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Results 1 - 10 of 14 > >>
EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.414-bromo-N-[(E)-(2-methyl-1H-indol-3-yl)methyleneamino]benzenesulfonamide uncompetitive inhibitor Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.414-methyl-3-oxo-2-(3-pyridylmethylene)benzo[3,4-b]furan-6-yl 4-chloro-benzenesulfonate mixed-type inhibitor Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.416-amino-2-((4-cyanobenzyl)thio)pyrimidin-4-yl 4-methylbenzenesulfonate uncompetitive inhibitor Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.41Ca2+ - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.41diethyldicarbonate 0.02-0.1 mM, complete inhibition, sphingomyelinase P1; 0.02-0.1 mM, complete inhibitionsphingomyelinase P2 Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.41EDTA strong Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.41EDTA - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.41Hg2+ - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.41more enzyme induced human platelet aggregation is inhibited by EDTA over a range of 0.6 to 3.0 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.1.4.41more inhibition of erythrocyte lysis by staphylococcal beta-haemolysin Go to the Ligand Summary Page
Results 1 - 10 of 14 > >>