大流行
2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019-20冠状病毒爆发
冠状病毒
药物发现
药物开发
计算生物学
病毒学
生物
病毒复制
药品
病毒
医学
生物信息学
药理学
传染病(医学专业)
疾病
爆发
病理
出处
期刊:ChemBioChem
[Wiley]
日期:2023-08-14
卷期号:24 (22)
被引量:1
标识
DOI:10.1002/cbic.202300301
摘要
Abstract 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 pro ) 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 pro in drug development and lists a series of design principles and relevant activities of advanced M pro inhibitors, hoping to provide some new directions and ideas for researchers.
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