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Compile Data Set for Download or QSAR

Found 1102 hits with Last Name = 'lapierre' and Initial = 'j'   
Target/Host
(Institution)		LigandTarget/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		pHTemp
°C
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143951
PNG
(1-Allyloxy-3-{4-[(4-chloro-phenyl)-phenyl-methyl]-...)
Show SMILES OC(COCC=C)CN1CCN(CC1)C(c1ccccc1)c1ccc(Cl)cc1
Show InChI InChI=1S/C23H29ClN2O2/c1-2-16-28-18-22(27)17-25-12-14-26(15-13-25)23(19-6-4-3-5-7-19)20-8-10-21(24)11-9-20/h2-11,22-23,27H,1,12-18H2
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 100n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143948
PNG
(1-Phenoxy-3-{4-[phenyl-(4-trifluoromethyl-phenyl)-...)
Show SMILES OC(COc1ccccc1)CN1CCN(CC1)C(c1ccccc1)c1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C27H29F3N2O2/c28-27(29,30)23-13-11-22(12-14-23)26(21-7-3-1-4-8-21)32-17-15-31(16-18-32)19-24(33)20-34-25-9-5-2-6-10-25/h1-14,24,26,33H,15-20H2
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ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143952
PNG
(CHEMBL59712 | N-{1-[2-Hydroxy-3-(4-methoxy-phenoxy...)
Show SMILES COc1ccc(OCC(O)CN2CCC(CC2)N(C(=O)c2ccc(OC)cc2)c2ccccc2)cc1
Show InChI InChI=1S/C29H34N2O5/c1-34-26-10-8-22(9-11-26)29(33)31(23-6-4-3-5-7-23)24-16-18-30(19-17-24)20-25(32)21-36-28-14-12-27(35-2)13-15-28/h3-15,24-25,32H,16-21H2,1-2H3
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 700n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143958
PNG
(CHEMBL63060 | N-(4-Fluoro-phenyl)-N-{1-[2-hydroxy-...)
Show SMILES COc1ccc(OCC(O)CN2CCC(CC2)N(C(=O)c2ccccc2)c2ccc(F)cc2)cc1
Show InChI InChI=1S/C28H31FN2O4/c1-34-26-11-13-27(14-12-26)35-20-25(32)19-30-17-15-24(16-18-30)31(23-9-7-22(29)8-10-23)28(33)21-5-3-2-4-6-21/h2-14,24-25,32H,15-20H2,1H3
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 1.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143949
PNG
(CHEMBL60843 | N-Benzyl-2-{4-[3-(2,6-dimethyl-pheno...)
Show SMILES Cc1cccc(C)c1OCC(O)CN1CCN(CC1)C(C(=O)NCc1ccccc1)c1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C31H36F3N3O3/c1-22-7-6-8-23(2)29(22)40-21-27(38)20-36-15-17-37(18-16-36)28(25-11-13-26(14-12-25)31(32,33)34)30(39)35-19-24-9-4-3-5-10-24/h3-14,27-28,38H,15-21H2,1-2H3,(H,35,39)
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 1.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143962
PNG
(CHEMBL62878 | N-(2-{4-[3-(4-Chloro-phenoxy)-2-hydr...)
Show SMILES OC(COc1ccc(Cl)cc1)CN1CCN(CC1)C(CNC(=O)c1ccc(cc1)C(F)(F)F)c1ccccc1
Show InChI InChI=1S/C29H31ClF3N3O3/c30-24-10-12-26(13-11-24)39-20-25(37)19-35-14-16-36(17-15-35)27(21-4-2-1-3-5-21)18-34-28(38)22-6-8-23(9-7-22)29(31,32)33/h1-13,25,27,37H,14-20H2,(H,34,38)
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 1.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143945
PNG
(4-Chloro-N-{1-[2-hydroxy-3-(4-methoxy-phenoxy)-pro...)
Show SMILES COc1ccc(OCC(O)CN2CCC(CC2)N(C(=O)c2ccc(Cl)cc2)c2ccccc2)cc1
Show InChI InChI=1S/C28H31ClN2O4/c1-34-26-11-13-27(14-12-26)35-20-25(32)19-30-17-15-24(16-18-30)31(23-5-3-2-4-6-23)28(33)21-7-9-22(29)10-8-21/h2-14,24-25,32H,15-20H2,1H3
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 1.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143961
PNG
(CHEMBL62240 | N-{1-[2-Hydroxy-3-(4-methoxy-phenoxy...)
Show SMILES COc1ccc(OCC(O)CN2CCC(CC2)N(C(=O)c2ccccc2)c2ccccc2)cc1
Show InChI InChI=1S/C28H32N2O4/c1-33-26-12-14-27(15-13-26)34-21-25(31)20-29-18-16-24(17-19-29)30(23-10-6-3-7-11-23)28(32)22-8-4-2-5-9-22/h2-15,24-25,31H,16-21H2,1H3
