CHEBI:75578 - 1-α-linolenoyl-2-oleoyl-sn-glycerol

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ChEBI Name 1-α-linolenoyl-2-oleoyl-sn-glycerol
ChEBI ID CHEBI:75578
ChEBI ASCII Name 1-alpha-linolenoyl-2-oleoyl-sn-glycerol
Definition A 1,2-diacyl-sn-glycerol where α-linolenoyl and oleoyl form the 1- and 2-acyl groups respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Lucila Aimo
Supplier Information
Download Molfile XML SDF
Formula C39H68O5
Net Charge 0
Average Mass 616.95420
Monoisotopic Mass 616.50668
InChI InChI=1S/C39H68O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-36-37(35-40)44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h5,7,11,13,17-20,37,40H,3-4,6,8-10,12,14-16,21-36H2,1-2H3/b7-5-,13-11-,19-17-,20-18-/t37-/m0/s1
InChIKey LYYSCXLWEIVEFO-LGRGBMOQSA-N
SMILES CCCCCCCC\C=C/CCCCCCCC(=O)O[C@@H](CO)COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
(via diglyceride )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via diglyceride )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-α-linolenoyl-2-oleoyl-sn-glycerol (CHEBI:75578) is a 1,2-diacyl-sn-glycerol (CHEBI:17815)
1-α-linolenoyl-2-oleoyl-sn-glycerol (CHEBI:75578) is a 1-α-linolenoyl-2-oleoylglycerol (CHEBI:75609)
1-α-linolenoyl-2-oleoyl-sn-glycerol (CHEBI:75578) is enantiomer of 2-oleoyl-3-α-linolenoyl-sn-glycerol (CHEBI:75580)
Incoming rac-1-α-linolenoyl-2-oleoylglycerol (CHEBI:75581) has part 1-α-linolenoyl-2-oleoyl-sn-glycerol (CHEBI:75578)
2-oleoyl-3-α-linolenoyl-sn-glycerol (CHEBI:75580) is enantiomer of 1-α-linolenoyl-2-oleoyl-sn-glycerol (CHEBI:75578)
IUPAC Name
(2S)-3-hydroxy-2-[(9Z)-octadec-9-enoyloxy]propyl (9Z,12Z,15Z)-octadeca-9,12,15-trienoate
Synonyms Sources
1-(9Z,12Z,15Z)-octadecatrienoyl-2-(9Z)-octadecenoyl-sn-glycerol UniProt
DG (18:3(n-3)/18:1(n-9)/0:0) SUBMITTER
sn-1-α-linolenoyl-2-oleoyl diglyceride SUBMITTER
Last Modified
23 October 2015