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苯并呋喃衍生物的天然来源、生物活性及合成

Natural source, bioactivity and synthesis of benzofuran derivatives.

作者信息

Miao Yu-Hang, Hu Yu-Heng, Yang Jie, Liu Teng, Sun Jie, Wang Xiao-Jing

机构信息

School of Medicine and Life Sciences, University of Jinan, Shandong Academy of Medical Sciences Jinan 250200 Shandong China

Institute of Materia Medica, Shandong Academy of Medical Sciences Jinan 250062 Shandong China.

出版信息

RSC Adv. 2019 Sep 2;9(47):27510-27540. doi: 10.1039/c9ra04917g. eCollection 2019 Aug 29.

Abstract

Benzofuran compounds are a class of compounds that are ubiquitous in nature. Numerous studies have shown that most benzofuran compounds have strong biological activities such as anti-tumor, antibacterial, anti-oxidative, and anti-viral activities. Owing to these biological activities and potential applications in many aspects, benzofuran compounds have attracted more and more attention of chemical and pharmaceutical researchers worldwide, making these substances potential natural drug lead compounds. For example, the recently discovered novel macrocyclic benzofuran compound has anti-hepatitis C virus activity and is expected to be an effective therapeutic drug for hepatitis C disease; novel scaffold compounds of benzothiophene and benzofuran have been developed and utilized as anticancer agents. Novel methods for constructing benzofuran rings have been discovered in recent years. A complex benzofuran derivative is constructed by a unique free radical cyclization cascade, which is an excellent method for the synthesis of a series of difficult-to-prepare polycyclic benzofuran compounds. Another benzofuran ring constructed by proton quantum tunneling has not only fewer side reactions, but also high yield, which is conducive to the construction of complex benzofuran ring systems. This review summarizes the recent studies on the various aspects of benzofuran derivatives including their important natural product sources, biological activities and drug prospects, and chemical synthesis, as well as the relationship between the bioactivities and structures.

摘要

苯并呋喃类化合物是一类在自然界中广泛存在的化合物。大量研究表明,大多数苯并呋喃类化合物具有抗肿瘤、抗菌、抗氧化和抗病毒等强大的生物活性。由于这些生物活性以及在许多方面的潜在应用,苯并呋喃类化合物已引起全球化学和制药研究人员越来越多的关注,使这些物质成为潜在的天然药物先导化合物。例如,最近发现的新型大环苯并呋喃化合物具有抗丙型肝炎病毒活性,有望成为丙型肝炎疾病的有效治疗药物;苯并噻吩和苯并呋喃的新型骨架化合物已被开发并用作抗癌剂。近年来发现了构建苯并呋喃环的新方法。通过独特的自由基环化级联反应构建了一种复杂的苯并呋喃衍生物,这是合成一系列难以制备的多环苯并呋喃化合物的优异方法。另一种通过质子量子隧穿构建的苯并呋喃环不仅副反应少,而且产率高,有利于构建复杂的苯并呋喃环系统。本综述总结了苯并呋喃衍生物在各个方面的最新研究,包括其重要的天然产物来源、生物活性和药物前景、化学合成以及生物活性与结构之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c85/9070854/9b594081e259/c9ra04917g-f1.jpg

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