Department of Mathematics, Michigan State University, East Lansing, Michigan 48824, United States.
Department of Chemistry and Pharmacology & Toxicology, Michigan State University, East Lansing, Michigan 48824, United States.
J Med Chem. 2021 Dec 9;64(23):16922-16955. doi: 10.1021/acs.jmedchem.1c00409. Epub 2021 Nov 19.
The main protease (M) plays a crucial role in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) replication and is highly conserved, rendering it one of the most attractive therapeutic targets for SARS-CoV-2 inhibition. Currently, although two drug candidates targeting SARS-CoV-2 M designed by Pfizer are under clinical trials, no SARS-CoV-2 medication is approved due to the long period of drug development. Here, we collect a comprehensive list of 817 available SARS-CoV-2 and SARS-CoV M inhibitors from the literature or databases and analyze their molecular mechanisms of action. The structure-activity relationships (SARs) among each series of inhibitors are discussed. Additionally, we broadly examine available antiviral activity, ADMET (absorption, distribution, metabolism, excretion, and toxicity), and animal tests of these inhibitors. We comment on their druggability or drawbacks that prevent them from becoming drugs. This Perspective sheds light on the future development of M inhibitors for SARS-CoV-2 and future coronavirus diseases.
主蛋白酶(M)在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)复制中起着至关重要的作用,并且高度保守,使其成为抑制 SARS-CoV-2 的最有吸引力的治疗靶标之一。目前,尽管辉瑞公司设计的两种针对 SARS-CoV-2 M 的药物候选物正在临床试验中,但由于药物开发周期长,尚未批准任何 SARS-CoV-2 药物。在这里,我们从文献或数据库中收集了 817 种可用的 SARS-CoV-2 和 SARS-CoV M 抑制剂,并分析了它们的作用机制。讨论了每个抑制剂系列之间的结构-活性关系(SAR)。此外,我们广泛研究了这些抑制剂的抗病毒活性、ADMET(吸收、分布、代谢、排泄和毒性)和动物试验。我们对它们的成药性或阻止它们成为药物的缺点进行了评论。本观点为 SARS-CoV-2 和未来的冠状病毒病的 M 抑制剂的未来发展提供了思路。