CHEBI:85292 - N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−)

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ChEBI Name N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−)
ChEBI ID CHEBI:85292
ChEBI ASCII Name N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1-)
Definition An N-acylphosphatidylethanolamine(1−) in which the N-acyl group is specified as stearoyl (octadecanoyl) 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 C59H111NO9P
Net Charge -1
Average Mass 1009.48830
Monoisotopic Mass 1008.80019
InChI InChI=1S/C59H112NO9P/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-57(61)60-52-53-67-70(64,65)68-55-56(69-59(63)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)54-66-58(62)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h26-27,29-30,56H,4-25,28,31-55H2,1-3H3,(H,60,61)(H,64,65)/p-1/b29-26-,30-27-/t56-/m1/s1
InChIKey GNAPJEPSPJZGSJ-WJOAKYJCSA-M
SMILES CCCCCCCCCCCCCCCCCC(=O)NCCOP([O-])(=O)OC[C@@H](COC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCCCC
ChEBI Ontology
Outgoing N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−) (CHEBI:85292) is a N-acylphosphatidylethanolamine(1−) (CHEBI:62537)
N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−) (CHEBI:85292) is conjugate base of N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (CHEBI:85791)
Incoming N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (CHEBI:85791) is conjugate acid of N-stearoyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine(1−) (CHEBI:85292)
IUPAC Name
(2R)-2,3-bis{[(9Z)-octadec-9-enoyl]oxy}propyl 2-(octadecanoylamino)ethyl phosphate
Synonyms Sources
N-octadecanoyl-1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine UniProt
N-octadecanoyl-1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine(1−) ChEBI
Citations Waiting for Citations Types Sources
14634025 PubMed citation SUBMITTER
16527816 PubMed citation SUBMITTER
Last Modified
11 April 2018