4518078 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 17 16 16 8 8 8 8 8 8 7 7 7 7 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 8 -1 13 1 1 2 2 2 2 3 3 3 3 8 9 10 10 11 11 12 12 13 14 14 14 14 15 15 15 17 17 18 18 19 19 20 21 21 22 22 23 23 24 25 25 26 27 28 28 29 26 4 5 10 18 6 7 12 22 13 13 16 36 16 17 19 38 27 15 16 30 31 17 32 33 34 35 20 21 20 23 37 24 39 25 26 24 40 41 27 42 28 29 29 43 44 1 2 2 1 1 2 2 1 1 1 2 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 2 1 1 1 1 1 2 2 1 1 2 1 1 1 2 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 2 5.4641 3.732 6.4641 4.4641 4.732 2.732 5.4641 6.3301 5.4641 7.2437 3.732 5.4641 6.4347 7.4128 6.3301 7.9128 5.4641 4.5981 4.5981 6.3301 3.732 5.4641 6.3301 4.5981 2.866 4.5981 2.866 3.732 6.3698 5.8147 7.9792 7.2212 8.3277 8.4144 4.9272 4.0611 3.1951 6.8671 5.4641 6.8671 5.135 2.3291 3.732 -2.3512 2.6488 -1.3512 2.6488 2.6488 -1.3512 -1.3512 -5.3512 -3.8512 3.6488 3.742 -0.3512 -4.3512 5.1433 5.3512 4.1488 4.4852 1.6488 0.1488 1.1488 1.1488 -2.3512 -0.3512 0.1488 -2.8512 -2.8512 -3.8512 -3.8512 -4.3512 5.7599 5.1433 5.6034 5.9409 4.0244 4.8496 3.9588 1.4588 -0.0412 1.4588 -0.9712 -0.1612 -2.5412 -4.1612 -4.9712 8 8 8 8 8 8 8 8 8 8 8 8 18 18 19 19 21 22 22 23 25 26 27 28 20 21 20 23 24 25 26 24 27 28 29 29 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 846 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 8 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 6 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 00000371C07BB800640000000000000000000000000100000000306000000000000000014000001C0614400000080AC1502431C182504002A10026626770C2001120070028881830668A08202281939180200460900008C8071000000000004000200000800000800040000100000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-chloro-N-[3-(3,4-dihydro-2H-pyrrol-5-ylsulfamoyl)phenyl]-5-nitro-benzenesulfonamide IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-chloro-N-[3-(3,4-dihydro-2H-pyrrol-5-ylsulfamoyl)phenyl]-5-nitrobenzenesulfonamide IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-chloro-<I>N</I>-[3-(3,4-dihydro-2<I>H</I>-pyrrol-5-ylsulfamoyl)phenyl]-5-nitrobenzenesulfonamide IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-chloro-N-[3-(3,4-dihydro-2H-pyrrol-5-ylsulfamoyl)phenyl]-5-nitrobenzenesulfonamide IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-chloranyl-N-[3-(3,4-dihydro-2H-pyrrol-5-ylsulfamoyl)phenyl]-5-nitro-benzenesulfonamide IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-chloro-5-nitro-N-[3-(1-pyrrolin-2-ylsulfamoyl)phenyl]benzenesulfonamide InChI Standard 1 1.0.6 InChI iupac.org 2021.05.07 InChI=1S/C16H15ClN4O6S2/c17-14-7-6-12(21(22)23)10-15(14)29(26,27)19-11-3-1-4-13(9-11)28(24,25)20-16-5-2-8-18-16/h1,3-4,6-7,9-10,19H,2,5,8H2,(H,18,20) InChIKey Standard 1 1.0.6 InChI iupac.org 2021.05.07 LKPSFDYVHGDOGW-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.05.07 1.6 Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 458.0121543 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 C16H15ClN4O6S2 Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 458.9 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C1CC(=NC1)NS(=O)(=O)C2=CC=CC(=C2)NS(=O)(=O)C3=C(C=CC(=C3)[N+](=O)[O-])Cl SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C1CC(=NC1)NS(=O)(=O)C2=CC=CC(=C2)NS(=O)(=O)C3=C(C=CC(=C3)[N+](=O)[O-])Cl Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 167 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 458.0121543 29 0 0 0 0 0 0 0 1 -1