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PubMed code 7608909

Compile data set for download or QSAR
Found 66 hits of Enzyme Inhibition Constant Data   
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
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031643
PNG
(1-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-prope...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C19H21NO2/c1-15(13-20(2)3)19(21)17-9-11-18(12-10-17)22-14-16-7-5-4-6-8-16/h4-12H,1,13-14H2,2-3H3
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n/an/a 180n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031651
PNG
(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(cc2)C(O)=O)cc1
Show InChI InChI=1S/C19H19NO6S/c1-13(12-20(2)3)18(21)14-4-8-16(9-5-14)26-27(24,25)17-10-6-15(7-11-17)19(22)23/h4-11H,1,12H2,2-3H3,(H,22,23)
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n/an/a 230n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031655
PNG
(1-[3-(4-Benzyloxy-phenyl)-3-oxo-propyl]-piperidine...)
Show SMILES CCOC(=O)C1CCN(CCC(=O)c2ccc(OCc3ccccc3)cc2)CC1
Show InChI InChI=1S/C24H29NO4/c1-2-28-24(27)21-12-15-25(16-13-21)17-14-23(26)20-8-10-22(11-9-20)29-18-19-6-4-3-5-7-19/h3-11,21H,2,12-18H2,1H3
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n/an/a 300n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031657
PNG
(1-(4-Benzyloxy-3-hydroxy-phenyl)-3-dimethylamino-p...)
Show SMILES CN(C)CCC(=O)c1ccc(OCc2ccccc2)c(O)c1
Show InChI InChI=1S/C18H21NO3/c1-19(2)11-10-16(20)15-8-9-18(17(21)12-15)22-13-14-6-4-3-5-7-14/h3-9,12,21H,10-11,13H2,1-2H3
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n/an/a 360n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031659
PNG
(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(C(O)=O)c(O)c2)cc1
Show InChI InChI=1S/C19H19NO7S/c1-12(11-20(2)3)18(22)13-4-6-14(7-5-13)27-28(25,26)15-8-9-16(19(23)24)17(21)10-15/h4-10,21H,1,11H2,2-3H3,(H,23,24)
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n/an/a 470n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031648
PNG
(1-(4-Benzyloxy-3-hydroxy-phenyl)-2-dimethylaminome...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OCc2ccccc2)c(O)c1
Show InChI InChI=1S/C19H21NO3/c1-14(12-20(2)3)19(22)16-9-10-18(17(21)11-16)23-13-15-7-5-4-6-8-15/h4-11,21H,1,12-13H2,2-3H3
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n/an/a 670n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031642
PNG
(4-Dimethylcarbamoyl-benzenesulfonic acid 4-(2-dime...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(cc2)C(=O)N(C)C)cc1
Show InChI InChI=1S/C21H24N2O5S/c1-15(14-22(2)3)20(24)16-6-10-18(11-7-16)28-29(26,27)19-12-8-17(9-13-19)21(25)23(4)5/h6-13H,1,14H2,2-5H3
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n/an/a 700n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM19459
PNG
(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)
Show SMILES Oc1ccc(cc1)-c1coc2cc(O)cc(O)c2c1=O
Show InChI InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H
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n/an/a 1.00E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031647
PNG
(1-(4-Benzyloxy-phenyl)-2-piperidin-1-ylmethyl-prop...)
Show SMILES C=C(CN1CCCCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C22H25NO2/c1-18(16-23-14-6-3-7-15-23)22(24)20-10-12-21(13-11-20)25-17-19-8-4-2-5-9-19/h2,4-5,8-13H,1,3,6-7,14-17H2
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n/an/a 1.10E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031662
PNG
(1-(4-Benzyloxy-phenyl)-2-morpholin-4-ylmethyl-prop...)
Show SMILES C=C(CN1CCOCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H23NO3/c1-17(15-22-11-13-24-14-12-22)21(23)19-7-9-20(10-8-19)25-16-18-5-3-2-4-6-18/h2-10H,1,11-16H2
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n/an/a 1.10E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031661
PNG
(1-(4-Benzyloxy-phenyl)-3-morpholin-4-yl-propan-1-o...)
