Zhou Kun, Chen Daquan
School of Pharmacy, Yantai University, Yantai, Shandong, RT 264005, P. R. China.
Chembiochem. 2023 Nov 16;24(22):e202300301. doi: 10.1002/cbic.202300301. Epub 2023 Oct 18.
The Coronavirus Disease 2019 (COVID-19) pandemic has brought a widespread influence on the world, especially in the face of sudden coronavirus infections, and there is still an urgent need for specific small molecule therapies to cope with possible future pandemics. The pathogen responsible for this pandemic is Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and understanding its structure and lifecycle is beneficial for designing specific drugs of treatment for COVID-19. The main protease (M ) which has conservative and specific advantages is essential for viral replication and transcription. It is regarded as one of the most potential targets for anti-SARS-CoV-2 drug development. This review introduces the popular knowledge of SARS-CoV-2 M in drug development and lists a series of design principles and relevant activities of advanced M inhibitors, hoping to provide some new directions and ideas for researchers.
2019年冠状病毒病(COVID-19)大流行对世界产生了广泛影响,尤其是面对突发的冠状病毒感染时,仍然迫切需要特定的小分子疗法来应对未来可能出现的大流行。引发此次大流行的病原体是严重急性呼吸综合征冠状病毒2(SARS-CoV-2),了解其结构和生命周期有助于设计针对COVID-19的特定治疗药物。具有保守性和特异性优势的主要蛋白酶(M)对于病毒复制和转录至关重要。它被视为抗SARS-CoV-2药物开发最具潜力的靶点之一。本文综述介绍了SARS-CoV-2 M在药物开发方面的通俗知识,并列举了一系列先进M抑制剂的设计原则及相关活性,希望能为研究人员提供一些新的方向和思路。