 C27 H55 N1 O9 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(5:0CHO_19:1)+CH3COO PC(5:0CHO_19:1)+CH3COO PC(24:1CHO)+CH3COO -1 692.4144255 3.847109219 PC aldehyde M+CH3COO - - - C34 H63 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(17:2_19:2COOH)+CH3COO PC(17:2_19:2COOH)+CH3COO PC(36:4COOH)+CH3COO -1 870.5501905 4.68712477 PC carboxylic M+CH3COO - - - C46 H81 N1 O12 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1COOH_18:3)+HCOO PC(19:1COOH_18:3)+HCOO PC(37:4COOH)+HCOO -1 870.5501905 4.653578595 PC carboxylic M+HCOO - - - C46 H81 N1 O12 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(23:7_18:0COOH)-H PE(23:7_18:0COOH)-H PE(41:7COOH)-H -1 832.5134105 10.90918884 PE carboxylic M-H - - - C46 H75 N1 O10 P1 CC=CC=CC=CC=CC=CC=CC=CCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O)O)COP(=O)(O)OCCN PE(18:0_18:2COOH)-H PE(18:0_18:2COOH)-H PE(36:2COOH)-H -1 772.5134105 6.510542776 PE carboxylic M-H - - - C41 H75 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(14:0_20:5)-CH3 PC(14:0_20:5)-CH3 PC(34:5)-CH3 -1 736.4922805 7.749317396 PC diacyl M-CH3 RM0171040 C41 H71 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(P-15:2)+CH3COO_1 LPC(P-15:2)+CH3COO LPC(P-15:2)+CH3COO -1 520.3044805 3.912386921 LPC monoalkenyl M+CH3COO - - - C25 H47 N1 O8 P1 CC=CC=CCCCCCCCCC=COC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_19:1COOH)-CH3 PC(16:0_19:1COOH)-CH3 PC(35:1COOH)-CH3 -1 788.5447105 12.39255129 PC carboxylic M-CH3 - - - C42 H79 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C LBPA(18:0_17:1)-H_1 LBPA(18:0_17:1)-H LBPA(35:1)-H -1 761.5338115 12.38810563 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H78 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCCC PC(9:1COOH_19:1)+HCOO PC(9:1COOH_19:1)+HCOO PC(28:2COOH)+HCOO -1 748.4406405 3.676486019 PC carboxylic M+HCOO - - - C37 H67 N1 O12 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_22:3COOH)-H PE(18:1_22:3COOH)-H PE(40:4COOH)-H -1 824.5447105 13.97985029 PE carboxylic M-H - - - C45 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)(O)OCCN PE(15:1_18:3)-H PE(15:1_18:3)-H PE(33:4)-H -1 696.4609805 8.043756256 PE diacyl M-H RM0001894 C38 H67 N1 O8 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN LPC(15:0)+CH3COO_2 LPC(15:0)+CH3COO LPC(15:0)+CH3COO -1 540.3306955 2.546834339 LPC monoacyl M+CH3COO RM0017309 C25 H51 N1 O9 P1 CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_19:2COOH)-CH3 PC(18:1_19:2COOH)-CH3 PC(37:3COOH)-CH3 -1 812.5447105 11.17616897 PC carboxylic M-CH3 - - - C44 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_20:1)+CH3COO PC(17:0_20:1)+CH3COO PC(37:1)+CH3COO -1 860.6386105 15.86781 PC diacyl M+CH3COO RM0097410 C47 H91 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(8:1COOH_19:1)+CH3COO PC(8:1COOH_19:1)+CH3COO PC(27:2COOH)+CH3COO -1 748.4406405 3.671980931 PC carboxylic M+CH3COO - - - C37 H67 N1 O12 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_18:2)+CH3COO_2 PC(17:0_18:2)+CH3COO PC(35:2)+CH3COO -1 830.5916605 12.11675575 PC diacyl M+CH3COO RM0000392 C45 H85 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_17:1)+CH3COO_2 PC(15:0_17:1)+CH3COO PC(32:1)+CH3COO -1 790.5603605 11.00995271 PC diacyl M+CH3COO RM0036654 C42 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1CHO)+CH3COO_1 PC(17:1_18:1CHO)+CH3COO PC(35:2CHO)+CH3COO -1 844.5709255 6.763660752 PC aldehyde M+CH3COO - - - C45 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_17:0)-H PE(O-18:1_17:0)-H PE(O-35:1)-H -1 716.5599655 17.28735605 PE alkyl-acyl M-H RM0008812 C40 H79 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(22:0_18:1)-H PE(22:0_18:1)-H PE(40:1)-H -1 800.6174805 18.18170854 PE diacyl M-H RM0043832 C45 H87 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN LPC(19:0)+CH3COO_1 LPC(19:0)+CH3COO LPC(19:0)+CH3COO -1 596.3932955 4.431408087 LPC monoacyl M+CH3COO RM0134490 C29 H59 N1 O9 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_18:3)+CH3COO_2 PC(18:0_18:3)+CH3COO PC(36:3)+CH3COO -1 842.5916605 12.21163084 PC diacyl M+CH3COO RM0000424 C46 H85 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_18:1)-H_1 PE(15:0_18:1)-H PE(33:1)-H -1 702.5079305 12.55333268 PE diacyl M-H RM0001835 C38 H73 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(20:5_20:5)-CH3_2 PC(20:5_20:5)-CH3 PC(40:10)-CH3 -1 810.5079305 6.36156602 PC diacyl M-CH3 RM0134892 C47 H73 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_17:0)-H_3 PE(16:0_17:0)-H PE(33:0)-H -1 704.5235805 14.18578753 PE diacyl M-H RM0001908 C38 H75 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(19:1_20:5)-CH3_4 PC(19:1_20:5)-CH3 PC(39:6)-CH3 -1 804.5548805 10.57155179 PC diacyl M-CH3 - - - C46 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-17:1_17:1)-H PE(O-17:1_17:1)-H PE(O-34:2)-H -1 700.5286655 15.35052811 PE alkyl-acyl M-H RM0054612 C39 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(15:0_16:0)-H_2 PE(15:0_16:0)-H PE(31:0)-H -1 676.4922805 11.61572321 PE diacyl M-H RM0001869 C36 H71 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:1_19:1COOH)+HCOO_2 PC(17:1_19:1COOH)+HCOO PC(36:2COOH)+HCOO -1 860.5658405 6.342294724 PC carboxylic M+HCOO - - - C45 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_18:1)-CH3_2 PC(17:0_18:1)-CH3 PC(35:1)-CH3 -1 758.5705305 14.06480914 PC diacyl M-CH3 RM0090135 C42 H81 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_9:2CHO)+CH3COO_1 PC(18:1_9:2CHO)+CH3COO PC(27:3CHO)+CH3COO -1 730.4300755 3.610887795 PC aldehyde M+CH3COO - - - C37 H65 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(O-16:1_18:1)-H PE(O-16:1_18:1)-H PE(O-34:2)-H -1 700.5286655 14.96893562 PE alkyl-acyl M-H RM0134798 C39 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PI(18:2_20:5)-H PI(18:2_20:5)-H PI(38:7)-H -1 879.5029065 6.336209747 PI diacyl M-H RM0013376 C47 H76 O13 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O LPE(14:0)-H LPE(14:0)-H LPE(14:0)-H -1 424.2469655 2.131215262 LPE monoacyl M-H RM0138793 C19 H39 N1 O7 P1 CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(17:1_17:1)-CH3_1 PC(17:1_17:1)-CH3 PC(34:2)-CH3 -1 742.5392305 12.0118114 PC diacyl M-CH3 RM0103999 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:0_18:2)-H PE(19:0_18:2)-H PE(37:2)-H -1 756.5548805 15.15793171 PE diacyl M-H RM0002040 C42 H79 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(19:1_20:3)-H_2 PE(19:1_20:3)-H PE(39:4)-H -1 780.5548805 14.42799571 PE diacyl M-H - - - C44 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(8:0CHO_18:1)+CH3COO PC(8:0CHO_18:1)+CH3COO PC(26:1CHO)+CH3COO -1 720.4457255 3.718802556 PC aldehyde M+CH3COO - - - C36 H67 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_20:4)-H_1 PE(19:1_20:4)-H PE(39:5)-H -1 778.5392305 12.32226319 PE diacyl M-H RM0001609 C44 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:1_19:1)+CH3COO_1 PC(18:1_19:1)+CH3COO PC(37:2)+CH3COO -1 858.6229605 14.75068254 PC diacyl M+CH3COO RM0042470 C47 H89 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_21:0)-H PE(15:0_21:0)-H PE(36:0)-H -1 746.5705305 16.94986266 PE diacyl M-H RM0001846 C41 H81 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(18:1_20:1COOH)-CH3 PC(18:1_20:1COOH)-CH3 PC(38:2COOH)-CH3 -1 828.5760105 14.34248851 PC carboxylic M-CH3 - - - C45 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_16:2)+CH3COO PC(15:0_16:2)+CH3COO PC(31:2)+CH3COO -1 774.5290605 7.738908235 PC diacyl M+CH3COO RM0171012 C41 H77 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:2_20:4)+CH3COO_2 PC(20:2_20:4)+CH3COO PC(40:6)+CH3COO -1 892.6073105 11.31360754 PC diacyl M+CH3COO RM0011314 C50 H87 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:2_18:2)-H PE(17:2_18:2)-H PE(35:4)-H -1 724.4922805 9.261713142 PE diacyl M-H RM0001278 C40 H71 N1 O8 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(17:1_18:1)-CH3_1 PC(17:1_18:1)-CH3 PC(35:2)-CH3 -1 756.5548805 11.96638611 PC diacyl M-CH3 RM0000418 C42 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(24:0_18:1)-H PE(24:0_18:1)-H PE(42:1)-H -1 828.6487805 19.01691725 PE diacyl M-H RM0001329 C47 H91 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN Cer(d17:1_16:0)-H Cer(d17:1_16:0)-H Cer(d33:1)-H -1 522.4891675 12.15688139 Cer acylsphingosines M-H 10256256 RM0038788 C33 H64 N1 O3 CCCCCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCC)O PC(18:1_18:1)-CH3_2 PC(18:1_18:1)-CH3 PC(36:2)-CH3 -1 770.5705305 13.86287998 PC diacyl M-CH3 RM0090053 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:1)-H_1 PE(18:1_18:1)-H PE(36:2)-H -1 742.5392305 15.24850229 PE diacyl M-H RM0134757 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_18:1)-H_2 PE(18:1_18:1)-H PE(36:2)-H -1 742.5392305 13.92484974 PE diacyl M-H RM0134757 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN LPE(15:0)-H LPE(15:0)-H LPE(15:0)-H -1 438.2626155 2.525068454 LPE monoacyl M-H RM0007290 C20 H41 N1 O7 P1 CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(19:1_10:2CHO)+CH3COO_1 PC(19:1_10:2CHO)+CH3COO PC(29:3CHO)+CH3COO -1 758.4613755 4.148150303 PC aldehyde M+CH3COO - - - C39 H69 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(17:2_20:5)+CH3COO_3 PC(17:2_20:5)+CH3COO PC(37:7)+CH3COO -1 848.5447105 7.02947562 PC diacyl M+CH3COO RM0171030 C47 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_18:1)-H_2 PE(15:0_18:1)-H PE(33:1)-H -1 702.5079305 12.1366118 PE diacyl M-H RM0001835 C38 H73 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(4:0CHO_18:1)+CH3COO PC(4:0CHO_18:1)+CH3COO PC(22:1CHO)+CH3COO -1 664.3831255 3.346646256 PC aldehyde M+CH3COO - - - C32 H59 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPE(15:1)-H LPE(15:1)-H LPE(15:1)-H -1 436.2469655 1.481833563 LPE monoacyl M-H RM0138796 C20 H39 N1 O7 P1 CC=CCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(17:0_17:1)-H_2 PE(17:0_17:1)-H PE(34:1)-H -1 716.5235805 13.93084967 PE diacyl M-H RM0103851 C39 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(20:5_20:5)-CH3_3 