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 2.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143974
PNG
(2-{4-[3-(2,6-Dimethyl-phenoxy)-2-hydroxy-propyl]-p...)
Show SMILES COc1ccc(CNC(=O)C(N2CCN(CC(O)COc3c(C)cccc3C)CC2)c2ccc(cc2)C(F)(F)F)cc1
Show InChI InChI=1S/C32H38F3N3O4/c1-22-5-4-6-23(2)30(22)42-21-27(39)20-37-15-17-38(18-16-37)29(25-9-11-26(12-10-25)32(33,34)35)31(40)36-19-24-7-13-28(41-3)14-8-24/h4-14,27,29,39H,15-21H2,1-3H3,(H,36,40)
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 2.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143950
PNG
(CHEMBL305591 | N-Benzyl-2-{4-[3-(2,6-dimethyl-phen...)
Show SMILES Cc1cccc(C)c1OCC(O)CN1CCN(CC1)C(C(=O)NCc1ccccc1)c1ccc(F)cc1
Show InChI InChI=1S/C30H36FN3O3/c1-22-7-6-8-23(2)29(22)37-21-27(35)20-33-15-17-34(18-16-33)28(25-11-13-26(31)14-12-25)30(36)32-19-24-9-4-3-5-10-24/h3-14,27-28,35H,15-21H2,1-2H3,(H,32,36)
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 2.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143964
PNG
(4-Chloro-N-(4-fluoro-phenyl)-N-{1-[2-hydroxy-3-(4-...)
Show SMILES COc1ccc(OCC(O)CN2CCC(CC2)N(C(=O)c2ccc(Cl)cc2)c2ccc(F)cc2)cc1
Show InChI InChI=1S/C28H30ClFN2O4/c1-35-26-10-12-27(13-11-26)36-19-25(33)18-31-16-14-24(15-17-31)32(23-8-6-22(30)7-9-23)28(34)20-2-4-21(29)5-3-20/h2-13,24-25,33H,14-19H2,1H3
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 2.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143967
PNG
(CHEMBL60568 | N-Benzyl-2-{4-[3-(2,6-dimethyl-pheno...)
Show SMILES Cc1ccc(cc1)C(N1CCN(CC(O)COc2c(C)cccc2C)CC1)C(=O)NCc1ccccc1
Show InChI InChI=1S/C31H39N3O3/c1-23-12-14-27(15-13-23)29(31(36)32-20-26-10-5-4-6-11-26)34-18-16-33(17-19-34)21-28(35)22-37-30-24(2)8-7-9-25(30)3/h4-15,28-29,35H,16-22H2,1-3H3,(H,32,36)
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 2.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143971
PNG
(CHEMBL59644 | N-Benzyl-2-{4-[2-hydroxy-3-(4-methox...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(C(=O)NCc2ccccc2)c2ccc(cc2)C(F)(F)F)cc1
Show InChI InChI=1S/C30H34F3N3O4/c1-39-26-11-13-27(14-12-26)40-21-25(37)20-35-15-17-36(18-16-35)28(23-7-9-24(10-8-23)30(31,32)33)29(38)34-19-22-5-3-2-4-6-22/h2-14,25,28,37H,15-21H2,1H3,(H,34,38)
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 2.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143954
PNG
(CHEMBL433100 | N-(4-Fluoro-phenyl)-N-{1-[2-hydroxy...)
Show SMILES COc1ccc(OCC(O)CN2CCC(CC2)N(C(=O)c2ccc(OC)cc2)c2ccc(F)cc2)cc1
Show InChI InChI=1S/C29H33FN2O5/c1-35-26-9-3-21(4-10-26)29(34)32(23-7-5-22(30)6-8-23)24-15-17-31(18-16-24)19-25(33)20-37-28-13-11-27(36-2)12-14-28/h3-14,24-25,33H,15-20H2,1-2H3
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 3.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143956
PNG
(2-{4-[3-(2,6-Dimethyl-phenoxy)-2-hydroxy-propyl]-p...)
Show SMILES COc1ccc(CNC(=O)C(N2CCN(CC(O)COc3c(C)cccc3C)CC2)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C32H41N3O4/c1-23-8-12-27(13-9-23)30(32(37)33-20-26-10-14-29(38-4)15-11-26)35-18-16-34(17-19-35)21-28(36)22-39-31-24(2)6-5-7-25(31)3/h5-15,28,30,36H,16-22H2,1-4H3,(H,33,37)
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 3.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143976
PNG
(2-{4-[3-(2,6-Dimethyl-phenoxy)-2-hydroxy-propyl]-p...)
Show SMILES COc1ccc(CNC(=O)C(N2CCN(CC(O)COc3c(C)cccc3C)CC2)c2ccc(F)cc2)cc1
Show InChI InChI=1S/C31H38FN3O4/c1-22-5-4-6-23(2)30(22)39-21-27(36)20-34-15-17-35(18-16-34)29(25-9-11-26(32)12-10-25)31(37)33-19-24-7-13-28(38-3)14-8-24/h4-14,27,29,36H,15-21H2,1-3H3,(H,33,37)
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 3.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143970
