Report error Found 10521 Enz. Inhib. hit(s) with Target = 'Prothrombin'
Affinity DatapH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:After substrate hydrolysis reaction, the absorbance at 405 nm was measured in a microplate reader. Percentages of inhibition at each concentration we...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Affinity DataEC50: 49nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 390nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 840nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 590nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 1.17E+3nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 880nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 5.60E+4nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 590nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 150nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataKon: 0.000220M-1s-1Assay Description:Compound was tested for the rate constant of deacylation against thrombinMore data for this Ligand-Target Pair
Affinity DataKon: 0.000100M-1s-1Assay Description:Compound was tested for the rate constant of deacylation against thrombinMore data for this Ligand-Target Pair
Affinity DataEC50: 50nMAssay Description:Inhibitory activity against human thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataEC50: 390nMAssay Description:Concentration required to inhibit thrombin hydrolysis of the chromogenic substrateMore data for this Ligand-Target Pair
Affinity DataKd: 1.00E+3nMAssay Description:Binding affinity to human fluorescence labelled FPRCK-alpha thrombin by fluorimetric methodMore data for this Ligand-Target Pair
Affinity DataKd: 2.80E+3nMAssay Description:Binding affinity to wild-type thrombin (unknown origin) by intrinsic fluorescence methodMore data for this Ligand-Target Pair
Affinity DataKd: 3.70E+3nMAssay Description:Binding affinity to human fluorescence labelled FPRCK-alpha thrombin by fluorimetric methodMore data for this Ligand-Target Pair
Affinity DataKd: 575nMAssay Description:Binding affinity against thrombinMore data for this Ligand-Target Pair
Affinity DataKd: 0.210nMAssay Description:Binding affinity to human thrombin after 30 mins by non-equilibrium capillary electrophoresisMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKd: 0.270nMAssay Description:Binding affinity to human thrombin after 30 mins by non-equilibrium capillary electrophoresisMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKd: 0.180nMAssay Description:Binding affinity to human thrombin after 30 mins by non-equilibrium capillary electrophoresisMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKd: 0.25nMAssay Description:Binding affinity to human thrombin after 30 mins by non-equilibrium capillary electrophoresisMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKd: 916nMAssay Description:Binding affinity to human alpha-thrombin in phosphate/HEPES/Tricine/Tris buffer by ITC methodMore data for this Ligand-Target Pair
Affinity DataKd: 3.68E+3nMAssay Description:Binding affinity to human alpha-thrombin in phosphate/HEPES/Tricine/Tris buffer by ITC methodMore data for this Ligand-Target Pair
