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Results 1 - 10 of 119 > >>
EC Number Inhibitors Commentary Structure
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2841,10-phenanthroline 1 mM, 30% inhibition Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.28412-oxododecanoic acid substrate inhibition Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.28412-oxododecanoic acid linear competitive Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2842,2'-dipyridyl 1 mM, 20% inhibition Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2842-mercaptoethanol inhibits both the reductase and dehydrogenase reactions by 30% at 1 mM Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2843-(1-tert-butyl-4-amino-1H-indazol-3-yl)phenol CBR1 inhibitor, does not inhibit NADH-dependent S-nitrosoglutathione reduction Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2843-(5-(4-(1H-imidazol-1-yl) phenyl)-1-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-2-yl) propionic acid N6022, a specific and potent GSNO-R inhibitor. N6022 inhibits the GSNO-R-mediated metabolism of GSNO and formaldehyde in the heart Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2843-(5-(4-(1H-imidazol-1-yl) phenyl)-1-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-2-yl) propionic acid N6022, a commercial potent and specific inhibitor of GSNOR Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2843-[1-(4-acetylphenyl)-5-phenyl-1H-pyrrol-2-yl]propanoic acid exhibits noncompetitive or uncompetitive inhibition against varied concentrations of S-nitrosoglutathione or NADH Go to the Ligand Summary Page
Show all pathways known for 1.1.1.284Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2843-[1-(4-acetylphenyl)-5-phenyl-1H-pyrrol-2-yl]propanoic acid 3-[1-(4-acetylphenyl)-5-phenyl-1H-pyrrol-2-yl]propanoic acid and 4-([2-[(2-cyanobenzyl)sulfanyl]-4-oxothieno[3,2-d]pyrimidin-3(4H)-yl]methyl)benzoic acid are more effective than 5-chloro-3-[2-[(4-ethoxyphenyl)(ethyl)amino]-2-oxoethyl]-1H-indole-2-carboxylic acid in inhibiting GSNOR inside the cells, dependence of S-nitrosothiols accumulation on the concentration of compound Go to the Ligand Summary Page
Results 1 - 10 of 119 > >>