CHEBI:45240 - 1,2-di-O-myristoyl-sn-glycero-3-phosphocholine

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ChEBI Name 1,2-di-O-myristoyl-sn-glycero-3-phosphocholine
ChEBI ID CHEBI:45240
ChEBI ASCII Name 1,2-di-O-myristoyl-sn-glycero-3-phosphocholine
Definition A 1,2-diacyl-sn-glycero-3-phosphocholine where the two phosphatidyl acyl groups are specified as tetradecanoyl (myristoyl).
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C36H72NO8P
Net Charge 0
Average Mass 677.93250
Monoisotopic Mass 677.49956
InChI InChI=1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1
InChIKey CITHEXJVPOWHKC-UUWRZZSWSA-N
SMILES CCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: MetaboLights Study
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
antigen
Any substance that stimulates an immune response in the body, such as through antibody production or by presentation to a T-cell receptor after binding to a major histocompability complex (MHC).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via phosphatidylcholine 28:0 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1,2-di-O-myristoyl-sn-glycero-3-phosphocholine (CHEBI:45240) has role antigen (CHEBI:59132)
1,2-di-O-myristoyl-sn-glycero-3-phosphocholine (CHEBI:45240) has role mouse metabolite (CHEBI:75771)
1,2-di-O-myristoyl-sn-glycero-3-phosphocholine (CHEBI:45240) is a 1,2-diacyl-sn-glycero-3-phosphocholine (CHEBI:57643)
1,2-di-O-myristoyl-sn-glycero-3-phosphocholine (CHEBI:45240) is a phosphatidylcholine 28:0 (CHEBI:65294)
1,2-di-O-myristoyl-sn-glycero-3-phosphocholine (CHEBI:45240) is a tetradecanoate ester (CHEBI:87691)
IUPAC Name
(2R)-2,3-bis(tetradecanoyloxy)propyl 2-(trimethylammonio)ethyl phosphate
Synonyms Sources
1,2-di-O-tetradecanoyl-sn-glycero-3-phosphocholine ChEBI
1,2-dimyristoyl-GPC ChEBI
1,2-Dimyristoyl-L-3-phosphatidylcholine LIPID MAPS
1,2-dimyristoyl-sn-glycero-3-phosphocholine ChEBI
1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHOCHOLINE PDBeChem
1,2-Dimyristoylphosphatidylcholine LIPID MAPS
1,2-ditetradecanoyl-sn-glycero-3-phosphocholine UniProt
1,2-ditetradecanoyl-sn-glycero-3-phosphocholine LIPID MAPS
Dimyristoyl lecithin ChemIDplus
Dimyristoyl phosphatidylcholine LIPID MAPS
dimyristoylphosphatidylcholine ChEBI
DMPC ChEBI
GPC(14:0/14:0) ChEBI
GPC(28:0) ChEBI
PC(14:0/14:0) LIPID MAPS
PC(28:0) ChEBI
phosphatidylcholine(14:0/14:0) ChEBI
phosphatidylcholine(28:0) ChEBI
Manual Xrefs Databases
HMDB0007866 HMDB
LMGP01010477 LIPID MAPS
PX4 PDBeChem
View more database links
Registry Numbers Types Sources
18194-24-6 CAS Registry Number ChemIDplus
3921768 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
2190620 PubMed citation Europe PMC
Last Modified
14 August 2017