CHEBI:83718 - 1,2-distearoyl-sn-glycero-3-phosphocholine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 1,2-distearoyl-sn-glycero-3-phosphocholine
ChEBI ID CHEBI:83718
ChEBI ASCII Name 1,2-distearoyl-sn-glycero-3-phosphocholine
Definition A phosphatidylcholine 36:0 in which both phosphatidyl acyl groups are specified as stearoyl (octadecanoyl).
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Lucila Aimo
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C44H88NO8P
Net Charge 0
Average Mass 790.14520
Monoisotopic Mass 789.62476
InChI InChI=1S/C44H88NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h42H,6-41H2,1-5H3/t42-/m1/s1
InChIKey NRJAVPSFFCBXDT-HUESYALOSA-N
SMILES CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via phosphatidylcholine 36:0 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1,2-distearoyl-sn-glycero-3-phosphocholine (CHEBI:83718) has functional parent octadecanoic acid (CHEBI:28842)
1,2-distearoyl-sn-glycero-3-phosphocholine (CHEBI:83718) is a phosphatidylcholine 36:0 (CHEBI:66858)
IUPAC Name
(2R)-2,3-bis(octadecanoyloxy)propyl 2-(trimethylazaniumyl)ethyl phosphate
Synonyms Sources
1,2-dioctadecanoyl-sn-glycero-3-phosphocholine UniProt
1,2-Distearoyl-sn-3-phosphacholine ChemIDplus
Distearoyl phosphatidylcholine LIPID MAPS
GPC(18:0/18:0) ChEBI
GPCho(18:0/18:0) HMDB
GPCho(36:0) HMDB
PC (18:0)2 SUBMITTER
PC 18:0/18:0 SUBMITTER
PC(18:0/18:0) LIPID MAPS
PC(36:0) HMDB
Phosphatidylcholine(18:0/18:0) HMDB
Phosphatidylcholine(36:0) HMDB
Manual Xrefs Databases
HMDB0008036 HMDB
LMGP01010006 LIPID MAPS
View more database links
Registry Numbers Types Sources
3923978 Reaxys Registry Number Reaxys
816-94-4 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
24792199 PubMed citation Europe PMC
Last Modified
11 August 2016