马拉维洛克
CCR5受体拮抗剂
药物开发
药物发现
病毒进入
病毒生命周期
病毒
寄主(生物学)
抗病毒药物
进入抑制剂
计算生物学
病毒学
生物
人类免疫缺陷病毒(HIV)
药品
病毒复制
趋化因子
生物信息学
趋化因子受体
药理学
免疫学
免疫系统
生态学
作者
Yong He,Jiahui Zhou,Huizhan Gao,Chuanfeng Liu,Peng Zhan,Xinyong Liu
标识
DOI:10.1016/j.ejmech.2023.116069
摘要
Viral infections are amongst the most prevalent diseases that pose a significant threat to human health. Targeting viral proteins or host factors represents two primary strategies for the development of antiviral drugs. In contrast to virus-targeting antivirals (VTAs), host-targeting antivirals (HTAs) offer advantages in terms of overcoming drug resistance and effectively combating a wide range of viruses, including newly emerging ones. Therefore, targeting host factors emerges as an extremely promising strategy with the potential to address critical challenges faced by VTAs. In recent years, extensive research has been conducted on the discovery and development of HTAs, leading to the approval of maraviroc, a chemokine receptor type 5 (CCR5) antagonist used for the treatment of HIV-1 infected individuals, with several other potential treatments in various stages of development for different viral infections. This review systematically summarizes advancements made in medicinal chemistry regarding various host targets and classifies them into four distinct catagories based on their involvement in the viral life cycle: virus attachment and entry, biosynthesis, nuclear import and export, and viral release.
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