Show SMILES O=C(CCN1CCOCC1)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C20H23NO3/c22-20(10-11-21-12-14-23-15-13-21)18-6-8-19(9-7-18)24-16-17-4-2-1-3-5-17/h1-9H,10-16H2
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n/an/a 1.50E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031646
PNG
(1-(4-Benzyloxy-phenyl)-2-piperazin-1-ylmethyl-prop...)
Show SMILES C=C(CN1CCNCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H24N2O2/c1-17(15-23-13-11-22-12-14-23)21(24)19-7-9-20(10-8-19)25-16-18-5-3-2-4-6-18/h2-10,22H,1,11-16H2
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n/an/a 1.50E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031660
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-propan-1-on...)
Show SMILES CN(C)CCC(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C18H21NO2/c1-19(2)13-12-18(20)16-8-10-17(11-9-16)21-14-15-6-4-3-5-7-15/h3-11H,12-14H2,1-2H3
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n/an/a 1.50E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031658
PNG
(1-(4-Benzyloxy-phenyl)-3-piperidin-1-yl-propan-1-o...)
Show SMILES O=C(CCN1CCCCC1)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H25NO2/c23-21(13-16-22-14-5-2-6-15-22)19-9-11-20(12-10-19)24-17-18-7-3-1-4-8-18/h1,3-4,7-12H,2,5-6,13-17H2
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n/an/a 1.80E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031644
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-(3,4-dime...)
Show SMILES CN(C)CC(CSc1ccc(C)c(C)c1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C27H31NO2S/c1-20-10-15-26(16-21(20)2)31-19-24(17-28(3)4)27(29)23-11-13-25(14-12-23)30-18-22-8-6-5-7-9-22/h5-16,24H,17-19H2,1-4H3
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n/an/a 2.10E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031649
PNG
(2-{3-(4-benzyloxy)-2-[(dimethylamino)methyl]-3-oxo...)
Show SMILES CN(C)CC(CNNC(N)=O)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C20H26N4O3/c1-24(2)13-17(12-22-23-20(21)26)19(25)16-8-10-18(11-9-16)27-14-15-6-4-3-5-7-15/h3-11,17,22H,12-14H2,1-2H3,(H3,21,23,26)
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n/an/a 3.90E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50369028
PNG
(CHEMBL468975)
Show SMILES CN(C)CC(=C)C(=O)c1ccccc1
Show InChI InChI=1S/C12H15NO/c1-10(9-13(2)3)12(14)11-7-5-4-6-8-11/h4-8H,1,9H2,2-3H3
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n/an/a 5.60E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031656
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-phenylsul...)
Show SMILES CN(C)CC(CSc1ccccc1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C25H27NO2S/c1-26(2)17-22(19-29-24-11-7-4-8-12-24)25(27)21-13-15-23(16-14-21)28-18-20-9-5-3-6-10-20/h3-16,22H,17-19H2,1-2H3
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n/an/a 7.30E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031653
PNG
(2-(2-Amino-ethylsulfanylmethyl)-1-(4-benzyloxy-phe...)
Show SMILES CN(C)CC(CSCCN)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H28N2O2S/c1-23(2)14-19(16-26-13-12-22)21(24)18-8-10-20(11-9-18)25-15-17-6-4-3-5-7-17/h3-11,19H,12-16,22H2,1-2H3
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n/an/a 8.80E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031650
PNG
(2-[3-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-3-...)
Show SMILES COC(=O)c1ccccc1SCC(CN(C)C)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C27H29NO4S/c1-28(2)17-22(19-33-25-12-8-7-11-24(25)27(30)31-3)26(29)21-13-15-23(16-14-21)32-18-20-9-5-4-6-10-20/h4-16,22H,17-19H2,1-3H3
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n/an/a 8.80E+3n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM19459
PNG
(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)
Show SMILES Oc1ccc(cc1)-c1coc2cc(O)cc(O)c2c1=O
Show InChI InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H
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n/an/a 1.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031656
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-phenylsul...)
Show SMILES CN(C)CC(CSc1ccccc1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C25H27NO2S/c1-26(2)17-22(19-29-24-11-7-4-8-12-24)25(27)21-13-15-23(16-14-21)28-18-20-9-5-3-6-10-20/h3-16,22H,17-19H2,1-2H3
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n/an/a>5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031648
PNG
(1-(4-Benzyloxy-3-hydroxy-phenyl)-2-dimethylaminome...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OCc2ccccc2)c(O)c1
Show InChI InChI=1S/C19H21NO3/c1-14(12-20(2)3)19(22)16-9-10-18(17(21)11-16)23-13-15-7-5-4-6-8-15/h4-11,21H,1,12-13H2,2-3H3
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n/an/a 5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031656
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-phenylsul...)
