Compile Data Set for Download or QSAR

Found 23 hits with Last Name = 'taylor' and Initial = 'pb'   

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
Cathepsin K (Homo sapiens (Human))	BDBM50260286 (CHEMBL508746 | cycloaltilisin 6) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]-[#6](-[#6])=[#6]-[#6]-c1c(-[#6]-[#6]-[#6](=O)-c2ccc(-[#8])cc2-[#8])cc(c(-[#8])c1-[#8])-c1cc(-[#8])c(-[#8])c(-[#6]-[#6]=[#6](-[#6])-[#6]-[#6]\[#6]=[#6](\[#6])-[#6])c1-[#6]-[#6]-[#6](=O)-c1ccc(-[#8])cc1-[#8] |w:38.39,8.8| Show InChI InChI=1S/C50H58O10/c1-29(2)9-7-11-31(5)13-18-36-33(15-23-43(53)39-20-16-34(51)26-45(39)55)25-42(50(60)49(36)59)41-28-47(57)48(58)38(19-14-32(6)12-8-10-30(3)4)37(41)22-24-44(54)40-21-17-35(52)27-46(40)56/h9-10,13-14,16-17,20-21,25-28,51-52,55-60H,7-8,11-12,15,18-19,22-24H2,1-6H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	98	n/a	n/a	n/a	n/a	n/a	n/a
Millennium Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibition of cathepsin K (unknown origin) by fluorimetric assay				J Nat Prod 65: 624-7 (2002) BindingDB Entry DOI: 10.7270/Q2FT8KRV
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029987 (12-Hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@H](O)[C@@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14-,21-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029982 (12-Hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@@H](O)[C@@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14-,21+/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase mutant (Tyr-181 to Cys)				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029982 (12-Hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@@H](O)[C@@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14-,21+/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase mutant (Tyr-181 to Cys)				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Cathepsin K (Homo sapiens (Human))	BDBM50260285 (1-(2,4-dihydroxyphenyl)-3-(2-(3,7-dimethylocta-2,6...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]-[#6](-[#6])=[#6]-[#6]-c1c(-[#6]-[#6]-[#6](=O)-c2ccc(-[#8])cc2-[#8])ccc(-[#8])c1-[#8] |w:8.8| Show InChI InChI=1S/C25H30O5/c1-16(2)5-4-6-17(3)7-11-20-18(9-14-23(28)25(20)30)8-13-22(27)21-12-10-19(26)15-24(21)29/h5,7,9-10,12,14-15,26,28-30H,4,6,8,11,13H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	170	n/a	n/a	n/a	n/a	n/a	n/a
Millennium Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibition of cathepsin K (unknown origin) by fluorimetric assay				J Nat Prod 65: 624-7 (2002) BindingDB Entry DOI: 10.7270/Q2FT8KRV
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029982 (12-Hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@@H](O)[C@@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14-,21+/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase mutant (Tyr-181 to Leu)				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50279762 ((5S)-9-chloro-5-methyl-6-(3-methylbut-2-enyl)-4,5,...) Show SMILES C[C@H]1Cn2c3c(CN1CC=C(C)C)cc(Cl)cc3[nH]c2=S |wD:1.0,(11.88,-16.19,;11.86,-14.64,;13.24,-13.98,;13.57,-12.47,;12.6,-11.27,;11.07,-11.28,;10.11,-12.49,;10.46,-13.99,;9.27,-14.97,;7.83,-14.43,;6.62,-15.39,;5.19,-14.85,;6.87,-16.91,;10.3,-9.95,;11.06,-8.61,;10.27,-7.28,;12.6,-8.61,;13.37,-9.95,;14.87,-10.27,;15.02,-11.79,;16.37,-12.56,)| Show InChI InChI=1S/C16H20ClN3S/c1-10(2)4-5-19-9-12-6-13(17)7-14-15(12)20(8-11(19)3)16(21)18-14/h4,6-7,11H,5,8-9H2,1-3H3,(H,18,21)/t11-/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	MMDB PDB PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair				3D Structure (crystal)
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029996 (Acetic acid 2,3,10,10-tetramethyl-6-oxo-8-phenyl-3...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@@H](OC(C)=O)[C@@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C27H26O6/c1-14-15(2)30-24-18-11-12-27(4,5)33-25(18)21-19(17-9-7-6-8-10-17)13-20(29)32-26(21)22(24)23(14)31-16(3)28/h6-15,23H,1-5H3/t14-,15-,23+/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	720	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Cathepsin K (Homo sapiens (Human))	BDBM50260287 (CHEMBL494579 | cycloaltilisin 7) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]C1([#6])[#8]-c2cc(-[#8])c3-[#6](=O)-[#6]-[#6](-[#8]-c3c2-[#6]=[#6]1)-c1ccc(-[#8])cc1 |c:23| Show InChI InChI=1S/C25H26O5/c1-15(2)5-4-11-25(3)12-10-18-22(30-25)14-20(28)23-19(27)13-21(29-24(18)23)16-6-8-17(26)9-7-16/h5-10,12,14,21,26,28H,4,11,13H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	840	n/a	n/a	n/a	n/a	n/a	n/a
Millennium Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibition of cathepsin K (unknown origin) by fluorimetric assay				J Nat Prod 65: 624-7 (2002) BindingDB Entry DOI: 10.7270/Q2FT8KRV
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029985 (6,6,10,11-Tetramethyl-4-phenyl-6H,10H-dipyrano[2,3...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2C=C1C)-c1ccccc1 |c:5,23| Show InChI InChI=1S/C25H22O4/c1-14-12-19-22(27-15(14)2)17-10-11-25(3,4)29-24(17)21-18(13-20(26)28-23(19)21)16-8-6-5-7-9-16/h5-13,15H,1-4H3/t15-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029988 (6,6,10,11-Tetramethyl-4-phenyl-10,11-dihydro-6H-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2C(=O)[C@@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H22O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14H,1-4H3/t13-,14-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029992 (12-Hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@H](O)[C@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14+,21+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Cathepsin K (Homo sapiens (Human))	BDBM50024210 (1H-indole-3-ethanamine | 2-(1H-indol-3-yl)ethanami...) Show SMILES NCCc1c[nH]c2ccccc12 Show InChI InChI=1S/C10H12N2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6,11H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Millennium Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibition of cathepsin K (unknown origin) by fluorimetric assay				J Nat Prod 65: 628-9 (2002) BindingDB Entry DOI: 10.7270/Q2B27V1V
					More data for this Ligand-Target Pair
Cathepsin K (Homo sapiens (Human))	BDBM50260288 (CHEMBL495256 | Haploscleridamine) Show SMILES C(C1NCCc2c1[nH]c1ccccc21)c1cnc[nH]1 Show InChI InChI=1S/C15H16N4/c1-2-4-13-11(3-1)12-5-6-17-14(15(12)19-13)7-10-8-16-9-18-10/h1-4,8-9,14,17,19H,5-7H2,(H,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Millennium Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibition of cathepsin K (unknown origin) by fluorimetric assay				J Nat Prod 65: 628-9 (2002) BindingDB Entry DOI: 10.7270/Q2B27V1V
