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针对 SARS-CoV-2 主蛋白酶的非肽类抑制剂:综述。

Non-peptidic inhibitors targeting SARS-CoV-2 main protease: A review.

机构信息

School of Chemical Engineering and Pharmacy, Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.

School of Chemical Engineering and Pharmacy, Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.

出版信息

Bioorg Chem. 2024 Jun;147:107380. doi: 10.1016/j.bioorg.2024.107380. Epub 2024 Apr 16.

Abstract

The COVID-19 pandemic continues to pose a threat to global health, and sounds the alarm for research & development of effective anti-coronavirus drugs, which are crucial for the patients and urgently needed for the current epidemic and future crisis. The main protease (M) stands as an essential enzyme in the maturation process of SARS-CoV-2, playing an irreplaceable role in regulating viral RNA replication and transcription. It has emerged as an ideal target for developing antiviral agents against SARS-CoV-2 due to its high conservation and the absence of homologous proteases in the human body. Among the SARS-CoV-2 M inhibitors, non-peptidic compounds hold promising prospects owing to their excellent antiviral activity and improved metabolic stability. In this review, we offer an overview of research progress concerning non-peptidic SARS-CoV-2 M inhibitors since 2020. The efforts delved into molecular structures, structure-activity relationships (SARs), biological activity, and binding modes of these inhibitors with M. This review aims to provide valuable clues and insights for the development of anti-SARS-CoV-2 agents as well as broad-spectrum coronavirus M inhibitors.

摘要

新冠疫情继续对全球健康构成威胁,促使人们加紧研发有效的抗冠状病毒药物,这对于患者至关重要,也是当前疫情和未来危机所急需的。主蛋白酶(M)是 SARS-CoV-2 成熟过程中的一种必需酶,在调节病毒 RNA 复制和转录方面发挥着不可替代的作用。由于其高度保守性和人体内不存在同源蛋白酶,它已成为开发抗 SARS-CoV-2 抗病毒药物的理想靶点。在 SARS-CoV-2 M 抑制剂中,非肽类化合物因其出色的抗病毒活性和改善的代谢稳定性而具有广阔的前景。本综述概述了自 2020 年以来非肽类 SARS-CoV-2 M 抑制剂的研究进展。研究深入探讨了这些抑制剂与 M 的分子结构、构效关系(SARs)、生物活性和结合模式。本综述旨在为开发抗 SARS-CoV-2 药物以及广谱冠状病毒 M 抑制剂提供有价值的线索和见解。

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