Compile Data Set for Download or QSAR

Found 28 hits Enz. Inhib. hit(s) with all data for entry = 50003397   

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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470139 (CHEMBL46745) Show SMILES Fc1ccc(OCC(=O)Nc2ccccc2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C21H16FNO3/c22-16-11-12-19(18(13-16)21(25)15-7-3-1-4-8-15)26-14-20(24)23-17-9-5-2-6-10-17/h1-13H,14H2,(H,23,24)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.59	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470155 (CHEMBL288971) Show SMILES Clc1ccc(OCC(=O)N2CCc3ccccc3C2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C24H20ClNO3/c25-20-10-11-22(21(14-20)24(28)18-7-2-1-3-8-18)29-16-23(27)26-13-12-17-6-4-5-9-19(17)15-26/h1-11,14H,12-13,15-16H2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	14.8	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470136 (CHEMBL296939 | GF-128590) Show SMILES Clc1ccc(OCC(=O)Nc2ccccc2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C21H16ClNO3/c22-16-11-12-19(18(13-16)21(25)15-7-3-1-4-8-15)26-14-20(24)23-17-9-5-2-6-10-17/h1-13H,14H2,(H,23,24)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid PDB UniChem	PDB Article PubMed	n/a	n/a	27.3	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair				3D Structure (crystal)
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470145 (CHEMBL46925) Show SMILES Clc1cc(OCC(=O)Nc2ccccc2)c(cc1Cl)C(=O)c1ccccc1 Show InChI InChI=1S/C21H15Cl2NO3/c22-17-11-16(21(26)14-7-3-1-4-8-14)19(12-18(17)23)27-13-20(25)24-15-9-5-2-6-10-15/h1-12H,13H2,(H,24,25)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	35	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470146 (CHEMBL417183) Show SMILES Clc1ccc(OCC(=O)c2cc3ccccc3[nH]2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C23H16ClNO3/c24-17-10-11-22(18(13-17)23(27)15-6-2-1-3-7-15)28-14-21(26)20-12-16-8-4-5-9-19(16)25-20/h1-13,25H,14H2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	161	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470138 (CHEMBL46650) Show SMILES CN(C)CCCOc1ccc(NC(=O)COc2ccc(Cl)cc2C(=O)c2ccccc2)cc1 Show InChI InChI=1S/C26H27ClN2O4/c1-29(2)15-6-16-32-22-12-10-21(11-13-22)28-25(30)18-33-24-14-9-20(27)17-23(24)26(31)19-7-4-3-5-8-19/h3-5,7-14,17H,6,15-16,18H2,1-2H3,(H,28,30)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	207	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470151 (CHEMBL297010) Show SMILES Clc1ccc(OCC(=O)Nc2ccccc2)c(c1)C(=O)c1cccnc1 Show InChI InChI=1S/C20H15ClN2O3/c21-15-8-9-18(17(11-15)20(25)14-5-4-10-22-12-14)26-13-19(24)23-16-6-2-1-3-7-16/h1-12H,13H2,(H,23,24)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	436	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470144 (CHEMBL43263) Show SMILES CN(C)CCCOc1ccc(NC(=O)Cc2ccc(Cl)cc2C(=O)c2ccccc2)cc1 Show InChI InChI=1S/C26H27ClN2O3/c1-29(2)15-6-16-32-23-13-11-22(12-14-23)28-25(30)17-20-9-10-21(27)18-24(20)26(31)19-7-4-3-5-8-19/h3-5,7-14,18H,6,15-17H2,1-2H3,(H,28,30)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	443	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470148 (CHEMBL42078) Show SMILES CN(C)CCCOc1ccc(NC(=O)Cc2ccc(Cl)cc2C(=O)c2ccccc2)c(C)c1 Show InChI