PNG
(CHEMBL61336 | N-(2-{4-[2-Hydroxy-3-(4-methoxy-phen...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(CNC(=O)c2ccc(cc2)C(F)(F)F)c2ccccc2)cc1
Show InChI InChI=1S/C30H34F3N3O4/c1-39-26-11-13-27(14-12-26)40-21-25(37)20-35-15-17-36(18-16-35)28(22-5-3-2-4-6-22)19-34-29(38)23-7-9-24(10-8-23)30(31,32)33/h2-14,25,28,37H,15-21H2,1H3,(H,34,38)
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 3.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143968
PNG
(4-Fluoro-N-(2-{4-[2-hydroxy-3-(4-methoxy-phenoxy)-...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(CNC(=O)c2ccc(F)cc2)c2ccccc2)cc1
Show InChI InChI=1S/C29H34FN3O4/c1-36-26-11-13-27(14-12-26)37-21-25(34)20-32-15-17-33(18-16-32)28(22-5-3-2-4-6-22)19-31-29(35)23-7-9-24(30)10-8-23/h2-14,25,28,34H,15-21H2,1H3,(H,31,35)
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 3.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143946
PNG
(CHEMBL64177 | N-(2-{4-[2-Hydroxy-3-(4-methoxy-phen...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(CNC(=O)c2ccccc2)c2ccccc2)cc1
Show InChI InChI=1S/C29H35N3O4/c1-35-26-12-14-27(15-13-26)36-22-25(33)21-31-16-18-32(19-17-31)28(23-8-4-2-5-9-23)20-30-29(34)24-10-6-3-7-11-24/h2-15,25,28,33H,16-22H2,1H3,(H,30,34)
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 4.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143973
PNG
(CHEMBL291629 | N-Benzyl-2-{4-[2-hydroxy-3-(4-metho...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(C(=O)NCc2ccccc2)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C30H37N3O4/c1-23-8-10-25(11-9-23)29(30(35)31-20-24-6-4-3-5-7-24)33-18-16-32(17-19-33)21-26(34)22-37-28-14-12-27(36-2)13-15-28/h3-15,26,29,34H,16-22H2,1-2H3,(H,31,35)
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 4.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143955
PNG
(2-{4-[2-Hydroxy-3-(4-methoxy-phenoxy)-propyl]-pipe...)
Show SMILES COc1ccc(CNC(=O)C(N2CCN(CC(O)COc3ccc(OC)cc3)CC2)c2ccc(cc2)C(F)(F)F)cc1
Show InChI InChI=1S/C31H36F3N3O5/c1-40-26-9-3-22(4-10-26)19-35-30(39)29(23-5-7-24(8-6-23)31(32,33)34)37-17-15-36(16-18-37)20-25(38)21-42-28-13-11-27(41-2)12-14-28/h3-14,25,29,38H,15-21H2,1-2H3,(H,35,39)
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 4.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143959
PNG
(CHEMBL61283 | N-(2-{4-[3-(4-Chloro-phenoxy)-2-hydr...)
Show SMILES COc1ccc(cc1)C(=O)NCC(N1CCN(CC(O)COc2ccc(Cl)cc2)CC1)c1ccccc1
Show InChI InChI=1S/C29H34ClN3O4/c1-36-26-11-7-23(8-12-26)29(35)31-19-28(22-5-3-2-4-6-22)33-17-15-32(16-18-33)20-25(34)21-37-27-13-9-24(30)10-14-27/h2-14,25,28,34H,15-21H2,1H3,(H,31,35)
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 4.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143957
PNG
(CHEMBL60847 | N-Benzyl-2-(4-fluoro-phenyl)-2-{4-[2...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(C(=O)NCc2ccccc2)c2ccc(F)cc2)cc1
Show InChI InChI=1S/C29H34FN3O4/c1-36-26-11-13-27(14-12-26)37-21-25(34)20-32-15-17-33(18-16-32)28(23-7-9-24(30)10-8-23)29(35)31-19-22-5-3-2-4-6-22/h2-14,25,28,34H,15-21H2,1H3,(H,31,35)
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 5.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143972
PNG
(2-{4-[3-(2,6-Dimethyl-phenoxy)-2-hydroxy-propyl]-p...)
Show SMILES COc1ccc(CNC(=O)C(N2CCN(CC(O)COc3c(C)cccc3C)CC2)c2ccc(OC)cc2)cc1
Show InChI InChI=1S/C32H41N3O5/c1-23-6-5-7-24(2)31(23)40-22-27(36)21-34-16-18-35(19-17-34)30(26-10-14-29(39-4)15-11-26)32(37)33-20-25-8-12-28(38-3)13-9-25/h5-15,27,30,36H,16-22H2,1-4H3,(H,33,37)
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 5.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143975
PNG
(2-(4-Fluoro-phenyl)-2-{4-[2-hydroxy-3-(4-methoxy-p...)
Show SMILES COc1ccc(CNC(=O)C(N2CCN(CC(O)COc3ccc(OC)cc3)CC2)c2ccc(F)cc2)cc1
Show InChI InChI=1S/C30H36FN3O5/c1-37-26-9-3-22(4-10-26)19-32-30(36)29(23-5-7-24(31)8-6-23)34-17-15-33(16-18-34)20-25(35)21-39-28-13-11-27(38-2)12-14-28/h3-14,25,29,35H,15-21H2,1-2H3,(H,32,36)
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 7.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143947
PNG
(4-Fluoro-N-{2-[4-(2-hydroxy-3-phenoxy-propyl)-pipe...)
Show SMILES OC(COc1ccccc1)CN1CCN(CC1)C(CNC(=O)c1ccc(F)cc1)c1ccccc1
Show InChI InChI=1S/C28H32FN3O3/c29-24-13-11-23(12-14-24)28(34)30-19-27(22-7-3-1-4-8-22)32-17-15-31(16-18-32)20-25(33)21-35-26-9-5-2-6-10-26/h1-14,25,27,33H,15-21H2,(H,30,34)
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 7.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143965
PNG
(CHEMBL60666 | N-(2-{4-[3-(4-Chloro-phenoxy)-2-hydr...)
Show SMILES COc1ccccc1C(=O)NCC(N1CCN(CC(O)COc2ccc(Cl)cc2)CC1)c1ccccc1
Show InChI InChI=1S/C29H34ClN3O4/c1-36-28-10-6-5-9-26(28)29(35)31-19-27(22-7-3-2-4-8-22)33-17-15-32(16-18-33)20-24(34)21-37-25-13-11-23(30)12-14-25/h2-14,24,27,34H,15-21H2,1H3,(H,31,35)
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 7.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143960
PNG
(CHEMBL64688 | N-(2-{4-[2-Hydroxy-3-(4-methoxy-phen...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(CNC(=O)c2ccccc2OC)c2ccccc2)cc1
Show InChI InChI=1S/C30H37N3O5/c1-36-25-12-14-26(15-13-25)38-22-24(34)21-32-16-18-33(19-17-32)28(23-8-4-3-5-9-23)20-31-30(35)27-10-6-7-11-29(27)37-2/h3-15,24,28,34H,16-22H2,1-2H3,(H,31,35)
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 8.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143953
PNG
(CHEMBL64831 | N-(2-{4-[2-Hydroxy-3-(4-methoxy-phen...)
Show SMILES COc1ccc(OCC(O)CN2CCN(CC2)C(CNC(=O)c2ccc(OC)cc2)c2ccccc2)cc1
Show InChI InChI=1S/C30H37N3O5/c1-36-26-10-8-24(9-11-26)30(35)31-20-29(23-6-4-3-5-7-23)33-18-16-32(17-19-33)21-25(34)22-38-28-14-12-27(37-2)13-15-28/h3-15,25,29,34H,16-22H2,1-2H3,(H,31,35)
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 8.00E+3n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143966
PNG
(2-Chloro-N-[2-{4-[3-(4-fluoro-phenoxy)-2-hydroxy-p...)
Show SMILES OC(COc1ccc(F)cc1)CN1CCN(CC1)C(CNS(=O)(=O)c1ccccc1Cl)c1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C28H30ClF4N3O4S/c29-25-3-1-2-4-27(25)41(38,39)34-17-26(20-5-7-21(8-6-20)28(31,32)33)36-15-13-35(14-16-36)18-23(37)19-40-24-11-9-22(30)10-12-24/h1-12,23,26,34,37H,13-19H2
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 1.00E+4n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143963
PNG
(CHEMBL64869 | N-[2-{4-[3-(4-Bromo-phenoxy)-2-hydro...)
Show SMILES Cc1cccc(c1)S(=O)(=O)NCC(N1CCN(CC(O)COc2ccc(Br)cc2)CC1)c1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C29H33BrF3N3O4S/c1-21-3-2-4-27(17-21)41(38,39)34-18-28(22-5-7-23(8-6-22)29(31,32)33)36-15-13-35(14-16-36)19-25(37)20-40-26-11-9-24(30)10-12-26/h2-12,17,25,28,34,37H,13-16,18-20H2,1H3
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 1.00E+4n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50223216
PNG
(CHEMBL3348562)
Show SMILES [H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])c3ccc(cc3CC[C@@]21[H])C(F)(F)C1N=NN=N1 |c:30,32|
Show InChI InChI=1S/C20H22F2N4O/c1-19-9-8-14-13-5-3-12(20(21,22)18-23-25-26-24-18)10-11(13)2-4-15(14)16(19)6-7-17(19)27/h3,5,10,14-16,18H,2,4,6-9H2,1H3/t14-,15-,16+,19+/m1/s1
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 1.60E+4n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibitory activity against steroid sulfatase (STS)

