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Results 1 - 10 of 10
EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.1271-(2-methylpropyl)-5-[4-([4-[3-(trifluoromethyl)-3H-diaziren-3-yl]benzyl]oxy)phenyl]-1H-imidazole bifunctional compound, inhibits juvenile hormone III synthesis by intact glands as well as methyl farnesoate epoxidation by gland homogenates. Using the compound, a radiolabeled and photoactivatable diazirine or benzophenone group can be introduced to label the hydrophobic substrate binding site of the enzyme Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.1275-(2-(benzyloxy)phenyl)-1-(3,7-dimethyloct-6-en-1-yl)-1H-imidazole - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.1275-(3-[[(2E)-3,7-dimethylocta-2,6-dien-1-yl]oxy]phenyl)-1-(2-methylpropyl)-1H-imidazole - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.1275-[3-(benzyloxy)phenyl]-1-(2-methylpropyl)-1H-imidazole - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.127carbon monoxide/oxygen atmosphere half-maximal inhibition at a CO/O ratio of 4.0. Inhibition is reversed by white-light irradiation Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.127cytochrome c inhibition by oxidized cytochrome c, 20 microM, 52.4% residual activity Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.127methyl (2E,6E)-3,7-dimethyl-8-(3,4-methylenedioxyphenoxy)-octadienoate inhibits juvenile hormone biosynthesis in vitro by spontaneously active glands, presumably by direct inhibition of the epoxidase, and also inhibits the production of total methyl ester Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.127more inhibition 1,5-disubstituted imidazoles Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.127NADP+ 2 mM, 57.2% residual activity Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.127[4-([4-[1-(2-methylpropyl)-1H-imidazol-5-yl]phenoxy]methyl)phenyl](phenyl)methanone bifunctional compound, inhibits juvenile hormone III synthesis by intact glands as well as methyl farnesoate epoxidation by gland homogenates. Using the compound, a radiolabeled and photoactivatable diazirine or benzophenone group can be introduced to label the hydrophobic substrate binding site of the enzyme Go to the Ligand Summary Page
Results 1 - 10 of 10