37632 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 17 7 7 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 2 2 2 3 3 3 4 4 5 5 6 7 7 8 9 10 10 11 11 12 12 13 14 14 15 15 16 16 17 17 19 19 19 20 20 20 21 21 22 22 23 23 24 24 25 18 7 8 9 11 19 20 12 13 6 8 9 10 14 11 12 13 15 26 27 28 29 16 17 30 18 31 21 22 18 32 33 34 35 36 37 38 23 39 24 40 25 41 25 42 43 1 1 1 1 1 1 1 1 2 1 2 2 2 1 1 1 1 1 1 1 1 1 1 2 1 2 1 2 1 1 1 1 1 1 1 1 1 1 1 2 1 2 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 2 5.8374 5.4906 6.3374 6.9517 7.4235 4.9365 5.9734 6.7384 4.7139 5.2518 6.9609 5.3374 4.1839 3.7234 4.9036 3.1862 2.9544 4.769 6.451 3.9063 5.4669 3.4725 5.033 4.0358 4.9068 4.6846 7.5195 7.3475 4.3288 3.5925 2.7334 4.3398 4.3216 5.1982 6.2781 7.0464 6.6238 3.5571 6.0851 2.8542 5.3822 3.7668 0.5504 -0.7766 -3.4247 1.4141 -1.9379 -1.063 -0.3427 -1.7613 -0.3427 0.6323 -2.4536 0.6323 1.4141 -1.0628 0.9546 2.3151 -0.7635 0.252 -4.117 -3.7034 2.3898 3.1413 3.2908 4.0423 4.117 -1.9385 -2.7039 0.3632 1.117 -1.6657 1.5606 -1.187 -3.6696 -4.5462 -4.5644 -4.2989 -3.8763 -3.108 1.8775 3.095 3.3371 4.5545 4.6756 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 2 2 5 5 6 7 7 10 14 15 16 16 17 21 22 23 24 8 9 6 8 9 10 14 15 17 18 21 22 18 23 24 25 25 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 490 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 0 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 3 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 00000371E07B800004000000000000000000000000016000000030600000040000000081D000001C02080000000C0AC11B2433D0870C1000A2032662640092802B2107A01D88003866988868A2C19B91942008608802C8C8271080C00E00004020000200000000804000040000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 1-(8-chloro-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)-N,N-dimethyl-methanamine IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 1-(8-chloro-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)-N,N-dimethylmethanamine IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 1-(8-chloro-6-phenyl-4<I>H</I>-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)-<I>N</I>,<I>N</I>-dimethylmethanamine IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 1-(8-chloro-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)-N,N-dimethylmethanamine IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 1-(8-chloranyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)-N,N-dimethyl-methanamine IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 (8-chloro-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)methyl-dimethyl-amine InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/C19H18ClN5/c1-24(2)12-18-23-22-17-11-21-19(13-6-4-3-5-7-13)15-10-14(20)8-9-16(15)25(17)18/h3-10H,11-12H2,1-2H3 InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 GJSLOMWRLALDCT-UHFFFAOYSA-N Log P XLogP3 7 3.0 sioc-ccbg.ac.cn 2021.10.14 1.6 Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 351.1250733 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 C19H18ClN5 Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 351.8 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 CN(C)CC1=NN=C2N1C3=C(C=C(C=C3)Cl)C(=NC2)C4=CC=CC=C4 SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 CN(C)CC1=NN=C2N1C3=C(C=C(C=C3)Cl)C(=NC2)C4=CC=CC=C4 Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 46.3 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 351.1250733 25 0 0 0 0 0 0 0 1 -1