Compile Data Set for Download or QSAR

Found 75 hits with Last Name = 'o''brien' and Initial = 'te'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326802 (1-(5-chloro-2-methoxyphenyl)-3-(2-(trifluoromethyl...) Show SMILES COc1ccc(Cl)cc1NC(=O)Nc1cc(nc2ccccc12)C(F)(F)F Show InChI InChI=1S/C18H13ClF3N3O2/c1-27-15-7-6-10(19)8-14(15)25-17(26)24-13-9-16(18(20,21)22)23-12-5-3-2-4-11(12)13/h2-9H,1H3,(H2,23,24,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326811 (1-(4-(6-methylpyrazin-2-yloxy)phenyl)-3-(2-(triflu...) Show SMILES Cc1cncc(Oc2ccc(NC(=O)Nc3cc(nc4ccccc34)C(F)(F)F)cc2)n1 Show InChI InChI=1S/C22H16F3N5O2/c1-13-11-26-12-20(27-13)32-15-8-6-14(7-9-15)28-21(31)30-18-10-19(22(23,24)25)29-17-5-3-2-4-16(17)18/h2-12H,1H3,(H2,28,29,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326801 (1-(4-(6-methylpyrazin-2-yloxy)phenyl)-3-(2-methylq...) Show SMILES Cc1cncc(Oc2ccc(NC(=O)Nc3cc(C)nc4ccccc34)cc2)n1 Show InChI InChI=1S/C22H19N5O2/c1-14-11-20(18-5-3-4-6-19(18)24-14)27-22(28)26-16-7-9-17(10-8-16)29-21-13-23-12-15(2)25-21/h3-13H,1-2H3,(H2,24,26,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326820 (1-(5-chloro-2-methoxyphenyl)-3-(2-oxo-1,2-dihydroq...) Show SMILES COc1ccc(Cl)cc1NC(=O)Nc1cc(=O)[nH]c2ccccc12 Show InChI InChI=1S/C17H14ClN3O3/c1-24-15-7-6-10(18)8-14(15)21-17(23)20-13-9-16(22)19-12-5-3-2-4-11(12)13/h2-9H,1H3,(H3,19,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326806 (1-(4-(trifluoromethoxy)phenyl)-3-(2-(trifluorometh...) Show SMILES FC(F)(F)Oc1ccc(NC(=O)Nc2cc(nc3ccccc23)C(F)(F)F)cc1 Show InChI InChI=1S/C18H11F6N3O2/c19-17(20,21)15-9-14(12-3-1-2-4-13(12)26-15)27-16(28)25-10-5-7-11(8-6-10)29-18(22,23)24/h1-9H,(H2,25,26,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326803 (1-(3-chloro-4-methoxyphenyl)-3-(2-(trifluoromethyl...) Show SMILES COc1ccc(NC(=O)Nc2cc(nc3ccccc23)C(F)(F)F)cc1Cl Show InChI InChI=1S/C18H13ClF3N3O2/c1-27-15-7-6-10(8-12(15)19)23-17(26)25-14-9-16(18(20,21)22)24-13-5-3-2-4-11(13)14/h2-9H,1H3,(H2,23,24,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086108 (CHEMBL3425702) Show SMILES [O-]C(=O)C(F)(F)F.[NH3+]CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2cc3ccccc3cc12 Show InChI InChI=1S/C22H19ClN4/c23-18-8-5-15(6-9-18)7-10-21-26-20-14-17-4-2-1-3-16(17)13-19(20)22(27-21)25-12-11-24/h1-10,13-14H,11-12,24H2,(H,25,26,27)/p+1/b10-7+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326822 (1-(2-methyl-1,8-naphthyridin-4-yl)-3-(4-(6-methylp...) Show SMILES Cc1cncc(Oc2ccc(NC(=O)Nc3cc(C)nc4ncccc34)cc2)n1 Show InChI InChI=1S/C21H18N6O2/c1-13-10-18(17-4-3-9-23-20(17)25-13)27-21(28)26-15-5-7-16(8-6-15)29-19-12-22-11-14(2)24-19/h3-12H,1-2H3,(H2,23,25,26,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326796 (1-(4-methoxyphenyl)-3-(2-methylquinolin-4-yl)urea ...) Show SMILES COc1ccc(NC(=O)Nc2cc(C)nc3ccccc23)cc1 Show InChI