CHEBI:495150 - 1-O-(α-D-galactopyranosyl)-N-tetracosanyl-2-aminononane-1,3,4-triol

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ChEBI Name 1-O-(α-D-galactopyranosyl)-N-tetracosanyl-2-aminononane-1,3,4-triol
ChEBI ID CHEBI:495150
ChEBI ASCII Name 1-O-(alpha-D-galactopyranosyl)-N-tetracosanyl-2-aminononane-1,3,4-triol
Definition A glycophytoceramide comprising (2S,3S,4R)-2-aminononane-1,3,4-triol having an α-D-galctopyranosyl residue at the O-1 position and an tetracosanoyl group attached to the nitrogen.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C39H77NO9
Net Charge 0
Average Mass 704.03000
Monoisotopic Mass 703.55983
InChI InChI=1S/C39H77NO9/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-26-28-34(43)40-31(35(44)32(42)27-25-6-4-2)30-48-39-38(47)37(46)36(45)33(29-41)49-39/h31-33,35-39,41-42,44-47H,3-30H2,1-2H3,(H,40,43)/t31-,32+,33+,35-,36-,37-,38+,39-/m0/s1
InChIKey MPKIDHIOYNMFES-CLTBVUQJSA-N
SMILES CCCCCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@H](O)CCCCC
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.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via N-acylphytosphingosine )
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ChEBI Ontology
Outgoing 1-O-(α-D-galactopyranosyl)-N-tetracosanyl-2-aminononane-1,3,4-triol (CHEBI:495150) has functional parent α-D-galactose (CHEBI:28061)
1-O-(α-D-galactopyranosyl)-N-tetracosanyl-2-aminononane-1,3,4-triol (CHEBI:495150) has role epitope (CHEBI:53000)
1-O-(α-D-galactopyranosyl)-N-tetracosanyl-2-aminononane-1,3,4-triol (CHEBI:495150) is a glycophytoceramide (CHEBI:59389)
IUPAC Name
N-[(2S,3S,4R)-1-(α-D-galactopyranosyloxy)-3,4-dihydroxynonan-2-yl]tetracosanamide
Synonyms Sources
(2S,3S,4R)-1-O-(α-D-galactopyranosyl)-N-tetracosanyl-2-aminononane-1,3,4-triol ChEBI
Galα-Cer(t9:0/24:0) ChEBI
OCH ChEBI
OCH (PBS 20) ChEBI
OCH9 ChEBI
Registry Number Type Source
9892753 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16007091 PubMed citation Europe PMC
23898038 PubMed citation Europe PMC
29351991 PubMed citation Europe PMC
Last Modified
26 February 2018