重新调整用途
蛋白酶
药物重新定位
人类免疫缺陷病毒(HIV)
蛋白酶抑制剂(药理学)
病毒学
医学
药理学
药物发现
药品
药物开发
计算生物学
生物
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
HIV-1蛋白酶
病毒疗法
慢病毒
作者
Dmitrii A. Iuzabchuk,Anastasia A. Andrianova,Ilia V. Yampolsky,Zinaida M. Kaskova,I. V. Smirnov
摘要
Development of de novo therapeutic agents is a complex, costly, and a high-risk process, whereas repurposing approved and investigational drugs for novel targets offers a more efficient and cost-effective strategy, likely yielding higher success rates. This approach demonstrated its effectiveness during SARS-CoV-2 pandemic, when existing drugs were repurposed to combat the virus. Originally pivotal in developing antiviral treatments against HIV and HCV, viral protease inhibitors represent a structurally privileged class of compounds capable of targeting difficult and non-classical protein sites. They have demonstrated promising biological activity against diverse alternative targets, including fungal pathogens, multidrug-resistant bacteria, and cancer, making them prime candidates for repurposing. This mini-review highlights the unique structural and physicochemical properties of approved HCV and HIV viral protease inhibitors that enable their repurposing for the development of new therapeutic agents.
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