InChI=1S/C27H29ClN2O3/c1-19-16-23(33-15-7-14-30(2)3)12-13-25(19)29-26(31)17-21-10-11-22(28)18-24(21)27(32)20-8-5-4-6-9-20/h4-6,8-13,16,18H,7,14-15,17H2,1-3H3,(H,29,31)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	752	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470137 (CHEMBL45100) Show SMILES CCN(CC)CCOc1ccc(NC(=O)COc2ccc(Cl)cc2C(=O)c2ccccc2)cc1 Show InChI InChI=1S/C27H29ClN2O4/c1-3-30(4-2)16-17-33-23-13-11-22(12-14-23)29-26(31)19-34-25-15-10-21(28)18-24(25)27(32)20-8-6-5-7-9-20/h5-15,18H,3-4,16-17,19H2,1-2H3,(H,29,31)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	935	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470166 (CHEMBL44002) Show SMILES Clc1ccc(OCc2nc3ccccc3[nH]2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C21H15ClN2O2/c22-15-10-11-19(16(12-15)21(25)14-6-2-1-3-7-14)26-13-20-23-17-8-4-5-9-18(17)24-20/h1-12H,13H2,(H,23,24)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470140 (CHEMBL42066) Show SMILES Clc1ccc(OCC(=O)Nc2ccccc2)c(c1)C(=O)C1CCCC1 Show InChI InChI=1S/C20H20ClNO3/c21-15-10-11-18(17(12-15)20(24)14-6-4-5-7-14)25-13-19(23)22-16-8-2-1-3-9-16/h1-3,8-12,14H,4-7,13H2,(H,22,23)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.03E+3	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470152 (CHEMBL42823) Show SMILES CCN(CC)CCOc1ccc(NC(=O)COc2ccccc2C(=O)c2ccccc2)cc1 Show InChI InChI=1S/C27H30N2O4/c1-3-29(4-2)18-19-32-23-16-14-22(15-17-23)28-26(30)20-33-25-13-9-8-12-24(25)27(31)21-10-6-5-7-11-21/h5-17H,3-4,18-20H2,1-2H3,(H,28,30)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470168 (CHEMBL46977) Show SMILES CCc1cc(OCCCN(C)C)ccc1NC(=O)Cc1ccc(Cl)cc1C(=O)c1ccccc1 Show InChI InChI=1S/C28H31ClN2O3/c1-4-20-17-24(34-16-8-15-31(2)3)13-14-26(20)30-27(32)18-22-11-12-23(29)19-25(22)28(33)21-9-6-5-7-10-21/h5-7,9-14,17,19H,4,8,15-16,18H2,1-3H3,(H,30,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.21E+3	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470142 (CHEMBL46675) Show SMILES Cc1ccccc1CNC(=O)COc1ccc(Cl)cc1C(=O)c1ccccc1 Show InChI InChI=1S/C23H20ClNO3/c1-16-7-5-6-10-18(16)14-25-22(26)15-28-21-12-11-19(24)13-20(21)23(27)17-8-3-2-4-9-17/h2-13H,14-15H2,1H3,(H,25,26)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.34E+3	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470154 (CHEMBL47214) Show SMILES CCN(CC)CCOc1ccc(NC(=O)COc2cc(OC)ccc2C(=O)c2ccccc2)cc1 Show InChI InChI=1S/C28H32N2O5/c1-4-30(5-2)17-18-34-23-13-11-22(12-14-23)29-27(31)20-35-26-19-24(33-3)15-16-25(26)28(32)21-9-7-6-8-10-21/h6-16,19H,4-5,17-18,20H2,1-3H3,(H,29,31)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.32E+4	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470153 (CHEMBL415908) Show SMILES CCN(CC)CCOc1ccc(NC(=O)COc2ccccc2C(=O)c2ccc(OC)cc2)cc1 Show InChI InChI=1S/C28H32N2O5/c1-4-30(5-2)18-19-34-24-16-12-22(13-17-24)29-27(31)20-35-26-9-7-6-8-25(26)28(32)21-10-14-23(33-3)15-11-21/h6-17H,4-5,18-20H2,1-3H3,(H,29,31)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470143 (CHEMBL295590) Show SMILES CCN(CC)CCOc1ccc(NC(=O)COc2ccccc2C(=O)c2ccc(F)cc2)cc1 Show InChI InChI=1S/C27H29FN2O4/c1-3-30(4-2)17-18-33-23-15-13-22(14-16-23)29-26(31)19-34-25-8-6-5-7-24(25)27(32)20-9-11-21(28)12-10-20/h5-16H,3-4,17-19H2,1-2H3,(H,29,31)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470135 (CHEMBL289000) Show SMILES O=C(COc1ccc(cc1C(=O)c1ccccc1)-n1ccnc1)Nc1ccccc1 Show InChI