Wang Jun, Shahed-Ai-Mahmud Md, Chen Angelo, Li Kan, Tan Haozhou, Joyce Ryan
Department of Medicinal Chemistry, Ernest Mario School of Pharmacy, Rutgers, the State University of New Jersey, Piscataway, New Jersey 08854, United States.
J Med Chem. 2023 Apr 13;66(7):4468-4490. doi: 10.1021/acs.jmedchem.3c00069. Epub 2023 Mar 24.
The current monkeypox outbreaks during the COVID-19 pandemic have reignited interest in orthopoxvirus antivirals. Monkeypox belongs to the genus of the Poxviridae family, which also includes the variola virus, vaccinia virus, and cowpox virus. Two orally bioavailable drugs, tecovirimat and brincidofovir, have been approved for treating smallpox infections. Given their human safety profiles and in vivo antiviral efficacy in animal models, both drugs have also been recommended to treat monkeypox infection. To facilitate the development of additional orthopoxvirus antivirals, we summarize the antiviral activity, mechanism of action, and mechanism of resistance of orthopoxvirus antivirals. This perspective covers both direct-acting and host-targeting antivirals with an emphasis on drug candidates showing in vivo antiviral efficacy in animal models. We hope to speed the orthopoxvirus antiviral drug discovery by providing medicinal chemists with insights into prioritizing proper drug targets and hits for further development.
在新冠疫情期间当前的猴痘疫情爆发重新点燃了人们对正痘病毒抗病毒药物的兴趣。猴痘属于痘病毒科,该科还包括天花病毒、牛痘病毒和痘苗病毒。两种口服生物可利用药物,即tecovirimat和brincidofovir,已被批准用于治疗天花感染。鉴于它们的人体安全性概况以及在动物模型中的体内抗病毒功效,这两种药物也被推荐用于治疗猴痘感染。为了促进更多正痘病毒抗病毒药物的开发,我们总结了正痘病毒抗病毒药物的抗病毒活性、作用机制和耐药机制。这一观点涵盖了直接作用和靶向宿主的抗病毒药物,重点是在动物模型中显示出体内抗病毒功效的候选药物。我们希望通过为药物化学家提供有关优先选择合适的药物靶点和命中物以进行进一步开发的见解,加速正痘病毒抗病毒药物的发现。