CHEBI:63008 - 1-O-(α-D-galactopyranosyl)-N-hexacosanoylsphinganine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 1-O-(α-D-galactopyranosyl)-N-hexacosanoylsphinganine
ChEBI ID CHEBI:63008
ChEBI ASCII Name 1-O-(alpha-D-galactopyranosyl)-N-hexacosanoylsphinganine
Definition A glycodihydroceramide having an α-D-galactopyranosyl residue at the O-1 position and an hexacosanoyl group attached to the nitrogen.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C50H99NO8
Net Charge 0
Average Mass 842.32300
Monoisotopic Mass 841.73707
InChI InChI=1S/C50H99NO8/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-26-28-30-32-34-36-38-40-46(54)51-43(42-58-50-49(57)48(56)47(55)45(41-52)59-50)44(53)39-37-35-33-31-29-27-16-14-12-10-8-6-4-2/h43-45,47-50,52-53,55-57H,3-42H2,1-2H3,(H,51,54)/t43-,44+,45+,47-,48-,49+,50-/m0/s1
InChIKey GTRFIKUZMLUSGB-LXQBDVMYSA-N
SMILES CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)CCCCCCCCCCCCCCC
Roles Classification
Biological Role(s): epitope
The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via N-acylsphinganine )
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via N-acylsphinganine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-O-(α-D-galactopyranosyl)-N-hexacosanoylsphinganine (CHEBI:63008) has functional parent α-D-galactose (CHEBI:28061)
1-O-(α-D-galactopyranosyl)-N-hexacosanoylsphinganine (CHEBI:63008) has role epitope (CHEBI:53000)
1-O-(α-D-galactopyranosyl)-N-hexacosanoylsphinganine (CHEBI:63008) is a glycodihydroceramide (CHEBI:60451)
IUPAC Name
N-[(2S,3R)-1-(α-D-galactopyranosyloxy)-3-hydroxyoctadecan-2-yl]hexacosanamide
Synonyms Sources
(2S,3R)-1-(α-D-galactopyranosyl)-2-hexacosanoylaminooctadecan-3-ol ChEBI
4''-deoxy-α-GalCer ChEBI
AH03-1 ChEBI
desoxy-KRN7000 ChEBI
Galα-Cer(d18:0/26:0) ChEBI
Registry Number Type Source
10235517 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
15722411 PubMed citation Europe PMC
16323834 PubMed citation Europe PMC
21376639 PubMed citation Europe PMC
29576533 PubMed citation Europe PMC
Last Modified
03 May 2018