RefMet Compound Details

RefMet ID, RefMet name, exact mass and formula
RefMet ID	RM0121145
RefMet name	Cer 43:0;O2
Alternative name	Cer(d43:0)
Sum Composition	Cer 43:0;O2	View other entries in RefMet with this sum composition
Exact mass	665.668594 (neutral)	Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M+2K-H]+ [M+Na]+ [M+2Na]2+ [M+2Na-H]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M.CH3]+ [M+Ag]+ [M+H+CH3OH]+ [M+H+CH3CN]+ [M+H+2CH3CN]+ [M+Na+CH3CN]+ [M.NaFormate+H]+ [M.NH4Formate+H]+ [M.TMSi]+ [M.tBuDMSi]+ [M+H-Hexose]+ [M+H-EtnP]+ [M+H-SerP]+ [M-H]- [M-H-H2O]- [M-CH3]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+Na-2H]- [M+K-2H]- [M.Formate]- [M.NaFormate-H]- [M.NH4Formate-H]- [M.F]- [M-H-Ser]- [M.HF2]- M(neutral)    View other RefMet entries with this exact (neutral) mass:   +/- 0.05 amu   +/- 0.1 amu   +/- 0.2 amu   +/- 0.5 amu
Formula	C43H87NO3	View other entries in RefMet with this formula
Chemical/Biochemical Classification
Super Class	Sphingolipids
Main Class	Ceramides
Sub Class	Cer (Ceramides)
Distribution of Cer 43:0;O2 in NMDR studies
Species	Plot Species distribution
Sample source	Plot Sample source(tissue) distribution
Platform	Platform (MS/NMR) used for detection
Chromatography	Chromatography methods used for detection
Studies	NMDR Studies reporting Cer 43:0;O2
External Links
KEGG ID	C12126
Structural annotation level
Annotation level	4   (1:Known structure; 2:Known regiochemistry; 3:Partial structure; 4:Sum-composition)

Abbrev	# of Studies	Refmet name(exact structures)	Systematic name
Cer 18:0;O2/25:0	14	Cer 18:0;O2/25:0	N-(pentacosanoyl)-sphinganine
Cer 19:0;O2/24:0	7	Cer 19:0;O2/24:0	N-(tetracosanoyl)-nonadecasphinganine
Cer 17:0;O2/26:0	2	Cer 17:0;O2/26:0	N-(hexacosanoyl)-heptadecasphinganine
Cer 20:0;O2/23:0	2	Cer 20:0;O2/23:0	N-(tricosanoyl)-eicosasphinganine
Cer 14:0;O2/29:0		Cer 14:0;O2/29:0	N-(nonacosanoyl)-tetradecasphinganine
Cer 15:0;O2/28:0		Cer 15:0;O2/28:0	N-(octacosanoyl)-pentadecasphinganine
Cer 16:0;O2/27:0		Cer 16:0;O2/27:0	N-(heptacosanoyl)-hexadecasphinganine
Cer 21:0;O2/22:0		Cer 21:0;O2/22:0	N-(docosanoyl)-heneicosasphinganine
Cer 22:0;O2/21:0		Cer 22:0;O2/21:0	N-(heneicosanoyl)-docosasphinganine

Table of KEGG reactions in human pathways involving Cer 43:0;O2

Rxn ID	KEGG Reaction	Enzyme
R06517	Acyl-CoA + Sphinganine <=> CoA + Dihydroceramide	acyl-CoA:sphingosine N-acyltransferase
R06518	Dihydroceramide + H2O <=> Fatty acid + Sphinganine	N-acylsphingosine amidohydrolase
R06519	Dihydroceramide + 2 Ferrocytochrome b5 + Oxygen + 2 H+ <=> N-Acylsphingosine + 2 Ferricytochrome b5 + 2 H2O	dihydroceramide,ferrocytochrome b5:oxygen oxidoreductase (4,5-dehydrogenating)
R06526	Dihydroceramide + 2 Ferrocytochrome b5 + Oxygen + 2 H+ <=> Phytoceramide + 2 Ferricytochrome b5 + H2O	dihydroceramide,ferrocytochrome b5:oxygen oxidoreductase (C4-hydroxylating)

Table of KEGG human pathways containing Cer 43:0;O2

Pathway ID	Human Pathway	# of reactions
hsa00600	Sphingolipid metabolism	4