InChI=1S/C24H19N3O3/c28-23(26-19-9-5-2-6-10-19)16-30-22-12-11-20(27-14-13-25-17-27)15-21(22)24(29)18-7-3-1-4-8-18/h1-15,17H,16H2,(H,26,28)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.51E+4	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470165 (CHEMBL441039) Show SMILES Clc1ccc(OCC(=O)Cc2ccccc2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C22H17ClO3/c23-18-11-12-21(20(14-18)22(25)17-9-5-2-6-10-17)26-15-19(24)13-16-7-3-1-4-8-16/h1-12,14H,13,15H2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.28E+4	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470164 (CHEMBL298060) Show SMILES Clc1ccc(OCC(=O)NC2CCCCC2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C21H22ClNO3/c22-16-11-12-19(18(13-16)21(25)15-7-3-1-4-8-15)26-14-20(24)23-17-9-5-2-6-10-17/h1,3-4,7-8,11-13,17H,2,5-6,9-10,14H2,(H,23,24)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.03E+4	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470147 (CHEMBL44592) Show SMILES CN(C)CCCOc1cc(C)c(NC(=O)Cc2ccc(Cl)cc2C(=O)c2ccccc2)c(C)c1 Show InChI InChI=1S/C28H31ClN2O3/c1-19-15-24(34-14-8-13-31(3)4)16-20(2)27(19)30-26(32)17-22-11-12-23(29)18-25(22)28(33)21-9-6-5-7-10-21/h5-7,9-12,15-16,18H,8,13-14,17H2,1-4H3,(H,30,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.04E+5	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470163 (CHEMBL46627) Show SMILES CN(C)CCCOc1ccc(NC(=O)c2ccc(Cl)cc2C(=O)c2ccccc2)c(C)c1 Show InChI InChI=1S/C26H27ClN2O3/c1-18-16-21(32-15-7-14-29(2)3)11-13-24(18)28-26(31)22-12-10-20(27)17-23(22)25(30)19-8-5-4-6-9-19/h4-6,8-13,16-17H,7,14-15H2,1-3H3,(H,28,31)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.21E+5	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470167 (CHEMBL44845) Show SMILES Clc1ccc(OCC(=O)Nc2ccccc2)c(C(=O)c2ccccc2)c1Cl Show InChI InChI=1S/C21H15Cl2NO3/c22-16-11-12-17(27-13-18(25)24-15-9-5-2-6-10-15)19(20(16)23)21(26)14-7-3-1-4-8-14/h1-12H,13H2,(H,24,25)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.49E+5	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470150 (CHEMBL46446) Show SMILES Clc1cc(Cl)c(OCC(=O)Nc2ccccc2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C21H15Cl2NO3/c22-15-11-17(20(26)14-7-3-1-4-8-14)21(18(23)12-15)27-13-19(25)24-16-9-5-2-6-10-16/h1-12H,13H2,(H,24,25)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.49E+5	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470141 (CHEMBL295678) Show SMILES OC(c1ccccc1)c1cc(Cl)ccc1OCC(=O)Nc1ccccc1 Show InChI InChI=1S/C21H18ClNO3/c22-16-11-12-19(18(13-16)21(25)15-7-3-1-4-8-15)26-14-20(24)23-17-9-5-2-6-10-17/h1-13,21,25H,14H2,(H,23,24)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.71E+5	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470134 (CHEMBL46865) Show SMILES Clc1ccc(OCCNc2ccccc2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C21H18ClNO2/c22-17-11-12-20(25-14-13-23-18-9-5-2-6-10-18)19(15-17)21(24)16-7-3-1-4-8-16/h1-12,15,23H,13-14H2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.84E+5	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470149 (CHEMBL46981) Show SMILES Clc1ccc(OC\C=C\c2ccccc2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C22H17ClO2/c23-19-13-14-21(25-15-7-10-17-8-3-1-4-9-17)20(16-19)22(24)18-11-5-2-6-12-18/h1-14,16H,15H2/b10-7+	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.86E+5	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair