The Basic Principles Of indazole-3-carboxylic acid
外观 资助维基百科 创建账号 登录 个人工具 资助维基百科7 μM, while 75 exhibited greater potency but a little bit reduced selectivity against human CSE. These inhibitors ended up synthesized utilizing a six-bromoindole scaffold, with different functional groups attached through Pd-catalyzed cross-coupling reactions. Compound 7