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Results 1 - 10 of 58 > >>
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EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B10(2R)-N4-hydroxy-N1-[(1S)-1-(1H-indol-3-ylmethyl)-2-(methylamino)-2-oxoethyl]-2-(2-methylpropyl)butanediamide IC50: 5930 nM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B10(4-(N-hydroxyamino)-2R-isobutyl-3S-methylsuccinyl)-L-phenylglycine-N-methylamide KB-R7785, 0.001mmol/l Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B101,10-phenanthroline - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B101,10-phenanthroline total inhibition when incubated with gelatin at 37 °C for either 2 or 18 h Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B104-[[[6-cyano-1-[(1-methyl-1H-imidazol-5-yl)methyl]-1,2,3,4,6,7-hexahydroquinolin-3-yl](pyridin-2-ylsulfonyl)amino]methyl]-N,N-dimethylpiperidine-1-carboxamide - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B10Aprotinin 0.1 mg/ml Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B10batimastat - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B10BB94 0.01 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B10Co2+ 0.01 mM Co2+ inhibits the activity by 80%, while increasing concentrations rescue the lost activity Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B10EDTA complete inhibition Go to the Ligand Summary Page
Results 1 - 10 of 58 > >>
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