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))		BDBM50143969
PNG
(CHEMBL64583 | N-(2-{4-[3-(4-Bromo-phenoxy)-2-hydro...)
Show SMILES COc1ccc(OC)c(c1)S(=O)(=O)NCC(N1CCN(CC(O)COc2ccc(Br)cc2)CC1)c1ccccc1
Show InChI InChI=1S/C29H36BrN3O6S/c1-37-26-12-13-28(38-2)29(18-26)40(35,36)31-19-27(22-6-4-3-5-7-22)33-16-14-32(15-17-33)20-24(34)21-39-25-10-8-23(30)9-11-25/h3-13,18,24,27,31,34H,14-17,19-21H2,1-2H3
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 3.00E+4n/an/an/an/an/an/an/an/a



ArQule Inc

Curated by ChEMBL


Assay Description
Predictive competitive inhibition of cytochrome P450 2D6 was determined in silico

Bioorg Med Chem Lett 14: 2025-30 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.078
BindingDB Entry DOI: 10.7270/Q22J6B8R
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50366887
PNG
(CHEMBL1627329)
Show SMILES C[C@]12CC[C@H]3[C@@H](CCc4cc(ccc34)C(F)(F)S(O)(=O)=O)[C@@H]1CCC2C=O |r|
Show InChI InChI=1S/C20H24F2O4S/c1-19-9-8-16-15-6-3-13(20(21,22)27(24,25)26)10-12(15)2-5-17(16)18(19)7-4-14(19)11-23/h3,6,10-11,14,16-18H,2,4-5,7-9H2,1H3,(H,24,25,26)/t14?,16-,17-,18+,19-/m1/s1
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 3.70E+4n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibitory activity against steroid sulfatase (STS)