Show SMILES CN(C)CC(CSc1ccccc1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C25H27NO2S/c1-26(2)17-22(19-29-24-11-7-4-8-12-24)25(27)21-13-15-23(16-14-21)28-18-20-9-5-3-6-10-20/h3-16,22H,17-19H2,1-2H3
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n/an/a>5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031651
PNG
(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(cc2)C(O)=O)cc1
Show InChI InChI=1S/C19H19NO6S/c1-13(12-20(2)3)18(21)14-4-8-16(9-5-14)26-27(24,25)17-10-6-15(7-11-17)19(22)23/h4-11H,1,12H2,2-3H3,(H,22,23)
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n/an/a 5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031659
PNG
(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(C(O)=O)c(O)c2)cc1
Show InChI InChI=1S/C19H19NO7S/c1-12(11-20(2)3)18(22)13-4-6-14(7-5-13)27-28(25,26)15-8-9-16(19(23)24)17(21)10-15/h4-10,21H,1,11H2,2-3H3,(H,23,24)
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n/an/a 5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031659
PNG
(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(C(O)=O)c(O)c2)cc1
Show InChI InChI=1S/C19H19NO7S/c1-12(11-20(2)3)18(22)13-4-6-14(7-5-13)27-28(25,26)15-8-9-16(19(23)24)17(21)10-15/h4-10,21H,1,11H2,2-3H3,(H,23,24)
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n/an/a>5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031657
PNG
(1-(4-Benzyloxy-3-hydroxy-phenyl)-3-dimethylamino-p...)
Show SMILES CN(C)CCC(=O)c1ccc(OCc2ccccc2)c(O)c1
Show InChI InChI=1S/C18H21NO3/c1-19(2)11-10-16(20)15-8-9-18(17(21)12-15)22-13-14-6-4-3-5-7-14/h3-9,12,21H,10-11,13H2,1-2H3
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n/an/a>5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031642
PNG
(4-Dimethylcarbamoyl-benzenesulfonic acid 4-(2-dime...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(cc2)C(=O)N(C)C)cc1
Show InChI InChI=1S/C21H24N2O5S/c1-15(14-22(2)3)20(24)16-6-10-18(11-7-16)28-29(26,27)19-12-8-17(9-13-19)21(25)23(4)5/h6-13H,1,14H2,2-5H3
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n/an/a>5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031653
PNG
(2-(2-Amino-ethylsulfanylmethyl)-1-(4-benzyloxy-phe...)
Show SMILES CN(C)CC(CSCCN)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H28N2O2S/c1-23(2)14-19(16-26-13-12-22)21(24)18-8-10-20(11-9-18)25-15-17-6-4-3-5-7-17/h3-11,19H,12-16,22H2,1-2H3
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n/an/a>5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031648
PNG
(1-(4-Benzyloxy-3-hydroxy-phenyl)-2-dimethylaminome...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OCc2ccccc2)c(O)c1
Show InChI InChI=1S/C19H21NO3/c1-14(12-20(2)3)19(22)16-9-10-18(17(21)11-16)23-13-15-7-5-4-6-8-15/h4-11,21H,1,12-13H2,2-3H3
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n/an/a>5.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031654
PNG
(2-Cyano-2-(3,4-dihydroxy-benzyl)-thioacetamide | C...)
Show SMILES NC(=S)C(Cc1ccc(O)c(O)c1)C#N
Show InChI InChI=1S/C10H10N2O2S/c11-5-7(10(12)15)3-6-1-2-8(13)9(14)4-6/h1-2,4,7,13-14H,3H2,(H2,12,15)
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n/an/a 7.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031642
PNG
(4-Dimethylcarbamoyl-benzenesulfonic acid 4-(2-dime...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(cc2)C(=O)N(C)C)cc1
Show InChI InChI=1S/C21H24N2O5S/c1-15(14-22(2)3)20(24)16-6-10-18(11-7-16)28-29(26,27)19-12-8-17(9-13-19)21(25)23(4)5/h6-13H,1,14H2,2-5H3
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n/an/a 7.00E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM19459
PNG
(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)
Show SMILES Oc1ccc(cc1)-c1coc2cc(O)cc(O)c2c1=O
Show InChI InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H
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n/an/a 7.50E+4n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031661
PNG
(1-(4-Benzyloxy-phenyl)-3-morpholin-4-yl-propan-1-o...)
