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新兴抗病毒药物发现策略:谨以此文献给 Erik De Clercq 教授 80 周年华诞

Newly Emerging Strategies in Antiviral Drug Discovery: Dedicated to Prof. Dr. Erik De Clercq on Occasion of His 80th Anniversary.

机构信息

Key Laboratory of Chemical Biology (Ministry of Education), Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Shandong University, 44 West Culture Road, Jinan 250012, China.

Department of Medicinal Chemistry, School of Pharmacy, Virginia Commonwealth University, 800 E Leigh Street, Richmond, VA 23298, USA.

出版信息

Molecules. 2022 Jan 27;27(3):850. doi: 10.3390/molecules27030850.

Abstract

Viral infections pose a persistent threat to human health. The relentless epidemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a global health problem, with millions of infections and fatalities so far. Traditional approaches such as random screening and optimization of lead compounds by organic synthesis have become extremely resource- and time-consuming. Various modern innovative methods or integrated paradigms are now being applied to drug discovery for significant resistance in order to simplify the drug process. This review provides an overview of newly emerging antiviral strategies, including proteolysis targeting chimera (PROTAC), ribonuclease targeting chimera (RIBOTAC), targeted covalent inhibitors, topology-matching design and antiviral drug delivery system. This article is dedicated to Prof. Dr. Erik De Clercq, an internationally renowned expert in the antiviral drug research field, on the occasion of his 80th anniversary.

摘要

病毒感染对人类健康构成持续威胁。严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)的无情流行已成为全球健康问题,迄今为止已感染数百万人并导致死亡。传统方法,如随机筛选和通过有机合成优化先导化合物,变得极其耗费资源和时间。现在正在应用各种现代创新方法或综合范式来进行药物发现,以应对重大抗性,从而简化药物研发过程。本文综述了新兴的抗病毒策略,包括蛋白水解靶向嵌合体(PROTAC)、核糖核酸酶靶向嵌合体(RIBOTAC)、靶向共价抑制剂、拓扑匹配设计和抗病毒药物传递系统。本文是为了纪念在抗病毒药物研究领域享有国际声誉的专家 Erik De Clercq 教授 80 周年而作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa6e/8839652/1131b658f876/molecules-27-00850-g001.jpg

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