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% Enzyme Activity of Urokinase in the Reaction Biology protease panel at 1.0 M
Assay data:1 Active, 1 Activity ≤ 1 µM, 1 Tested
SummaryRelated BioAssays by Target
% Enzyme Activity of Trypsin in the Reaction Biology protease panel at 1.0 M
% Enzyme Activity of Plasmin in the Reaction Biology protease panel at 1.0 M
Inhibition of human recombinant plasmin using Boc-Val-Leu-Lys-MCA as substrate pretreated with compound followed by substrate addition incubated for 60 mins by multilabel plate reader method
Assay data:1 Tested
Inhibition of human recombinant trypsin using Boc-phe-Ser-Arg-MCA as substrate pretreated with compound followed by substrate addition incubated for 60 mins by multilabel plate reader method
Assay data:2 Tested
Binding affinity to trypsin (unknown origin) assessed as inhibition constant
Inhibition of trypsin (unknown origin) at 50 uM using 4-nitrophenyl acetate as substrate and measured for 1 min by spectrophotometric analysis relative to control
Assay data:6 Tested
Inhibition of trypsin (unknown origin) assessed as residual enzyme activity at 50 uM using 4-nitrophenyl acetate as substrate and measured for 1 min by spectrophotometric analysis relative to control
Inhibition of trypsin (unknown origin) assessed as residual enzyme activity at 20 uM using 4-nitrophenyl acetate as substrate and measured for 1 min by spectrophotometric analysis relative to control
Inhibition of trypsin (unknown origin) assessed as residual enzyme activity at 10 uM using 4-nitrophenyl acetate as substrate and measured for 1 min by spectrophotometric analysis relative to control
Assay data:7 Tested
Inhibition of human plasma trypsin using Boc-Ile-Glu-Gly-Arg-AMC as substrate assessed as fold change in inhibition measured for 30 mins by fluorometric assay
Inhibition of human plasmin using MeOSuc-Ala-Phe-Lys-AMC as substrate assessed as fold change in inhibition measured for 30 mins by fluorometric assay
Inhibition of human plasma trypsin using Boc-Ile-Glu-Gly-Arg-AMC as substrate measured for 30 mins by fluorometric assay
Inhibition of trypsin (unknown origin) assessed as inhibition of casein hydrolysis using S2238 as chromogenic substrate preincubated for 5 mins followed by substrate addition and measured after 11 mins by absorbance based analysis
Binding affinity to trypsin (unknown origin) assessed as dissociation constant by surface plasmon resonance imaging method
Assay data:1 Active, 1 Tested
Binding affinity to trypsin (unknown origin) assessed as inhibition constant by Lineweaver-Burk plot analysis
Inhibition of trypsin (unknown origin) using S-2765 as chromogenic substrate preincubated for 10 mins followed by substrate addition and measured after 10 mins
Inhibition of plasmin (unknown origin) using S-2251 as chromogenic substrate preincubated for 10 mins followed by substrate addition and measured after 10 mins
Assay data:1 Active, 2 Tested
Stability of the compound assessed as trypsin (unknown origin) mediated compound degradation incubated for 60 mins by UV-based HPLC analysis
Assay data:4 Active, 4 Tested
Inhibition of trypsin (unknown origin) at 50 uM by biochemical assay relative to control
Assay data:28 Tested
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