Show SMILES O=C(CCN1CCOCC1)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C20H23NO3/c22-20(10-11-21-12-14-23-15-13-21)18-6-8-19(9-7-18)24-16-17-4-2-1-3-5-17/h1-9H,10-16H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031658
PNG
(1-(4-Benzyloxy-phenyl)-3-piperidin-1-yl-propan-1-o...)
Show SMILES O=C(CCN1CCCCC1)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H25NO2/c23-21(13-16-22-14-5-2-6-15-22)19-9-11-20(12-10-19)24-17-18-7-3-1-4-8-18/h1,3-4,7-12H,2,5-6,13-17H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031654
PNG
(2-Cyano-2-(3,4-dihydroxy-benzyl)-thioacetamide | C...)
Show SMILES NC(=S)C(Cc1ccc(O)c(O)c1)C#N
Show InChI InChI=1S/C10H10N2O2S/c11-5-7(10(12)15)3-6-1-2-8(13)9(14)4-6/h1-2,4,7,13-14H,3H2,(H2,12,15)
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031655
PNG
(1-[3-(4-Benzyloxy-phenyl)-3-oxo-propyl]-piperidine...)
Show SMILES CCOC(=O)C1CCN(CCC(=O)c2ccc(OCc3ccccc3)cc2)CC1
Show InChI InChI=1S/C24H29NO4/c1-2-28-24(27)21-12-15-25(16-13-21)17-14-23(26)20-8-10-22(11-9-20)29-18-19-6-4-3-5-7-19/h3-11,21H,2,12-18H2,1H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031654
PNG
(2-Cyano-2-(3,4-dihydroxy-benzyl)-thioacetamide | C...)
Show SMILES NC(=S)C(Cc1ccc(O)c(O)c1)C#N
Show InChI InChI=1S/C10H10N2O2S/c11-5-7(10(12)15)3-6-1-2-8(13)9(14)4-6/h1-2,4,7,13-14H,3H2,(H2,12,15)
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031652
PNG
(4-[4-(3-Dimethylamino-2-methyl-propionyl)-phenoxys...)
Show SMILES CC(CN(C)C)C(=O)c1ccc(OS(=O)(=O)c2ccc(cc2)C(O)=O)cc1
Show InChI InChI=1S/C19H21NO6S/c1-13(12-20(2)3)18(21)14-4-8-16(9-5-14)26-27(24,25)17-10-6-15(7-11-17)19(22)23/h4-11,13H,12H2,1-3H3,(H,22,23)
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n/an/a 1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031650
PNG
(2-[3-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-3-...)
Show SMILES COC(=O)c1ccccc1SCC(CN(C)C)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C27H29NO4S/c1-28(2)17-22(19-33-25-12-8-7-11-24(25)27(30)31-3)26(29)21-13-15-23(16-14-21)32-18-20-9-5-4-6-10-20/h4-16,22H,17-19H2,1-3H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031660
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-propan-1-on...)
Show SMILES CN(C)CCC(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C18H21NO2/c1-19(2)13-12-18(20)16-8-10-17(11-9-16)21-14-15-6-4-3-5-7-15/h3-11H,12-14H2,1-2H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031644
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-(3,4-dime...)
Show SMILES CN(C)CC(CSc1ccc(C)c(C)c1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C27H31NO2S/c1-20-10-15-26(16-21(20)2)31-19-24(17-28(3)4)27(29)23-11-13-25(14-12-23)30-18-22-8-6-5-7-9-22/h5-16,24H,17-19H2,1-4H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031644
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-(3,4-dime...)
