Compile Data Set for Download or QSAR

Found 78 hits of Enzyme Inhibition Constant Data   

TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345617(3-(2-(cyclohexylamino)pyridin-4-yl)-4-(naphthalen-...)copy SMILEScopy InChI
Affinity DataIC50: 52.2nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345617(3-(2-(cyclohexylamino)pyridin-4-yl)-4-(naphthalen-...)copy SMILEScopy InChI
Affinity DataIC50: 66.5nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345607(4-(5-(naphthalen-2-yl)-1H-pyrazol-4-yl)pyridine | ...)copy SMILEScopy InChI
Affinity DataIC50: 245nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345606(4-(4-(naphthalen-2-yl)-1H-1,2,3-triazol-5-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 364nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345616(3-(2-aminopyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,2...)copy SMILEScopy InChI
Affinity DataIC50: 504nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345609(4-(naphthalen-2-yl)-3-(pyridin-4-yl)-1H-1,2,4-tria...)copy SMILEScopy InChI
Affinity DataIC50: 559nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345607(4-(5-(naphthalen-2-yl)-1H-pyrazol-4-yl)pyridine | ...)copy SMILEScopy InChI
Affinity DataIC50: 864nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345618(3-(2-(cyclopropylmethylamino)pyridin-4-yl)-4-(naph...)copy SMILEScopy InChI
Affinity DataIC50: 945nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345616(3-(2-aminopyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,2...)copy SMILEScopy InChI
Affinity DataIC50: 1.03E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345606(4-(4-(naphthalen-2-yl)-1H-1,2,3-triazol-5-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 1.22E+3nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345602(4-(1-(naphthalen-2-yl)-1H-pyrazol-5-yl)pyridine | ...)copy SMILEScopy InChI
Affinity DataIC50: 1.23E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345604(4-(1-(naphthalen-2-yl)-1H-imidazol-2-yl)pyridine |...)copy SMILEScopy InChI
Affinity DataIC50: 1.91E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345618(3-(2-(cyclopropylmethylamino)pyridin-4-yl)-4-(naph...)copy SMILEScopy InChI
Affinity DataIC50: 2.25E+3nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345601(4-(5-(naphthalen-2-yl)-2,5-dihydro-1H-pyrazol-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 2.46E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345605(4-(1-(naphthalen-2-yl)-1H-1,2,3-triazol-5-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 2.67E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345609(4-(naphthalen-2-yl)-3-(pyridin-4-yl)-1H-1,2,4-tria...)copy SMILEScopy InChI
Affinity DataIC50: 2.98E+3nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345608(4-(naphthalen-2-yl)-5-(pyridin-4-yl)pyrimidine | C...)copy SMILEScopy InChI
Affinity DataIC50: 4.13E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345620(4-(4-(naphthalen-2-yl)-4H-1,2,4-triazol-3-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 4.48E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345600(4-(5-(naphthalen-2-yl)-1H-1,2,3-triazol-1-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 4.81E+3nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345602(4-(1-(naphthalen-2-yl)-1H-pyrazol-5-yl)pyridine | ...)copy SMILEScopy InChI
Affinity DataIC50: 4.88E+3nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345604(4-(1-(naphthalen-2-yl)-1H-imidazol-2-yl)pyridine |...)copy SMILEScopy InChI
Affinity DataIC50: 6.39E+3nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345606(4-(4-(naphthalen-2-yl)-1H-1,2,3-triazol-5-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 6.85E+3nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345607(4-(5-(naphthalen-2-yl)-1H-pyrazol-4-yl)pyridine | ...)copy SMILEScopy InChI
Affinity DataIC50: 7.15E+3nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345605(4-(1-(naphthalen-2-yl)-1H-1,2,3-triazol-5-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 9.14E+3nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345601(4-(5-(naphthalen-2-yl)-2,5-dihydro-1H-pyrazol-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 9.31E+3nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345609(4-(naphthalen-2-yl)-3-(pyridin-4-yl)-1H-1,2,4-tria...)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345599(4-(4-chloro-5-(naphthalen-2-yl)-1H-1,2,3-triazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 1.26E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345611(3-(2-methylpyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,...)copy SMILEScopy InChI
Affinity DataIC50: 1.48E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345598(4-(5-hydrazono-4-(naphthalen-2-yl)-4,5-dihydro-1H-...)copy SMILEScopy InChI
Affinity DataIC50: 1.49E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345611(3-(2-methylpyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,...)copy SMILEScopy InChI
Affinity DataIC50: 1.53E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345608(4-(naphthalen-2-yl)-5-(pyridin-4-yl)pyrimidine | C...)copy SMILEScopy InChI
Affinity DataIC50: 1.81E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345621(4-(5-methyl-4-(naphthalen-2-yl)-4H-1,2,4-triazol-3...)copy SMILEScopy InChI
Affinity DataIC50: 1.83E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345600(4-(5-(naphthalen-2-yl)-1H-1,2,3-triazol-1-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 1.86E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345620(4-(4-(naphthalen-2-yl)-4H-1,2,4-triazol-3-yl)pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345616(3-(2-aminopyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,2...)copy SMILEScopy InChI
Affinity DataIC50: 2.43E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345613(3-(3-fluoropyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,...)copy SMILEScopy InChI
Affinity DataIC50: 2.74E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345597(4-(5-chloro-4-(naphthalen-2-yl)-4H-1,2,4-triazol-3...)copy SMILEScopy InChI
Affinity DataIC50: 3.04E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345615(3-(pyridin-4-yl)-4-(quinolin-6-yl)-1H-1,2,4-triazo...)copy SMILEScopy InChI
Affinity DataIC50: 3.18E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345598(4-(5-hydrazono-4-(naphthalen-2-yl)-4,5-dihydro-1H-...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345613(3-(3-fluoropyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,...)copy SMILEScopy InChI
Affinity DataIC50: 3.46E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345599(4-(4-chloro-5-(naphthalen-2-yl)-1H-1,2,3-triazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 3.79E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345601(4-(5-(naphthalen-2-yl)-2,5-dihydro-1H-pyrazol-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 4.19E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345621(4-(5-methyl-4-(naphthalen-2-yl)-4H-1,2,4-triazol-3...)copy SMILEScopy InChI
Affinity DataIC50: 4.62E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345622(4-(1-(naphthalen-2-yl)-1H-tetrazol-5-yl)pyridine |...)copy SMILEScopy InChI
Affinity DataIC50: 4.91E+4nMAssay Description:Inhibition of JNK3 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345615(3-(pyridin-4-yl)-4-(quinolin-6-yl)-1H-1,2,4-triazo...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345617(3-(2-(cyclohexylamino)pyridin-4-yl)-4-(naphthalen-...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345621(4-(5-methyl-4-(naphthalen-2-yl)-4H-1,2,4-triazol-3...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345604(4-(1-(naphthalen-2-yl)-1H-imidazol-2-yl)pyridine |...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345610(3-(pyridin-4-yl)-4-(quinolin-3-yl)-1H-1,2,4-triazo...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of JNK2 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Elan Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50345611(3-(2-methylpyridin-4-yl)-4-(naphthalen-2-yl)-1H-1,...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ044CPubMed
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