重新调整用途
2019年冠状病毒病(COVID-19)
小分子
药物开发
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
药物重新定位
药物发现
药品
蛋白酵素
医学
计算生物学
药理学
生物
生物信息学
传染病(医学专业)
疾病
酶
遗传学
生态学
病理
生物化学
作者
Sibei Lei,Xiaohua Chen,Jieping Wu,Xingmei Duan,Ke Men
标识
DOI:10.1038/s41392-022-01249-8
摘要
Abstract The outbreak of COVID-19 has become a global crisis, and brought severe disruptions to societies and economies. Until now, effective therapeutics against COVID-19 are in high demand. Along with our improved understanding of the structure, function, and pathogenic process of SARS-CoV-2, many small molecules with potential anti-COVID-19 effects have been developed. So far, several antiviral strategies were explored. Besides directly inhibition of viral proteins such as RdRp and M pro , interference of host enzymes including ACE2 and proteases, and blocking relevant immunoregulatory pathways represented by JAK/STAT, BTK, NF-κB, and NLRP3 pathways, are regarded feasible in drug development. The development of small molecules to treat COVID-19 has been achieved by several strategies, including computer-aided lead compound design and screening, natural product discovery, drug repurposing, and combination therapy. Several small molecules representative by remdesivir and paxlovid have been proved or authorized emergency use in many countries. And many candidates have entered clinical-trial stage. Nevertheless, due to the epidemiological features and variability issues of SARS-CoV-2, it is necessary to continue exploring novel strategies against COVID-19. This review discusses the current findings in the development of small molecules for COVID-19 treatment. Moreover, their detailed mechanism of action, chemical structures, and preclinical and clinical efficacies are discussed.
科研通智能强力驱动
Strongly Powered by AbleSci AI