CHEBI:84160 - 1-O-(α-D-galactosyl)-N-decanoylphytosphingosine

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ChEBI Name 1-O-(α-D-galactosyl)-N-decanoylphytosphingosine
ChEBI ID CHEBI:84160
ChEBI ASCII Name 1-O-(alpha-D-galactosyl)-N-decanoylphytosphingosine
Definition A glycophytoceramide having an α-D-galactopyranosyl residue at the O-1 position and a decanoyl group attached to the nitrogen.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C34H67NO9
Net Charge 0
Average Mass 633.89710
Monoisotopic Mass 633.48158
InChI InChI=1S/C34H67NO9/c1-3-5-7-9-11-12-13-14-15-17-18-20-22-27(37)30(39)26(35-29(38)23-21-19-16-10-8-6-4-2)25-43-34-33(42)32(41)31(40)28(24-36)44-34/h26-28,30-34,36-37,39-42H,3-25H2,1-2H3,(H,35,38)/t26-,27+,28+,30-,31-,32-,33+,34-/m0/s1
InChIKey KOVUZRDYDHABCN-HVPSFVGRSA-N
SMILES CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@H](CO[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)NC(=O)CCCCCCCCC
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via N-acylphytosphingosine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-O-(α-D-galactosyl)-N-decanoylphytosphingosine (CHEBI:84160) has functional parent α-D-galactose (CHEBI:28061)
1-O-(α-D-galactosyl)-N-decanoylphytosphingosine (CHEBI:84160) has functional parent decanoic acid (CHEBI:30813)
1-O-(α-D-galactosyl)-N-decanoylphytosphingosine (CHEBI:84160) is a glycophytoceramide (CHEBI:59389)
IUPAC Name
N-[(2S,3S,4R)-1-(α-D-galactopyranosyloxy)-3,4-dihydroxyoctadecan-2-yl]decanamide
Synonyms Sources
(2S,3S,4R)-N-decanoyl-1-[(α-D-galactopyranosyl)oxy]-2-amino-octadecane-3,4-diol ChEBI
1-O-(α-D-galactopyranosyl)-N-decanoylphytosphingosine ChEBI
α-GC (C10:0) ChEBI
α-GC (C10:0/C18:0) ChEBI
α-GC(C10:0/C18:0) ChEBI
α-GC, C10:0/C18:0 ChEBI
αGC (C10) ChEBI
αGC(C10) ChEBI
Registry Number Type Source
11628401 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21425779 PubMed citation Europe PMC
21910729 PubMed citation Europe PMC
29351991 PubMed citation Europe PMC
Last Modified
26 February 2018