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Results 1 - 10 of 14 > >>
EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.473-bromo-7-nitroindazole - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.473-[2,4-di(6-amino-4-methylpyridin-2-yl)ethyl]benzonitrile inhibitor binds to heme propionate A through a bifurcated H-bond and a pi-pi stacking interaction between the conserved Tyr and aminopyridine group Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.474-methylquinolin-2-amine among the most potent aminoquinoline inhibitors tested, KS value 0.00080 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.476,6'-[(5-amino-1,3-phenylene)di(ethane-2,1-diyl)]bis(4-methylpyridin-2-amine) compound interacts with the active site Glu243 and heme propionate D through a series of hydrogen bonds between the aminopyridine functional groups. Comparison with inhibition of mammalian NOS isoforms Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.476,6'-[[(2S,3S)-2-aminobutane-1,3-diyl]bis(oxymethanediyl)]bis(4-methylpyridin-2-amine) compound impedes the growth of Bacillus subtilis under oxidative stress an is able to displace the tetrahydrobiopterin cofactor in the Bacillus subtilis enzyme but not in the mouse enzyme Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.476,6'-[[5-(aminomethyl)-1,3-phenylene]di(ethane-2,1-diyl)]bis(4-methylpyridin-2-amine) compound interacts with the active site Glu243 and heme propionate D through a series of hydrogen bonds between the aminopyridine functional groups. Comparison with inhibition of mammalian NOS isoforms Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.476-([(3R,5S)-5-][[[[(6-amino-4-methylpyridin-2-yl)methoxy]methyl]pyrrolidin-3-yl]oxy]methyl)-4-methylpyridin-2-amine compound impedes the growth of Bacillus subtilis under oxidative stress Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.476-[5-([4-[(6-amino-4-methylpyridin-2-yl)methyl]pyrrolidin-3-yl]oxy)pentyl]-4-methylpyridin-2-amine binding is stabilized by a 3.2 A H-bond between the pyrrolidine ring and the carbonyl group of tetrahydrobiopterin Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.477-nitroindazole - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.47N,N'-[[(2S)-3-aminopropane-1,2-diyl]bis(oxymethylene-3,1-phenylene)]di(thiophene-2-carboximidamide) inhibitor binds by extending outside the active site to interact with a surface adjacent to residue Y357 Go to the Ligand Summary Page
Results 1 - 10 of 14 > >>