化学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
对偶(语法数字)
2019年冠状病毒病(COVID-19)
2019-20冠状病毒爆发
计算生物学
病毒学
内科学
传染病(医学专业)
疾病
医学
艺术
文学类
爆发
生物
作者
Wenyi Zhang,Lecheng Xiao,D. Li,Yuxuan Hu,Wenying Yu
标识
DOI:10.1021/acs.jmedchem.4c00384
摘要
The 2019 coronavirus disease (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in millions of deaths, posing a serious threat to public health and safety. Rapid mutations of SARS-CoV-2 and complex interactions among multiple targets during infection pose a risk of expiry for small molecule inhibitors. This suggests that the traditional concept of "one bug, one drug" could be ineffective in dealing with the coronavirus. The dual-target drug strategy is expected to be the key to ending coronavirus infections. However, the lack of design method and improper combination of dual-targets poses obstacle to the discovery of new dual-target drugs. In this Perspective, we summarized the profiles concerning drug design methods, structure-activity relationships, and pharmacological parameters of dual-target drugs for the treatment of COVID-19. Importantly, we underscored how target combination and rational drug design illuminate the development of dual-target drugs for SARS-CoV-2.
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