Compile Data Set for Download or QSAR

Found 23 hits of Enzyme Inhibition Constant Data   

TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50339059(3-cyclobutyl-1-(2-phenylquinolin-7-yl)-imidazo[1,5...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of IGF-1R by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:Inhibition of cRafMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50199683(3-(8-amino-3-cyclobutylimidazo[1,5-a]pyrazin-1-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 520nMAssay Description:Inhibition of IGF-1R by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 770nMAssay Description:Inhibition of SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 960nMAssay Description:Inhibition of MEK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of cRafMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 1.96E+3nMAssay Description:Inhibition of AblMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 2.72E+3nMAssay Description:Inhibition of IGF-1R by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 3.58E+3nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 4.21E+3nMAssay Description:Inhibition of KDRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 5.30E+3nMAssay Description:Inhibition of SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AblMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340953(3-cyclobutyl-1-(quinolin-7-yl)imidazo[1,5-a]pyrazi...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of IGF-1R by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of MEK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
Target3-phosphoinositide-dependent protein kinase 1(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 1.12E+4nMAssay Description:Inhibition of PDK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetInsulin receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 2.26E+4nMAssay Description:Inhibition of IRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
Target3-phosphoinositide-dependent protein kinase 1(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of PDK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetInsulin receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of IRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of IGF-1R by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340954(CHEMBL1762110 | Trans-N-((-4-(8-amino-1-(1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of PI3KgammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
OSI Pharmaceuticals, Inc

Curated by ChEMBL
LigandPNGBDBM50340952(4-(8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of PI3KgammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23QHPubMed
* indicates data uncertainty>20%