24761624 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 17 16 16 8 8 8 8 7 7 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 6 -1 9 1 1 2 2 3 4 5 5 6 7 8 8 8 9 10 10 10 11 11 12 13 15 15 16 16 17 17 18 18 19 19 20 21 22 22 23 23 24 24 26 25 13 14 14 12 20 37 9 9 10 12 14 21 11 27 28 17 18 13 15 16 29 19 20 22 30 23 31 21 32 24 26 25 33 25 34 26 35 36 1 1 1 2 2 1 1 1 2 1 1 1 1 1 1 1 2 1 1 2 1 1 1 2 1 1 2 1 2 1 1 1 2 1 1 1 2 1 1 13 2 12 15 29 16 2 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 10.0634 5.2395 6.6244 6.2565 2.5369 6.001 6.8671 6.7177 6.001 7.7122 8.3 6.0486 5.135 6.2177 4.269 4.269 7.8933 9.2945 5.135 3.403 5.135 8.481 9.8823 3.403 9.4756 4.269 7.5413 8.2695 3.732 7.2767 9.5467 5.672 8.2289 10.4989 2.866 4.269 2 3.984 1.5106 2.632 -0.8689 -0.984 -3.984 -2.484 0.8524 -2.984 0.7479 1.5569 0.1093 0.516 1.7185 0.016 -0.984 2.4705 1.4524 -1.484 -1.484 -2.484 3.2795 2.2614 -2.484 3.175 -2.984 0.1519 0.4761 0.326 2.5353 0.886 -1.174 3.8459 2.1966 -2.794 -3.604 -1.294 8 8 8 8 8 8 8 8 8 8 8 8 11 11 16 16 17 18 19 20 21 22 23 24 17 18 19 20 22 23 21 24 26 25 25 26 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 616 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 6 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 3 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 00000371C07B3800640000000000000000000000000160000000306000000000000000014000001E06040800000C0EC1D82430C6831042088D02255253008200006027182888000E6ECA08262283939384700864C61188D987B0C0200E04400040000800000880008000100000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 (5E)-3-[(4-chlorophenyl)methyl]-5-[(2-hydroxy-5-nitro-phenyl)methylene]-2-thioxo-thiazolidin-4-one IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 (5E)-3-[(4-chlorophenyl)methyl]-5-[(2-hydroxy-5-nitrophenyl)methylidene]-2-sulfanylidene-4-thiazolidinone IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 (5<I>E</I>)-3-[(4-chlorophenyl)methyl]-5-[(2-hydroxy-5-nitrophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 (5E)-3-[(4-chlorophenyl)methyl]-5-[(2-hydroxy-5-nitrophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 (5E)-3-[(4-chlorophenyl)methyl]-5-[(5-nitro-2-oxidanyl-phenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 (5E)-3-(4-chlorobenzyl)-5-(2-hydroxy-5-nitro-benzylidene)-2-thioxo-thiazolidin-4-one InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/C17H11ClN2O4S2/c18-12-3-1-10(2-4-12)9-19-16(22)15(26-17(19)25)8-11-7-13(20(23)24)5-6-14(11)21/h1-8,21H,9H2/b15-8+ InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 PQXPUDSXKHSHBY-OVCLIPMQSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.10.14 4.6 Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 405.9848769 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 C17H11ClN2O4S2 Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 406.9 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 C1=CC(=CC=C1CN2C(=O)C(=CC3=C(C=CC(=C3)[N+](=O)[O-])O)SC2=S)Cl SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 C1=CC(=CC=C1CN2C(=O)/C(=C\C3=C(C=CC(=C3)[N+](=O)[O-])O)/SC2=S)Cl Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 144 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 405.9848769 26 0 0 0 1 1 0 0 1 -1