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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 11 hits in this display   

TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  190nMAssay Description:Inhibition of Src by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  280nMAssay Description:Inhibition of EGFR by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  310nMAssay Description:Inhibition of IGF1R by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEphrin type-B receptor 4(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  610nMAssay Description:Inhibition of EphB4 by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  700nMAssay Description:Inhibition of CDK2 by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin receptor(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  900nMAssay Description:Inhibition of insulin receptor by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  900nMAssay Description:Inhibition of FAK by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of PDGFRbeta by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of VEGFR3 by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiopoietin-1 receptor(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of TIE2 by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(CHEMBL460746 | N-(3-(benzo[d]thiazol-2-yl)-4-hydro...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of VEGFR2 by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed