1.0 2026-09-21 19:28:33 UTC 2026-09-21 19:28:33 UTC FDB116969 3-cyclohexyl-1-[2-[methyl-[[(3R)-1-methyl-3-piperidyl]methyl]amino]-2-oxo-ethyl]-2-phenyl-indole-6-carboxylic acid 3-cyclohexyl-1-[2-[methyl-[[(3R)-1-methylpiperidin-3-yl]methyl]amino]-2-oxoethyl]-2-phenylindole-6-carboxylic acid C31H39N3O3 501.6597 501.299142129 3-cyclohexyl-1-{[methyl({[(3R)-1-methylpiperidin-3-yl]methyl})carbamoyl]methyl}-2-phenyl-1H-indole-6-carboxylic acid 3-cyclohexyl-1-{[methyl({[(3R)-1-methylpiperidin-3-yl]methyl})carbamoyl]methyl}-2-phenylindole-6-carboxylic acid [H][C@@]1(CN(C)C(=O)CN2C3=C(C=CC(=C3)C(O)=O)C(C3CCCCC3)=C2C2=CC=CC=C2)CCCN(C)C1 InChI=1S/C31H39N3O3/c1-32-17-9-10-22(19-32)20-33(2)28(35)21-34-27-18-25(31(36)37)15-16-26(27)29(23-11-5-3-6-12-23)30(34)24-13-7-4-8-14-24/h4,7-8,13-16,18,22-23H,3,5-6,9-12,17,19-21H2,1-2H3,(H,36,37)/t22-/m1/s1 AWVLDLUQVKNAMT-JOCHJYFZSA-N belongs to the class of organic compounds known as 2-phenylindoles. These are indoles substituted at the 2-position with a phenyl group. 2-phenylindoles Organic compounds Organoheterocyclic compounds Indoles and derivatives Indoles Aromatic heteropolycyclic compounds 3-alkylindoles Amino acids Azacyclic compounds Benzene and substituted derivatives Carbonyl compounds Carboxylic acids Heteroaromatic compounds Hydrocarbon derivatives Indolecarboxylic acids N-alkylindoles Organic oxides Phenylpyrroles Piperidines Tertiary carboxylic acid amides Trialkylamines 2-phenylindole 2-phenylpyrrole 3-alkylindole Amine Amino acid Amino acid or derivatives Aromatic heteropolycyclic compound Azacycle Benzenoid Carbonyl group Carboxamide group Carboxylic acid Carboxylic acid derivative Heteroaromatic compound Hydrocarbon derivative Indolecarboxylic acid Indolecarboxylic acid derivative Monocyclic benzene moiety N-alkylindole Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Piperidine Pyrrole Substituted pyrrole Tertiary aliphatic amine Tertiary amine Tertiary carboxylic acid amide indolecarboxylic acid piperidines logp 5.17 ALOGPS logs -5.85 ALOGPS solubility 7.11e-04 g/l ALOGPS logp 2.55 ChemAxon pka_strongest_acidic 3.9 ChemAxon pka_strongest_basic 8.92 ChemAxon iupac 3-cyclohexyl-1-{[methyl({[(3R)-1-methylpiperidin-3-yl]methyl})carbamoyl]methyl}-2-phenyl-1H-indole-6-carboxylic acid ChemAxon average_mass 501.6597 ChemAxon mono_mass 501.299142129 ChemAxon smiles [H][C@@]1(CN(C)C(=O)CN2C3=C(C=CC(=C3)C(O)=O)C(C3CCCCC3)=C2C2=CC=CC=C2)CCCN(C)C1 ChemAxon formula C31H39N3O3 ChemAxon inchi InChI=1S/C31H39N3O3/c1-32-17-9-10-22(19-32)20-33(2)28(35)21-34-27-18-25(31(36)37)15-16-26(27)29(23-11-5-3-6-12-23)30(34)24-13-7-4-8-14-24/h4,7-8,13-16,18,22-23H,3,5-6,9-12,17,19-21H2,1-2H3,(H,36,37)/t22-/m1/s1 ChemAxon inchikey AWVLDLUQVKNAMT-JOCHJYFZSA-N ChemAxon polar_surface_area 65.78 ChemAxon refractivity 148.37 ChemAxon polarizability 57.08 ChemAxon rotatable_bond_count 7 ChemAxon acceptor_count 4 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon