Department of Chemistry, Wichita State University, Wichita, KS 67260, USA.
Bioorg Med Chem Lett. 2013 Jul 1;23(13):3709-12. doi: 10.1016/j.bmcl.2013.05.021. Epub 2013 May 16.
The design, synthesis, and in vitro evaluation of the first macrocyclic inhibitor of 3C and 3C-like proteases of picornavirus, norovirus, and coronavirus are reported. The in vitro inhibitory activity (50% effective concentration) of the macrocyclic inhibitor toward enterovirus 3C protease (CVB3 Nancy strain), and coronavirus (SARS-CoV) and norovirus 3C-like proteases, was determined to be 1.8, 15.5 and 5.1 μM, respectively.
本文报道了第一个针对小核糖核酸病毒科的 3C 和 3C 样蛋白酶的大环抑制剂的设计、合成和体外评价。该大环抑制剂对肠道病毒 3C 蛋白酶(CVB3 Nancy 株)、冠状病毒(SARS-CoV)和诺如病毒 3C 样蛋白酶的体外抑制活性(50%有效浓度)分别为 1.8、15.5 和 5.1 μM。