开发 N-杂环衍生物作为抗 SARS-CoV-2 抑制剂的最新进展:综述

IF 1.3 4区 生物学 Q4 CHEMISTRY, MEDICINAL
Walid Ettahiri , Mohamed Adardour , Siham Alaoui , Abderrazzak Elmoutaouakil Ala Allah , Maryem Aichouch , Rajae Salim , Youssef Ramli , Abdelhakim Bouyahya , Mustapha Taleb
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引用次数: 0

摘要

由 COVID-19 引起的大流行阻碍了地球上的一切,包括身心健康、日常生活和全球经济。目前,市场上还没有抗击 SARS-CoV-2 的明确药物和疫苗。已经设计并测试了一些有机化合物来对付这种病毒,但它们并没有显示出良好的活性。自然界中含量丰富的 N-杂环是药理活性化合物的重要来源。N-heterocycles 具有通过各种抗病毒机制发挥抗 SARS-CoV-2 活性的潜力,其中一些已经用于临床或正在进行临床评估,以处理 COVID-19。因此,N-杂环在发现新型抗 SARS-CoV-2 药物中占有重要地位。本研究旨在收集从 2019 年到 2022 年初发表的有关 N-杂环衍生物(吲唑、三唑并嘧啶、吡唑并嘧啶、喹喔啉、苯并咪唑、苯并二氮杂卓、吲哚和喹啉)作为潜在抗 SARS-CoV-2 药物的最新进展、其结构-活性关系和作用机制的文章信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recent advance in the development of N-heterocyclic derivatives as anti-SARS-CoV-2 inhibitors: A review

Recent advance in the development of N-heterocyclic derivatives as anti-SARS-CoV-2 inhibitors: A review

The pandemic caused by COVID-19 hinders everything on earth, including physical and mental health, daily life and the global economy. Currently, there are no defined drugs and few vaccines available on the market to combat SARS-CoV-2. A number of organic compounds have been designed and tested against the virus, but they have not shown promising activities. N-heterocycles, which are abundant in nature, is a significant source of pharmacologically active compounds. N-heterocycles have the potential to exert Anti- SARS-CoV-2 activity via various antiviral mechanisms, and some of them, have already used in clinics or under clinical evaluations for the processing of COVID-19. Therefore, N-heterocycles occupies an important position in the discovery of novel anti-SARS-CoV-2 agents. The current study is an effort to collect information’s covering the articles published from 2019 to the beginning of this year 2022, regarding the recent development of N-heterocycles derivatives; indazole, triazolopyrimidine, pyrazolopyrimidine, quinoxaline, benzimidazole, benzodiazepine, indole, and quinoline, as potential anti-SARS-CoV-2 agents, their structure-activity relationship and mechanisms of action.

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来源期刊
Phytochemistry Letters
Phytochemistry Letters 生物-生化与分子生物学
CiteScore
3.00
自引率
11.80%
发文量
190
审稿时长
34 days
期刊介绍: Phytochemistry Letters invites rapid communications on all aspects of natural product research including: • Structural elucidation of natural products • Analytical evaluation of herbal medicines • Clinical efficacy, safety and pharmacovigilance of herbal medicines • Natural product biosynthesis • Natural product synthesis and chemical modification • Natural product metabolism • Chemical ecology • Biotechnology • Bioassay-guided isolation • Pharmacognosy • Pharmacology of natural products • Metabolomics • Ethnobotany and traditional usage • Genetics of natural products Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.
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