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50366886
PNG
(CHEMBL1628110)
Show SMILES C[C@]12CC[C@H]3[C@@H](CCc4cc(ccc34)C(F)(F)S(O)(=O)=O)[C@@H]1CCC2=O |r|
Show InChI InChI=1S/C19H22F2O4S/c1-18-9-8-14-13-5-3-12(19(20,21)26(23,24)25)10-11(13)2-4-15(14)16(18)6-7-17(18)22/h3,5,10,14-16H,2,4,6-9H2,1H3,(H,23,24,25)/t14-,15-,16+,18+/m1/s1
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 5.70E+4n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Competitive inhibitory activity against steroid sulfatase (STS)

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50366524
PNG
(ESTRONE | ESTROPIPATE | Estrone 3-sulfate | Estron...)
Show SMILES C[C@]12CC[C@H]3[C@@H](CCc4cc(OS(O)(=O)=O)ccc34)[C@@H]1CCC2=O
Show InChI InChI=1S/C18H22O5S/c1-18-9-8-14-13-5-3-12(23-24(20,21)22)10-11(13)2-4-15(14)16(18)6-7-17(18)19/h3,5,10,14-16H,2,4,6-9H2,1H3,(H,20,21,22)/t14-,15-,16+,18+/m1/s1
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 6.00E+4n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibitory activity against steroid sulfatase (STS) desulfation of 4-MUS

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50366888
PNG
(CHEMBL1627836)
Show SMILES C[C@]12CC[C@H]3[C@@H](CCc4cc(Cc5nnn[nH]5)ccc34)[C@@H]1CCC2=O
Show InChI InChI=1S/C20H24N4O/c1-20-9-8-15-14-4-2-12(11-19-21-23-24-22-19)10-13(14)3-5-16(15)17(20)6-7-18(20)25/h2,4,10,15-17H,3,5-9,11H2,1H3,(H,21,22,23,24)/t15-,16-,17+,20+/m1/s1
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 7.27E+4n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibitory activity against steroid sulfatase (STS)

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50366884
PNG
(CHEMBL1628109)
Show SMILES C[C@]12CC[C@H]3[C@@H](CCc4cc(CS(O)(=O)=O)ccc34)[C@@H]1CCC2=O |r|
Show InChI InChI=1S/C19H24O4S/c1-19-9-8-15-14-4-2-12(11-24(21,22)23)10-13(14)3-5-16(15)17(19)6-7-18(19)20/h2,4,10,15-17H,3,5-9,11H2,1H3,(H,21,22,23)/t15-,16-,17+,19+/m1/s1
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 1.40E+5n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibitory activity against steroid sulfatase (STS)

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50366885
PNG
(CHEMBL1628114)
Show SMILES C[C@]12CC[C@H]3[C@@H](CCc4cc(CS(O)(=O)=O)ccc34)[C@@H]1CCC2C=O |r|
Show InChI InChI=1S/C20H26O4S/c1-20-9-8-17-16-5-2-13(12-25(22,23)24)10-14(16)3-6-18(17)19(20)7-4-15(20)11-21/h2,5,10-11,15,17-19H,3-4,6-9,12H2,1H3,(H,22,23,24)/t15?,17-,18-,19+,20-/m1/s1
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 1.40E+5n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibitory activity against steroid sulfatase (STS)

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Steryl-sulfatase


(Homo sapiens (Human))		BDBM50366884
PNG
(CHEMBL1628109)
Show SMILES C[C@]12CC[C@H]3[C@@H](CCc4cc(CS(O)(=O)=O)ccc34)[C@@H]1CCC2=O |r|
Show InChI InChI=1S/C19H24O4S/c1-19-9-8-15-14-4-2-12(11-24(21,22)23)10-13(14)3-5-16(15)17(19)6-7-18(19)20/h2,4,10,15-17H,3,5-9,11H2,1H3,(H,21,22,23)/t15-,16-,17+,19+/m1/s1
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 6.00E+5n/an/an/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibitory activity against steroid sulfatase (STS) using methodology of Li et al.

