Bulut Haydar
The Experimental Retrovirology Section, HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Glob Health Med. 2022 Dec 31;4(6):296-300. doi: 10.35772/ghm.2022.01066.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its variants are responsible for the devastating coronavirus disease 2019 (COVID-19) pandemic with more than 6.5 million deaths since 2019. Although a number of vaccines significantly reduced the mortality rate, a large number of the world population is yet being infected with highly contagious omicron variants/subvarints. Additional therapeutic interventions are needed to reduce hospitalization and curb the ongoing pandemic. The activity of the SARS-CoV-2 enzyme; chymotrypsin-like main protease (M) is essential for the cleavage of viral nonstructural polypeptides into individual functional proteins and therefore M is an attractive drug target. The aim of this review is to summarize recent progress toward the development of therapeutic drugs against M protease.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)及其变种导致了具有毁灭性的2019冠状病毒病(COVID-19)大流行,自2019年以来已造成超过650万人死亡。尽管多种疫苗显著降低了死亡率,但世界上仍有大量人口感染具有高度传染性的奥密克戎变种/亚变种。需要额外的治疗干预措施来减少住院率并遏制当前的大流行。SARS-CoV-2酶——类胰凝乳蛋白酶样主要蛋白酶(M)的活性对于将病毒非结构多肽切割成单个功能蛋白至关重要,因此M是一个有吸引力的药物靶点。本综述的目的是总结针对M蛋白酶的治疗药物开发的最新进展。