CHEBI:75219 - 1-palmitoyl-2-acetyl-sn-glycero-3-phosphocholine

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ChEBI Name 1-palmitoyl-2-acetyl-sn-glycero-3-phosphocholine
ChEBI ID CHEBI:75219
ChEBI ASCII Name 1-palmitoyl-2-acetyl-sn-glycero-3-phosphocholine
Definition A 1,2-diacyl-sn-glycero-3-phosphocholine in which the two acyl substituents at positions 1 and 2 are specified as palmitoyl and acetyl respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Lucila Aimo
Supplier Information
Download Molfile XML SDF
Formula C26H52NO8P
Net Charge 0
Average Mass 537.66670
Monoisotopic Mass 537.34305
InChI InChI=1S/C26H52NO8P/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-26(29)32-22-25(35-24(2)28)23-34-36(30,31)33-21-20-27(3,4)5/h25H,6-23H2,1-5H3/t25-/m1/s1
InChIKey XPAXRSJGGFVTFM-RUZDIDTESA-N
SMILES CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(C)=O
Roles Classification
Biological Role(s): platelet-activating factor receptor agonist
An agonist that binds to and activates platelet-activating factor receptors.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-palmitoyl-2-acetyl-sn-glycero-3-phosphocholine (CHEBI:75219) has functional parent acetic acid (CHEBI:15366)
1-palmitoyl-2-acetyl-sn-glycero-3-phosphocholine (CHEBI:75219) has functional parent hexadecanoic acid (CHEBI:15756)
1-palmitoyl-2-acetyl-sn-glycero-3-phosphocholine (CHEBI:75219) has role platelet-activating factor receptor agonist (CHEBI:75414)
1-palmitoyl-2-acetyl-sn-glycero-3-phosphocholine (CHEBI:75219) is a 1,2-diacyl-sn-glycero-3-phosphocholine (CHEBI:57643)
IUPAC Name
(2R)-2-acetoxy-3-(hexadecanoyloxy)propyl 2-(trimethylazaniumyl)ethyl phosphate
Synonyms Sources
(2R)-2-acetoxy-3-(palmitoyloxy)propyl 2-(trimethylazaniumyl)ethyl phosphate IUPAC
1-hexadecanoyl-2-acetyl-sn-glycero-3-phosphocholine SUBMITTER
1-hexadecanoyl-2-acetyl-sn-glycero-3-phosphocholine UniProt
1-O-Palmitoyl-2-O-acetyl-sn-glyceryl-3-phosphorylcholine LIPID MAPS
1-Palmitoyl-2-acetyl-sn-glycero-3-phosphorylcholine LIPID MAPS
1-palmitoyl-2-acetyl-sn-phosphatidylcholine SUBMITTER
PC(16:0/2:0) SUBMITTER
Manual Xref Database
LMGP01010612 LIPID MAPS
View more database links
Registry Numbers Types Sources
4040861 Reaxys Registry Number Reaxys
84062-61-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
1819698 PubMed citation Europe PMC
8283038 PubMed citation Europe PMC
Last Modified
30 August 2013