InChI=1S/C41H68O5/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-36-41(44)46-39(37-42)38-45-40(43)35-33-31-29-27-25-23-21-18-16-14-12-10-8-6-4-2/h6,8,12,14,17-19,21-22,24,28,30,39,42H,3-5,7,9-11,13,15-16,20,23,25-27,29,31-38H2,1-2H3/b8-6-,14-12-,19-17-,21-18-,24-22-,30-28-/t39-/m0/s1 |
XPXCMAYRPSSBKG-VRRKQHPASA-N |
C(CCC(O[C@@H](CO)COC(CCCCCCC/C=C\C/C=C\C/C=C\CC)=O)=O)/C=C\C/C=C\C/C=C\CCCCCCCC |
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human blood serum metabolite
Any metabolite (endogenous or exogenous) found in human blood serum samples.
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 )
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View more via ChEBI Ontology
Outgoing
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1-α-linolenoyl-2-[(5Z,8Z,11Z)-icosatrienoyl]-sn-glycerol
(CHEBI:89238)
has functional parent
α-linolenic acid
(CHEBI:27432)
1-α-linolenoyl-2-[(5Z,8Z,11Z)-icosatrienoyl]-sn-glycerol
(CHEBI:89238)
has functional parent
(5Z,8Z,11Z)-icosatrienoic acid
(CHEBI:72865)
1-α-linolenoyl-2-[(5Z,8Z,11Z)-icosatrienoyl]-sn-glycerol
(CHEBI:89238)
has role
human blood serum metabolite
(CHEBI:85234)
1-α-linolenoyl-2-[(5Z,8Z,11Z)-icosatrienoyl]-sn-glycerol
(CHEBI:89238)
is a
1,2-diacyl-sn-glycerol
(CHEBI:17815)
1-α-linolenoyl-2-[(5Z,8Z,11Z)-icosatrienoyl]-sn-glycerol
(CHEBI:89238)
is a
diacylglycerol 38:6
(CHEBI:85703)
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(2S)-1-hydroxy-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propan-2-yl (5Z,8Z,11Z)-icosa-5,8,11-trienoate
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1-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyl]-2-[(5Z,8Z,11Z)-icosa-5,8,11-trienoyl]-sn-glycerol
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ChEBI
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1-[(9Z,12Z,15Z)-octadecatrienoyl]-2-[(5Z,8Z,11Z)-icosatrienoyl]-sn-glycerol
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ChEBI
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DAG(18:3/20:3)
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HMDB
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DAG(18:3n3/20:3n9)
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HMDB
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DAG(18:3w3/20:3w9)
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HMDB
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DAG(38:6)
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HMDB
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DG(18:3(9Z,12Z,15Z)/20:3(5Z,8Z,11Z)/0:0)
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HMDB
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DG(18:3/20:3)
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HMDB
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DG(18:3n3/20:3n9)
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HMDB
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DG(18:3w3/20:3w9)
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HMDB
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DG(38:6)
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HMDB
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Diacylglycerol(18:3/20:3)
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HMDB
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Diacylglycerol(18:3n3/20:3n9)
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HMDB
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Diacylglycerol(18:3w3/20:3w9)
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HMDB
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Diacylglycerol(38:6)
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HMDB
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20671299
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PubMed citation
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Europe PMC
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25880480
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PubMed citation
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Europe PMC
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