RefMet Compound Details

RefMet ID	RM0124995
MW structure	87898 (View MW Metabolite Database details)
RefMet name	Cer 19:0;O3/37:0
Alternative name	Cer(t19:0/37:0)
Systematic name	N-(heptatriacontanoyl)-4R-hydroxynonadecasphinganine
SMILES	CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@@H]([C@@H](CCCCCCCCCCCCCCC)O)O   Run Tanimoto similarity search (with similarity coefficient >=0.6)
Sum Composition	Cer 56:0;O3	View other entries in RefMet with this sum composition
Exact mass	863.866959 (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	C56H113NO4	View other entries in RefMet with this formula
InChI	InChI=1S/C56H113NO4/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32-33-34-35-36-37-39-41-43-45-47-49-51-55(60) 57-53(52-58)56(61)54(59)50-48-46-44-42-40-38-16-14-12-10-8-6-4-2/h53-54,56,58-59,61H,3-52H2,1-2H3,(H,57,60)/t53-,54+,56-/m0/s1
InChIKey	URXRETGHQJQXER-JJEZHPPHSA-N	View other enantiomers/diastereomers of this metabolite in RefMet
Super Class	Sphingolipids
Main Class	Ceramides
Sub Class	PhytoCer (Phytoceramides)
Pubchem CID	145715058
Annotation level	1   (1:Known structure; 2:Known regiochemistry; 3:Partial structure; 4:Sum-composition)

Table of KEGG reactions in human pathways involving Cer 19:0;O3/37:0

Rxn ID	KEGG Reaction	Enzyme
R06526	Dihydroceramide + 2 Ferrocytochrome b5 + Oxygen + 2 H+ <=> Phytoceramide + 2 Ferricytochrome b5 + H2O	dihydroceramide,ferrocytochrome b5:oxygen oxidoreductase (C4-hydroxylating)
R06527	C26-CoA + Phytosphingosine <=> CoA + Phytoceramide	acyl-CoA: phytosphingosine N-acyltransferase
R06528	Phytoceramide + H2O <=> Fatty acid + Phytosphingosine	Phytoceramide amidohydrolase

Table of KEGG human pathways containing Cer 19:0;O3/37:0

Pathway ID	Human Pathway	# of reactions
hsa00600	Sphingolipid metabolism	2
hsa01100	Metabolic pathways	1