CHEBI:132256 - N-arachidonoyl-2-oxoserotonin

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ChEBI Name N-arachidonoyl-2-oxoserotonin
ChEBI ID CHEBI:132256
ChEBI ASCII Name N-arachidonoyl-2-oxoserotonin
Definition A fatty amide obtained by formal condensation of the carboxy group of arachidonic acid with the amino group of 2-oxoserotonin.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Nevila Nouspikel
Supplier Information
Download Molfile XML SDF
Formula C30H42N2O3
Net Charge 0
Average Mass 478.667
Monoisotopic Mass 478.31954
InChI InChI=1S/C30H42N2O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-29(34)31-23-22-26-27-24-25(33)20-21-28(27)32-30(26)35/h6-7,9-10,12-13,15-16,20-21,24,26,33H,2-5,8,11,14,17-19,22-23H2,1H3,(H,31,34)(H,32,35)/b7-6-,10-9-,13-12-,16-15-
InChIKey NTJHTZJPDOWXMN-DOFZRALJSA-N
SMILES N1C(C(CCNC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)C2=C1C=CC(O)=C2)=O
Roles Classification
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
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ChEBI Ontology
Outgoing N-arachidonoyl-2-oxoserotonin (CHEBI:132256) has functional parent arachidonic acid (CHEBI:15843)
N-arachidonoyl-2-oxoserotonin (CHEBI:132256) has functional parent serotonin (CHEBI:28790)
N-arachidonoyl-2-oxoserotonin (CHEBI:132256) has role human metabolite (CHEBI:77746)
N-arachidonoyl-2-oxoserotonin (CHEBI:132256) is a fatty amide (CHEBI:29348)
N-arachidonoyl-2-oxoserotonin (CHEBI:132256) is a hydroxyindoles (CHEBI:84729)
N-arachidonoyl-2-oxoserotonin (CHEBI:132256) is a oxindoles (CHEBI:38459)
N-arachidonoyl-2-oxoserotonin (CHEBI:132256) is a phenols (CHEBI:33853)
IUPAC Name
(5Z,8Z,11Z,14Z)-N-[2-(5-hydroxy-2-oxo-2,3-dihydro-1H-indol-3-yl)ethyl]icosa-5,8,11,14-tetraenamide
Synonyms Sources
2-oxo-N-[(5Z,8Z,11Z,14Z)-eicosatetraenoyl]-serotonin UniProt
arachidonoyl 2-oxoserotonin ChEBI
arachidonoyl-2-oxoserotonin ChEBI
N-[(5Z,8Z,11Z,14Z)-eicosatetraenoyl]-2-oxoserotonin ChEBI
N-[(5Z,8Z,11Z,14Z)-icosatetraenoyl]-2-oxoserotonin ChEBI
Citation Waiting for Citations Type Source
24563460 PubMed citation SUBMITTER
Last Modified
18 October 2016