CHEBI:139539 - (S,S)-bis-(3-oleoylglycero)-1-phosphate

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ChEBI Name (S,S)-bis-(3-oleoylglycero)-1-phosphate ChEBI ID CHEBI:139539 ChEBI ASCII Name (S,S)-bis-(3-oleoylglycero)-1-phosphate Definition A 2,2'-lysobisphosphatidic acid in which both acyl groups are specified as oleoyl. 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 C42H79O10P Net Charge 0 Average Mass 775.046 Monoisotopic Mass 774.54109 InChI InChI=1S/C42H79O10P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-41(45)49-35-39(43)37-51-53(47,48)52-38-40(44)36-50-42(46)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20,39-40,43-44H,3-16,21-38H2,1-2H3,(H,47,48)/b19-17-,20-18-/t39-,40-/m0/s1 InChIKey GNCZTBXGLUHKAP-JOZUOZHYSA-N SMILES O(C[C@@H](COP(O)(=O)OC[C@H](COC(CCCCCCC/C=C\CCCCCCCC)=O)O)O)C(CCCCCCC/C=C\CCCCCCCC)=O Roles Classification Biological Role(s): mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). (via monoacylglycerol phosphate ) View more via ChEBI Ontology ChEBI Ontology Outgoing (S,S)-bis-(3-oleoylglycero)-1-phosphate (CHEBI:139539) has functional parent oleic acid (CHEBI:16196) (S,S)-bis-(3-oleoylglycero)-1-phosphate (CHEBI:139539) is a 2,2'-lysobisphosphatidic acid (CHEBI:60818) (S,S)-bis-(3-oleoylglycero)-1-phosphate (CHEBI:139539) is conjugate acid of (S,S)-bis-(3-oleoylglycero)-1-phosphate(1−) (CHEBI:139150) Incoming (S,S)-bis-(3-oleoylglycero)-1-phosphate(1−) (CHEBI:139150) is conjugate base of (S,S)-bis-(3-oleoylglycero)-1-phosphate (CHEBI:139539) IUPAC Name (hydroxyphosphoryl)bis[oxy(2S)-2-hydroxypropane-3,1-diyl] (9Z,9'Z)di-octadec-9-enoate Synonyms Sources (S,S) 18:1(9Z) BMP ChEBI (S,S)-bis-(3-oleoyl-sn-glycero)-1-phosphate ChEBI (S,S)-bis-[3-(9Z-octadecenoyl)-sn-glycero]-1-phosphate ChEBI (S,S)-bis-[3-(9Z-octadecenoyl)glycero]-1-phosphate ChEBI Registry Number Type Source 28957883 Reaxys Registry Number Reaxys Citation Type Source 21788486 PubMed citation Europe PMC Last Modified 30 January 2018