1.0 2011-09-21 00:32:39 UTC 2015-07-21 06:57:47 UTC FDB023629 N-Arachidonoyl glycine A human metabolite taken as a putative food compound of mammalian origin [HMDB] N-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-glycine N-arachidonoyl glycine N-arachidonoylglycine N-arachidonyl-L-glycine N-arachidonylglycine NAGly C22H35NO3 361.5182 361.261693991 2-[(1-hydroxyicosa-5,8,11,14-tetraen-1-ylidene)amino]acetic acid [(1-hydroxyicosa-5,8,11,14-tetraen-1-ylidene)amino]acetic acid CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCC(O)=O InChI=1S/C22H35NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-21(24)23-20-22(25)26/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-20H2,1H3,(H,23,24)(H,25,26) YLEARPUNMCCKMP-UHFFFAOYSA-N belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. N-acyl-alpha amino acids Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Aliphatic acyclic compounds Carbonyl compounds Carboximidic acids Carboxylic acids Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Propargyl-type 1,3-dipolar organic compounds Aliphatic acyclic compound Carbonyl group Carboximidic acid Carboximidic acid derivative Carboxylic acid Hydrocarbon derivative Monocarboxylic acid or derivatives N-acyl-alpha-amino acid Organic 1,3-dipolar compound Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Propargyl-type 1,3-dipolar organic compound Solid logp 6.45 ALOGPS logs -6.34 ALOGPS solubility 1.66e-04 g/l ALOGPS logp 6.3 ChemAxon pka_strongest_acidic 4.03 ChemAxon pka_strongest_basic 1.98 ChemAxon iupac 2-[(1-hydroxyicosa-5,8,11,14-tetraen-1-ylidene)amino]acetic acid ChemAxon average_mass 361.5182 ChemAxon mono_mass 361.261693991 ChemAxon smiles CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCC(O)=O ChemAxon formula C22H35NO3 ChemAxon inchi InChI=1S/C22H35NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-21(24)23-20-22(25)26/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-20H2,1H3,(H,23,24)(H,25,26) ChemAxon inchikey YLEARPUNMCCKMP-UHFFFAOYSA-N ChemAxon polar_surface_area 69.89 ChemAxon refractivity 113.28 ChemAxon polarizability 42.76 ChemAxon rotatable_bond_count 16 ChemAxon acceptor_count 4 ChemAxon donor_count 2 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon HMDB05096 #<Reference:0x000055ce3186e598> Glycine N-acyltransferase Q6IB77 GLYAT Glycine N-acyltransferase-like protein 1 Q969I3 GLYATL1 Glycine N-acyltransferase-like protein 2 Q8WU03 GLYATL2