InChI=1S/C18H17N3O2/c1-12-11-17(15-5-3-4-6-16(15)19-12)21-18(22)20-13-7-9-14(23-2)10-8-13/h3-11H,1-2H3,(H2,19,20,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.39E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086088 (CHEMBL3425706) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(cc2)N=[N+]=[N-])nc2cc3ccccc3cc12 Show InChI InChI=1S/C24H23N7/c1-31(2)14-13-26-24-21-15-18-5-3-4-6-19(18)16-22(21)27-23(28-24)12-9-17-7-10-20(11-8-17)29-30-25/h3-12,15-16H,13-14H2,1-2H3,(H,26,27,28)/b12-9+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326812 (1-(5-chloro-2-methoxyphenyl)-3-(2-chloroquinolin-4...) Show SMILES COc1ccc(Cl)cc1NC(=O)Nc1cc(Cl)nc2ccccc12 Show InChI InChI=1S/C17H13Cl2N3O2/c1-24-15-7-6-10(18)8-14(15)22-17(23)21-13-9-16(19)20-12-5-3-2-4-11(12)13/h2-9H,1H3,(H2,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.49E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326807 (1-(5-chloro-2,4-dimethoxyphenyl)-3-(2-(trifluorome...) Show SMILES COc1cc(OC)c(NC(=O)Nc2cc(nc3ccccc23)C(F)(F)F)cc1Cl Show InChI InChI=1S/C19H15ClF3N3O3/c1-28-15-9-16(29-2)14(7-11(15)20)26-18(27)25-13-8-17(19(21,22)23)24-12-6-4-3-5-10(12)13/h3-9H,1-2H3,(H2,24,25,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50230005 (1-(5-chloro-2-methoxyphenyl)-3-(2-methylquinolin-4...) Show SMILES COc1ccc(Cl)cc1NC(=O)Nc1cc(C)nc2ccccc12 Show InChI InChI=1S/C18H16ClN3O2/c1-11-9-15(13-5-3-4-6-14(13)20-11)21-18(23)22-16-10-12(19)7-8-17(16)24-2/h3-10H,1-2H3,(H2,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.87E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326809 (1-(4-(pyrimidin-2-yl)phenyl)-3-(2-(trifluoromethyl...) Show SMILES FC(F)(F)c1cc(NC(=O)Nc2ccc(cc2)-c2ncccn2)c2ccccc2n1 Show InChI InChI=1S/C21H14F3N5O/c22-21(23,24)18-12-17(15-4-1-2-5-16(15)28-18)29-20(30)27-14-8-6-13(7-9-14)19-25-10-3-11-26-19/h1-12H,(H2,27,28,29,30)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.93E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326823 (1-(5-chloro-2-methoxyphenyl)-3-(2-methyl-5,6,7,8-t...) Show SMILES COc1ccc(Cl)cc1NC(=O)Nc1cc(C)nc2NCCCc12 Show InChI InChI=1S/C17H19ClN4O2/c1-10-8-13(12-4-3-7-19-16(12)20-10)21-17(23)22-14-9-11(18)5-6-15(14)24-2/h5-6,8-9H,3-4,7H2,1-2H3,(H3,19,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.05E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326815 (1-(4-chlorophenyl)-3-(2-chloroquinolin-4-yl)urea |...) Show SMILES Clc1ccc(NC(=O)Nc2cc(Cl)nc3ccccc23)cc1 Show InChI InChI=1S/C16H11Cl2N3O/c17-10-5-7-11(8-6-10)19-16(22)21-14-9-15(18)20-13-4-2-1-3-12(13)14/h1-9H,(H2,19,20,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.11E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326816 (1-(2-chloroquinolin-4-yl)-3-(4-(trifluoromethoxy)p...) Show SMILES FC(F)(F)Oc1ccc(NC(=O)Nc2cc(Cl)nc3ccccc23)cc1 Show InChI