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Results 1 - 10 of 114 > >>
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EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10 phenanthroline - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10-phenanthroline half-maximal inhibition at 1.8 mM, competitive and reversible inhibition is reversed by ZnCl2, increases 20fold the inhibition by EDTA Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10-phenanthroline - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10-phenanthroline inactivation Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10-phenanthroline complete inhibition Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10-phenanthroline 86.3% inhibition at 5 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10-phenanthroline 87.8% inhibition at 5 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221,10-phenanthroline 3% residual activity at 10 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221-ethyl-3-(3-dimethylaminopropyl)carbodiimide inactivation by modification of pK 5.8 carboxylate, presence arginine hydroxamate decreases inhibitory potency, hydroxylamine does not recover enzyme activity Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.11.221-Phenyl-2-thiourea competitive Go to the Ligand Summary Page
Results 1 - 10 of 114 > >>
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