CHEBI:84719 - β-D-glucosyl-N-octadecanoylsphingosine

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ChEBI Name β-D-glucosyl-N-octadecanoylsphingosine
ChEBI ID CHEBI:84719
ChEBI ASCII Name beta-D-glucosyl-N-octadecanoylsphingosine
Definition A β-D-glucosyl-N-acylsphingosine in which the acyl group is specified as octadecanoyl.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C42H81NO8
Net Charge 0
Average Mass 728.09440
Monoisotopic Mass 727.59622
InChI InChI=1S/C42H81NO8/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-38(46)43-35(34-50-42-41(49)40(48)39(47)37(33-44)51-42)36(45)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h29,31,35-37,39-42,44-45,47-49H,3-28,30,32-34H2,1-2H3,(H,43,46)/b31-29+/t35-,36+,37+,39+,40-,41+,42+/m0/s1
InChIKey YMYQEDCYNANIPI-DYJXBSQNSA-N
SMILES CCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)\C=C\CCCCCCCCCCCCC
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: MetaboLights Study
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via D-glucosyl-N-acylsphingosine )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via D-glucosyl-N-acylsphingosine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-D-glucosyl-N-octadecanoylsphingosine (CHEBI:84719) has functional parent octadecanoic acid (CHEBI:28842)
β-D-glucosyl-N-octadecanoylsphingosine (CHEBI:84719) has role mouse metabolite (CHEBI:75771)
β-D-glucosyl-N-octadecanoylsphingosine (CHEBI:84719) is a β-D-glucosyl-N-acylsphingosine (CHEBI:22801)
IUPAC Name
N-[(2S,3R,4E)-1-(β-D-glucopyranosyloxy)-3-hydroxyoctadec-4-en-2-yl]octadecanamide
Synonyms Sources
β-D-glucosyl-(1↔1)-N-octadecanoylsphing-4-enine UniProt
β-D-glucosyl-N-stearoylsphingosine ChEBI
C18 GlcCer LIPID MAPS
GlcCer(d18:1/18:0) LIPID MAPS
N-(octadecanoyl)-1-β-glucosyl-sphing-4-enine LIPID MAPS
Manual Xref Database
LMSP0501AA05 LIPID MAPS
View more database links
Last Modified
08 February 2019