InChI=1S/C17H11ClF3N3O2/c18-15-9-14(12-3-1-2-4-13(12)23-15)24-16(25)22-10-5-7-11(8-6-10)26-17(19,20)21/h1-9H,(H2,22,23,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086098 (CHEMBL3425705) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(I)cc2)nc2cc3ccccc3cc12 Show InChI InChI=1S/C24H23IN4/c1-29(2)14-13-26-24-21-15-18-5-3-4-6-19(18)16-22(21)27-23(28-24)12-9-17-7-10-20(25)11-8-17/h3-12,15-16H,13-14H2,1-2H3,(H,26,27,28)/b12-9+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086206 (CHEMBL3425606) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(C)cc12 Show InChI InChI=1S/C21H23ClN4/c1-15-4-10-19-18(14-15)21(23-12-13-26(2)3)25-20(24-19)11-7-16-5-8-17(22)9-6-16/h4-11,14H,12-13H2,1-3H3,(H,23,24,25)/b11-7+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326821 (1-(5-chloro-2-methoxyphenyl)-3-(2-methyl-1,8-napht...) Show SMILES COc1ccc(Cl)cc1NC(=O)Nc1cc(C)nc2ncccc12 Show InChI InChI=1S/C17H15ClN4O2/c1-10-8-13(12-4-3-7-19-16(12)20-10)21-17(23)22-14-9-11(18)5-6-15(14)24-2/h3-9H,1-2H3,(H2,19,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.47E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086123 (CHEMBL3425694) Show SMILES CN(C)CCOc1nc(\C=C\c2ccc(Cl)cc2)nc2cc3ccccc3cc12 Show InChI InChI=1S/C24H22ClN3O/c1-28(2)13-14-29-24-21-15-18-5-3-4-6-19(18)16-22(21)26-23(27-24)12-9-17-7-10-20(25)11-8-17/h3-12,15-16H,13-14H2,1-2H3/b12-9+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086124 (CHEMBL3425693) Show SMILES [O-]C(=O)C(F)(F)F.Cc1ccc2nc(\C=C\c3ccc(Cl)cc3)nc(NCC[NH3+])c2c1 Show InChI InChI=1S/C19H19ClN4/c1-13-2-8-17-16(12-13)19(22-11-10-21)24-18(23-17)9-5-14-3-6-15(20)7-4-14/h2-9,12H,10-11,21H2,1H3,(H,22,23,24)/p+1/b9-5+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326808 (1-(4-nitrophenyl)-3-(2-(trifluoromethyl)quinolin-4...) Show SMILES [O-][N+](=O)c1ccc(NC(=O)Nc2cc(nc3ccccc23)C(F)(F)F)cc1 Show InChI InChI=1S/C17H11F3N4O3/c18-17(19,20)15-9-14(12-3-1-2-4-13(12)22-15)23-16(25)21-10-5-7-11(8-6-10)24(26)27/h1-9H,(H2,21,22,23,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.71E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086201 (CHEMBL3425611) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(cc12)-c1ccccc1 Show InChI InChI=1S/C26H25ClN4/c1-31(2)17-16-28-26-23-18-21(20-6-4-3-5-7-20)11-14-24(23)29-25(30-26)15-10-19-8-12-22(27)13-9-19/h3-15,18H,16-17H2,1-2H3,(H,28,29,30)/b15-10+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326805 (1-(4-chlorophenyl)-3-(2-(trifluoromethyl)quinolin-...) Show SMILES FC(F)(F)c1cc(NC(=O)Nc2ccc(Cl)cc2)c2ccccc2n1 Show InChI InChI=1S/C17H11ClF3N3O/c18-10-5-7-11(8-6-10)22-16(25)24-14-9-15(17(19,20)21)23-13-4-2-1-3-12(13)14/h1-9H,(H2,22,23,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.81E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326810 (1-(3-(pyrimidin-2-yl)phenyl)-3-(2-(trifluoromethyl...) Show SMILES FC(F)(F)c1cc(NC(=O)Nc2cccc(c2)-c2ncccn2)c2ccccc2n1 Show