Bioorg Med Chem Lett 14: 151-5 (2003)


BindingDB Entry DOI: 10.7270/Q28K79NV
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK [C481S]


(Homo sapiens (Human))		BDBM499813
PNG
((2-chloro-4-phenoxyphenyl)(4- (((3R,6R)-6-(hydroxy...)
Show SMILES OC[C@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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US Patent
n/an/a 0.370n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Enzyme assay using full length recombinant active form of wild-type BTK and BTK-C481S was measured as described previously (Anastassiadis T, et al., ...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK [C481S]


(Homo sapiens (Human))		BDBM499811
PNG
(US11020398, Compound I-123 | US20230364079, Exampl...)
Show SMILES OC[C@@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.390n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Enzyme assay using full length recombinant active form of wild-type BTK and BTK-C481S was measured as described previously (Anastassiadis T, et al., ...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair		3D
3D Structure (crystal)
Tyrosine-protein kinase BTK


(Homo sapiens (Human))		BDBM499813
PNG
((2-chloro-4-phenoxyphenyl)(4- (((3R,6R)-6-(hydroxy...)
Show SMILES OC[C@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.560n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Enzyme assay using full length recombinant active form of wild-type BTK and BTK-C481S was measured as described previously (Anastassiadis T, et al., ...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))		BDBM499813
PNG
((2-chloro-4-phenoxyphenyl)(4- (((3R,6R)-6-(hydroxy...)
Show SMILES OC[C@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.560n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Enzyme assay using full length recombinant active form of wild-type BTK and BTK-C481S was measured as described previously (Anastassiadis T, et al., ...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))		BDBM499810
PNG
(N-((S)-1-((2S,5R)-5-((5-(2-chloro-4- phenoxybenzoy...)
Show SMILES C[C@H](NC(C)=O)[C@@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.770n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Full length unphosphorylated form of BTK expressed in Sf9 cells was employed to test inhibitory activity in the inactive BTK assay. The assay was mea...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK [C481S]


(Homo sapiens (Human))		BDBM499814
PNG
((2-chloro-4-phenoxyphenyl)(4- (((3S,6S)-6-(hydroxy...)
Show SMILES OC[C@@H]1CC[C@@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.790n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Enzyme assay using full length recombinant active form of wild-type BTK and BTK-C481S was measured as described previously (Anastassiadis T, et al., ...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))		BDBM499811
PNG
(US11020398, Compound I-123 | US20230364079, Exampl...)
Show SMILES OC[C@@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.850n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Enzyme assay using full length recombinant active form of wild-type BTK and BTK-C481S was measured as described previously (Anastassiadis T, et al., ...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair		3D
3D Structure (crystal)
Tyrosine-protein kinase BTK


(Homo sapiens (Human))		BDBM499811
PNG
(US11020398, Compound I-123 | US20230364079, Exampl...)
Show SMILES OC[C@@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.850n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Enzyme assay using full length recombinant active form of wild-type BTK and BTK-C481S was measured as described previously (Anastassiadis T, et al., ...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair		3D
3D Structure (crystal)
Tyrosine-protein kinase BTK


(Homo sapiens (Human))		BDBM499838
PNG
((2-chloro-4-phenoxyphenyl)(4- (((3R,6S)-6-((R)-1- ...)
Show SMILES C[C@@H](O)[C@@H]1CC[C@H](CO1)Nc1ncnc2[nH]cc(C(=O)c3ccc(Oc4ccccc4)cc3Cl)c12 |r|
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n/an/a 0.930n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Full length unphosphorylated form of BTK expressed in Sf9 cells was employed to test inhibitory activity in the inactive BTK assay. The assay was mea...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))		BDBM499976
PNG
((racemic)-1-(2-(((5-(2-chloro-4- phenoxybenzoyl)-7...)
Show SMILES Clc1cc(Oc2ccccc2)ccc1C(=O)c1c[nH]c2ncnc(NCC3CCCN3C(=O)C=C)c12 |w:25.27|
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n/an/a 0.980n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Purified full-length inactive BTK (wild type and C481 mutant, N-terminal 6XHIS tagged BTK, Mwt=78.2 kDa) were activated using soluble inositol hexaki...

US Patent US11020398 (2021)


BindingDB Entry DOI: 10.7270/Q2DZ0CFC
More data for this
Ligand-Target Pair
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