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将细胞周期蛋白依赖性激酶(CDK)抑制剂重新用作宿主靶向抗病毒药物:一篇综述。

Repurposing of CDK Inhibitors as Host Targeting Antivirals: A Mini- Review.

作者信息

Liu Miao, Peng Wei, Ji Xingyue

机构信息

Jiangsu Province Engineering Research Center of Precision Diagnostics and Therapeutics Development, College of Pharmaceutical Science, Soochow University, Suzhou, Jiangsu, 215021, China.

Department of Gastrointestinal Surgery, Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, 215004, China.

出版信息

Mini Rev Med Chem. 2025;25(3):178-189. doi: 10.2174/0113895575311618240820103549.

Abstract

Most of the antiviral drugs in the market are designed to target viral proteins directly. They are generally considered safe for human use. However, they also suffer from several inherent limitations, in particular, narrow-spectrum antiviral profiles and liability to drug resistance. The other strategy for antiviral drug development is targeting host factors, which are highly involved at different stages in the viral life cycle. In contrast to direct-acting antiviral agents, host-targeting antiviral ones normally exhibit broad-spectrum antiviral properties along with a much higher genetic barrier to drug resistance. Cyclin-dependent kinases (CDKs) represent one such host factor. In this review, we summarized a number of CDK inhibitors (CDKIs) of varied chemical scaffolds with demonstrated antiviral activity. Challenges and issues associated with the repurposing of CDKIs as antiviral agents were also discussed.

摘要

市场上的大多数抗病毒药物都是直接针对病毒蛋白设计的。它们通常被认为对人类使用是安全的。然而,它们也存在一些固有的局限性,特别是抗病毒谱窄和容易产生耐药性。抗病毒药物开发的另一种策略是针对宿主因子,宿主因子在病毒生命周期的不同阶段高度参与。与直接作用的抗病毒药物不同,靶向宿主的抗病毒药物通常具有广谱抗病毒特性,并且对耐药性具有更高的遗传屏障。细胞周期蛋白依赖性激酶(CDKs)就是这样一种宿主因子。在本综述中,我们总结了许多具有不同化学骨架且已证明具有抗病毒活性的CDK抑制剂(CDKIs)。还讨论了将CDKIs重新用作抗病毒药物相关的挑战和问题。

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