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Results 1 - 10 of 55 > >>
EC Number Inhibitors Commentary Structure
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.3(E)-N'-(4-butyl-2-methylphenyl)-N-hydroxyformimidamide HET0016, almost completely abolishes hypotonic solutions- or 2,4,6-trinitrophenol-induced enhancement of receptor-activated cationic current I(TRPC6) Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.3(E)-N'-(4-butyl-2-methylphenyl)-N-hydroxyformimidamide HET0016, diminishes TRPC6-like channel activity in myocytes Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.31,1-dichloroethene 50% of BMO activity is irreversibly lost after oxidation of approximately 25 nmol/mg protein Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.31,2-cis-dichloroethene 50% of BMO activity is lost after oxidation of 120 nmol/mg protein Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.31,2-trans-dichloroethene 50% of BMO activity is lost after oxidation of 20 nmol/mg protein Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.31,7-octadiyne inhibits oxidation of methyl tert-butyl ether; putative mechanism-based inactivator, strongly inhibitory at 0.1% (v/v) Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.31-octyne acts as a mechanism-based inhibitor of AlkB Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.31-octyne irreversible inhibition, oxidation product hexylketene or its equivalent, covalently binds to AlkB Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.311-dodecynoic acid completely inhibited lauric acid omega-hydroxylation Go to the Ligand Summary Page
Show all pathways known for 1.14.15.3Display the word mapDisplay the reaction diagram Show all sequences 1.14.15.317-octadecynoic acid almost completely abolishes hypotonic solutions- or 2,4,6-trinitrophenol-induced enhancement of receptor-activated cationic current I(TRPC6) Go to the Ligand Summary Page
Results 1 - 10 of 55 > >>