Affinity DataKi: 31nMAssay Description:In vitro binding affinity by measuring the inhibition of bovine trypsinMore data for this Ligand-Target Pair
Affinity DataKi: 31nMAssay Description:Inhibitory Activity against bovine trypsinMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Inhibitory concentration against human Coagulation factor Xa (fXa)More data for this Ligand-Target Pair
Affinity DataKi: 300nMAssay Description:In vitro binding affinity by measuring the inhibition of human thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 300nMAssay Description:Inhibitory Activity against human thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 410nMAssay Description:Binding affinity of the compound was evaluated against Coagulation factor XMore data for this Ligand-Target Pair
Affinity DataKi: 1.24E+3nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 1.24E+3nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 4.00E+3nMAssay Description:Reversible competitive inhibition of boar spermatozoa acrosin using BzArgOEt as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
TargetIonotropic glutamate receptor subunit Delta2(Xenopus)
State University Of New York
Curated by PDSP Ki Database
State University Of New York
Curated by PDSP Ki Database
Affinity DataKi: 1.84E+4nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
Affinity DataKi: 1.84E+4nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
Affinity DataKi: 2.00E+4nMAssay Description:Inhibitory concentration against bovine trypsinMore data for this Ligand-Target Pair
Affinity DataKi: 3.20E+4nMAssay Description:Competitive inhibition of bovine beta trypsin using Bz-Arg-NH-Np as substrate at pH 7 at 30 degCMore data for this Ligand-Target Pair
Affinity DataKi: 3.50E+4nMpH: 7.5Assay Description:Tested for the Inhibition of the catalytic activity of bovine trypsin at 25 degree C and pH 7.5.More data for this Ligand-Target Pair
Affinity DataKi: 3.90E+4nMAssay Description:Inhibitory activity against bovine trypsin expressed as dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 1.60E+5nMAssay Description:Inhibitory activity against bovine coagulation factor X expressed as dissociation constantMore data for this Ligand-Target Pair
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Institut FüR Biochemie
Curated by ChEMBL
Institut FüR Biochemie
Curated by ChEMBL
Affinity DataKi: 1.80E+5nMAssay Description:Inhibitory activity against human urokinase plasminogen activator expressed as dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 2.20E+5nMpH: 7.5Assay Description:Tested for the Inhibition of the catalytic activity of human Thrombin at 25 degree C and pH 7.5.More data for this Ligand-Target Pair
TargetCoagulation factor VII/Tissue factor(Homo sapiens (Human))
Bristol-Myers Squibb
Curated by ChEMBL
Bristol-Myers Squibb
Curated by ChEMBL
Affinity DataKi: 2.40E+5nMAssay Description:Inhibition of human soluble tissue factor/factor VIIa expressed in Origami B (DE3) using D-Ile-Pro-Arg-pNA as substrate after 30 mins by spectrophoto...More data for this Ligand-Target Pair
Affinity DataKi: 2.58E+5nMAssay Description:Binding affinity to thrombin (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 3.16E+5nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair
Affinity DataKi: 3.50E+5nMpH: 7.5Assay Description:Tested for the Inhibition of the catalytic activity of human plasmin at 25 degree C and pH 7.5.More data for this Ligand-Target Pair
Affinity DataKi: 3.98E+5nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Aurigene Discovery Technologies
Curated by ChEMBL
Aurigene Discovery Technologies
Curated by ChEMBL
Affinity DataKi: 4.00E+5nMAssay Description:Inhibition of matriptase-SP1 (615 to 855) (unknown origin) expressed in Escherichia coli BL21(DE3) using Boc-Gln-Ala-Arg-7-amido-4-methyl coumarin hy...More data for this Ligand-Target Pair
Affinity DataKi: 5.00E+5nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair
Affinity DataKi: 8.90E+5nMAssay Description:Inhibitory activity against bovine thrombin expressed as dissociation constantMore data for this Ligand-Target Pair
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Institut FüR Biochemie
Curated by ChEMBL
Institut FüR Biochemie
Curated by ChEMBL
Affinity DataKi: 9.10E+5nMAssay Description:Inhibitory activity against human tissue-type plasminogen activator expressed as dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 2.51E+6nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair