Compile Data Set for Download or QSAR

Found 29 hits with Last Name = 'amblard' and Initial = 'mc'   

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
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286545 (3-Benzenesulfonyl-5-chloro-2-(1H-imidazol-2-yl)-1H...) Show SMILES Clc1ccc2[nH]c(-c3ncc[nH]3)c(c2c1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C17H12ClN3O2S/c18-11-6-7-14-13(10-11)16(15(21-14)17-19-8-9-20-17)24(22,23)12-4-2-1-3-5-12/h1-10,21H,(H,19,20)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50230553 (3-Benzenesulfonyl-5-chloro-2-(5-methyl-1H-imidazol...) Show SMILES Cc1c[nH]c(n1)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C18H14ClN3O2S/c1-11-10-20-18(21-11)16-17(14-9-12(19)7-8-15(14)22-16)25(23,24)13-5-3-2-4-6-13/h2-10,22H,1H3,(H,20,21)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	4.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286549 (3-Benzenesulfonyl-5-chloro-2-(4,5-dimethyl-1H-imid...) Show SMILES Cc1nc([nH]c1C)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C19H16ClN3O2S/c1-11-12(2)22-19(21-11)17-18(15-10-13(20)8-9-16(15)23-17)26(24,25)14-6-4-3-5-7-14/h3-10,23H,1-2H3,(H,21,22)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	5.10	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286550 (3-Benzenesulfonyl-5-chloro-2-(4,5-dihydro-1H-imida...) Show SMILES Clc1ccc2[nH]c(C3=NCCN3)c(c2c1)S(=O)(=O)c1ccccc1 |t:7| Show InChI InChI=1S/C17H14ClN3O2S/c18-11-6-7-14-13(10-11)16(15(21-14)17-19-8-9-20-17)24(22,23)12-4-2-1-3-5-12/h1-7,10,21H,8-9H2,(H,19,20)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	6.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286551 (2-(3-Benzenesulfonyl-5-chloro-1H-indol-2-yl)-4,5,6...) Show SMILES Clc1ccc2[nH]c(-c3nc4CCCCc4[nH]3)c(c2c1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H18ClN3O2S/c22-13-10-11-16-15(12-13)20(28(26,27)14-6-2-1-3-7-14)19(23-16)21-24-17-8-4-5-9-18(17)25-21/h1-3,6-7,10-12,23H,4-5,8-9H2,(H,24,25)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	8.10	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50230553 (3-Benzenesulfonyl-5-chloro-2-(5-methyl-1H-imidazol...) Show SMILES Cc1c[nH]c(n1)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C18H14ClN3O2S/c1-11-10-20-18(21-11)16-17(14-9-12(19)7-8-15(14)22-16)25(23,24)13-5-3-2-4-6-13/h2-10,22H,1H3,(H,20,21)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	9	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286543 (3-Benzenesulfonyl-5-chloro-2-(4-methyl-5-propyl-1H...) Show SMILES CCCc1[nH]c(nc1C)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H20ClN3O2S/c1-3-7-17-13(2)23-21(25-17)19-20(16-12-14(22)10-11-18(16)24-19)28(26,27)15-8-5-4-6-9-15/h4-6,8-12,24H,3,7H2,1-2H3,(H,23,25)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	9.40	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286548 (3-Benzenesulfonyl-5-chloro-2-(4,5-diethyl-1H-imida...) Show SMILES CCc1nc([nH]c1CC)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H20ClN3O2S/c1-3-16-17(4-2)25-21(24-16)19-20(15-12-13(22)10-11-18(15)23-19)28(26,27)14-8-6-5-7-9-14/h5-12,23H,3-4H2,1-2H3,(H,24,25)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286542 (3-Benzenesulfonyl-5-chloro-2-(4,5-dihydro-thiazol-...) Show SMILES Clc1ccc2[nH]c(C3=NCCS3)c(c2c1)S(=O)(=O)c1ccccc1 |t:7| Show InChI InChI=1S/C17H13ClN2O2S2/c18-11-6-7-14-13(10-11)16(15(20-14)17-19-8-9-23-17)24(21,22)12-4-2-1-3-5-12/h1-7,10,20H,8-9H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286546 (4-(3-Benzenesulfonyl-5-chloro-1H-indol-2-yl)-4H-1l...) Show SMILES Nc1nc(cs1)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C17H12ClN3O2S2/c18-10-6-7-13-12(8-10)16(15(20-13)14-9-24-17(19)21-14)25(22,23)11-4-2-1-3-5-11/h1-9,20H,(H2,19,21)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286549 (3-Benzenesulfonyl-5-chloro-2-(4,5-dimethyl-1H-imid...) Show SMILES Cc1nc([nH]c1C)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C19H16ClN3O2S/c1-11-12(2)22-19(21-11)17-18(15-10-13(20)8-9-16(15)23-17)26(24,25)14-6-4-3-5-7-14/h3-10,23H,1-2H3,(H,21,22)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-2 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286545 (3-Benzenesulfonyl-5-chloro-2-(1H-imidazol-2-yl)-1H...) Show SMILES Clc1ccc2[nH]c(-c3ncc[nH]3)c(c2c1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C17H12ClN3O2S/c18-11-6-7-14-13(10-11)16(15(21-14)17-19-8-9-20-17)24(22,23)12-4-2-1-3-5-12/h1-10,21H,(H,19,20)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-2 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286552 ((3aS,7aS)-2-(3-Benzenesulfonyl-5-chloro-1H-indol-2...) Show SMILES Clc1ccc2[nH]c(C3=N[C@H]4CCCC[C@@H]4N3)c(c2c1)S(=O)(=O)c1ccccc1 |t:7| Show InChI InChI=1S/C21H20ClN3O2S/c22-13-10-11-16-15(12-13)20(28(26,27)14-6-2-1-3-7-14)19(23-16)21-24-17-8-4-5-9-18(17)25-21/h1-3,6-7,10-12,17-18,23H,4-5,8-9H2,(H,24,25)/t17-,18-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286544 (3-Benzenesulfonyl-5-chloro-2-(5,5-dimethyl-4,5-dih...) Show SMILES CC1(C)CN=C(N1)c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 |c:4| Show InChI InChI=1S/C19H18ClN3O2S/c1-19(2)11-21-18(23-19)16-17(14-10-12(20)8-9-15(14)22-16)26(24,25)13-6-4-3-5-7-13/h3-10,22H,11H2,1-2H3,(H,21,23)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286543 (3-Benzenesulfonyl-5-chloro-2-(4-methyl-5-propyl-1H...) Show SMILES CCCc1[nH]c(nc1C)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H20ClN3O2S/c1-3-7-17-13(2)23-21(25-17)19-20(16-12-14(22)10-11-18(16)24-19)28(26,27)15-8-5-4-6-9-15/h4-6,8-12,24H,3,7H2,1-2H3,(H,23,25)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	210	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-2 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286546 (4-(3-Benzenesulfonyl-5-chloro-1H-indol-2-yl)-4H-1l...) Show SMILES Nc1nc(cs1)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C17H12ClN3O2S2/c18-10-6-7-13-12(8-10)16(15(20-13)14-9-24-17(19)21-14)25(22,23)11-4-2-1-3-5-11/h1-9,20H,(H2,19,21)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	222	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286550 (3-Benzenesulfonyl-5-chloro-2-(4,5-dihydro-1H-imida...) Show SMILES Clc1ccc2[nH]c(C3=NCCN3)c(c2c1)S(=O)(=O)c1ccccc1 |t:7| Show InChI InChI=1S/C17H14ClN3O2S/c18-11-6-7-14-13(10-11)16(15(21-14)17-19-8-9-20-17)24(22,23)12-4-2-1-3-5-12/h1-7,10,21H,8-9H2,(H,19,20)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	358	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-2 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286545 (3-Benzenesulfonyl-5-chloro-2-(1H-imidazol-2-yl)-1H...) Show SMILES Clc1ccc2[nH]c(-c3ncc[nH]3)c(c2c1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C17H12ClN3O2S/c18-11-6-7-14-13(10-11)16(15(21-14)17-19-8-9-20-17)24(22,23)12-4-2-1-3-5-12/h1-10,21H,(H,19,20)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N/Y181C double mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286542 (3-Benzenesulfonyl-5-chloro-2-(4,5-dihydro-thiazol-...) Show SMILES Clc1ccc2[nH]c(C3=NCCS3)c(c2c1)S(=O)(=O)c1ccccc1 |t:7| Show InChI InChI=1S/C17H13ClN2O2S2/c18-11-6-7-14-13(10-11)16(15(20-14)17-19-8-9-23-17)24(21,22)12-4-2-1-3-5-12/h1-7,10,20H,8-9H2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	1.25E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286547 (3-Benzenesulfonyl-5-chloro-2-(1,4,5,6-tetrahydro-p...) Show SMILES Clc1ccc2[nH]c(c(c2c1)S(=O)(=O)c1ccccc1)C1=NCCCN1 |t:22| Show InChI InChI=1S/C18H16ClN3O2S/c19-12-7-8-15-14(11-12)17(16(22-15)18-20-9-4-10-21-18)25(23,24)13-5-2-1-3-6-13/h1-3,5-8,11,22H,4,9-10H2,(H,20,21)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.29E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50286553 (3-Benzenesulfonyl-5-chloro-2-imidazol-1-yl-1H-indo...) Show SMILES Clc1ccc2[nH]c(c(c2c1)S(=O)(=O)c1ccccc1)-n1ccnc1 Show InChI InChI=1S/C17H12ClN3O2S/c18-12-6-7-15-14(10-12)16(17(20-15)21-9-8-19-11-21)24(22,23)13-4-2-1-3-5-13/h1-11,20H	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	2.39E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primer				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286549 (3-Benzenesulfonyl-5-chloro-2-(4,5-dimethyl-1H-imid...) Show SMILES Cc1nc([nH]c1C)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C19H16ClN3O2S/c1-11-12(2)22-19(21-11)17-18(15-10-13(20)8-9-16(15)23-17)26(24,25)14-6-4-3-5-7-14/h3-10,23H,1-2H3,(H,21,22)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N/Y181C double mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286545 (3-Benzenesulfonyl-5-chloro-2-(1H-imidazol-2-yl)-1H...) Show SMILES Clc1ccc2[nH]c(-c3ncc[nH]3)c(c2c1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C17H12ClN3O2S/c18-11-6-7-14-13(10-11)16(15(21-14)17-19-8-9-20-17)24(22,23)12-4-2-1-3-5-12/h1-10,21H,(H,19,20)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-2 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286542 (3-Benzenesulfonyl-5-chloro-2-(4,5-dihydro-thiazol-...) Show SMILES Clc1ccc2[nH]c(C3=NCCS3)c(c2c1)S(=O)(=O)c1ccccc1 |t:7| Show InChI InChI=1S/C17H13ClN2O2S2/c18-11-6-7-14-13(10-11)16(15(20-14)17-19-8-9-23-17)24(21,22)12-4-2-1-3-5-12/h1-7,10,20H,8-9H2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286549 (3-Benzenesulfonyl-5-chloro-2-(4,5-dimethyl-1H-imid...) Show SMILES Cc1nc([nH]c1C)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C19H16ClN3O2S/c1-11-12(2)22-19(21-11)17-18(15-10-13(20)8-9-16(15)23-17)26(24,25)14-6-4-3-5-7-14/h3-10,23H,1-2H3,(H,21,22)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286550 (3-Benzenesulfonyl-5-chloro-2-(4,5-dihydro-1H-imida...) Show SMILES Clc1ccc2[nH]c(C3=NCCN3)c(c2c1)S(=O)(=O)c1ccccc1 |t:7| Show InChI InChI=1S/C17H14ClN3O2S/c18-11-6-7-14-13(10-11)16(15(21-14)17-19-8-9-20-17)24(22,23)12-4-2-1-3-5-12/h1-7,10,21H,8-9H2,(H,19,20)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-2 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286543 (3-Benzenesulfonyl-5-chloro-2-(4-methyl-5-propyl-1H...) Show SMILES CCCc1[nH]c(nc1C)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H20ClN3O2S/c1-3-7-17-13(2)23-21(25-17)19-20(16-12-14(22)10-11-18(16)24-19)28(26,27)15-8-5-4-6-9-15/h4-6,8-12,24H,3,7H2,1-2H3,(H,23,25)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against HIV-2 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50230553 (3-Benzenesulfonyl-5-chloro-2-(5-methyl-1H-imidazol...) Show SMILES Cc1c[nH]c(n1)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C18H14ClN3O2S/c1-11-10-20-18(21-11)16-17(14-9-12(19)7-8-15(14)22-16)25(23,24)13-5-3-2-4-6-13/h2-10,22H,1H3,(H,20,21)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50286546 (4-(3-Benzenesulfonyl-5-chloro-1H-indol-2-yl)-4H-1l...) Show SMILES Nc1nc(cs1)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C17H12ClN3O2S2/c18-10-6-7-13-12(8-10)16(15(20-13)14-9-24-17(19)21-14)25(22,23)11-4-2-1-3-5-11/h1-9,20H,(H2,19,21)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against K103N mutant of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 5: 491-496 (1995) Article DOI: 10.1016/0960-894X(95)00059-3 BindingDB Entry DOI: 10.7270/Q28052KF
					More data for this Ligand-Target Pair