Compile Data Set for Download or QSAR

Found 16 hits of Enzyme Inhibition Constant Data   

TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268240(2-(6-Methoxy-9H-purine-9-yl)-1-phenylethanone | CH...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268224(2-(6-Amino-7H-purine-7-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268223(2-(6-Amino-9H-purine-9-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+4nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268240(2-(6-Methoxy-9H-purine-9-yl)-1-phenylethanone | CH...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+4nMAssay Description:Inhibition of VEGFR3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268239(2-(6-Amino-9H-purine-9-yl)-1-(pyridine-3-yl)ethano...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+4nMAssay Description:Inhibition of VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetAurora kinase B(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268223(2-(6-Amino-9H-purine-9-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+4nMAssay Description:Inhibition of Aurora BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268239(2-(6-Amino-9H-purine-9-yl)-1-(pyridine-3-yl)ethano...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+4nMAssay Description:Inhibition of SRCMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268225(2-(6-Amino-9H-purine-9-yl)-1-phenylethanone | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+4nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268223(2-(6-Amino-9H-purine-9-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 8.10E+4nMAssay Description:Inhibition of VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268224(2-(6-Amino-7H-purine-7-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 8.20E+4nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268224(2-(6-Amino-7H-purine-7-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 8.20E+4nMAssay Description:Inhibition of SRCMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetAngiopoietin-1 receptor(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268223(2-(6-Amino-9H-purine-9-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 8.50E+4nMAssay Description:Inhibition of TIE2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268226(2-(6-Amino-9H-purine-9-yl)-1-(pyridine-2-yl)ethano...)copy SMILEScopy InChI
Affinity DataIC50: 8.90E+4nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268239(2-(6-Amino-9H-purine-9-yl)-1-(pyridine-3-yl)ethano...)copy SMILEScopy InChI
Affinity DataIC50: 9.30E+4nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268223(2-(6-Amino-9H-purine-9-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 9.50E+4nMAssay Description:Inhibition of ERBB2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
TargetAngiopoietin-1 receptor(Homo sapiens (Human))
Eberhard-Karls-University

Curated by ChEMBL
LigandPNGBDBM50268224(2-(6-Amino-7H-purine-7-yl)-1-(1H-indole-3-yl)ethan...)copy SMILEScopy InChI
Affinity DataIC50: 9.50E+4nMAssay Description:Inhibition of TIE2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K78WKPubMed
* indicates data uncertainty>20%