Anandamide

FAAH (fatty acid acyl hydrolase not an A/B hydrolase) terminates action of Anandamide both substrates are natural ligand of cannabinoid receptors and both give arachidonic acid

General

Type : Acyl-Glycerol, Natural, Arachidonate, Not AlphaBeta Hydrolase target

Chemical_Nomenclature : (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide

Canonical SMILES : CCCCC\/C=CC\/C=CC\/C=CC\/C=CCCCC(=O)NCCO

InChI : InChI=1S\/C22H37NO2\/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22(25)23-20-21-24\/h6-7,9-10,12-13,15-16,24H,2-5,8,11,14,17-21H2,1H3,(H,23,25)\/b7-6-,10-9-,13-12-,16-15-

InChIKey : LGEQQWMQCRIYKG-DOFZRALJSA-N

Other name(s) : AEA  ||  Arachidonylethanolamide  ||  Arachidonoyl ethanolamide  ||  N-Arachidonoylethanolamine  ||  CHEMBL15848  ||  CHEBI:2700  ||  SCHEMBL43143


MW : 347.5

Formula : C22H37NO2

CAS_number : 94421-68-8

PubChem : 5281969

UniChem : LGEQQWMQCRIYKG-DOFZRALJSA-N

Target

Structures : No structure

Families : No family

References (1)

Title : Low level chlorpyrifos exposure increases anandamide accumulation in juvenile rat brain in the absence of brain cholinesterase inhibition - Carr_2014_Neurotoxicol_43_82
Author(s) : Carr RL , Graves CA , Mangum LC , Nail CA , Ross MK
Ref : Neurotoxicology , 43 :82 , 2014
Abstract :
PubMedSearch : Carr_2014_Neurotoxicol_43_82
PubMedID: 24373905