4037244 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 16 8 8 8 7 7 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 4 5 5 6 6 6 7 7 7 8 8 8 9 9 9 10 10 10 11 11 12 12 13 13 14 14 15 15 16 16 17 17 17 18 20 20 20 21 21 22 22 23 23 24 24 24 25 26 27 27 27 2 3 5 12 19 7 8 19 20 44 9 28 29 10 30 31 11 32 33 11 34 35 36 37 13 14 16 17 15 38 18 19 18 39 40 41 42 43 21 45 46 22 23 25 47 26 48 25 26 27 49 50 51 52 53 2 2 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 2 1 1 1 2 1 1 1 1 1 1 1 1 2 1 1 1 2 1 2 1 1 1 1 1 1 1 1 5 255 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 3.732 4.732 2.732 6.3301 3.732 5.4641 4.5981 2.866 4.5981 2.866 3.732 3.732 2.866 4.5981 4.5981 2.866 2 3.732 5.4641 6.3301 6.3301 5.4641 7.1962 6.3301 5.4641 7.1962 6.3301 4.8101 5.2087 2.2554 2.654 5.2087 4.8101 2.654 2.2554 4.1306 3.3335 5.135 2.3291 2.31 1.4631 1.69 3.732 4.9272 6.9407 6.5422 4.9272 7.7331 4.9272 7.7331 5.7101 6.3301 6.9501 2.75 2.75 2.75 0.25 3.75 -1.25 4.25 4.25 5.25 5.25 5.75 1.75 1.25 1.25 0.25 0.25 1.75 -0.25 -0.25 -1.75 -2.75 -3.25 -3.25 -4.75 -4.25 -4.25 -5.75 3.6674 4.3577 4.3577 3.6674 5.1423 5.8326 5.8326 5.1423 6.225 6.225 1.56 -0.06 2.2869 2.06 1.2131 -0.87 -1.56 -1.8577 -1.1674 -2.94 -2.94 -4.56 -4.56 -5.75 -6.37 -5.75 8 8 8 8 8 8 8 8 8 8 8 8 12 12 13 14 15 16 21 21 22 23 24 24 13 14 16 15 18 18 22 23 25 26 25 26 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 587 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 4 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 1 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 5 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 00000371E07B30004000000000000000000000000000000000003C6080000000000000014000001E04104000000C00C1D804320182C00002880221521070C200102400000888990804C80820328095118421086086008889871888008E40000080000400008000010000080000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-methyl-3-(1-piperidylsulfonyl)-N-(p-tolylmethyl)benzamide IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-methyl-N-[(4-methylphenyl)methyl]-3-(1-piperidinylsulfonyl)benzamide IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-methyl-<I>N</I>-[(4-methylphenyl)methyl]-3-piperidin-1-ylsulfonylbenzamide IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-methyl-N-[(4-methylphenyl)methyl]-3-piperidin-1-ylsulfonylbenzamide IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-methyl-N-[(4-methylphenyl)methyl]-3-piperidin-1-ylsulfonyl-benzamide IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-methyl-N-(4-methylbenzyl)-3-piperidinosulfonyl-benzamide InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/C21H26N2O3S/c1-16-6-9-18(10-7-16)15-22-21(24)19-11-8-17(2)20(14-19)27(25,26)23-12-4-3-5-13-23/h6-11,14H,3-5,12-13,15H2,1-2H3,(H,22,24) InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 SYGVCRXMTGAMFE-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.10.14 3.4 Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 386.16641387 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 C21H26N2O3S Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 386.5 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 CC1=CC=C(C=C1)CNC(=O)C2=CC(=C(C=C2)C)S(=O)(=O)N3CCCCC3 SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 CC1=CC=C(C=C1)CNC(=O)C2=CC(=C(C=C2)C)S(=O)(=O)N3CCCCC3 Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 74.9 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 386.16641387 27 0 0 0 0 0 0 0 1 -1