1.0 2016-10-03 18:35:00 UTC 2020-04-22 15:49:18 UTC BMDB0012252 BMDB12252 Linoleoyl ethanolamide (9Z,12Z)-N-(2-Hydroxyethyl)octadeca-9,12-dien-1-amide Anandamide (18:2, N-6) Linoleamide mea Linoleic ethanolamide Linoleoyl monoethanolamide Monoethanolamine linoleic acid amide N-(2-Hydroxyethyl)-9,12-octadecadienamide N-(2-Hydroxyethyl)linoleamide N-(9Z,12Z-Octadecadienoyl)-ethanolamine N-cis-9-cis-12-Octadecadienoylethanolamine Monoethanolamine linoleate amide LEA N-(2-Hydroxyethyl)-linoleamide Linoleoylethanolamide Linoleoyl ethanolamide C20H37NO2 323.5133 323.282429433 (9Z,12Z)-N-(2-hydroxyethyl)octadeca-9,12-dienamide linoleamide mea 68171-52-8 CCCCC\C=C/C\C=C/CCCCCCCC(=O)NCCO InChI=1S/C20H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)21-18-19-22/h6-7,9-10,22H,2-5,8,11-19H2,1H3,(H,21,23)/b7-6-,10-9- KQXDGUVSAAQARU-HZJYTTRNSA-N belongs to the class of organic compounds known as n-acylethanolamines. N-acylethanolamines are compounds containing an N-acyethanolamine moiety, which is characterized by an acyl group is linked to the nitrogen atom of ethanolamine. Organic compounds Organic nitrogen compounds Organonitrogen compounds Amines N-acylethanolamines Carbonyl compounds Hydrocarbon derivatives N-acyl amines Organic oxides Organopnictogen compounds Primary alcohols Secondary carboxylic acid amides Alcohol Aliphatic acyclic compound Carbonyl group Carboxamide group Carboxylic acid derivative Fatty acyl Fatty amide Hydrocarbon derivative N-acyl-amine N-acylethanolamine Organic oxide Organic oxygen compound Organooxygen compound Organopnictogen compound Primary alcohol Secondary carboxylic acid amide Aliphatic acyclic compounds N-(long-chain-acyl)ethanolamine N-(polyunsaturated fatty acyl)ethanolamine N-acyl ethanolamines (endocannabinoids) Solid logp 6.26 ALOGPS logs -5.89 ALOGPS logp 5.15 ChemAxon pka_strongest_acidic 15.47 ChemAxon pka_strongest_basic -1.3 ChemAxon iupac (9Z,12Z)-N-(2-hydroxyethyl)octadeca-9,12-dienamide ChemAxon average_mass 323.5133 ChemAxon mono_mass 323.282429433 ChemAxon smiles CCCCC\C=C/C\C=C/CCCCCCCC(=O)NCCO ChemAxon formula C20H37NO2 ChemAxon inchi InChI=1S/C20H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)21-18-19-22/h6-7,9-10,22H,2-5,8,11-19H2,1H3,(H,21,23)/b7-6-,10-9- ChemAxon inchikey KQXDGUVSAAQARU-HZJYTTRNSA-N ChemAxon polar_surface_area 49.33 ChemAxon refractivity 101.53 ChemAxon polarizability 41.41 ChemAxon rotatable_bond_count 16 ChemAxon acceptor_count 2 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 0 ChemAxon bioavailability 0 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::MsMs 310006 Specdb::MsMs 310007 Specdb::MsMs 310008 Specdb::MsMs 354577 Specdb::MsMs 354578 Specdb::MsMs 354579 Specdb::MsMs 2823302 Specdb::MsMs 2823303 Specdb::MsMs 2823304 Specdb::MsMs 2859233 Specdb::MsMs 2859234 Specdb::MsMs 2859235 Specdb::NmrOneD 330382 Specdb::NmrOneD 330383 Specdb::NmrOneD 330384 Specdb::NmrOneD 330385 Specdb::NmrOneD 330386 Specdb::NmrOneD 330387 Specdb::NmrOneD 330388 Specdb::NmrOneD 330389 Specdb::NmrOneD 330390 Specdb::NmrOneD 330391 Specdb::NmrOneD 330392 Specdb::NmrOneD 330393 Specdb::NmrOneD 330394 Specdb::NmrOneD 330395 Specdb::NmrOneD 330396 Specdb::NmrOneD 330397 Specdb::NmrOneD 330398 Specdb::NmrOneD 330399 Specdb::NmrOneD 330400 Specdb::NmrOneD 330401 Specdb::CMs 19771 Specdb::CMs 39887 Specdb::CMs 149100 FDB028893 4446566 64032 5283446 CPD6666-4