InChI InChI=1S/C21H14F3N5O/c22-21(23,24)18-12-17(15-7-1-2-8-16(15)28-18)29-20(30)27-14-6-3-5-13(11-14)19-25-9-4-10-26-19/h1-12H,(H2,27,28,29,30)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326804 (1-(4-methoxyphenyl)-3-(2-(trifluoromethyl)quinolin...) Show SMILES COc1ccc(NC(=O)Nc2cc(nc3ccccc23)C(F)(F)F)cc1 Show InChI InChI=1S/C18H14F3N3O2/c1-26-12-8-6-11(7-9-12)22-17(25)24-15-10-16(18(19,20)21)23-14-5-3-2-4-13(14)15/h2-10H,1H3,(H2,22,23,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326800 (1-(2-methylquinolin-4-yl)-3-(3-(pyrimidin-2-yl)phe...) Show SMILES Cc1cc(NC(=O)Nc2cccc(c2)-c2ncccn2)c2ccccc2n1 Show InChI InChI=1S/C21H17N5O/c1-14-12-19(17-8-2-3-9-18(17)24-14)26-21(27)25-16-7-4-6-15(13-16)20-22-10-5-11-23-20/h2-13H,1H3,(H2,24,25,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326799 (1-(2-methylquinolin-4-yl)-3-(4-(pyrimidin-2-yl)phe...) Show SMILES Cc1cc(NC(=O)Nc2ccc(cc2)-c2ncccn2)c2ccccc2n1 Show InChI InChI=1S/C21H17N5O/c1-14-13-19(17-5-2-3-6-18(17)24-14)26-21(27)25-16-9-7-15(8-10-16)20-22-11-4-12-23-20/h2-13H,1H3,(H2,24,25,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326798 (1-(2-methylquinolin-4-yl)-3-(4-(trifluoromethoxy)p...) Show SMILES Cc1cc(NC(=O)Nc2ccc(OC(F)(F)F)cc2)c2ccccc2n1 Show InChI InChI=1S/C18H14F3N3O2/c1-11-10-16(14-4-2-3-5-15(14)22-11)24-17(25)23-12-6-8-13(9-7-12)26-18(19,20)21/h2-10H,1H3,(H2,22,23,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326797 (1-(4-chlorophenyl)-3-(2-methylquinolin-4-yl)urea |...) Show SMILES Cc1cc(NC(=O)Nc2ccc(Cl)cc2)c2ccccc2n1 Show InChI InChI=1S/C17H14ClN3O/c1-11-10-16(14-4-2-3-5-15(14)19-11)21-17(22)20-13-8-6-12(18)7-9-13/h2-10H,1H3,(H2,19,20,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326795 (1-(3-chloro-4-methoxyphenyl)-3-(2-methylquinolin-4...) Show SMILES COc1ccc(NC(=O)Nc2cc(C)nc3ccccc23)cc1Cl Show InChI InChI=1S/C18H16ClN3O2/c1-11-9-16(13-5-3-4-6-15(13)20-11)22-18(23)21-12-7-8-17(24-2)14(19)10-12/h3-10H,1-2H3,(H2,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086203 (CHEMBL3425609) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(Br)cc12 Show InChI InChI=1S/C20H20BrClN4/c1-26(2)12-11-23-20-17-13-15(21)6-9-18(17)24-19(25-20)10-5-14-3-7-16(22)8-4-14/h3-10,13H,11-12H2,1-2H3,(H,23,24,25)/b10-5+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086200 (CHEMBL3425612) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(cc12)-c1ccncc1 Show InChI InChI=1S/C25H24ClN5/c1-31(2)16-15-28-25-22-17-20(19-11-13-27-14-12-19)6-9-23(22)29-24(30-25)10-5-18-3-7-21(26)8-4-18/h3-14,17H,15-16H2,1-2H3,(H,28,29,30)/b10-5+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326824 (1-(5-chloro-2-methoxyphenyl)-3-(2-methyl-1,7-napht...) Show SMILES COc1ccc(Cl)cc1NC(=O)Nc1cc(C)nc2cnccc12 Show InChI InChI=1S/C17H15ClN4O2/c1-10-7-13(12-5-6-19-9-15(12)20-10)21-17(23)22-14-8-11(18)3-4-16(14)24-2/h3-9H,1-2H3,(H2,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326825 (1-(5-chloro-2,4-dimethoxyphenyl)-3-(2-methyl-1,7-n...) Show SMILES COc1cc(OC)c(NC(=O)Nc2cc(C)nc3cnccc23)cc1Cl Show InChI InChI=1S/C18H17ClN4O3/c1-10-6-13(11-4-5-20-9-15(11)21-10)22-18(24)23-14-7-12(19)16(25-2)8-17(14)26-3/h4-9H,1-3H3,(H2,21,22,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326819 (1-(2-chloroquinolin-4-yl)-3-(4-(6-methylpyrazin-2-...) Show SMILES Cc1cncc(Oc2ccc(NC(=O)Nc3cc(Cl)nc4ccccc34)cc2)n1 Show InChI InChI=1S/C21H16ClN5O2/c1-13-11-23-12-20(24-13)29-15-8-6-14(7-9-15)25-21(28)27-18-10-19(22)26-17-5-3-2-4-16(17)18/h2-12H,1H3,(H2,25,26,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326818 (1-(2-chloroquinolin-4-yl)-3-(3-(pyrimidin-2-yl)phe...) Show SMILES Clc1cc(NC(=O)Nc2cccc(c2)-c2ncccn2)c2ccccc2n1 Show InChI InChI=1S/C20H14ClN5O/c21-18-12-17(15-7-1-2-8-16(15)25-18)26-20(27)24-14-6-3-5-13(11-14)19-22-9-4-10-23-19/h1-12H,(H2,24,25,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326817 (1-(2-chloroquinolin-4-yl)-3-(4-(pyrimidin-2-yl)phe...) Show SMILES Clc1cc(NC(=O)Nc2ccc(cc2)-c2ncccn2)c2ccccc2n1 Show InChI InChI=1S/C20H14ClN5O/c21-18-12-17(15-4-1-2-5-16(15)25-18)26-20(27)24-14-8-6-13(7-9-14)19-22-10-3-11-23-19/h1-12H,(H2,24,25,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326814 (1-(2-chloroquinolin-4-yl)-3-(4-methoxyphenyl)urea ...) Show SMILES COc1ccc(NC(=O)Nc2cc(Cl)nc3ccccc23)cc1 Show InChI InChI=1S/C17H14ClN3O2/c1-23-12-8-6-11(7-9-12)19-17(22)21-15-10-16(18)20-14-5-3-2-4-13(14)15/h2-10H,1H3,(H2,19,20,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Insulin-like growth factor 1 receptor (Homo sapiens (Human))	BDBM50326813 (1-(3-chloro-4-methoxyphenyl)-3-(2-chloroquinolin-4...) Show SMILES COc1ccc(NC(=O)Nc2cc(Cl)nc3ccccc23)cc1Cl Show InChI InChI=1S/C17H13Cl2N3O2/c1-24-15-7-6-10(8-12(15)18)20-17(23)22-14-9-16(19)21-13-5-3-2-4-11(13)14/h2-9H,1H3,(H2,20,21,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
San Francisco State University Curated by ChEMBL					Assay Description Inhibition of recombinant IGF1R by ELISA				Bioorg Med Chem 18: 5995-6005 (2010) Article DOI: 10.1016/j.bmc.2010.06.071 BindingDB Entry DOI: 10.7270/Q27944WQ
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086197 (CHEMBL3425615) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(cc12)C1=CCCCC1 |t:28| Show InChI InChI=1S/C26H29ClN4/c1-31(2)17-16-28-26-23-18-21(20-6-4-3-5-7-20)11-14-24(23)29-25(30-26)15-10-19-8-12-22(27)13-9-19/h6,8-15,18H,3-5,7,16-17H2,1-2H3,(H,28,29,30)/b15-10+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086109 (CHEMBL3425701) Show SMILES [I-].C[N+](C)(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2cc3ccccc3cc12 Show InChI InChI=1S/C25H26ClN4/c1-30(2,3)15-14-27-25-22-16-19-6-4-5-7-20(19)17-23(22)28-24(29-25)13-10-18-8-11-21(26)12-9-18/h4-13,16-17H,14-15H2,1-3H3,(H,27,28,29)/q+1/b13-10+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086199 (CHEMBL3425613) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(cc12)-c1ccc2ccccc2c1 Show InChI InChI=1S/C30H27ClN4/c1-35(2)18-17-32-30-27-20-25(24-11-10-22-5-3-4-6-23(22)19-24)12-15-28(27)33-29(34-30)16-9-21-7-13-26(31)14-8-21/h3-16,19-20H,17-18H2,1-2H3,(H,32,33,34)/b16-9+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086120 (CHEMBL3425697) Show SMILES CN(C)CCCNc1nc(\C=C\c2ccc(Cl)cc2)nc2cc3ccccc3cc12 Show InChI InChI=1S/C25H25ClN4/c1-30(2)15-5-14-27-25-22-16-19-6-3-4-7-20(19)17-23(22)28-24(29-25)13-10-18-8-11-21(26)12-9-18/h3-4,6-13,16-17H,5,14-15H2,1-2H3,(H,27,28,29)/b13-10+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086105 (CHEMBL3425704) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(cc12)C(=O)c1ccccc1 Show InChI InChI=1S/C27H25ClN4O/c1-32(2)17-16-29-27-23-18-21(26(33)20-6-4-3-5-7-20)11-14-24(23)30-25(31-27)15-10-19-8-12-22(28)13-9-19/h3-15,18H,16-17H2,1-2H3,(H,29,30,31)/b15-10+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086202 (CHEMBL3425610) Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(Cl)cc2)nc2ccc(I)cc12 Show InChI InChI=1S/C20H20ClIN4/c1-26(2)12-11-23-20-17-13-16(22)8-9-18(17)24-19(25-20)10-5-14-3-6-15(21)7-4-14/h3-10,13H,11-12H2,1-2H3,(H,23,24,25)/b10-5+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Escherichia coli)	BDBM50086204 (CHEMBL3425608) Show SMILES COc1cc2nc(\C=C\c3ccc(Cl)cc3)nc(NCCN(C)C)c2cc1OC Show InChI InChI=1S/C22H25ClN4O2/c1-27(2)12-11-24-22-17-13-19(28-3)20(29-4)14-18(17)25-21(26-22)10-7-15-5-8-16(23)9-6-15/h5-10,13-14H,11-12H2,1-4H3,(H,24,25,26)/b10-7+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Escherichia coli FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Bacillus subtilis)	BDBM50085931 (CHEMBL3425688) Show SMILES CN(C)CCNc1nc(nc2ccc(C)cc12)-c1cccs1 Show InChI InChI=1S/C17H20N4S/c1-12-6-7-14-13(11-12)16(18-8-9-21(2)3)20-17(19-14)15-5-4-10-22-15/h4-7,10-11H,8-9H2,1-3H3,(H,18,19,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.28E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Bacillus subtilis FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair
Cell division protein FtsZ (Bacillus subtilis)	BDBM50085932 (CHEMBL3425687) Show SMILES CN(C)CCNc1nc(nc2ccc(C)cc12)-c1cc2ccccc2o1 Show InChI InChI=1S/C21H22N4O/c1-14-8-9-17-16(12-14)20(22-10-11-25(2)3)24-21(23-17)19-13-15-6-4-5-7-18(15)26-19/h4-9,12-13H,10-11H2,1-3H3,(H,22,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.28E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of Bacillus subtilis FtsZ GTPase activity after 5 mins by enzyme-coupled inhibition assay				ACS Med Chem Lett 6: 308-12 (2015) Article DOI: 10.1021/ml500497s BindingDB Entry DOI: 10.7270/Q2PV6N4C
					More data for this Ligand-Target Pair

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