BDBM50100891 2-Phenyl-1H-benzoimidazole-5-carboxamidine::2-Phenyl-3H-benzoimidazole-5-carboxamidine::CHEMBL96917
SMILES NC(=N)c1ccc2nc([nH]c2c1)-c1ccccc1
InChI Key InChIKey=YOGKYTKBSDBMTL-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50100891
Affinity DataKi: 5.50E+4nMAssay Description:Compound was tested against Human Serine Protease TrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 5.50E+4nMAssay Description:ComInhibition of Human Serine Protease Urokinase Plasminogen Activator (u-PA).More data for this Ligand-Target Pair
Affinity DataKi: 1.25E+5nMAssay Description:Binding affinity against human coagulation factor XMore data for this Ligand-Target Pair
Affinity DataKi: 3.40E+5nMAssay Description:Inhibition of Human Serine Protease Thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 3.50E+5nMAssay Description:Inhibition of Human Serine Protease Plasmin.More data for this Ligand-Target Pair
Affinity DataKi: 3.81E+5nMAssay Description:Inhibition of Human Serine Protease tissue type Plasminogen Activator (t-PA).More data for this Ligand-Target Pair
TargetSporulation kinase A(Bacillus subtilis (strain 168))
The R. W. Johnson Pharmaceutical Research Institute
Curated by ChEMBL
The R. W. Johnson Pharmaceutical Research Institute
Curated by ChEMBL
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of KinA/Sp0F system two component (TCS) from Bacillus subtilis.More data for this Ligand-Target Pair
