CHEBI:85293 - N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−)

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−)
ChEBI ID CHEBI:85293
ChEBI ASCII Name N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1-)
Definition An N-acylphosphatidylethanolamine(1−) in which the N-acyl group is specified as myristoyl (tetradecanoyl) while the phosphatidyl acyl groups are both specified as oleoyl (9Z-octadecenoyl); major species at pH 7.3.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Nevila Nouspikel
Supplier Information
Download Molfile XML SDF
Formula C55H103NO9P
Net Charge -1
Average Mass 953.38190
Monoisotopic Mass 952.73759
InChI InChI=1S/C55H104NO9P/c1-4-7-10-13-16-19-22-24-26-28-31-34-37-40-43-46-54(58)62-50-52(65-55(59)47-44-41-38-35-32-29-27-25-23-20-17-14-11-8-5-2)51-64-66(60,61)63-49-48-56-53(57)45-42-39-36-33-30-21-18-15-12-9-6-3/h24-27,52H,4-23,28-51H2,1-3H3,(H,56,57)(H,60,61)/p-1/b26-24-,27-25-/t52-/m1/s1
InChIKey ODIMKKAAMGFUTD-FVKUMAIZSA-M
SMILES CCCCCCCCCCCCCC(=O)NCCOP([O-])(=O)OC[C@@H](COC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCCCC
ChEBI Ontology
Outgoing N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−) (CHEBI:85293) is a N-acylphosphatidylethanolamine(1−) (CHEBI:62537)
N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−) (CHEBI:85293) is conjugate base of N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (CHEBI:85793)
Incoming N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (CHEBI:85793) is conjugate acid of N-myristoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−) (CHEBI:85293)
IUPAC Name
(2R)-2,3-bis{[(9Z)-octadec-9-enoyl]oxy}propyl 2-(tetradecanoylamino)ethyl phosphate
Synonyms Sources
N-tetradecanoyl-1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine UniProt
N-tetradecanoyl-1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine(1−) ChEBI
Citation Waiting for Citations Type Source
16527816 PubMed citation SUBMITTER
Last Modified
11 April 2018