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029981 (12-Hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@@H](O)[C@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14+,21-/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029986 (12-(4-Bromo-benzoyl)-6,6,10,11-tetramethyl-4-pheny...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@H]([C@H]1C)C(=O)c1ccc(Br)cc1)-c1ccccc1 |c:5| Show InChI InChI=1S/C32H27BrO5/c1-17-18(2)36-29-22-14-15-32(3,4)38-30(22)26-23(19-8-6-5-7-9-19)16-24(34)37-31(26)27(29)25(17)28(35)20-10-12-21(33)13-11-20/h5-18,25H,1-4H3/t17-,18+,25-/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029994 (4-hydroxy-2,3,10,10-tetramethyl-8-phenyl-(2R,3S,4S...) Show SMILES C[C@H]1Oc2c3[C@@H]4[C@H](Oc3c3c(cc(=O)oc3c2[C@@H](O)[C@H]1C)-c1ccccc1)C4(C)C Show InChI InChI=1S/C25H24O5/c1-11-12(2)28-23-17-19-24(25(19,3)4)30-21(17)16-14(13-8-6-5-7-9-13)10-15(26)29-22(16)18(23)20(11)27/h5-12,19-20,24,27H,1-4H3/t11-,12+,19+,20-,24-/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029983 (3-[7-Hydroxy-5-methoxy-2,2-dimethyl-6-(2-methyl-bu...) Show SMILES COc1c2C=CC(C)(C)Oc2c(C(=CC(O)=O)c2ccccc2)c(O)c1C(=O)C(C)=CC |w:13.14,30.33,c:4| Show InChI InChI=1S/C26H26O6/c1-6-15(2)22(29)21-23(30)20(18(14-19(27)28)16-10-8-7-9-11-16)25-17(24(21)31-5)12-13-26(3,4)32-25/h6-14,30H,1-5H3,(H,27,28)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029991 (Acetic acid 2,3,10,10-tetramethyl-6-oxo-8-phenyl-3...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2[C@H](OC(C)=O)[C@@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C27H26O6/c1-14-15(2)30-24-18-11-12-27(4,5)33-25(18)21-19(17-9-7-6-8-10-17)13-20(29)32-26(21)22(24)23(14)31-16(3)28/h6-15,23H,1-5H3/t14-,15-,23-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029984 (4-hydroxy-2,3,10,10-tetramethyl-8-phenyl-(2R,3S,4S...) Show SMILES C[C@H]1Oc2c3[C@H]4[C@@H](Oc3c3c(cc(=O)oc3c2[C@@H](O)[C@H]1C)-c1ccccc1)C4(C)C Show InChI InChI=1S/C25H24O5/c1-11-12(2)28-23-17-19-24(25(19,3)4)30-21(17)16-14(13-8-6-5-7-9-13)10-15(26)29-22(16)18(23)20(11)27/h5-12,19-20,24,27H,1-4H3/t11-,12+,19-,20-,24+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029995 (6,6,10,11-Tetramethyl-4-phenyl-10,11-dihydro-6H-di...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c3c(cc(=O)oc3c2C(=O)[C@H]1C)-c1ccccc1 |c:5| Show InChI InChI=1S/C25H22O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14H,1-4H3/t13-,14+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029990 (3-(5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-3,4-dihydro...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c(C(=CC(O)=O)c3ccccc3)c(O)c2C(=O)[C@H]1C |w:14.15,c:5| Show InChI InChI=1S/C25H24O6/c1-13-14(2)30-23-16-10-11-25(3,4)31-24(16)19(22(29)20(23)21(13)28)17(12-18(26)27)15-8-6-5-7-9-15/h5-14,29H,1-4H3,(H,26,27)/t13-,14+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50029993 (3-(5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-3,4-dihydro...) Show SMILES C[C@H]1Oc2c3C=CC(C)(C)Oc3c(C(=CC(O)=O)c3ccccc3)c(O)c2C(=O)[C@@H]1C |w:14.15,c:5| Show InChI InChI=1S/C25H24O6/c1-13-14(2)30-23-16-10-11-25(3,4)31-24(16)19(22(29)20(23)21(13)28)17(12-18(26)27)15-8-6-5-7-9-15/h5-14,29H,1-4H3,(H,26,27)/t13-,14-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals R& D Curated by ChEMBL					Assay Description Inhibitory concentration against HIV-1 reverse transcriptase in scintillation proximity assay				J Med Chem 36: 4131-8 (1994) BindingDB Entry DOI: 10.7270/Q269746K
					More data for this Ligand-Target Pair