PC(20:5_20:5)-CH3 PC(40:10)-CH3 -1 810.5079305 6.263645987 PC diacyl M-CH3 RM0134892 C47 H73 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_10:2CHO)+CH3COO_2 PC(19:1_10:2CHO)+CH3COO PC(29:3CHO)+CH3COO -1 758.4613755 4.023708613 PC aldehyde M+CH3COO - - - C39 H69 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:1COOH)-H_2 PE(18:1_18:1COOH)-H PE(36:2COOH)-H -1 772.5134105 6.399525427 PE carboxylic M-H - - - C41 H75 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PE(14:0_17:1)-H_1 PE(14:0_17:1)-H PE(31:1)-H -1 674.4766305 10.49369853 PE diacyl M-H RM0001317 C36 H69 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(7:1CHO_18:1)+CH3COO_1 PC(7:1CHO_18:1)+CH3COO PC(25:2CHO)+CH3COO -1 704.4144255 3.605151574 PC aldehyde M+CH3COO - - - C35 H63 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:0_20:5)-H_2 PE(O-19:0_20:5)-H PE(O-39:5)-H -1 764.5599655 14.60242201 PE alkyl-acyl M-H - - - C44 H79 N1 O7 P1 CCCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:1_18:1)-CH3_2 PC(17:1_18:1)-CH3 PC(35:2)-CH3 -1 756.5548805 12.37056314 PC diacyl M-CH3 RM0000418 C42 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_18:0)-H PE(16:0_18:0)-H PE(34:0)-H -1 718.5392305 15.79951228 PE diacyl M-H RM0011528 C39 H77 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(O-18:2_18:1)-H_1 PE(O-18:2_18:1)-H PE(O-36:3)-H -1 726.5443155 15.00075041 PE alkyl-acyl M-H RM0054694 C41 H77 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_17:1)+CH3COO_2 PC(17:1_17:1)+CH3COO PC(34:2)+CH3COO -1 816.5760105 14.95454959 PC diacyl M+CH3COO RM0103999 C44 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1COOH)-CH3_1 PC(17:1_19:1COOH)-CH3 PC(36:2COOH)-CH3 -1 800.5447105 12.09697843 PC carboxylic M-CH3 - - - C43 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:5)-CH3_1 PC(18:1_20:5)-CH3 PC(38:6)-CH3 -1 790.5392305 9.413968582 PC diacyl M-CH3 RM0000028 C45 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_20:1COOH)-CH3 PC(17:0_20:1COOH)-CH3 PC(37:1COOH)-CH3 -1 816.5760105 14.98195 PC carboxylic M-CH3 - - - C44 H83 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_18:0)-H PE(17:0_18:0)-H PE(35:0)-H -1 732.5548805 16.27475944 PE diacyl M-H RM0028163 C40 H79 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(O-19:1_18:1)-H_1 PE(O-19:1_18:1)-H PE(O-37:2)-H -1 742.5756155 17.17931542 PE alkyl-acyl M-H RM0182188 C42 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(O-18:1_16:0)-H PE(O-18:1_16:0)-H PE(O-34:1)-H -1 702.5443155 16.57735325 PE alkyl-acyl M-H RM0008809 C39 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(19:1_20:3)-H_3 PE(19:1_20:3)-H PE(39:4)-H -1 780.5548805 14.01137159 PE diacyl M-H - - - C44 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(17:1_20:4)+CH3COO_3 PC(17:1_20:4)+CH3COO PC(37:5)+CH3COO -1 852.5760105 9.376192891 PC diacyl M+CH3COO RM0001068 C47 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(8:0CHO_19:1)+CH3COO PC(8:0CHO_19:1)+CH3COO PC(27:1CHO)+CH3COO -1 734.4613755 4.146575443 PC aldehyde M+CH3COO - - - C37 H69 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPC(19:1)+CH3COO LPC(19:1)+CH3COO LPC(19:1)+CH3COO -1 594.3776455 3.79944648 LPC monoacyl M+CH3COO RM0048604 C29 H57 N1 O9 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_17:1)-H_2 PE(O-18:1_17:1)-H PE(O-35:2)-H -1 714.5443155 15.67672427 PE alkyl-acyl M-H RM0008813 C40 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(4:1CHO_20:5)-H PE(4:1CHO_20:5)-H PE(24:6CHO)-H -1 580.2680955 1.833394505 PE aldehyde M-H - - - C29 H43 N1 O9 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)C=CC(=O))COP(=O)(O)OCCN PC(18:1_13:2CHO)+HCOO PC(18:1_13:2CHO)+HCOO PC(31:3CHO)+HCOO -1 772.4770255 4.079815272 PC aldehyde M+HCOO - - - C40 H71 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(14:0_17:1)-H_2 PE(14:0_17:1)-H PE(31:1)-H -1 674.4766305 10.10162224 PE diacyl M-H RM0001317 C36 H69 N1 O8 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PG(18:3_20:5)-H PG(18:3_20:5)-H PG(38:8)-H -1 789.4712115 5.915945529 PG diacyl M-H RM0008010 C44 H70 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCC(CO)O PC(17:1_18:1)+CH3COO_4 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 15.79055455 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_16:1)+CH3COO_2 PC(15:0_16:1)+CH3COO PC(31:1)+CH3COO -1 776.5447105 9.401391078 PC diacyl M+CH3COO RM0024964 C41 H79 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:4)-H_1 PE(18:1_18:4)-H PE(36:5)-H -1 736.4922805 9.338406939 PE diacyl M-H RM0001181 C41 H71 N1 O8 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_20:4)-CH3_3 PC(18:1_20:4)-CH3 PC(38:5)-CH3 -1 792.5548805 10.65934236 PC diacyl M-CH3 RM0134948 C45 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PG(17:0_18:1)-H PG(17:0_18:1)-H PG(35:1)-H -1 761.5338115 11.9759451 PG diacyl M-H RM0008278 C41 H78 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O PC(17:0_20:5)+CH3COO_3 PC(17:0_20:5)+CH3COO PC(37:5)+CH3COO -1 852.5760105 9.98497011 PC diacyl M+CH3COO RM0001077 C47 H83 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:5)-CH3_3 PC(17:1_20:5)-CH3 PC(37:6)-CH3 -1 776.5235805 8.28491284 PC diacyl M-CH3 RM0104001 C44 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_17:1)+CH3COO_1 PC(16:0_17:1)+CH3COO PC(33:1)+CH3COO -1 804.5760105 11.85157917 PC diacyl M+CH3COO RM0134943 C43 H83 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_17:1)+CH3COO_3 PC(15:0_17:1)+CH3COO PC(32:1)+CH3COO -1 790.5603605 10.3242582 PC diacyl M+CH3COO RM0036654 C42 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_19:4)+CH3COO_1 PC(19:1_19:4)+CH3COO PC(38:5)+CH3COO -1 866.5916605 11.61053607 PC diacyl M+CH3COO - - - C48 H85 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_17:1)-H_1 PE(16:0_17:1)-H PE(33:1)-H -1 702.5079305 13.07097718 PE diacyl M-H RM0001944 C38 H73 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN LPE(18:2)-H_2 LPE(18:2)-H LPE(18:2)-H -1 476.2782655 2.641268888 LPE monoacyl M-H RM0048672 C23 H43 N1 O7 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(O-18:1_18:2)-H_2 PE(O-18:1_18:2)-H PE(O-36:3)-H -1 726.5443155 15.7213875 PE alkyl-acyl M-H RM0054646 C41 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(18:1_18:3)-H_2 PE(18:1_18:3)-H PE(36:4)-H -1 738.5079305 10.4542316 PE diacyl M-H RM0001279 C41 H73 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(17:2_2:0)-H PE(17:2_2:0)-H PE(19:2)-H -1 504.2731805 2.721488199 PE diacyl M-H - - - C24 H43 N1 O8 P1 CC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PE(O-18:0_20:4)-H_2 PE(O-18:0_20:4)-H PE(O-38:4)-H -1 752.5599655 14.71462304 PE alkyl-acyl M-H RM0017815 C43 H79 N1 O7 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(24:2_18:1)-H PE(24:2_18:1)-H PE(42:3)-H -1 824.6174805 17.13981553 PE diacyl M-H RM0182703 C47 H87 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN LPE(20:3)-H_2 LPE(20:3)-H LPE(20:3)-H -1 502.2939155 3.002108829 LPE monoacyl M-H RM0012621 C25 H45 N1 O7 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(20:1_20:4)-H PE(20:1_20:4)-H PE(40:5)-H -1 792.5548805 13.55571084 PE diacyl M-H RM0043761 C45 H79 N1 O8 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN LBPA(16:0_17:1)-H LBPA(16:0_17:1)-H LBPA(33:1)-H -1 733.5025115 10.08022643 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C39 H74 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCC=CC PE(17:1_18:2)-H PE(17:1_18:2)-H PE(35:3)-H -1 726.5079305 11.27904495 PE diacyl M-H RM0001941 C40 H73 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(18:1CHO_20:5)+CH3COO_4 PC(18:1CHO_20:5)+CH3COO PC(38:6CHO)+CH3COO -1 878.5552755 4.509751044 PC aldehyde M+CH3COO - - - C48 H81 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(20:0_20:2)-H PE(20:0_20:2)-H PE(40:2)-H -1 798.6018305 17.35313257 PE diacyl M-H RM0011468 C45 H85 N1 O8 P1 CC=CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(22:2COOH_20:5)-H PE(22:2COOH_20:5)-H PE(42:7COOH)-H -1 846.5290605 12.62352211 PE carboxylic M-H - - - C47 H77 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(18:1_19:1)+CH3COO_2 PC(18:1_19:1)+CH3COO PC(37:2)+CH3COO -1 858.6229605 15.1016256 PC diacyl M+CH3COO RM0042470 C47 H89 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_16:2)-H PE(16:0_16:2)-H PE(32:2)-H -1 686.4766305 9.790157591 PE diacyl M-H RM0182615 C37 H69 N1 O8 P1 CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(15:0_18:1)+CH3COO PC(15:0_18:1)+CH3COO PC(33:1)+CH3COO -1 804.5760105 11.36201386 PC diacyl M+CH3COO RM0000544 C43 H83 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_20:5)-H_2 PE(19:1_20:5)-H PE(39:6)-H -1 776.5235805 11.78386467 PE diacyl M-H - - - C44 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PG(18:0_18:1)-H PG(18:0_18:1)-H PG(36:1)-H -1 775.5494615 13.18976877 PG diacyl M-H RM0134551 C42 H80 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCC(CO)O PE(22:2COOH_20:3)-H PE(22:2COOH_20:3)-H PE(42:5COOH)-H -1 850.5603605 15.04956926 PE carboxylic M-H - - - C47 H81 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PE(18:0_18:3)-H_2 PE(18:0_18:3)-H PE(36:3)-H -1 740.5235805 12.93745727 PE diacyl M-H RM0001967 C41 H75 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(17:0_20:0)-H PE(17:0_20:0)-H PE(37:0)-H -1 760.5861805 17.5043866 PE diacyl M-H RM0097440 C42 H83 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(18:1_19:1)+CH3COO_3 PC(18:1_19:1)+CH3COO PC(37:2)+CH3COO -1 858.6229605 14.36823861 PC diacyl M+CH3COO RM0042470 C47 H89 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C OAHFA(2:0_23:0)-H OAHFA(2:0_23:0)-H OAHFA(25:0)-H -1 411.3479835 6.367929419 OAHFA Fatty ethers M-H - - - C25 H47 O4 CC(=O)OCCCCCCCCCCCCCCCCCCCCCCC(=O)O LBPA(17:0_18:1)-H_2 LBPA(17:0_18:1)-H LBPA(35:1)-H -1 761.5338115 11.95599446 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H78 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC=CC PC(6:0COOH_19:1)-CH3 PC(6:0COOH_19:1)-CH3 PC(25:1COOH)-CH3 -1 648.3882105 3.579107737 PC carboxylic