CHEBI:85385 - 1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate

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ChEBI Name 1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate
ChEBI ID CHEBI:85385
ChEBI ASCII Name 1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate
Definition A 1,2-diacyl-sn-glycerol 3-phosphate in which the phosphatidyl acyl groups at postions 1 and 2 are specified as heptadecanoyl and stearoyl respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C38H75O8P
Net Charge 0
Average Mass 690.97110
Monoisotopic Mass 690.51996
InChI InChI=1S/C38H75O8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(40)46-36(35-45-47(41,42)43)34-44-37(39)32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h36H,3-35H2,1-2H3,(H2,41,42,43)/t36-/m1/s1
InChIKey VEIHRUNGGHIRIO-PSXMRANNSA-N
SMILES CCCCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCC)COP(O)(O)=O
Roles Classification
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via phosphatidic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate (CHEBI:85385) has functional parent heptadecanoic acid (CHEBI:32365)
1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate (CHEBI:85385) has functional parent octadecanoic acid (CHEBI:28842)
1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate (CHEBI:85385) is a 1,2-diacyl-sn-glycerol 3-phosphate (CHEBI:29089)
1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate (CHEBI:85385) is conjugate acid of 1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate(2−) (CHEBI:84429)
Incoming 1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate(2−) (CHEBI:84429) is conjugate base of 1-heptadecanoyl-2-stearoyl-sn-glycero-3-phosphate (CHEBI:85385)
IUPAC Name
(2R)-1-(heptadecanoyloxy)-3-(phosphonooxy)propan-2-yl octadecanoate
Synonyms Sources
1-heptadecanoyl-2-octadecanoyl-glycero-3-phosphate LIPID MAPS
1-heptadecanoyl-2-octadecanoyl-sn-glycero-3-phosphate ChEBI
PA(17:0/18:0) LIPID MAPS
Manual Xref Database
LMGP10010895 LIPID MAPS
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Last Modified
23 February 2022