69736115 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 16 8 7 7 7 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 2 3 3 3 4 4 4 5 5 5 6 6 6 6 7 7 8 8 9 9 9 10 10 11 11 12 13 13 14 14 15 15 16 16 17 17 19 19 20 20 21 21 22 23 23 24 18 19 12 8 10 11 7 12 35 22 44 45 7 8 9 25 10 26 27 28 11 29 30 31 32 33 34 13 14 15 16 36 17 37 18 38 18 39 20 21 22 40 23 41 24 24 42 43 1 1 2 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 2 1 1 1 2 1 2 1 1 1 1 2 2 1 1 1 1 2 1 1 6 7 9 8 25 2 1 7 4 6 10 26 3 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 5.4553 6.5722 10.1961 8.1419 2.6176 9.9373 8.5646 9.4595 11.3362 8.2225 11.595 7.1457 6.7231 7.2967 5.7269 6.8741 5.3043 5.8779 4.4591 4.0364 3.8855 3.0403 2.8893 2.4667 9.7173 8.9965 9.7773 8.8463 11.1413 11.9302 8.0282 7.6368 12.189 11.7899 8.4976 7.9143 5.3713 7.2297 4.6867 4.3921 4.1475 2.5337 1.849 2 2.9733 -2.3322 2.1122 3.8444 1.3802 -4.3191 2.8785 2.2865 4.827 2.3697 3.2262 3.3356 1.293 0.3867 -0.4325 0.2995 -1.3388 -0.6068 -1.4259 -2.4194 -3.3257 -1.6002 -3.4128 -1.6874 -2.5937 2.0574 1.8417 5.3594 4.919 1.7811 2.1919 3.8149 3.023 3.1578 3.9242 0.8723 -0.3784 0.8074 -1.8466 -0.6608 -3.8336 -1.0383 -1.1795 -2.6477 -4.3732 -4.827 5 3 8 8 8 8 8 8 8 8 8 8 8 8 6 7 13 13 14 15 16 17 19 19 20 21 22 23 25 4 14 15 16 17 18 18 20 21 22 23 24 24 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 452 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 4 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 2 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 4 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 00000371E07B2000400000000000000000000000000162C000003C6080000000000000014000001E04100000000D28C1D80430C183C00008880225525000820000240A100888990864C8086032A0D59194210C609600A8C9871888008E10000000200000002000000040000000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 4-(3-aminophenyl)sulfanyl-N-[(4S)-1-azabicyclo[2.2.1]heptan-3-yl]benzamide IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 4-[(3-aminophenyl)thio]-N-[(4S)-1-azabicyclo[2.2.1]heptan-3-yl]benzamide IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 4-(3-aminophenyl)sulfanyl-<I>N</I>-[(4<I>S</I>)-1-azabicyclo[2.2.1]heptan-3-yl]benzamide IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 4-(3-aminophenyl)sulfanyl-N-[(4S)-1-azabicyclo[2.2.1]heptan-3-yl]benzamide IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 4-(3-aminophenyl)sulfanyl-N-[(4S)-1-azabicyclo[2.2.1]heptan-3-yl]benzamide IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 4-[(3-aminophenyl)thio]-N-[(4S)-1-azabicyclo[2.2.1]heptan-3-yl]benzamide InChI Standard 1 1.0.6 InChI iupac.org 2021.05.07 InChI=1S/C19H21N3OS/c20-15-2-1-3-17(10-15)24-16-6-4-13(5-7-16)19(23)21-18-12-22-9-8-14(18)11-22/h1-7,10,14,18H,8-9,11-12,20H2,(H,21,23)/t14-,18?/m0/s1 InChIKey Standard 1 1.0.6 InChI iupac.org 2021.05.07 HZJHJNNTDHMJHP-PIVQAISJSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.05.07 2.9 Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 339.14053348 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 C19H21N3OS Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 339.5 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C1CN2CC1C(C2)NC(=O)C3=CC=C(C=C3)SC4=CC=CC(=C4)N SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C1CN2C[C@H]1C(C2)NC(=O)C3=CC=C(C=C3)SC4=CC=CC(=C4)N Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 83.7 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 339.14053348 24 2 1 1 0 0 0 0 1 -1