Report error Found 21 Enz. Inhib. hit(s) with all data for entry = 50019567
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 19nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 39nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 48nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 107nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 262nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 366nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 424nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 494nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 504nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 655nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 850nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 1.08E+3nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 2.46E+3nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 12(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 3.62E+3nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C9 in human liver microsomes using diclofenac as substrate incubated for 10 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2D6 in human liver microsomes using bufuralol as substrate incubated for 10 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using testosterone as substrate incubated for 5 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C19 in human liver microsomes using S-mephenytoin as substrate incubated for 45 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of hERG expressed in CHO cells at -80 mV holding potential by QPatch automated electrophysiology assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of hERG expressed in CHO cells at -80 mV holding potential by QPatch automated electrophysiology assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Human)
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
The University of Texas Md Anderson Cancer Center
Curated by ChEMBL
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of hERG expressed in CHO cells at -80 mV holding potential by QPatch automated electrophysiology assayMore data for this Ligand-Target Pair
