CHEBI:82751 - cholesteryl arachidonate

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ChEBI Name cholesteryl arachidonate
ChEBI ID CHEBI:82751
Definition A cholesterol ester obtained by the formal condensation of the hydroxy group in cholesterol with the carboxy group of arachidonic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter AnneNiknejad
Supplier Information
Download Molfile XML SDF
Formula C47H76O2
Net Charge 0
Average Mass 673.10510
Monoisotopic Mass 672.58453
InChI InChI=1S/C47H76O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-27-45(48)49-40-32-34-46(5)39(36-40)28-29-41-43-31-30-42(38(4)26-24-25-37(2)3)47(43,6)35-33-44(41)46/h11-12,14-15,17-18,20-21,28,37-38,40-44H,7-10,13,16,19,22-27,29-36H2,1-6H3/b12-11-,15-14-,18-17-,21-20-/t38-,40+,41+,42-,43+,44+,46+,47-/m1/s1
InChIKey IMXSFYNMSOULQS-BEDFLICRSA-N
SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@H](CC[C@H]4[C@@H]3CC=C2C1)[C@H](C)CCCC(C)C
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: MetaboLights Study
Roles Classification
Biological Role(s): antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing cholesteryl arachidonate (CHEBI:82751) has functional parent arachidonic acid (CHEBI:15843)
cholesteryl arachidonate (CHEBI:82751) has role antibacterial agent (CHEBI:33282)
cholesteryl arachidonate (CHEBI:82751) has role mouse metabolite (CHEBI:75771)
cholesteryl arachidonate (CHEBI:82751) is a cholesteryl icosatetraenoate (CHEBI:132006)
IUPAC Name
(3β)-cholest-5-en-3-yl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate
Synonyms Sources
20:4 Cholesteryl ester LIPID MAPS
CE(20:4(5Z,8Z,11Z,14Z)) LIPID MAPS
CE(20:4) LIPID MAPS
cholest-5-en-3β-yl (5Z,8Z,11Z,14Z-eicosatetraenoate) LIPID MAPS
cholest-5-en-3β-yl (5Z,8Z,11Z,14Z-icosatetraenoate) SUBMITTER
cholesterol arachidonate SUBMITTER
cholesteryl (5Z,8Z,11Z,14Z)-eicosatetraenoate UniProt
Manual Xrefs Databases
HMDB0006726 HMDB
LMST01020014 LIPID MAPS
View more database links
Registry Numbers Types Sources
2343317 Reaxys Registry Number Reaxys
604-34-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12083928 PubMed citation Europe PMC
12605870 PubMed citation Europe PMC
18768875 PubMed citation Europe PMC
7213606 PubMed citation Europe PMC
9020103 PubMed citation SUBMITTER
Last Modified
12 June 2017