BDBM50193810 CHEMBL3972653
SMILES CNC(=O)c1ccccc1Nc1nc(Nc2ccc3C[C@@H](CCCc3c2OC)N2CCN(CCO)CC2)ncc1Cl
InChI Key InChIKey=BCSHRERPHLTPEE-OAQYLSRUSA-N
Data 10 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 10 hits for monomerid = 50193810
TargetCytochrome P450 1A2(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: >5.60E+3nMAssay Description:Inhibition of CYP1A2 in human liver microsomes using phenacetin as substrate in presence of NADPH by LC/MS/MS analysisMore data for this Ligand-Target Pair
TargetCytochrome P450 3A4(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: >5.60E+3nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using testosterone/midazolam as substrate in presence of NADPH by LC/MS/MS analysisMore data for this Ligand-Target Pair
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: 5.70nMAssay Description:Inhibition of human ALK expressed in baculovirus using recombinant GST PLC-gamma as substrate assessed as phosphorylation of the substrate after 15 m...More data for this Ligand-Target Pair
TargetInsulin receptor(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: 81nMAssay Description:Inhibition of recombinant human INSR expressed in baculovirus using ATP as substrate after 15 mins by TRF assayMore data for this Ligand-Target Pair
TargetCytochrome P450 2C19(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: >5.60E+3nMAssay Description:Inhibition of CYP2C19 in human liver microsomes using S-mephenytoin as substrate in presence of NADPH by LC/MS/MS analysisMore data for this Ligand-Target Pair
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: 1nMAssay Description:Inhibition of human FAK expressed in baculovirus after 30 mins using biotinyl-amino-hexanoyl-EQEDEPEGDYFEWLE-amide as substrate by TRF assayMore data for this Ligand-Target Pair
TargetCytochrome P450 2D6(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: >5.60E+3nMAssay Description:Inhibition of CYP2D6 in human liver microsomes using dextromethorphan as substrate in presence of NADPH by LC/MS/MS analysisMore data for this Ligand-Target Pair
TargetCytochrome P450 2C9(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: >5.60E+3nMAssay Description:Inhibition of CYP2C9 in human liver microsomes using diclofenac as substrate in presence of NADPH by LC/MS/MS analysisMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Teva Branded Pharmaceutical Products R & D
Curated by ChEMBL
Affinity DataIC50: 50nMAssay Description:Inhibition of NPM-ALK phosphorylation in human SUP-M2 cells after 2 to 3 hrs by ELISAMore data for this Ligand-Target Pair