RefMet Compound Details

RefMet ID, RefMet name, exact mass and formula
RefMet ID	RM0044751
RefMet name	GlcCer 28:0;O2;O
Alternative name	GlcCer(d28:0(OH))
Sum Composition	GlcCer 28:0;O3	View other entries in RefMet with this sum composition
Exact mass	633.481584 (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	C34H67NO9	View other entries in RefMet with this formula
Chemical/Biochemical Classification
Super Class	Sphingolipids
Main Class	Glycosphingolipids
Sub Class	HexCer (Hexosyl ceramides)
Distribution of GlcCer 28:0;O2;O 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 GlcCer 28:0;O2;O
External Links
KEGG ID	C01190
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
GlcCer 14:0;O3/14:0		GlcCer 14:0;O3/14:0	N-(tetradecanoyl)-1-beta-glucosyl-4R-hydroxytetradecasphinganine
GlcCer 15:0;O3/13:0		GlcCer 15:0;O3/13:0	N-(tridecanoyl)-1-beta-glucosyl-4R-hydroxypentadecasphinganine
GlcCer 16:0;O3/12:0		GlcCer 16:0;O3/12:0	N-(dodecanoyl)-1-beta-glucosyl-4R-hydroxyhexadecasphinganine
GlcCer 17:0;O3/11:0		GlcCer 17:0;O3/11:0	N-(undecanoyl)-1-beta-glucosyl-4R-hydroxyheptadecasphinganine
GlcCer 18:0;O3/10:0		GlcCer 18:0;O3/10:0	N-(decanoyl)-1-beta-glucosyl-4R-hydroxysphinganine

Table of KEGG reactions in human pathways involving GlcCer 28:0;O2;O

Rxn ID	KEGG Reaction	Enzyme
R01497	UDP-glucose + N-Acylsphingosine <=> UDP + Glucosylceramide	UDP-glucose:N-acylsphingosine D-glucosyltransferase
R01498	Glucosylceramide + H2O <=> D-Glucose + N-Acylsphingosine	D-Glucosyl-N-acylsphingosine glucohydrolase
R03354	Glucosylceramide + UDP-alpha-D-galactose <=> Lactosylceramide + UDP	UDP-alpha-D-galactose:beta-D-glucosyl-(1<->1)-ceramide 4-beta-D-galactosyltransferase
R03355	Lactosylceramide + H2O <=> Glucosylceramide + D-Galactose	beta-D-Galactosyl-1,4-beta-D-glucosylceramide galactohydrolase

Table of KEGG human pathways containing GlcCer 28:0;O2;O

Pathway ID	Human Pathway	# of reactions
hsa00600	Sphingolipid metabolism	4