M-CH3 - - - C32 H59 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_20:5)+HCOO_2 PC(18:3_20:5)+HCOO PC(38:8)+HCOO -1 846.5290605 6.875087908 PC diacyl M+HCOO RM0024946 C47 H77 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:0_16:0)-H PE(O-18:0_16:0)-H PE(O-34:0)-H -1 704.5599655 16.55472727 PE alkyl-acyl M-H 52925029 RM0135084 C39 H79 N1 O7 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(19:0_18:1)-H_2 PE(19:0_18:1)-H PE(37:1)-H -1 758.5705305 16.42057907 PE diacyl M-H RM0103853 C42 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(7:1CHO_19:1)+CH3COO PC(7:1CHO_19:1)+CH3COO PC(26:2CHO)+CH3COO -1 718.4300755 3.893172196 PC aldehyde M+CH3COO - - - C36 H65 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_17:1)-CH3_2 PC(17:1_17:1)-CH3 PC(34:2)-CH3 -1 742.5392305 13.80200963 PC diacyl M-CH3 RM0103999 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_17:1)-CH3 PC(16:0_17:1)-CH3 PC(33:1)-CH3 -1 730.5392305 15.34005429 PC diacyl M-CH3 RM0134943 C40 H77 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(26:0_18:1)-H PE(26:0_18:1)-H PE(44:1)-H -1 856.6800805 19.70487676 PE diacyl M-H RM0002038 C49 H95 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(18:0_17:1)-H PE(18:0_17:1)-H PE(35:1)-H -1 730.5392305 15.33231406 PE diacyl M-H RM0001940 C40 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:1_20:5)+CH3COO_4 PC(17:1_20:5)+CH3COO PC(37:6)+CH3COO -1 850.5603605 8.28491284 PC diacyl M+CH3COO RM0104001 C47 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:0COOH_17:1)-H PC(19:0COOH_17:1)-H PC(36:1COOH)-H -1 816.5760105 14.98504737 PC carboxylic M-H - - - C44 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1)+CH3COO_3 PC(17:1_19:1)+CH3COO PC(36:2)+CH3COO -1 844.6073105 14.73139943 PC diacyl M+CH3COO RM0181295 C46 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0CHO_18:1)-H_1 PE(18:0CHO_18:1)-H PE(36:1CHO)-H -1 758.5341455 8.720672478 PE aldehyde M-H - - - C41 H77 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O))COP(=O)(O)OCCN PC(13:0CHO_20:5)+CH3COO PC(13:0CHO_20:5)+CH3COO PC(33:5CHO)+CH3COO -1 810.4926755 6.601421273 PC aldehyde M+CH3COO - - - C43 H73 N1 O11 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_17:1)-H_3 PE(17:0_17:1)-H PE(34:1)-H -1 716.5235805 14.32917656 PE diacyl M-H RM0103851 C39 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PI(18:0_20:5)-H_1 PI(18:0_20:5)-H PI(38:5)-H -1 883.5342065 9.260538646 PI diacyl M-H RM0056629 C47 H80 O13 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O LPE(16:0)-H_1 LPE(16:0)-H LPE(16:0)-H -1 452.2782655 3.144076582 LPE monoacyl M-H RM0134456 C21 H43 N1 O7 P1 CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(18:1_18:1CHO)+CH3COO_1 PC(18:1_18:1CHO)+CH3COO PC(36:2CHO)+CH3COO -1 858.5865755 7.263532211 PC aldehyde M+CH3COO - - - C46 H85 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(18:2_20:5)+CH3COO_2 PC(18:2_20:5)+CH3COO PC(38:7)+CH3COO -1 862.5603605 8.628401171 PC diacyl M+CH3COO RM0171080 C48 H81 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PI(19:1_20:5)-H_2 PI(19:1_20:5)-H PI(39:6)-H -1 895.5342065 8.282673015 PI diacyl M-H - - - C48 H80 O13 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(19:1_19:1)+CH3COO_3 PC(19:1_19:1)+CH3COO PC(38:2)+CH3COO -1 872.6386105 16.01542648 PC diacyl M+CH3COO RM0001025 C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(25:2_18:1COOH)-H PE(25:2_18:1COOH)-H PE(43:3COOH)-H -1 868.6073105 17.9062333 PE carboxylic M-H - - - C48 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(19:1_19:4)+CH3COO_2 PC(19:1_19:4)+CH3COO PC(38:5)+CH3COO -1 866.5916605 11.50732828 PC diacyl M+CH3COO - - - C48 H85 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0CHO_15:0)-CH3 PC(18:0CHO_15:0)-CH3 PC(33:0CHO)-CH3 -1 746.5341455 13.08799315 PC aldehyde M-CH3 - - - C40 H77 N1 O9 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_19:2)-H PE(19:1_19:2)-H PE(38:3)-H -1 768.5548805 14.76671166 PE diacyl M-H - - - C43 H79 N1 O8 P1 CC=CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(19:1_20:4)-H_2 PE(19:1_20:4)-H PE(39:5)-H -1 778.5392305 12.80692262 PE diacyl M-H RM0001609 C44 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(15:1_16:2)+CH3COO_2 PC(15:1_16:2)+CH3COO PC(31:3)+CH3COO -1 772.5134105 7.07805787 PC diacyl M+CH3COO - - - C41 H75 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:0_18:1)+CH3COO PC(19:0_18:1)+CH3COO PC(37:1)+CH3COO -1 860.6386105 16.15370414 PC diacyl M+CH3COO RM0011000 C47 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_19:1)+CH3COO_4 PC(19:1_19:1)+CH3COO PC(38:2)+CH3COO -1 872.6386105 15.90894397 PC diacyl M+CH3COO RM0001025 C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_16:1)-H_1 PE(17:0_16:1)-H PE(33:1)-H -1 702.5079305 12.31847314 PE diacyl M-H RM0001922 C38 H73 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(O-18:0_20:5)+CH3COO PC(O-18:0_20:5)+CH3COO PC(O-38:5)+CH3COO -1 852.6123955 13.47893702 PC alkyl-acyl M+CH3COO RM0052298 C48 H87 N1 O9 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(d14:1_30:0)-H Cer(d14:1_30:0)-H Cer(d44:1)-H -1 676.6613175 19.72409479 Cer acylsphingosines M-H 145714681 RM0048131 C44 H86 N1 O3 CCCCCCCCCC=CC(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCCCCCCCCCCCC)O PC(19:1_18:2)+CH3COO_5 PC(19:1_18:2)+CH3COO PC(37:3)+CH3COO -1 856.6073105 13.57585929 PC diacyl M+CH3COO RM0104145 C47 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_18:2COOH)-H PE(16:0_18:2COOH)-H PE(34:2COOH)-H -1 744.4821105 5.265611865 PE carboxylic M-H - - - C39 H71 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN LPE(17:0)-H_1 LPE(17:0)-H LPE(17:0)-H -1 466.2939155 3.630623111 LPE monoacyl M-H RM0012607 C22 H45 N1 O7 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(16:0_20:5)+CH3COO_3 PC(16:0_20:5)+CH3COO PC(36:5)+CH3COO -1 838.5603605 9.095041755 PC diacyl M+CH3COO RM0171098 C46 H81 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C OAHFA(2:0_25:0)-H OAHFA(2:0_25:0)-H OAHFA(27:0)-H -1 439.3792835 8.124640353 OAHFA Fatty ethers M-H - - - C27 H51 O4 CC(=O)OCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O PC(17:1_18:1CHO)+CH3COO_2 PC(17:1_18:1CHO)+CH3COO PC(35:2CHO)+CH3COO -1 844.5709255 5.594959461 PC aldehyde M+CH3COO - - - C45 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C LBPA(16:0_16:1)-H LBPA(16:0_16:1)-H LBPA(32:1)-H -1 719.4868615 8.803814644 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H RM0188191 C38 H72 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC LPC(20:5)+CH3COO_1 LPC(20:5)+CH3COO LPC(20:5)+CH3COO -1 600.3306955 1.857818376 LPC monoacyl M+CH3COO RM0106165 C30 H51 N1 O9 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(20:0CHO_18:2)-H PE(20:0CHO_18:2)-H PE(38:2CHO)-H -1 784.5497955 13.02215989 PE aldehyde M-H - - - C43 H79 N1 O9 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC(=O))COP(=O)(O)OCCN LPC(20:4)+CH3COO_3 LPC(20:4)+CH3COO LPC(20:4)+CH3COO -1 602.3463455 2.105118753 LPC monoacyl M+CH3COO RM0048636 C30 H53 N1 O9 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4)+CH3COO_3 PC(18:1_20:4)+CH3COO PC(38:5)+CH3COO -1 866.5916605 10.84881052 PC diacyl M+CH3COO RM0134948 C48 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_19:1)+HCOO PC(18:1_19:1)+HCOO PC(37:2)+HCOO -1 844.6073105 14.75068254 PC diacyl M+HCOO RM0042470 C46 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(18:1)-H_1 LPE(18:1)-H LPE(18:1)-H -1 478.2939155 3.894648687 LPE monoacyl M-H RM0104274 C23 H45 N1 O7 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PG(16:0_17:1)-H PG(16:0_17:1)-H PG(33:1)-H -1 733.5025115 10.08241487 PG diacyl M-H RM0035513 C39 H74 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(CO)O PC(18:3_18:3)+CH3COO PC(18:3_18:3)+CH3COO PC(36:6)+CH3COO -1 836.5447105 7.12556941 PC diacyl M+CH3COO RM0134888 C46 H79 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PI(17:0_20:5)-H PI(17:0_20:5)-H PI(37:5)-H -1 869.5185565 7.966682904 PI diacyl M-H RM0089991 C46 H78 O13 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PS(17:1_18:1)-H PS(17:1_18:1)-H PS(35:2)-H -1 772.5134105 9.869843455 PS diacyl M-H RM0058002 C41 H75 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCC(C(=O)O)N PE(O-19:1_20:3)-H_2 PE(O-19:1_20:3)-H PE(O-39:4)-H -1 766.5756155 15.3708075 PE alkyl-acyl M-H - - - C44 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(20:3_20:4)+CH3COO_2 PC(20:3_20:4)+CH3COO PC(40:7)+CH3COO -1 890.5916605 9.834111862 PC diacyl M+CH3COO RM0000550 C50 H85 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(7:0CHO_19:1)+CH3COO PC(7:0CHO_19:1)+CH3COO PC(26:1CHO)+CH3COO -1 720.4457255 4.006732771 PC aldehyde M+CH3COO - - - C36 H67 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(12:1_18:1)+CH3COO PC(12:1_18:1)+CH3COO PC(30:2)+CH3COO -1 760.5134105 9.713777461 PC diacyl M+CH3COO RM0181001 C40 H75 N1 O10 P1 CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:0_19:1)-H PE(O-18:0_19:1)-H PE(O-37:1)-H -1 744.5912655 17.39232931 PE alkyl-acyl M-H - - - C42 H83 N1 O7 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(20:5_21:6)+HCOO PC(20:5_21:6)+HCOO PC(41:11)+HCOO -1 882.5290605 6.259021518 PC diacyl M+HCOO - - - C50 H77 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCC=CC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:3_17:1)-H PE(18:3_17:1)-H PE(35:4)-H -1 724.4922805 9.723459253 PE diacyl M-H RM0011549 C40 H71 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(15:0_16:1)-H PE(15:0_16:1)-H PE(31:1)-H -1 674.4766305 9.849118155 PE diacyl M-H RM0044193 C36 H69 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_18:1)+CH3COO PC(18:1_18:1)+CH3COO PC(36:2)+CH3COO -1 844.6073105 16.80745272 PC diacyl M+CH3COO RM0090053 C46 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1)+CH3COO_4 PC(17:1_19:1)+CH3COO PC(36:2)+CH3COO -1 844.6073105 14.82393613 PC diacyl M+CH3COO RM0181295 C46 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:0_20:4)+CH3COO PC(19:0_20:4)+CH3COO PC(39:4)+CH3COO -1 882.6229605 14.1350834 PC diacyl M+CH3COO RM0011026 C49 H89 N1 O10 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:1_20:5)-H PE(17:1_20:5)-H PE(37:6)-H -1 748.4922805 8.82469576 PE diacyl M-H RM0001325 C42 H71 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(18:0_10:2COOH)-H PE(18:0_10:2COOH)-H PE(28:2COOH)-H -1 660.3882105 4.094650173 PE carboxylic M-H - - - C33 H59 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(17:1_18:2COOH)+CH3COO_1 PC(17:1_18:2COOH)+CH3COO PC(35:3COOH)+CH3COO -1 858.5501905 4.845534599 PC carboxylic M+CH3COO - - - C45 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(23:2_19:1COOH)-H PE(23:2_19:1COOH)-H PE(42:3COOH)-H -1 854.5916605 17.14092142 PE carboxylic M-H - - - C47 H85 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PE(19:0_18:1)-H_3 PE(19:0_18:1)-H PE(37:1)-H -1 758.5705305 16.28744958 PE diacyl M-H RM0103853 C42 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(18:3_18:4)+CH3COO_2 PC(18:3_18:4)+CH3COO PC(36:7)+CH3COO -1 834.5290605 6.336588994 PC diacyl M+CH3COO RM0010988 C46 H77 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_17:2)+CH3COO_2 PC(17:1_17:2)+CH3COO PC(34:3)+CH3COO -1 814.5603605 9.945239292 PC diacyl M+CH3COO RM0041846 C44 H81 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_17:1)-H_1 PE(15:0_17:1)-H PE(32:1)-H -1 688.4922805 11.35303661 PE diacyl M-H RM0011409 C37 H71 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_18:1)-H_3 PE(18:1_18:1)-H PE(36:2)-H -1 742.5392305 13.02452223 PE diacyl M-H RM0134757 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(16:1_20:5)-H PE(16:1_20:5)-H PE(36:6)-H -1 734.4766305 7.802304232 PE diacyl M-H RM0001902 C41 H69 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(18:3_18:4)+CH3COO_3 PC(18:3_18:4)+CH3COO PC(36:7)+CH3COO -1 834.5290605 6.271687311 PC diacyl M+CH3COO RM0010988 C46 H77 N1 O10 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1)+CH3COO_5 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 13.39046957 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:2_18:4)+CH3COO PC(16:2_18:4)+CH3COO PC(34:6)+CH3COO -1 808.5134105 5.946937354 PC diacyl M+CH3COO - - - C44 H75 N1 O10 P1 CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_17:0)-CH3_2 PC(15:0_17:0)-CH3 PC(32:0)-CH3 -1 718.5392305 15.49912254 PC diacyl M-CH3 RM0171217 C39 H77 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_19:1)-H_3 PE(18:1_19:1)-H PE(37:2)-H -1 756.5548805 15.2898355 PE diacyl M-H RM0097460 C42 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(19:1_19:1)+CH3COO_5 PC(19:1_19:1)+CH3COO PC(38:2)+CH3COO -1 872.6386105 16.11981984 PC diacyl M+CH3COO RM0001025 C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_19:3COOH)-CH3 PC(17:0_19:3COOH)-CH3 PC(36:3COOH)-CH3 -1 798.5290605 10.71591987 PC carboxylic M-CH3 - - - C43 H77 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_17:1)+CH3COO_2 PC(14:0_17:1)+CH3COO PC(31:1)+CH3COO -1 776.5447105 9.481542567 PC diacyl M+CH3COO RM0097915 C41 H79 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:1_18:1)-H_2 PE(O-19:1_18:1)-H PE(O-37:2)-H -1 742.5756155 16.97026011 PE alkyl-acyl M-H RM0182188 C42 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_20:5)-CH3_2 PC(18:1_20:5)-CH3 PC(38:6)-CH3 -1 790.5392305 9.49475573 PC diacyl M-CH3 RM0000028 C45 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_20:1)-H PE(18:1_20:1)-H PE(38:2)-H -1 770.5705305 15.75494071 PE diacyl M-H RM0001945 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_10:2CHO)+CH3COO PC(17:1_10:2CHO)+CH3COO PC(27:3CHO)+CH3COO -1 730.4300755 3.568961909 PC aldehyde M+CH3COO - - - C37 H65 N1 O11 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(19:1_18:2)-H_2 PE(19:1_18:2)-H PE(37:3)-H -1 754.5392305 13.33136955 PE diacyl M-H RM0044057 C42 H77 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:0CHO_18:1)-H_2 PE(18:0CHO_18:1)-H PE(36:1CHO)-H -1 758.5341455 11.48314299 PE aldehyde M-H - - - C41 H77 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O))COP(=O)(O)OCCN PE(O-18:1_18:1)-H_2 PE(O-18:1_18:1)-H PE(O-36:2)-H -1 728.5599655 16.84672179 PE alkyl-acyl M-H RM0134800 C41 H79 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:0CHO_18:2)-CH3 PC(18:0CHO_18:2)-CH3 PC(36:2CHO)-CH3 -1 784.5497955 13.01715426 PC aldehyde M-CH3 - - - C43 H79 N1 O9 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:5)-CH3_4 PC(17:1_20:5)-CH3 PC(37:6)-CH3 -1 776.5235805 8.207218793 PC diacyl M-CH3 RM0104001 C44 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_19:3)-H PE(18:1_19:3)-H PE(37:4)-H -1 752.5235805 11.6188627 PE diacyl M-H RM0182699 C42 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(16:0_16:1)-H PE(16:0_16:1)-H PE(32:1)-H -1 688.4922805 11.4638854 PE diacyl M-H RM0011556 C37 H71 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(18:4_20:5)-CH3 PC(18:4_20:5)-CH3 PC(38:9)-CH3 -1 784.4922805 6.295375188 PC diacyl M-CH3 RM0011025 C45 H71 N1 O8 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(7:1CHO_18:1)-H PE(7:1CHO_18:1)-H PE(25:2CHO)-H -1 602.3463455 3.643202201 PE aldehyde M-H - - - C30 H53 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC(=O))COP(=O)(O)OCCN LPE(18:0)-H_1 LPE(18:0)-H LPE(18:0)-H -1 480.3095655 3.965664259 LPE monoacyl M-H RM0017276 C23 H47 N1 O7 P1 CCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(17:1_20:4)-H PE(17:1_20:4)-H PE(37:5)-H -1 750.5079305 10.33629988 PE diacyl M-H RM0001900 C42 H73 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN LPC(20:5)+CH3COO_2 LPC(20:5)+CH3COO LPC(20:5)+CH3COO -1 600.3306955 1.777552159 LPC monoacyl M+CH3COO RM0106165 C30 H51 N1 O9 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(22:0_19:1)-H PE(22:0_19:1)-H PE(41:1)-H -1 814.6331305 18.77816333 PE diacyl M-H RM0182782 C46 H89 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(17:0_18:2COOH)-H_1 PE(17:0_18:2COOH)-H PE(35:2COOH)-H -1 758.4977605 5.651621253 PE carboxylic M-H - - - C40 H73 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PE(18:1_18:1CHO)-H PE(18:1_18:1CHO)-H PE(36:2CHO)-H -1 756.5184955 7.188697063 PE aldehyde M-H - - - C41 H75 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)(O)OCCN PE(18:0_20:1)-H PE(18:0_20:1)-H PE(38:1)-H -1 772.5861805 17.08704383 PE diacyl M-H RM0011551 C43 H83 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(22:1CHO_18:1)-H PE(22:1CHO_18:1)-H PE(40:2CHO)-H -1 812.5810955 14.92663933 PE aldehyde M-H - - - C45 H83 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC=CC(=O))COP(=O)(O)OCCN PC(O-18:0_19:1)+CH3COO PC(O-18:0_19:1)+CH3COO PC(O-37:1)+CH3COO -1 846.6593455 17.26660432 PC alkyl-acyl M+CH3COO RM0180461 C47 H93 N1 O9 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_18:2)-H_2 PE(18:0_18:2)-H PE(36:2)-H -1 742.5392305 15.03633749 PE diacyl M-H RM0001471 C41 H77 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(14:0_17:1)+CH3COO_3 PC(14:0_17:1)+CH3COO PC(31:1)+CH3COO -1 776.5447105 9.555694323 PC diacyl M+CH3COO RM0097915 C41 H79 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:2COOH)+CH3COO PC(17:1_19:2COOH)+CH3COO PC(36:3COOH)+CH3COO -1 872.5658405 5.295251398 PC carboxylic M+CH3COO - - - C46 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:2)+CH3COO_2 PC(19:1_20:2)+CH3COO PC(39:3)+CH3COO -1 884.6386105 14.81511333 PC diacyl M+CH3COO - - - C49 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(20:1)+CH3COO LPC(20:1)+CH3COO LPC(20:1)+CH3COO -1 608.3932955 4.045594237 LPC monoacyl M+CH3COO RM0048599 C30 H59 N1 O9 P1 CC=CCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(17:2_18:3)+CH3COO_2 PC(17:2_18:3)+CH3COO PC(35:5)+CH3COO -1 824.5447105 7.92821766 PC diacyl M+CH3COO RM0171256 C45 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:1_17:1)-H_1 PE(16:1_17:1)-H PE(33:2)-H -1 700.4922805 11.2625796 PE diacyl M-H RM0041005 C38 H71 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_18:1)-CH3_3 PC(18:1_18:1)-CH3 PC(36:2)-CH3 -1 770.5705305 14.29145954 PC diacyl M-CH3 RM0090053 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_16:1)-H PE(O-18:1_16:1)-H PE(O-34:2)-H -1 700.5286655 15.12595738 PE alkyl-acyl M-H RM0008810 C39 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_18:2)+CH3COO_2 PC(17:1_18:2)+CH3COO PC(35:3)+CH3COO -1 828.5760105 11.16801472 PC diacyl M+CH3COO RM0025431 C45 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_20:5)-H_2 PE(O-18:1_20:5)-H PE(O-38:6)-H -1 748.5286655 13.97319494 PE alkyl-acyl M-H RM0008821 C43 H75 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(16:1_18:2)-H PE(16:1_18:2)-H PE(34:3)-H -1 712.4922805 9.821216197 PE diacyl M-H RM0087626 C39 H71 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(O-18:0_18:2)+CH3COO PC(O-18:0_18:2)+CH3COO PC(O-36:2)+CH3COO -1 830.6280455 15.21424908 PC alkyl-acyl M+CH3COO RM0052323 C46 H89 N1 O9 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:1_18:1)-H_1 PE(17:1_18:1)-H PE(35:2)-H -1 728.5235805 13.11694478 PE diacyl M-H RM0001943 C40 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_18:1COOH)-H_3 PE(18:1_18:1COOH)-H PE(36:2COOH)-H -1 772.5134105 5.223971883 PE carboxylic M-H - - - C41 H75 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PE(22:3COOH_18:2)-H PE(22:3COOH_18:2)-H PE(40:5COOH)-H -1 822.5290605 12.09389813 PE carboxylic M-H - - - C45 H77 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC=CC(=O)O)COP(=O)(O)OCCN PE(18:0_20:5)-H_2 PE(18:0_20:5)-H PE(38:5)-H -1 764.5235805 12.79841432 PE diacyl M-H RM0043840 C43 H75 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(18:1_19:1)-H_4 PE(18:1_19:1)-H PE(37:2)-H -1 756.5548805 15.59021879 PE diacyl M-H RM0097460 C42 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(21:1_18:2)-H PE(21:1_18:2)-H PE(39:3)-H -1 782.5705305 16.06964269 PE diacyl M-H - - - C44 H81 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_17:1)+CH3COO_3 PC(17:1_17:1)+CH3COO PC(34:2)+CH3COO -1 816.5760105 11.82785933 PC diacyl M+CH3COO RM0103999 C44 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1)-CH3 