CHEBI:84158 - 1-O-(α-D-galactopyranosyl)-N-tetradecanoylphytosphingosine

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ChEBI Name 1-O-(α-D-galactopyranosyl)-N-tetradecanoylphytosphingosine ChEBI ID CHEBI:84158 ChEBI ASCII Name 1-O-(alpha-D-galactopyranosyl)-N-tetradecanoylphytosphingosine Definition A glycophytoceramide having an α-D-galactopyranosyl residue at the O-1 position and a tetradecanoyl group attached to the nitrogen. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C38H75NO9 Net Charge 0 Average Mass 690.00340 Monoisotopic Mass 689.54418 InChI InChI=1S/C38H75NO9/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-31(41)34(43)30(29-47-38-37(46)36(45)35(44)32(28-40)48-38)39-33(42)27-25-23-21-19-16-14-12-10-8-6-4-2/h30-32,34-38,40-41,43-46H,3-29H2,1-2H3,(H,39,42)/t30-,31+,32+,34-,35-,36-,37+,38-/m0/s1 InChIKey RDQPYNDNISLBGF-ZORUMLJWSA-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)CCCCCCCCCCCCC 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-galactopyranosyl)-N-tetradecanoylphytosphingosine (CHEBI:84158) has functional parent α-D-galactose (CHEBI:28061) 1-O-(α-D-galactopyranosyl)-N-tetradecanoylphytosphingosine (CHEBI:84158) has functional parent tetradecanoic acid (CHEBI:28875) 1-O-(α-D-galactopyranosyl)-N-tetradecanoylphytosphingosine (CHEBI:84158) is a glycophytoceramide (CHEBI:59389) IUPAC Name N-[(2S,3S,4R)-1-(α-D-galactopyranosyloxy)-3,4-dihydroxyoctadecan-2-yl]tetradecanamide Synonyms Sources (2S,3S,4R)-N-tetradecanoyl-1-[(α-D-galactopyranosyl)oxy]-2-amino-octadecane-3,4-diol ChEBI α-GC (C14:0) ChEBI α-GC (C14:0/C18:0) ChEBI α-GC(C14:0/C18:0) ChEBI α-GC, C14:0/C18:0 ChEBI Registry Number Type Source 11628403 Reaxys Registry Number Reaxys Citation Type Source 21910729 PubMed citation Europe PMC Last Modified 23 December 2014