Compile Data Set for Download or QSAR

Found 66 hits of Enzyme Inhibition Constant Data   

TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031643(1-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-prope...)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031651(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031655(1-[3-(4-Benzyloxy-phenyl)-3-oxo-propyl]-piperidine...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031657(1-(4-Benzyloxy-3-hydroxy-phenyl)-3-dimethylamino-p...)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031659(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)copy SMILEScopy InChI
Affinity DataIC50: 470nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031648(1-(4-Benzyloxy-3-hydroxy-phenyl)-2-dimethylaminome...)copy SMILEScopy InChI
Affinity DataIC50: 670nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031642(4-Dimethylcarbamoyl-benzenesulfonic acid 4-(2-dime...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM19459(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031647(1-(4-Benzyloxy-phenyl)-2-piperidin-1-ylmethyl-prop...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031662(1-(4-Benzyloxy-phenyl)-2-morpholin-4-ylmethyl-prop...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031661(1-(4-Benzyloxy-phenyl)-3-morpholin-4-yl-propan-1-o...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031646(1-(4-Benzyloxy-phenyl)-2-piperazin-1-ylmethyl-prop...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031660(1-(4-Benzyloxy-phenyl)-3-dimethylamino-propan-1-on...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031658(1-(4-Benzyloxy-phenyl)-3-piperidin-1-yl-propan-1-o...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031644(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-(3,4-dime...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031649(2-{3-(4-benzyloxy)-2-[(dimethylamino)methyl]-3-oxo...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50369028(CHEMBL468975)copy SMILEScopy InChI
Affinity DataIC50: 5.60E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031656(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-phenylsul...)copy SMILEScopy InChI
Affinity DataIC50: 7.30E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031653(2-(2-Amino-ethylsulfanylmethyl)-1-(4-benzyloxy-phe...)copy SMILEScopy InChI
Affinity DataIC50: 8.80E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031650(2-[3-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-3-...)copy SMILEScopy InChI
Affinity DataIC50: 8.80E+3nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM19459(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031656(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-phenylsul...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031648(1-(4-Benzyloxy-3-hydroxy-phenyl)-2-dimethylaminome...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031656(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-phenylsul...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031651(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031659(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031659(4-[4-(2-Dimethylaminomethyl-acryloyl)-phenoxysulfo...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031657(1-(4-Benzyloxy-3-hydroxy-phenyl)-3-dimethylamino-p...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031642(4-Dimethylcarbamoyl-benzenesulfonic acid 4-(2-dime...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031653(2-(2-Amino-ethylsulfanylmethyl)-1-(4-benzyloxy-phe...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031648(1-(4-Benzyloxy-3-hydroxy-phenyl)-2-dimethylaminome...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031654(2-Cyano-2-(3,4-dihydroxy-benzyl)-thioacetamide | C...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+4nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031642(4-Dimethylcarbamoyl-benzenesulfonic acid 4-(2-dime...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+4nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM19459(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+4nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031661(1-(4-Benzyloxy-phenyl)-3-morpholin-4-yl-propan-1-o...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031658(1-(4-Benzyloxy-phenyl)-3-piperidin-1-yl-propan-1-o...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031654(2-Cyano-2-(3,4-dihydroxy-benzyl)-thioacetamide | C...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031655(1-[3-(4-Benzyloxy-phenyl)-3-oxo-propyl]-piperidine...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031654(2-Cyano-2-(3,4-dihydroxy-benzyl)-thioacetamide | C...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031652(4-[4-(3-Dimethylamino-2-methyl-propionyl)-phenoxys...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the Epidermal growth factor receptor activity in A431 membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031650(2-[3-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-3-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031660(1-(4-Benzyloxy-phenyl)-3-dimethylamino-propan-1-on...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031644(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-(3,4-dime...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031644(1-(4-Benzyloxy-phenyl)-3-dimethylamino-2-(3,4-dime...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50369028(CHEMBL468975)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the c-src tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031658(1-(4-Benzyloxy-phenyl)-3-piperidin-1-yl-propan-1-o...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031655(1-[3-(4-Benzyloxy-phenyl)-3-oxo-propyl]-piperidine...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031647(1-(4-Benzyloxy-phenyl)-2-piperidin-1-ylmethyl-prop...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031650(2-[3-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-3-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
CIBA Limited

Curated by ChEMBL
LigandPNGBDBM50031643(1-(4-Benzyloxy-phenyl)-2-dimethylaminomethyl-prope...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of the v-abl tyrosine kinase activity in A431 membranes using angiotensin II as phosphate acceptor as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MS3TDKPubMed
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