Compile Data Set for Download or QSAR
Report error Found 24 Enz. Inhib. hit(s) with all data for entry = 50039007
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303639BDBM50303639(N-(4-(2-(4-(1H-1,2,3-Triazol-1-yl)phenylamino)pyri...)
Affinity DataIC50: 4nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303638BDBM50303638(4-(4-(4-(Methylsulfonamido)phenyl)pyrimidin-2-ylam...)
Affinity DataIC50: 7nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303639BDBM50303639(N-(4-(2-(4-(1H-1,2,3-Triazol-1-yl)phenylamino)pyri...)
Affinity DataIC50: 16nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303638BDBM50303638(4-(4-(4-(Methylsulfonamido)phenyl)pyrimidin-2-ylam...)
Affinity DataIC50: 19nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303644BDBM50303644(3-Morpholino-5-(2-(4-(3-(pyridin-2-yl)-1H-1,2,4-tr...)
Affinity DataIC50: 39nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303642BDBM50303642(3-(2-(4-(2-Methyl-2H-tetrazol-5-yl)phenylamino)pyr...)
Affinity DataIC50: 45nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303641BDBM50303641(3-(2-(4-(3-Methyl-1H-1,2,4-triazol-1-yl)phenylamin...)
Affinity DataIC50: 54nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303641BDBM50303641(3-(2-(4-(3-Methyl-1H-1,2,4-triazol-1-yl)phenylamin...)
Affinity DataIC50: 79nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303644BDBM50303644(3-Morpholino-5-(2-(4-(3-(pyridin-2-yl)-1H-1,2,4-tr...)
Affinity DataIC50: 79nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303643BDBM50303643(4-(3-Morpholinophenyl)-N-(4-(3-(pyridin-3-yl)-1H-1...)
Affinity DataIC50: 85nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303643BDBM50303643(4-(3-Morpholinophenyl)-N-(4-(3-(pyridin-3-yl)-1H-1...)
Affinity DataIC50: 97nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303646BDBM50303646(N-[(2Z)-4-(3-fluoro-5-morpholin-4-ylphenyl)pyrimid...)
Affinity DataIC50: 99nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303645BDBM50303645(4-(3-Fluoro-5-morpholinophenyl)-N-(4-(3-(4-methylp...)
Affinity DataIC50: 102nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303640BDBM50303640(N-(4-(3-Methyl-1H-1,2,4-triazol-1-yl)phenyl)-4-(3-...)
Affinity DataIC50: 113nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50169959BDBM50169959([3H-Benzothiazol-(2Z)-ylidene]-[2-(2-pyridin-3-yl-...)
Affinity DataIC50: 120nMAssay Description:Inhibition of JNK3More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303637BDBM50303637(N-(4-(1H-1,2,3-Triazol-1-yl)phenyl)-4-(3-morpholin...)
Affinity DataIC50: 123nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303645BDBM50303645(4-(3-Fluoro-5-morpholinophenyl)-N-(4-(3-(4-methylp...)
Affinity DataIC50: 133nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303642BDBM50303642(3-(2-(4-(2-Methyl-2H-tetrazol-5-yl)phenylamino)pyr...)
Affinity DataIC50: 140nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303646BDBM50303646(N-[(2Z)-4-(3-fluoro-5-morpholin-4-ylphenyl)pyrimid...)
Affinity DataIC50: 148nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303647BDBM50303647(N-(4-(1H-1,2,4-Triazol-1-yl)phenyl)-4-phenylpyrimi...)
Affinity DataIC50: 297nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303637BDBM50303637(N-(4-(1H-1,2,3-Triazol-1-yl)phenyl)-4-(3-morpholin...)
Affinity DataIC50: 365nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303640BDBM50303640(N-(4-(3-Methyl-1H-1,2,4-triazol-1-yl)phenyl)-4-(3-...)
Affinity DataIC50: 390nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 10(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303636BDBM50303636(4-(4-Phenylpyrimidin-2-ylamino)benzamide | CHEMBL5...)
Affinity DataIC50: 491nMAssay Description:Inhibition of JNK3 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed
TargetMitogen-activated protein kinase 8(Human)
Translational Research Institute

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50303636BDBM50303636(4-(4-Phenylpyrimidin-2-ylamino)benzamide | CHEMBL5...)
Affinity DataIC50: 535nMAssay Description:Inhibition of JNK1 by time resolved fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/27/2012
Entry Details Article
PubMed