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Results 1 - 10 of 64 > >>
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EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2(3R,4R)-4-[3-(4-chlorophenyl)-1H-pyrazol-5-yl]-1-(2,2-dimethylpropyl)-3-(4-fluorophenyl)piperidine compound shows improved oral bioavailabilities Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.22-[4-[3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1-(2-phenylethyl)piperidin-4-yl]pyridine most potent compound in the series Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2angiotensin I inhibits the mutant DELTA317-496 in a dose-dependent manner Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2angiotensin II IC50: 3 mM, inhibits hydrolysis of Gly-Pro-4-nitroanilide Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2angiotensin II IC50: 0.1 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2angiotensin II IC50: 0.002 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2angiotensin II - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2angiotensin III inhibits the mutant DELTA317-496 in a dose-dependent manner Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2anti-PRCP - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.16.2antipain IC50: 0.05 mM Go to the Ligand Summary Page
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