Show SMILES CN(C)CC(CSc1ccc(C)c(C)c1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C27H31NO2S/c1-20-10-15-26(16-21(20)2)31-19-24(17-28(3)4)27(29)23-11-13-25(14-12-23)30-18-22-8-6-5-7-9-22/h5-16,24H,17-19H2,1-4H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50369028
PNG
(CHEMBL468975)
Show SMILES CN(C)CC(=C)C(=O)c1ccccc1
Show InChI InChI=1S/C12H15NO/c1-10(9-13(2)3)12(14)11-7-5-4-6-8-11/h4-8H,1,9H2,2-3H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031658
PNG
(1-(4-Benzyloxy-phenyl)-3-piperidin-1-yl-propan-1-o...)
Show SMILES O=C(CCN1CCCCC1)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H25NO2/c23-21(13-16-22-14-5-2-6-15-22)19-9-11-20(12-10-19)24-17-18-7-3-1-4-8-18/h1,3-4,7-12H,2,5-6,13-17H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031655
PNG
(1-[3-(4-Benzyloxy-phenyl)-3-oxo-propyl]-piperidine...)
Show SMILES CCOC(=O)C1CCN(CCC(=O)c2ccc(OCc3ccccc3)cc2)CC1
Show InChI InChI=1S/C24H29NO4/c1-2-28-24(27)21-12-15-25(16-13-21)17-14-23(26)20-8-10-22(11-9-20)29-18-19-6-4-3-5-7-19/h3-11,21H,2,12-18H2,1H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031647
PNG
(1-(4-Benzyloxy-phenyl)-2-piperidin-1-ylmethyl-prop...)
Show SMILES C=C(CN1CCCCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C22H25NO2/c1-18(16-23-14-6-3-7-15-23)22(24)20-10-12-21(13-11-20)25-17-19-8-4-2-5-9-19/h2,4-5,8-13H,1,3,6-7,14-17H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031650
PNG
(2-[3-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-3-...)
Show SMILES COC(=O)c1ccccc1SCC(CN(C)C)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C27H29NO4S/c1-28(2)17-22(19-33-25-12-8-7-11-24(25)27(30)31-3)26(29)21-13-15-23(16-14-21)32-18-20-9-5-4-6-10-20/h4-16,22H,17-19H2,1-3H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031643
PNG
(1-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-prope...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C19H21NO2/c1-15(13-20(2)3)19(21)17-9-11-18(12-10-17)22-14-16-7-5-4-6-8-16/h4-12H,1,13-14H2,2-3H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))		BDBM50031645
PNG
(1-(4-Benzyloxy-phenyl)-4-dimethylamino-butan-1-one...)
Show SMILES CN(C)CCCC(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C19H23NO2/c1-20(2)14-6-9-19(21)17-10-12-18(13-11-17)22-15-16-7-4-3-5-8-16/h3-5,7-8,10-13H,6,9,14-15H2,1-2H3
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranes

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031653
PNG
(2-(2-Amino-ethylsulfanylmethyl)-1-(4-benzyloxy-phe...)
Show SMILES CN(C)CC(CSCCN)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H28N2O2S/c1-23(2)14-19(16-26-13-12-22)21(24)18-8-10-20(11-9-18)25-15-17-6-4-3-5-7-17/h3-11,19H,12-16,22H2,1-2H3
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031649
PNG
(2-{3-(4-benzyloxy)-2-[(dimethylamino)methyl]-3-oxo...)
Show SMILES CN(C)CC(CNNC(N)=O)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C20H26N4O3/c1-24(2)13-17(12-22-23-20(21)26)19(25)16-8-10-18(11-9-16)27-14-15-6-4-3-5-7-15/h3-11,17,22H,12-14H2,1-2H3,(H3,21,23,26)
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031662
PNG
(1-(4-Benzyloxy-phenyl)-2-morpholin-4-ylmethyl-prop...)
Show SMILES C=C(CN1CCOCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H23NO3/c1-17(15-22-11-13-24-14-12-22)21(23)19-7-9-20(10-8-19)25-16-18-5-3-2-4-6-18/h2-10H,1,11-16H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031657
PNG
(1-(4-Benzyloxy-3-hydroxy-phenyl)-3-dimethylamino-p...)
Show SMILES CN(C)CCC(=O)c1ccc(OCc2ccccc2)c(O)c1
Show InChI InChI=1S/C18H21NO3/c1-19(2)11-10-16(20)15-8-9-18(17(21)12-15)22-13-14-6-4-3-5-7-14/h3-9,12,21H,10-11,13H2,1-2H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031646
PNG
(1-(4-Benzyloxy-phenyl)-2-piperazin-1-ylmethyl-prop...)
Show SMILES C=C(CN1CCNCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H24N2O2/c1-17(15-23-13-11-22-12-14-23)21(24)19-7-9-20(10-8-19)25-16-18-5-3-2-4-6-18/h2-10,22H,1,11-16H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031643
PNG
(1-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-prope...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C19H21NO2/c1-15(13-20(2)3)19(21)17-9-11-18(12-10-17)22-14-16-7-5-4-6-8-16/h4-12H,1,13-14H2,2-3H3
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031646
PNG
(1-(4-Benzyloxy-phenyl)-2-piperazin-1-ylmethyl-prop...)
Show SMILES C=C(CN1CCNCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H24N2O2/c1-17(15-23-13-11-22-12-14-23)21(24)19-7-9-20(10-8-19)25-16-18-5-3-2-4-6-18/h2-10,22H,1,11-16H2
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031649
PNG
(2-{3-(4-benzyloxy)-2-[(dimethylamino)methyl]-3-oxo...)
Show SMILES CN(C)CC(CNNC(N)=O)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C20H26N4O3/c1-24(2)13-17(12-22-23-20(21)26)19(25)16-8-10-18(11-9-16)27-14-15-6-4-3-5-7-15/h3-11,17,22H,12-14H2,1-2H3,(H3,21,23,26)
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031660
PNG
(1-(4-Benzyloxy-phenyl)-3-dimethylamino-propan-1-on...)
Show SMILES CN(C)CCC(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C18H21NO2/c1-19(2)13-12-18(20)16-8-10-17(11-9-16)21-14-15-6-4-3-5-7-15/h3-11H,12-14H2,1-2H3
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031651
PNG
(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)
Show SMILES CN(C)CC(=C)C(=O)c1ccc(OS(=O)(=O)c2ccc(cc2)C(O)=O)cc1
Show InChI InChI=1S/C19H19NO6S/c1-13(12-20(2)3)18(21)14-4-8-16(9-5-14)26-27(24,25)17-10-6-15(7-11-17)19(22)23/h4-11H,1,12H2,2-3H3,(H,22,23)
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031661
PNG
(1-(4-Benzyloxy-phenyl)-3-morpholin-4-yl-propan-1-o...)
Show SMILES O=C(CCN1CCOCC1)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C20H23NO3/c22-20(10-11-21-12-14-23-15-13-21)18-6-8-19(9-7-18)24-16-17-4-2-1-3-5-17/h1-9H,10-16H2
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031662
PNG
(1-(4-Benzyloxy-phenyl)-2-morpholin-4-ylmethyl-prop...)
Show SMILES C=C(CN1CCOCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H23NO3/c1-17(15-22-11-13-24-14-12-22)21(23)19-7-9-20(10-8-19)25-16-18-5-3-2-4-6-18/h2-10H,1,11-16H2
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CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))		BDBM50031647
PNG
(1-(4-Benzyloxy-phenyl)-2-piperidin-1-ylmethyl-prop...)
Show SMILES C=C(CN1CCCCC1)C(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C22H25NO2/c1-18(16-23-14-6-3-7-15-23)22(24)20-10-12-21(13-11-20)25-17-19-8-4-2-5-9-19/h2,4-5,8-13H,1,3,6-7,14-17H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50369028
PNG
(CHEMBL468975)
Show SMILES CN(C)CC(=C)C(=O)c1ccccc1
Show InChI InChI=1S/C12H15NO/c1-10(9-13(2)3)12(14)11-7-5-4-6-8-11/h4-8H,1,9H2,2-3H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))		BDBM50031645
PNG
(1-(4-Benzyloxy-phenyl)-4-dimethylamino-butan-1-one...)
Show SMILES CN(C)CCCC(=O)c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C19H23NO2/c1-20(2)14-6-9-19(21)17-10-12-18(13-11-17)22-15-16-7-4-3-5-8-16/h3-5,7-8,10-13H,6,9,14-15H2,1-2H3
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n/an/a>1.00E+5n/an/an/an/an/an/a



CIBA Limited

Curated by ChEMBL


Assay Description
In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrate

J Med Chem 38: 2441-8 (1995)


BindingDB Entry DOI: 10.7270/Q2MS3TDK
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%