PC(17:1_19:1)-CH3 PC(36:2)-CH3 -1 770.5705305 14.08542153 PC diacyl M-CH3 RM0181295 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_7:1CHO)-H PE(16:0_7:1CHO)-H PE(23:1CHO)-H -1 576.3306955 3.537081862 PE aldehyde M-H - - - C28 H51 N1 O9 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC(=O))COP(=O)(O)OCCN PC(17:2_18:3)+CH3COO_3 PC(17:2_18:3)+CH3COO PC(35:5)+CH3COO -1 824.5447105 7.877422789 PC diacyl M+CH3COO RM0171256 C45 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_19:1COOH)-CH3 PC(14:0_19:1COOH)-CH3 PC(33:1COOH)-CH3 -1 760.5134105 9.687361106 PC carboxylic M-CH3 - - - C40 H75 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_19:1COOH)-H PE(17:0_19:1COOH)-H PE(36:1COOH)-H -1 774.5290605 6.681019927 PE carboxylic M-H - - - C41 H77 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(18:1_19:1COOH)-CH3 PC(18:1_19:1COOH)-CH3 PC(37:2COOH)-CH3 -1 814.5603605 12.41575012 PC carboxylic M-CH3 - - - C44 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0_20:5)+CH3COO_3 PC(18:0_20:5)+CH3COO PC(38:5)+CH3COO -1 866.5916605 12.06626296 PC diacyl M+CH3COO RM0025394 C48 H85 N1 O10 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(25:2_19:2COOH)-H PE(25:2_19:2COOH)-H PE(44:4COOH)-H -1 880.6073105 17.47676316 PE carboxylic M-H - - - C49 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN LPE(17:0)-H_2 LPE(17:0)-H LPE(17:0)-H -1 466.2939155 3.477328849 LPE monoacyl M-H RM0012607 C22 H45 N1 O7 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(O-20:1_18:1)-H PE(O-20:1_18:1)-H PE(O-38:2)-H -1 756.5912655 16.43805187 PE alkyl-acyl M-H RM0054756 C43 H83 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN CL(18:2_18:2_20:3_20:4)-H CL(18:2_18:2_20:3_20:4)-H CL(76:11)-H -1 1497.980605 19.50157363 CL diacyl-diacyl M-H RM0179310 C85 H143 O17 P2 CC=CC=CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC=CC)COC(=O)CCCCCCCCCCC=CC=CC=CC=CC PI(18:0_20:5)-H_2 PI(18:0_20:5)-H PI(38:5)-H -1 883.5342065 9.075818747 PI diacyl M-H RM0056629 C47 H80 O13 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(8:1COOH_20:5)+CH3COO PC(8:1COOH_20:5)+CH3COO PC(28:6COOH)+CH3COO -1 754.3936905 1.684561207 PC carboxylic M+CH3COO - - - C38 H61 N1 O12 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PI(18:1_20:5)-H_1 PI(18:1_20:5)-H PI(38:6)-H -1 881.5185565 7.28308482 PI diacyl M-H RM0056657 C47 H78 O13 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(17:0_4:1CHO)-H_1 PE(17:0_4:1CHO)-H PE(21:1CHO)-H -1 548.2993955 3.612449815 PE aldehyde M-H - - - C26 H47 N1 O9 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)C=CC(=O))COP(=O)(O)OCCN PE(17:0_18:2COOH)-H_2 PE(17:0_18:2COOH)-H PE(35:2COOH)-H -1 758.4977605 5.837951743 PE carboxylic M-H - - - C40 H73 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(15:0_18:4)+CH3COO PC(15:0_18:4)+CH3COO PC(33:4)+CH3COO -1 798.5290605 7.424009499 PC diacyl M+CH3COO RM0025581 C43 H77 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_18:3)-H_2 PE(16:0_18:3)-H PE(34:3)-H -1 712.4922805 10.19722249 PE diacyl M-H RM0001916 C39 H71 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(20:1_18:2)-H PE(20:1_18:2)-H PE(38:3)-H -1 768.5548805 14.47599317 PE diacyl M-H RM0134781 C43 H79 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(24:2_19:1COOH)-H PE(24:2_19:1COOH)-H PE(43:3COOH)-H -1 868.6073105 17.70037841 PE carboxylic M-H - - - C48 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PC(7:0CHO_18:1)+CH3COO PC(7:0CHO_18:1)+CH3COO PC(25:1CHO)+CH3COO -1 706.4300755 3.594901428 PC aldehyde M+CH3COO - - - C35 H65 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPE(20:2)-H_1 LPE(20:2)-H LPE(20:2)-H -1 504.3095655 3.496386504 LPE monoacyl M-H RM0097979 C25 H47 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(16:0_18:1)-CH3 PC(16:0_18:1)-CH3 PC(34:1)-CH3 -1 744.5548805 13.10571457 PC diacyl M-CH3 RM0090134 C41 H79 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(21:1CHO_18:1)-H PE(21:1CHO_18:1)-H PE(39:2CHO)-H -1 798.5654455 13.94509906 PE aldehyde M-H - - - C44 H81 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC=CC(=O))COP(=O)(O)OCCN PC(15:0_17:1)+CH3COO_4 PC(15:0_17:1)+CH3COO PC(32:1)+CH3COO -1 790.5603605 9.988770972 PC diacyl M+CH3COO RM0036654 C42 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:2COOH)-H_2 PE(18:1_18:2COOH)-H PE(36:3COOH)-H -1 770.4977605 5.523949192 PE carboxylic M-H - - - C41 H73 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(O-18:0_20:4)+CH3COO PC(O-18:0_20:4)+CH3COO PC(O-38:4)+CH3COO -1 854.6280455 14.45783357 PC alkyl-acyl M+CH3COO RM0134871 C48 H89 N1 O9 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_20:4COOH)+CH3COO_4 PC(17:1_20:4COOH)+CH3COO PC(37:5COOH)+CH3COO -1 882.5501905 5.083617076 PC carboxylic M+CH3COO - - - C47 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CCC=CCC=CCC=CCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_17:2)-H PE(17:0_17:2)-H PE(34:2)-H -1 714.5079305 11.69118995 PE diacyl M-H RM0098688 C39 H73 N1 O8 P1 CC=CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN LPE(18:1)-H_2 LPE(18:1)-H LPE(18:1)-H -1 478.2939155 3.431270116 LPE monoacyl M-H RM0104274 C23 H45 N1 O7 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(18:1_11:2COOH)+CH3COO PC(18:1_11:2COOH)+CH3COO PC(29:3COOH)+CH3COO -1 774.4562905 3.503957785 PC carboxylic M+CH3COO - - - C39 H69 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C LPE(16:0)-H_2 LPE(16:0)-H LPE(16:0)-H -1 452.2782655 3.293421155 LPE monoacyl M-H RM0134456 C21 H43 N1 O7 P1 CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(20:0_18:1)-H PE(20:0_18:1)-H PE(38:1)-H -1 772.5861805 17.17489914 PE diacyl M-H RM0001950 C43 H83 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(25:2_19:1COOH)-H PE(25:2_19:1COOH)-H PE(44:3COOH)-H -1 882.6229605 18.17410712 PE carboxylic M-H - - - C49 H89 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)(O)OCCN PE(18:2_18:3)-H PE(18:2_18:3)-H PE(36:5)-H -1 736.4922805 8.851759082 PE diacyl M-H RM0001182 C41 H71 N1 O8 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(O-19:1_18:1)+CH3COO PC(O-19:1_18:1)+CH3COO PC(O-37:2)+CH3COO -1 844.6436955 15.88737344 PC alkyl-acyl M+CH3COO RM0180530 C47 H91 N1 O9 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(5:0CHO_18:2)+CH3COO PC(5:0CHO_18:2)+CH3COO PC(23:2CHO)+CH3COO -1 676.3831255 2.680473265 PC aldehyde M+CH3COO - - - C33 H59 N1 O11 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:2CHO)+CH3COO_1 PC(18:1_18:2CHO)+CH3COO PC(36:3CHO)+CH3COO -1 856.5709255 6.16795147 PC aldehyde M+CH3COO - - - C46 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_18:2)+CH3COO_6 PC(19:1_18:2)+CH3COO PC(37:3)+CH3COO -1 856.6073105 12.65822752 PC diacyl M+CH3COO RM0104145 C47 H87 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1CHO_18:2)+CH3COO PC(18:1CHO_18:2)+CH3COO PC(36:3CHO)+CH3COO -1 856.5709255 5.93269334 PC aldehyde M+CH3COO - - - C46 H83 N1 O11 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_18:2COOH)-H_3 PE(18:1_18:2COOH)-H PE(36:3COOH)-H -1 770.4977605 5.836110662 PE carboxylic M-H - - - C41 H73 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(19:1_20:4)+CH3COO_6 PC(19:1_20:4)+CH3COO PC(39:5)+CH3COO -1 880.6073105 12.8558463 PC diacyl M+CH3COO RM0000618 C49 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:0COOH_18:1)+CH3COO PC(18:0COOH_18:1)+CH3COO PC(36:1COOH)+CH3COO -1 876.5971405 6.268054232 PC carboxylic M+CH3COO - - - C46 H87 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PI(16:0_20:5)-H PI(16:0_20:5)-H PI(36:5)-H -1 855.5029065 7.374043745 PI diacyl M-H RM0096571 C45 H76 O13 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PE(4:0CHO_18:0)-H PE(4:0CHO_18:0)-H PE(22:0CHO)-H -1 564.3306955 4.061070995 PE aldehyde M-H - - - C27 H51 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCC(=O))COP(=O)(O)OCCN PC(17:1_19:1)+CH3COO_5 PC(17:1_19:1)+CH3COO PC(36:2)+CH3COO -1 844.6073105 14.45099079 PC diacyl M+CH3COO RM0181295 C46 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0COOH_17:0)-CH3 PC(16:0COOH_17:0)-CH3 PC(33:0COOH)-CH3 -1 762.5290605 11.9313313 PC carboxylic M-CH3 - - - C40 H77 N1 O10 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(20:0_4:1CHO)-H PE(20:0_4:1CHO)-H PE(24:1CHO)-H -1 590.3463455 5.094380065 PE aldehyde M-H - - - C29 H53 N1 O9 P1 CCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)C=CC(=O))COP(=O)(O)OCCN LPE(17:0)-H_3 LPE(17:0)-H LPE(17:0)-H -1 466.2939155 3.726979662 LPE monoacyl M-H RM0012607 C22 H45 N1 O7 P1 CCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(O-19:1_20:5)+CH3COO PC(O-19:1_20:5)+CH3COO PC(O-39:6)+CH3COO -1 864.6123955 12.62367209 PC alkyl-acyl M+CH3COO - - - C49 H87 N1 O9 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_17:1)-CH3 PC(16:1_17:1)-CH3 PC(33:2)-CH3 -1 728.5235805 13.27290912 PC diacyl M-CH3 RM0025143 C40 H75 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:2_18:1)-H PE(O-19:2_18:1)-H PE(O-37:3)-H -1 740.5599655 16.12967647 PE alkyl-acyl M-H RM0182193 C42 H79 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_18:1)-H_4 PE(18:1_18:1)-H PE(36:2)-H -1 742.5392305 14.32093129 PE diacyl M-H RM0134757 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_19:2COOH)+HCOO_1 PC(17:1_19:2COOH)+HCOO PC(36:3COOH)+HCOO -1 858.5501905 5.393125651 PC carboxylic M+HCOO - - - C45 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(21:0_18:2)+CH3COO_2 PC(21:0_18:2)+CH3COO PC(39:2)+CH3COO -1 886.6542605 16.53847515 PC diacyl M+CH3COO RM0000027 C49 H93 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_22:5)+CH3COO PC(18:1_22:5)+CH3COO PC(40:6)+CH3COO -1 892.6073105 11.15502076 PC diacyl M+CH3COO RM0171147 C50 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C Cer(t17:1_22:1)-H Cer(t17:1_22:1)-H Cer(t39:2)-H -1 620.5623325 17.9178959 Cer phytoceramides M-H - - - C39 H74 N1 O4 CCCCCCCCCCCC=CC(O)C(C(CO)NC(=O)CCCCCCCCCCCCCCCCCCC=CC)O PC(17:1_18:2CHO)+CH3COO_1 PC(17:1_18:2CHO)+CH3COO PC(35:3CHO)+CH3COO -1 842.5552755 5.750190632 PC aldehyde M+CH3COO - - - C45 H81 N1 O11 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C LBPA(18:0_17:1)-H_2 LBPA(18:0_17:1)-H LBPA(35:1)-H -1 761.5338115 12.43891299 LBPA Monoacylglycerophosphomonoradylglycerolsá M-H - - - C41 H78 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCCC PE(27:0_18:1)-H PE(27:0_18:1)-H PE(45:1)-H -1 870.6957305 19.86106348 PE diacyl M-H RM0002041 C50 H97 N1 O8 P1 CCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_18:2CHO)+CH3COO_2 PC(18:1_18:2CHO)+CH3COO PC(36:3CHO)+CH3COO -1 856.5709255 6.371223175 PC aldehyde M+CH3COO - - - C46 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(17:1_17:1)-H PE(17:1_17:1)-H PE(34:2)-H -1 714.5079305 12.32929708 PE diacyl M-H RM0134771 C39 H73 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(20:4_20:5)-H_3 PE(20:4_20:5)-H PE(40:9)-H -1 784.4922805 7.957804474 PE diacyl M-H RM0043955 C45 H71 N1 O8 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:1_18:1)+CH3COO_6 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 11.65510794 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPC(15:0)+CH3COO_3 LPC(15:0)+CH3COO LPC(15:0)+CH3COO -1 540.3306955 2.171202235 LPC monoacyl M+CH3COO RM0017309 C25 H51 N1 O9 P1 CCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_20:4)-H_3 PE(18:0_20:4)-H PE(38:4)-H -1 766.5392305 13.81532135 PE diacyl M-H RM0134782 C43 H77 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCCN PE(21:2COOH_18:1)-H PE(21:2COOH_18:1)-H PE(39:3COOH)-H -1 812.5447105 14.64382178 PE carboxylic M-H - - - C44 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN LPE(19:0)-H_1 LPE(19:0)-H LPE(19:0)-H -1 494.3252155 4.574488947 LPE monoacyl M-H RM0097987 C24 H49 N1 O7 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(20:0_18:3)+CH3COO PC(20:0_18:3)+CH3COO PC(38:3)+CH3COO -1 870.6229605 14.9474097 PC diacyl M+CH3COO RM0103846 C48 H89 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_18:3)-H_3 PE(15:0_18:3)-H PE(33:3)-H -1 698.4766305 9.082131868 PE diacyl M-H RM0024692 C38 H69 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PE(16:1_17:1)-H_2 PE(16:1_17:1)-H PE(33:2)-H -1 700.4922805 10.58040215 PE diacyl M-H RM0041005 C38 H71 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(16:1_17:1)+CH3COO_2 PC(16:1_17:1)+CH3COO PC(33:2)+CH3COO -1 802.5603605 9.095326151 PC diacyl M+CH3COO RM0025143 C43 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_17:1)-H_2 PE(16:0_17:1)-H PE(33:1)-H -1 702.5079305 11.92242599 PE diacyl M-H RM0001944 C38 H73 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:0_22:5CHO)-CH3 PC(18:0_22:5CHO)-CH3 PC(40:5CHO)-CH3 -1 834.5654455 15.878623 PC aldehyde M-CH3 - - - C47 H81 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_17:2)-H PE(16:0_17:2)-H PE(33:2)-H -1 700.4922805 11.80833899 PE diacyl M-H RM0099068 C38 H71 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(15:0_18:1)+HCOO PC(15:0_18:1)+HCOO PC(33:1)+HCOO -1 790.5603605 9.975763395 PC diacyl M+HCOO RM0000544 C42 H81 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(18:0)-H_2 LPE(18:0)-H LPE(18:0)-H -1 480.3095655 4.121031873 LPE monoacyl M-H RM0017276 C23 H47 N1 O7 P1 CCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(18:0_17:1)+CH3COO_2 PC(18:0_17:1)+CH3COO PC(35:1)+CH3COO -1 832.6073105 14.96065021 PC diacyl M+CH3COO RM0001080 C45 H87 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:2)+CH3COO_3 PC(17:1_18:2)+CH3COO PC(35:3)+CH3COO -1 828.5760105 11.2435117 PC diacyl M+CH3COO RM0025431 C45 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1)+HCOO_1 PC(17:1_19:1)+HCOO PC(36:2)+HCOO -1 830.5916605 14.45099079 PC diacyl M+HCOO RM0181295 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_20:5)-H_3 PE(17:0_20:5)-H PE(37:5)-H -1 750.5079305 11.10817423 PE diacyl M-H RM0028171 C42 H73 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(19:1_19:1)+CH3COO_6 PC(19:1_19:1)+CH3COO PC(38:2)+CH3COO -1 872.6386105 15.53025869 PC diacyl M+CH3COO RM0001025 C48 H91 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(14:0_18:1COOH)-CH3 PC(14:0_18:1COOH)-CH3 PC(32:1COOH)-CH3 -1 746.4977605 9.06819 PC carboxylic M-CH3 - - - C39 H73 N1 O10 P1 CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:1CHO)+CH3COO_2 PC(18:1_18:1CHO)+CH3COO PC(36:2CHO)+CH3COO -1 858.5865755 6.01973967 PC aldehyde M+CH3COO - - - C46 H85 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_20:5)+CH3COO_3 PC(18:3_20:5)+CH3COO PC(38:8)+CH3COO -1 860.5447105 7.320085875 PC diacyl M+CH3COO RM0024946 C48 H79 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_19:1)+HCOO_2 PC(17:1_19:1)+HCOO PC(36:2)+HCOO -1 830.5916605 14.39332771 PC diacyl M+HCOO RM0181295 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:2_18:1)-H_2 PE(O-18:2_18:1)-H PE(O-36:3)-H -1 726.5443155 15.31710579 PE alkyl-acyl M-H RM0054694 C41 H77 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_19:1)-CH3_1 PC(18:1_19:1)-CH3 PC(37:2)-CH3 -1 784.5861805 14.18785929 PC diacyl M-CH3 RM0042470 C44 H83 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:1_18:1)+CH3COO_2 PC(O-18:1_18:1)+CH3COO PC(O-36:2)+CH3COO -1 830.6280455 14.65957266 PC alkyl-acyl M+CH3COO RM0017287 C46 H89 N1 O9 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(16:0_20:0)-H PE(16:0_20:0)-H PE(36:0)-H -1 746.5705305 17.16413662 PE diacyl M-H RM0001907 C41 H81 N1 O8 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(O-17:0_18:1)-H_1 PE(O-17:0_18:1)-H PE(O-35:1)-H -1 716.5599655 16.41796233 PE alkyl-acyl M-H RM0043666 C40 H79 N1 O7 P1 CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN LPE(16:1)-H LPE(16:1)-H LPE(16:1)-H -1 450.2626155 1.837894903 LPE monoacyl M-H RM0090013 C21 H41 N1 O7 P1 CC=CCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(17:1_18:2)+CH3COO_4 PC(17:1_18:2)+CH3COO PC(35:3)+CH3COO -1 828.5760105 10.08265429 PC diacyl M+CH3COO RM0025431 C45 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(22:0_17:1)-H PE(22:0_17:1)-H PE(39:1)-H -1 786.6018305 17.91246741 PE diacyl M-H RM0007157 C44 H85 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(17:1_18:1)+CH3COO_7 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 12.98014867 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1)+CH3COO_8 PC(17:1_18:1)+CH3COO PC(35:2)+CH3COO -1 830.5916605 13.03975417 PC diacyl M+CH3COO RM0000418 C45 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_22:1CHO)-H PE(18:1_22:1CHO)-H PE(40:2CHO)-H -1 812.5810955 14.54073104 PE aldehyde M-H - - - C45 H83 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC=CC(=O))COP(=O)(O)OCCN LPC(18:3)+CH3COO LPC(18:3)+CH3COO LPC(18:3)+CH3COO -1 576.3306955 1.960718212 LPC monoacyl M+CH3COO RM0134471 C28 H51 N1 O9 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_21:2COOH)-H PE(18:1_21:2COOH)-H PE(39:3COOH)-H -1 812.5447105 14.97057208 PE carboxylic M-H - - - C44 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(15:1_20:5)+CH3COO_5 PC(15:1_20:5)+CH3COO PC(35:6)+CH3COO -1 822.5290605 7.207639065 PC diacyl M+CH3COO RM0171229 C45 H77 N1 O10 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(15:0_20:5)+CH3COO PC(15:0_20:5)+CH3COO PC(35:5)+CH3COO -1 824.5447105 8.758002197 PC diacyl M+CH3COO RM0036657 C45 H79 N1 O10 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(O-19:1_18:2)+CH3COO PC(O-19:1_18:2)+CH3COO PC(O-37:3)+CH3COO -1 842.6280455 14.6012803 PC alkyl-acyl M+CH3COO - - - C47 H89 N1 O9 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_20:4)+CH3COO_4 PC(18:1_20:4)+CH3COO PC(38:5)+CH3COO -1 866.5916605 10.65934236 PC diacyl M+CH3COO RM0134948 C48 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(22:0)-H_1 LPE(22:0)-H LPE(22:0)-H -1 536.3721655 6.648538908 LPE monoacyl M-H RM0017246 C27 H55 N1 O7 P1 CCCCCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(17:1_18:1COOH)+CH3COO_3 PC(17:1_18:1COOH)+CH3COO PC(35:2COOH)+CH3COO -1 860.5658405 4.708710028 PC carboxylic M+CH3COO - - - C45 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_20:4)+CH3COO PC(16:1_20:4)+CH3COO PC(36:5)+CH3COO -1 838.5603605 8.904717683 PC diacyl M+CH3COO RM0171100 C46 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0CHO_18:2)-CH3 PC(17:0CHO_18:2)-CH3 PC(35:2CHO)-CH3 -1 770.5341455 11.45048098 PC aldehyde M-CH3 - - - C42 H77 N1 O9 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_18:1COOH)-CH3 PC(16:1_18:1COOH)-CH3 PC(34:2COOH)-CH3 -1 772.5134105 9.23158426 PC carboxylic M-CH3 - - - C41 H75 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:5)+CH3COO_6 PC(19:1_20:5)+CH3COO PC(39:6)+CH3COO -1 878.5916605 10.90656482 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_20:5)+CH3COO_7 PC(19:1_20:5)+CH3COO PC(39:6)+CH3COO -1 878.5916605 10.92332552 PC diacyl M+CH3COO - - - C49 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(7:1CHO_18:1)+CH3COO_2 PC(7:1CHO_18:1)+CH3COO PC(25:2CHO)+CH3COO -1 704.4144255 3.496688926 PC aldehyde M+CH3COO - - - C35 H63 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(18:0CHO_18:1)-H_3 PE(18:0CHO_18:1)-H PE(36:1CHO)-H -1 758.5341455 8.522346966 PE aldehyde M-H - - - C41 H77 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O))COP(=O)(O)OCCN PE(18:1_18:2COOH)-H_4 PE(18:1_18:2COOH)-H PE(36:3COOH)-H -1 770.4977605 5.340804023 PE carboxylic M-H - - - C41 H73 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PE(18:2_21:2COOH)-H PE(18:2_21:2COOH)-H PE(39:4COOH)-H -1 810.5290605 12.89861649 PE carboxylic M-H - - - C44 H77 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PE(18:2_20:3)-H PE(18:2_20:3)-H PE(38:5)-H -1 764.5235805 10.9243679 PE diacyl M-H RM0104576 C43 H75 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(17:0CHO_20:5)-CH3 PC(17:0CHO_20:5)-CH3 PC(37:5CHO)-CH3 -1 792.5184955 9.675855572 PC aldehyde M-CH3 - - - C44 H75 N1 O9 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPC(21:1)+CH3COO LPC(21:1)+CH3COO LPC(21:1)+CH3COO -1 622.4089455 4.633933508 LPC monoacyl M+CH3COO RM0180211 C31 H61 N1 O9 P1 CC=CCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_17:1)+CH3COO_2 PC(16:0_17:1)+CH3COO