Compile Data Set for Download or QSAR
Found 9 with Last Name = 'verbinnen' and Initial = 't'
TargetTGF-beta receptor type-1(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204832(4-(2-(5-bromo-2-fluorophenyl)pteridin-4-ylamino)-N...)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:Inhibition of TGFBR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204832(4-(2-(5-bromo-2-fluorophenyl)pteridin-4-ylamino)-N...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Inhibition of human JNK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed
TargetVascular endothelial growth factor receptor 1(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204832(4-(2-(5-bromo-2-fluorophenyl)pteridin-4-ylamino)-N...)copy SMILEScopy InChI
Affinity DataIC50: 47nMAssay Description:Inhibition of human VEGFR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed
TargetTGF-beta receptor type-1(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204834(2-(5-chloro-2-fluorophenyl)-N-(pyridin-4-yl)pterid...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibition of TGFBR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204832(4-(2-(5-bromo-2-fluorophenyl)pteridin-4-ylamino)-N...)copy SMILEScopy InChI
Affinity DataIC50: 59nMAssay Description:Inhibition of human JNK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed
TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204832(4-(2-(5-bromo-2-fluorophenyl)pteridin-4-ylamino)-N...)copy SMILEScopy InChI
Affinity DataIC50: 123nMAssay Description:Inhibition of human VEGFR3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204832(4-(2-(5-bromo-2-fluorophenyl)pteridin-4-ylamino)-N...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of human VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed
TargetCathepsin S(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336504((2R,3aR,10Z,11aS,12aR,14aR)-N-(cyclopropylsulfonyl...)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of human cathepsin S in human JY cells assessed as p10 accumulation by fluorescence-based assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZWZPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50204832(4-(2-(5-bromo-2-fluorophenyl)pteridin-4-ylamino)-N...)copy SMILEScopy InChI
Affinity DataIC50: 1.05E+4nMAssay Description:Inhibition of JNK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JM2999PubMed