Compile Data Set for Download or QSAR

Found 60 hits of Enzyme Inhibition Constant Data   

TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037393(5,7-Diamino-2-(3-amino-phenyl)-6-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 7.80E+3nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037413(6-Amino-2-(4-amino-phenyl)-chromen-4-one | CHEMBL1...)copy SMILEScopy InChI
Affinity DataIC50: 8.70E+3nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037408(6-Amino-2-(4-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037395(5,7-Diamino-2-(4-amino-phenyl)-6-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037413(6-Amino-2-(4-amino-phenyl)-chromen-4-one | CHEMBL1...)copy SMILEScopy InChI
Affinity DataIC50: 2.88E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037393(5,7-Diamino-2-(3-amino-phenyl)-6-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 3.84E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037393(5,7-Diamino-2-(3-amino-phenyl)-6-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+4nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037410(8-Amino-2-(4-amino-phenyl)-chromen-4-one | CHEMBL3...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037396(8-Amino-2-(4-amino-phenyl)-5-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037408(6-Amino-2-(4-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037405(6-Amino-2-(4-amino-phenyl)-5-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037392(8-Amino-2-(3-amino-phenyl)-6-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037402(8-Amino-2-(4-amino-phenyl)-5-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037395(5,7-Diamino-2-(4-amino-phenyl)-6-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037399(6-Amino-2-(3-amino-phenyl)-chromen-4-one | CHEMBL1...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037407(8-Amino-2-(4-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037401(8-Amino-2-(4-amino-phenyl)-6-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037397(6-Amino-2-(3-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037406(8-Amino-2-(4-amino-phenyl)-6-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037409(6,8-Diamino-2-(4-amino-phenyl)-7-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037394(6,8-Diamino-2-(4-amino-phenyl)-chromen-4-one | CHE...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037392(8-Amino-2-(3-amino-phenyl)-6-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.60E+4nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037409(6,8-Diamino-2-(4-amino-phenyl)-7-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037410(8-Amino-2-(4-amino-phenyl)-chromen-4-one | CHEMBL3...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037394(6,8-Diamino-2-(4-amino-phenyl)-chromen-4-one | CHE...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037392(8-Amino-2-(3-amino-phenyl)-6-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037397(6-Amino-2-(3-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037396(8-Amino-2-(4-amino-phenyl)-5-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037405(6-Amino-2-(4-amino-phenyl)-5-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037401(8-Amino-2-(4-amino-phenyl)-6-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037395(5,7-Diamino-2-(4-amino-phenyl)-6-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037402(8-Amino-2-(4-amino-phenyl)-5-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037407(8-Amino-2-(4-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037406(8-Amino-2-(4-amino-phenyl)-6-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037399(6-Amino-2-(3-amino-phenyl)-chromen-4-one | CHEMBL1...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037413(6-Amino-2-(4-amino-phenyl)-chromen-4-one | CHEMBL1...)copy SMILEScopy InChI
Affinity DataIC50: 1.03E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037394(6,8-Diamino-2-(4-amino-phenyl)-chromen-4-one | CHE...)copy SMILEScopy InChI
Affinity DataIC50: 1.06E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037406(8-Amino-2-(4-amino-phenyl)-6-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.17E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037410(8-Amino-2-(4-amino-phenyl)-chromen-4-one | CHEMBL3...)copy SMILEScopy InChI
Affinity DataIC50: 1.23E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037408(6-Amino-2-(4-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.41E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037399(6-Amino-2-(3-amino-phenyl)-chromen-4-one | CHEMBL1...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037405(6-Amino-2-(4-amino-phenyl)-5-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 2.23E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037402(8-Amino-2-(4-amino-phenyl)-5-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 3.26E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037407(8-Amino-2-(4-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 3.28E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037401(8-Amino-2-(4-amino-phenyl)-6-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 3.82E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037397(6-Amino-2-(3-amino-phenyl)-7-hydroxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 5.02E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037409(6,8-Diamino-2-(4-amino-phenyl)-7-hydroxy-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 7.54E+5nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037411(7-Hydroxy-6,8-dinitro-2-(4-nitro-phenyl)-chromen-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.57E+6nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037396(8-Amino-2-(4-amino-phenyl)-5-methoxy-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.62E+6nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50037417(7-Hydroxy-8-nitro-2-(4-nitro-phenyl)-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 1.88E+6nMAssay Description:In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WNPPubMed
Displayed 1 to 50 (of 60 total ) | Next | Last >>* indicates data uncertainty>20%