PC(33:1)+CH3COO -1 804.5760105 11.53585807 PC diacyl M+CH3COO RM0134943 C43 H83 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(O-18:0_18:1)+CH3COO PC(O-18:0_18:1)+CH3COO PC(O-36:1)+CH3COO -1 832.6436955 16.39540518 PC alkyl-acyl M+CH3COO RM0020660 C46 H91 N1 O9 P1 CCCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:3_20:5)+CH3COO_4 PC(18:3_20:5)+CH3COO PC(38:8)+CH3COO -1 860.5447105 6.875087908 PC diacyl M+CH3COO RM0024946 C48 H79 N1 O10 P1 CC=CC=CC=CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_4:1CHO)-H_2 PE(17:0_4:1CHO)-H PE(21:1CHO)-H -1 548.2993955 3.737423609 PE aldehyde M-H - - - C26 H47 N1 O9 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)C=CC(=O))COP(=O)(O)OCCN PC(16:0_18:1)+CH3COO_2 PC(16:0_18:1)+CH3COO PC(34:1)+CH3COO -1 818.5916605 12.67982604 PC diacyl M+CH3COO RM0090134 C44 H85 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(15:1_17:1)-H PE(15:1_17:1)-H PE(32:2)-H -1 686.4766305 9.997441238 PE diacyl M-H RM0044205 C37 H69 N1 O8 P1 CC=CCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:2_19:2)+CH3COO PC(18:2_19:2)+CH3COO PC(37:4)+CH3COO -1 854.5916605 10.72195327 PC diacyl M+CH3COO RM0181394 C47 H85 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1COOH_18:2)+HCOO_3 PC(19:1COOH_18:2)+HCOO PC(37:3COOH)+HCOO -1 872.5658405 5.870506625 PC carboxylic M+HCOO - - - C46 H83 N1 O12 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C LPC(20:4)+CH3COO_4 LPC(20:4)+CH3COO LPC(20:4)+CH3COO -1 602.3463455 1.996529042 LPC monoacyl M+CH3COO RM0048636 C30 H53 N1 O9 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C LPE(19:0)-H_2 LPE(19:0)-H LPE(19:0)-H -1 494.3252155 4.429056969 LPE monoacyl M-H RM0097987 C24 H49 N1 O7 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(17:1_19:2COOH)+HCOO_2 PC(17:1_19:2COOH)+HCOO PC(36:3COOH)+HCOO -1 858.5501905 5.295251398 PC carboxylic M+HCOO - - - C45 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(15:0_17:1)-H_2 PE(15:0_17:1)-H PE(32:1)-H -1 688.4922805 10.65885635 PE diacyl M-H RM0011409 C37 H71 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_20:5)-CH3_5 PC(17:1_20:5)-CH3 PC(37:6)-CH3 -1 776.5235805 10.21862337 PC diacyl M-CH3 RM0104001 C44 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(18:1_21:1)-H PE(18:1_21:1)-H PE(39:2)-H -1 784.5861805 16.73350768 PE diacyl M-H - - - C44 H83 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_18:1)-CH3_3 PC(17:1_18:1)-CH3 PC(35:2)-CH3 -1 756.5548805 11.86859135 PC diacyl M-CH3 RM0000418 C42 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(20:0_18:2)-H PE(20:0_18:2)-H PE(38:2)-H -1 770.5705305 16.25810968 PE diacyl M-H RM0001998 C43 H81 N1 O8 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(19:1_19:1)-H_2 PE(19:1_19:1)-H PE(38:2)-H -1 770.5705305 16.31250335 PE diacyl M-H RM0182777 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:1_18:2COOH)+CH3COO_2 PC(17:1_18:2COOH)+CH3COO PC(35:3COOH)+CH3COO -1 858.5501905 4.727430897 PC carboxylic M+CH3COO - - - C45 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(4:1CHO_19:1)-H PE(4:1CHO_19:1)-H PE(23:2CHO)-H -1 574.3150455 3.922708603 PE aldehyde M-H - - - C28 H49 N1 O9 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)C=CC(=O))COP(=O)(O)OCCN PC(17:1_20:5)+HCOO_2 PC(17:1_20:5)+HCOO PC(37:6)+HCOO -1 836.5447105 8.28491284 PC diacyl M+HCOO RM0104001 C46 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(20:4_20:4)+CH3COO_3 PC(20:4_20:4)+CH3COO PC(40:8)+CH3COO -1 888.5760105 8.231335472 PC diacyl M+CH3COO RM0136719 C50 H83 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C OAHFA(2:0_24:0)-H_2 OAHFA(2:0_24:0)-H OAHFA(26:0)-H -1 425.3636335 7.40987349 OAHFA Fatty ethers M-H - - - C26 H49 O4 CC(=O)OCCCCCCCCCCCCCCCCCCCCCCCC(=O)O PC(16:1_17:1)+CH3COO_3 PC(16:1_17:1)+CH3COO PC(33:2)+CH3COO -1 802.5603605 10.12037893 PC diacyl M+CH3COO RM0025143 C43 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_17:1)+CH3COO_4 PC(16:1_17:1)+CH3COO PC(33:2)+CH3COO -1 802.5603605 10.14432544 PC diacyl M+CH3COO RM0025143 C43 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(5:0CHO_17:1)+CH3COO PC(5:0CHO_17:1)+CH3COO PC(22:1CHO)+CH3COO -1 664.3831255 3.012655503 PC aldehyde M+CH3COO - - - C32 H59 N1 O11 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(16:0_18:1COOH)-CH3 PC(16:0_18:1COOH)-CH3 PC(34:1COOH)-CH3 -1 774.5290605 11.21949503 PC carboxylic M-CH3 - - - C41 H77 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:2CHO)+CH3COO_2 PC(17:1_18:2CHO)+CH3COO PC(35:3CHO)+CH3COO -1 842.5552755 6.069432139 PC aldehyde M+CH3COO - - - C45 H81 N1 O11 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PS(18:2_20:2)-H PS(18:2_20:2)-H PS(38:4)-H -1 810.5290605 12.89399293 PS diacyl M-H RM0057537 C44 H77 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCC(C(=O)O)N PC(O-17:0_18:1)+CH3COO PC(O-17:0_18:1)+CH3COO PC(O-35:1)+CH3COO -1 818.6280455 15.61944445 PC alkyl-acyl M+CH3COO RM0180436 C45 H89 N1 O9 P1 CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:1COOH)+CH3COO_1 PC(18:1_18:1COOH)+CH3COO PC(36:2COOH)+CH3COO -1 874.5814905 4.827345707 PC carboxylic M+CH3COO - - - C46 H85 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C LPE(18:1)-H_3 LPE(18:1)-H LPE(18:1)-H -1 478.2939155 3.080720102 LPE monoacyl M-H RM0104274 C23 H45 N1 O7 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(16:1_20:5)+CH3COO PC(16:1_20:5)+CH3COO PC(36:6)+CH3COO -1 836.5447105 7.639862902 PC diacyl M+CH3COO RM0103865 C46 H79 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C LPE(21:0)-H LPE(21:0)-H LPE(21:0)-H -1 522.3565155 5.753244606 LPE monoacyl M-H RM0007284 C26 H53 N1 O7 P1 CCCCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(O-19:2_18:2)-H_2 PE(O-19:2_18:2)-H PE(O-37:4)-H -1 738.5443155 14.42382438 PE alkyl-acyl M-H - - - C42 H77 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCCN PC(17:1_19:1COOH)-CH3_2 PC(17:1_19:1COOH)-CH3 PC(36:2COOH)-CH3 -1 800.5447105 11.67241779 PC carboxylic M-CH3 - - - C43 H79 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(23:2_19:2COOH)-H PE(23:2_19:2COOH)-H PE(42:4COOH)-H -1 852.5760105 16.26259823 PE carboxylic M-H - - - C47 H83 N1 O10 P1 CC=CC=CCCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PE(16:1_18:1)-H PE(16:1_18:1)-H PE(34:2)-H -1 714.5079305 11.54036455 PE diacyl M-H RM0134804 C39 H73 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(20:1_20:5)+CH3COO_2 PC(20:1_20:5)+CH3COO PC(40:6)+CH3COO -1 892.6073105 12.30523205 PC diacyl M+CH3COO RM0000886 C50 H87 N1 O10 P1 CC=CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1COOH)-CH3 PC(17:1_18:1COOH)-CH3 PC(35:2COOH)-CH3 -1 786.5290605 10.54429439 PC carboxylic M-CH3 - - - C42 H77 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:1)-CH3_4 PC(18:1_18:1)-CH3 PC(36:2)-CH3 -1 770.5705305 13.17994553 PC diacyl M-CH3 RM0090053 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(17:0_16:1)-H_2 PE(17:0_16:1)-H PE(33:1)-H -1 702.5079305 12.7654035 PE diacyl M-H RM0001922 C38 H73 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN LPC(P-15:2)+CH3COO_2 LPC(P-15:2)+CH3COO LPC(P-15:2)+CH3COO -1 520.3044805 3.806223701 LPC monoalkenyl M+CH3COO - - - C25 H47 N1 O8 P1 CC=CC=CCCCCCCCCC=COC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1CHO_18:2)-CH3 PC(18:1CHO_18:2)-CH3 PC(36:3CHO)-CH3 -1 782.5341455 10.68827871 PC aldehyde M-CH3 - - - C43 H77 N1 O9 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(16:1_17:1)+CH3COO_5 PC(16:1_17:1)+CH3COO PC(33:2)+CH3COO -1 802.5603605 9.980342134 PC diacyl M+CH3COO RM0025143 C43 H81 N1 O10 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-18:1_19:1)-H PE(O-18:1_19:1)-H PE(O-37:2)-H -1 742.5756155 17.3990779 PE alkyl-acyl M-H RM0054648 C42 H81 N1 O7 P1 CC=CCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(7:0CHO_17:0)-H PE(7:0CHO_17:0)-H PE(24:0CHO)-H -1 592.3619955 3.867512017 PE aldehyde M-H - - - C29 H55 N1 O9 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCC(=O))COP(=O)(O)OCCN LPC(16:0)+CH3COO_2 LPC(16:0)+CH3COO LPC(16:0)+CH3COO -1 554.3463455 2.936966619 LPC monoacyl M+CH3COO RM0134475 C26 H53 N1 O9 P1 CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PE(17:1_19:1)-H_2 PE(17:1_19:1)-H PE(36:2)-H -1 742.5392305 14.70855246 PE diacyl M-H RM0098138 C41 H77 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_18:4)-H_2 PE(18:1_18:4)-H PE(36:5)-H -1 736.4922805 9.53983572 PE diacyl M-H RM0001181 C41 H71 N1 O8 P1 CC=CC=CC=CC=CCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PI(17:1_20:5)-H PI(17:1_20:5)-H PI(37:6)-H -1 867.5029065 6.917798798 PI diacyl M-H RM0056210 C46 H76 O13 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O LPE(22:0)-H_2 LPE(22:0)-H LPE(22:0)-H -1 536.3721655 6.490593785 LPE monoacyl M-H RM0017246 C27 H55 N1 O7 P1 CCCCCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN LPE(20:0)-H LPE(20:0)-H LPE(20:0)-H -1 508.3408655 5.126831903 LPE monoacyl M-H RM0134453 C25 H51 N1 O7 P1 CCCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(O-17:0_18:1)-H_2 PE(O-17:0_18:1)-H PE(O-35:1)-H -1 716.5599655 16.07425017 PE alkyl-acyl M-H RM0043666 C40 H79 N1 O7 P1 CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(18:1_18:1)-CH3_5 PC(18:1_18:1)-CH3 PC(36:2)-CH3 -1 770.5705305 13.08838838 PC diacyl M-CH3 RM0090053 C43 H81 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0CHO_18:1)-CH3 PC(17:0CHO_18:1)-CH3 PC(35:1CHO)-CH3 -1 772.5497955 13.5436802 PC aldehyde M-CH3 - - - C42 H79 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_18:2CHO)-H PE(18:0_18:2CHO)-H PE(36:2CHO)-H -1 756.5184955 7.577735174 PE aldehyde M-H - - - C41 H75 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O))COP(=O)(O)OCCN LPE(20:2)-H_2 LPE(20:2)-H LPE(20:2)-H -1 504.3095655 3.432849815 LPE monoacyl M-H RM0097979 C25 H47 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(17:0_17:1)-H_4 PE(17:0_17:1)-H PE(34:1)-H -1 716.5235805 13.2353758 PE diacyl M-H RM0103851 C39 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(17:0_19:1)-H PE(17:0_19:1)-H PE(36:1)-H -1 744.5548805 15.26960802 PE diacyl M-H RM0182657 C41 H79 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(10:1CHO_19:1)+CH3COO PC(10:1CHO_19:1)+CH3COO PC(29:2CHO)+CH3COO -1 760.4770255 4.274703809 PC aldehyde M+CH3COO - - - C39 H71 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(6:0COOH_18:1)-CH3 PC(6:0COOH_18:1)-CH3 PC(24:1COOH)-CH3 -1 634.3725605 2.978549196 PC carboxylic M-CH3 - - - C31 H57 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(22:2COOH_20:4)-H PE(22:2COOH_20:4)-H PE(42:6COOH)-H -1 848.5447105 14.21766301 PE carboxylic M-H - - - C47 H79 N1 O10 P1 CCCCCCC=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(16:0_20:1COOH)-CH3 PC(16:0_20:1COOH)-CH3 PC(36:1COOH)-CH3 -1 802.5603605 13.99217288 PC carboxylic M-CH3 - - - C43 H81 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C CL(18:2_18:2_20:4_20:4)-H CL(18:2_18:2_20:4_20:4)-H CL(76:12)-H -1 1495.964955 19.09213029 CL diacyl-diacyl M-H RM0179312 C85 H141 O17 P2 CC=CC=CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COC(=O)CCCCCCCCCCC=CC=CC=CC=CC PE(O-19:1_15:0)-H PE(O-19:1_15:0)-H PE(O-34:1)-H -1 702.5443155 16.3480343 PE alkyl-acyl M-H - - - C39 H77 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCC)COP(=O)(O)OCCN PE(7:0CHO_18:0)-H PE(7:0CHO_18:0)-H PE(25:0CHO)-H -1 606.3776455 4.361731931 PE aldehyde M-H - - - C30 H57 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCC(=O))COP(=O)(O)OCCN PE(18:0_19:1)-H PE(18:0_19:1)-H PE(37:1)-H -1 758.5705305 16.76935452 PE diacyl M-H RM0104573 C42 H81 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(15:0_17:1)-H_3 PE(15:0_17:1)-H PE(32:1)-H -1 688.4922805 11.06532095 PE diacyl M-H RM0011409 C37 H71 N1 O8 P1 CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:1_20:5)-H PE(18:1_20:5)-H PE(38:6)-H -1 762.5079305 9.998528188 PE diacyl M-H RM0090268 C43 H73 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OCCN PC(17:0_17:1)+CH3COO_2 PC(17:0_17:1)+CH3COO PC(34:1)+CH3COO -1 818.5916605 12.45429528 PC diacyl M+CH3COO RM0025585 C44 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_18:2CHO)+CH3COO_3 PC(18:1_18:2CHO)+CH3COO PC(36:3CHO)+CH3COO -1 856.5709255 6.717252233 PC aldehyde M+CH3COO - - - C46 H83 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(16:1_16:1)-H PE(16:1_16:1)-H PE(32:2)-H -1 686.4766305 9.326459906 PE diacyl M-H RM0134770 C37 H69 N1 O8 P1 CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PC(17:0_18:2)-CH3_2 PC(17:0_18:2)-CH3 PC(35:2)-CH3 -1 756.5548805 12.11675575 PC diacyl M-CH3 RM0000392 C42 H79 N1 O8 P1 CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C OAHFA(2:0_18:0)-H OAHFA(2:0_18:0)-H OAHFA(20:0)-H -1 341.2697335 3.78853466 OAHFA Fatty ethers M-H - - - C20 H37 O4 CC(=O)OCCCCCCCCCCCCCCCCCC(=O)O PC(17:1_18:2COOH)+CH3COO_3 PC(17:1_18:2COOH)+CH3COO PC(35:3COOH)+CH3COO -1 858.5501905 4.976265646 PC carboxylic M+CH3COO - - - C45 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(17:0_17:1)+CH3COO_3 PC(17:0_17:1)+CH3COO PC(34:1)+CH3COO -1 818.5916605 12.81486787 PC diacyl M+CH3COO RM0025585 C44 H85 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C PE(22:2COOH_18:2)-H PE(22:2COOH_18:2)-H PE(40:4COOH)-H -1 824.5447105 14.55083069 PE carboxylic M-H - - - C45 H79 N1 O10 P1 CC=CC=CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)(O)OCCN PC(17:1_17:1)+CH3COO_4 PC(17:1_17:1)+CH3COO PC(34:2)+CH3COO -1 816.5760105 10.2073965 PC diacyl M+CH3COO RM0103999 C44 H83 N1 O10 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PE(O-19:1_19:1)-H_2 PE(O-19:1_19:1)-H PE(O-38:2)-H -1 756.5912655 17.63965593 PE alkyl-acyl M-H - - - C43 H83 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCOC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PI(18:0_20:4)-H_2 PI(18:0_20:4)-H PI(38:4)-H -1 885.5498565 10.54590726 PI diacyl M-H RM0134537 C47 H82 O13 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(18:1_9:2CHO)+CH3COO_2 PC(18:1_9:2CHO)+CH3COO PC(27:3CHO)+CH3COO -1 730.4300755 3.659095282 PC aldehyde M+CH3COO - - - C37 H65 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPC(19:0)+CH3COO_2 LPC(19:0)+CH3COO LPC(19:0)+CH3COO -1 596.3932955 4.290631113 LPC monoacyl M+CH3COO RM0134490 C29 H59 N1 O9 P1 CCCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:1COOH)+CH3COO_4 PC(17:1_18:1COOH)+CH3COO PC(35:2COOH)+CH3COO -1 860.5658405 4.562103172 PC carboxylic M+CH3COO - - - C45 H83 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_19:1COOH)+HCOO_3 PC(18:1_19:1COOH)+HCOO PC(37:2COOH)+HCOO -1 874.5814905 6.28013973 PC carboxylic M+HCOO - - - C46 H85 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(18:1_19:1)-CH3_2 PC(18:1_19:1)-CH3 PC(37:2)-CH3 -1 784.5861805 14.75068254 PC diacyl M-CH3 RM0042470 C44 H83 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(5:0CHO_18:1)+CH3COO_2 PC(5:0CHO_18:1)+CH3COO PC(23:1CHO)+CH3COO -1 678.3987755 3.559491204 PC aldehyde M+CH3COO - - - C33 H61 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PC(5:0CHO_18:1)+CH3COO_3 PC(5:0CHO_18:1)+CH3COO PC(23:1CHO)+CH3COO -1 678.3987755 3.423384094 PC aldehyde M+CH3COO - - - C33 H61 N1 O11 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC(=O))COP(=O)([O-])OCC[N+](C)(C)C PE(16:1_2:0)-H PE(16:1_2:0)-H PE(18:1)-H -1 492.2731805 1.212151145 PE diacyl M-H - - - C23 H43 N1 O8 P1 CC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PE(18:0_18:1)-H PE(18:0_18:1)-H PE(36:1)-H -1 744.5548805 15.83662986 PE diacyl M-H RM0134779 C41 H79 N1 O8 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN PC(18:0COOH_18:1)-CH3 PC(18:0COOH_18:1)-CH3 PC(36:1COOH)-CH3 -1 802.5603605 13.62355646 PC carboxylic M-CH3 - - - C43 H81 N1 O10 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(17:1_18:1)-H_2 PE(17:1_18:1)-H PE(35:2)-H -1 728.5235805 13.58915861 PE diacyl M-H RM0001943 C40 H75 N1 O8 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC)COP(=O)(O)OCCN PI(18:1_20:5)-H_2 PI(18:1_20:5)-H PI(38:6)-H -1 881.5185565 7.408657416 PI diacyl M-H RM0056657 C47 H78 O13 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O PC(16:0_20:5)+CH3COO_4 PC(16:0_20:5)+CH3COO PC(36:5)+CH3COO -1 838.5603605 9.008396898 PC diacyl M+CH3COO RM0171098 C46 H81 N1 O10 P1 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC)COP(=O)([O-])OCC[N+](C)(C)C PC(17:1_18:2COOH)+CH3COO_4 PC(17:1_18:2COOH)+CH3COO PC(35:3COOH)+CH3COO -1 858.5501905 5.00865641 PC carboxylic M+CH3COO - - - C45 H81 N1 O12 P1 CC=CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PC(19:1_9:2CHO)+CH3COO PC(19:1_9:2CHO)+CH3COO PC(28:3CHO)+CH3COO -1 744.4457255 4.033924064 PC aldehyde M+CH3COO - - - C38 H67 N1 O11 P1 CC=CCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPE(20:2)-H_3 LPE(20:2)-H LPE(20:2)-H -1 504.3095655 3.632327601 LPE monoacyl M-H RM0097979 C25 H47 N1 O7 P1 CC=CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN LPE(20:1)-H LPE(20:1)-H LPE(20:1)-H -1 506.3252155 4.168084312 LPE monoacyl M-H RM0104269 C25 H49 N1 O7 P1 CC=CCCCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PC(18:1_18:1COOH)+CH3COO_2 PC(18:1_18:1COOH)+CH3COO PC(36:2COOH)+CH3COO -1 874.5814905 4.991848415 PC carboxylic M+CH3COO - - - C46 H85 N1 O12 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC=CC(=O)O)COP(=O)([O-])OCC[N+](C)(C)C PE(18:0_20:3)-H_2 PE(18:0_20:3)-H PE(38:3)-H -1 768.5548805 14.90765614 PE diacyl M-H RM0001660 C43 H79 N1 O8 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCCN PC(18:0_22:6CHO)-CH3 PC(18:0_22:6CHO)-CH3 PC(40:6CHO)-CH3 -1 832.5497955 14.69038479 PC aldehyde M-CH3 - - - C47 H79 N1 O9 P1 CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCC=CC=CC=CC=CC=CC=CC(=O))COP(=O)([O-])OCC[N+](C)(C)C LPE(18:1)-H_4 LPE(18:1)-H LPE(18:1)-H -1 478.2939155 3.218677289 LPE monoacyl M-H RM0104274 C23 H45 N1 O7 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(CO)COP(=O)(O)OCCN PE(18:0CHO_18:1)-H_4 PE(18:0CHO_18:1)-H PE(36:1CHO)-H -1 758.5341455 6.675421125 PE aldehyde M-H - - - C41 H77 N1 O9 P1 CC=CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCCC(=O))COP(=O)(O)OCCN CL(20:3_20:3_20:4_20:4)-2H CL(20:3_20:3_20:4_20:4)-2H CL(80:14)-2H -2 773.494489 19.32099088 CL diacyl-diacyl M-2H - - - C89 H144 O17 P2 CC=CC=CC=CC=CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC=CC)COC(=O)CCCCCCCCCCCCC=CC=CC=CC CL(20:3_20:3_20:3_20:4)-2H CL(20:3_20:3_20:3_20:4)-2H CL(80:13)-2H -2 774.502314 19.6663267 CL diacyl-diacyl M-2H - - - C89 H146 O17 P2 CC=CC=CC=CC=CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC=CC)COC(=O)CCCCCCCCCCCCC=CC=CC=CC CL(20:4_20:4_20:4_20:4)-2H_1 CL(20:4_20:4_20:4_20:4)-2H CL(80:16)-2H -2 771.478839 18.52957214 CL diacyl-diacyl M-2H - - - C89 H140 O17 P2 CC=CC=CC=CC=CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COC(=O)CCCCCCCCCCC=CC=CC=CC=CC CL(20:3_20:4_20:4_20:4)-2H CL(20:3_20:4_20:4_20:4)-2H CL(80:15)-2H -2 772.486664 18.92983332 CL diacyl-diacyl M-2H - - - C89 H142 O17 P2 CC=CC=CC=CC=CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC=CC)COC(=O)CCCCCCCCCCC=CC=CC=CC=CC CL(20:4_20:4_20:4_20:4)-2H_2 CL(20:4_20:4_20:4_20:4)-2H CL(80:16)-2H -2 771.478839 18.70129642 CL diacyl-diacyl M-2H - - - C89 H140 O17 P2 CC=CC=CC=CC=CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COC(=O)CCCCCCCCCCC=CC=CC=CC=CC CL(18:2_20:4_20:4_20:4)-2H CL(18:2_20:4_20:4_20:4)-2H CL(78:14)-2H -2 759.478839 18.81531751 CL diacyl-diacyl M-2H - - - C87 H140 O17 P2 CC=CC=CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COC(=O)CCCCCCCCCCC=CC=CC=CC=CC CL(18:2_20:3_20:4_20:4)-2H CL(18:2_20:3_20:4_20:4)-2H CL(78:13)-2H -2 760.486664 19.22181576 CL diacyl-diacyl M-2H - - - C87 H142 O17 P2 CC=CC=CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC=CC)COC(=O)CCCCCCCCCCC=CC=CC=CC=CC CL(18:2_20:3_20:3_20:4)-2H CL(18:2_20:3_20:3_20:4)-2H CL(78:12)-2H -2 761.494489 19.56961583 CL diacyl-diacyl M-2H - - - C87 H144 O17 P2 CC=CC=CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC=CC=CC=CC=CC)COP(=O)(O)OCC(O)COP(=O)(O)OCC(OC(=O)CCCCCCCCCCCCC=CC=CC=CC)COC(=O)CCCCCCCCCCCCC=CC=CC=CC METABOLITES_END #END