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Results 1 - 10 of 114 > >>
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EC Number Inhibitors Commentary Structure
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.213(2E)-3-(4-bromophenyl)-2-[4-(methylsulfonyl)phenyl]prop-2-enoic acid 93.3% inhibition at 0.1 mM Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.213(2E)-3-(4-ethylphenyl)-2-[4-(methylsulfonyl)phenyl]prop-2-enoic acid 89.1% inhibition at 0.1 mM Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.213(2E)-3-(4-methylphenyl)-2-[4-(methylsulfonyl)phenyl]prop-2-enoic acid 92.7% inhibition at 0.1 mM Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.213(2E)-3-[4-(methylsulfanyl)phenyl]-2-[4-(methylsulfonyl)phenyl]prop-2-enoic acid 93.5% inhibition at 0.1 mM Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.213(E/Z)-sulfindac wild-type, W86Y and W227Y Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2131,10-phenanthroline wild-type, W86Y and W227Y Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2131,7-phenanthroline wild-type, W86Y and W227Y Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2131-(4'nitrophenyl)prop-2-en-1-ol inactivation dependent on NAD+ concentration, optimal at 0.5-1.0 mM NAD+, 2-mercaptoethanol prvides a concentration-dependent protection Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2131-(4'nitrophenyl)prop-2-en-1-one inactivation can be retarded markedly in a concentration-dependent manner by both NADH and NADPH. Competitive inhibitor of NAD+ binding, measured for androsterone oxidation Go to the Ligand Summary Page
Show all pathways known for 1.1.1.213Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2131-(4'nitrophenyl)prop-2-yn-1-one competitive inhibitor of NAD+ binding, measured for androsterone oxidation Go to the Ligand Summary Page
Results 1 - 10 of 114 > >>
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