Affinity DataKi: 0.0400nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.0700nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.0900nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: <0.100nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.160nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.190nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.190nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.220nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.230nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.240nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.25nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.270nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.290nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.320nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.360nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.420nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.430nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.450nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.460nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.580nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.780nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.800nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.800nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 0.850nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 1.80nMAssay Description:Binding affinity to human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 3.10nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 5.60nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 30nMAssay Description:Compound was evaluated for the inhibitory activity against thrombin.More data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center
Curated by ChEMBL
Bayer Research Center
Curated by ChEMBL
Affinity DataIC50: 6nMAssay Description:Inhibitory activity against human Raf-1 kinaseMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Cgi Pharmaceuticals
Curated by ChEMBL
Cgi Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 7nMAssay Description:Inhibition of VEGFR2 after 1 hrMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Cgi Pharmaceuticals
Curated by ChEMBL
Cgi Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of VEGFR2 autophosphorylation by cell based assayMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center
Curated by ChEMBL
Bayer Research Center
Curated by ChEMBL
Affinity DataIC50: 12nMAssay Description:Inhibitory activity against human Raf-1 kinaseMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Cgi Pharmaceuticals
Curated by ChEMBL
Cgi Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 13nMAssay Description:Inhibition of VEGFR2 autophosphorylation by cell based assayMore data for this Ligand-Target Pair
Affinity DataIC50: 26nMAssay Description:Inhibition of EphB4 autophosphorylation by cell based assayMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center
Curated by ChEMBL
Bayer Research Center
Curated by ChEMBL
Affinity DataIC50: 26nMAssay Description:Inhibitory activity against human Raf-1 kinaseMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center
Curated by ChEMBL
Bayer Research Center
Curated by ChEMBL
Affinity DataIC50: 27nMAssay Description:Inhibitory activity against human Raf-1 kinaseMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Cgi Pharmaceuticals
Curated by ChEMBL
Cgi Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 33nMAssay Description:Inhibition of VEGFR2 autophosphorylation by cell based assayMore data for this Ligand-Target Pair
Affinity DataIC50: 33nMAssay Description:Inhibition of Tie2 after 1 hrMore data for this Ligand-Target Pair
Affinity DataIC50: 35nMAssay Description:Inhibition of EPHA2 after 1 hrMore data for this Ligand-Target Pair
Affinity DataIC50: 37nMAssay Description:Inhibition of EphB4 after 1 hrMore data for this Ligand-Target Pair
Affinity DataIC50: 37nMAssay Description:Inhibition of Tie2 after 1 hrMore data for this Ligand-Target Pair
Affinity DataIC50: 37nMAssay Description:Inhibition of EphB4 autophosphorylation by cell based assayMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center
Curated by ChEMBL
Bayer Research Center
Curated by ChEMBL
Affinity DataIC50: 38nMAssay Description:Inhibitory activity against human Raf-1 kinaseMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center
Curated by ChEMBL
Bayer Research Center
Curated by ChEMBL
Affinity DataIC50: 44nMAssay Description:Inhibitory activity against human Raf-1 kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 49nMAssay Description:Inhibition of EphB4 after 1 hrMore data for this Ligand-Target Pair
Affinity DataIC50: 50nMAssay Description:Inhibition of Tie2 autophosphorylation by cell based assayMore data for this Ligand-Target Pair
Affinity DataIC50: 50nMAssay Description:Inhibition of EphB4 autophosphorylation by cell based assayMore data for this Ligand-Target Pair
Affinity DataIC50: 50nMAssay Description:Inhibition of EphB4 autophosphorylation by cell based assayMore data for this Ligand-Target Pair