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苯乙烯基色酮:生物活性和构效关系。

Styrylchromones: Biological Activities and Structure-Activity Relationship.

机构信息

LAQV, REQUIMTE, Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.

LAQV-REQUIMTE & QOPNA, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.

出版信息

Oxid Med Cell Longev. 2021 Dec 22;2021:2804521. doi: 10.1155/2021/2804521. eCollection 2021.

DOI:10.1155/2021/2804521
PMID:34987699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8720608/
Abstract

Styrylchromones (SC) are a group of oxygen-containing heterocyclic compounds, which are characterized by the attachment of a styryl group to the chromone core. SC can be found in nature or can be chemically synthesized in the laboratory. As their presence in nature is scarce, the synthetic origin is the most common. Two types of SC are known: 2-styrylchromones and 3-styrylchromones. However, 2-styrylchromones are the most common, being more commonly found in nature and which chemical synthesis is more commonly described. A wide variety of SC has been described in the literature, with different substituents in different positions, the majority of which are distributed on the A- and/or B-rings. Over the years, several biological activities have been attributed to SC. This work presents a comprehensive review of the biological activities attributed to SC and their structure-activity relationship, based on a published literature search, since 1989. The following biological activities are thoroughly revised and discussed in this review: antioxidant, antiallergic, antiviral, antibacterial, antifungal, anti-inflammatory, and antitumoral, affinity and selectivity for A adenosine receptors, neuroprotective, and -glucosidase inhibition. In general, SC are composed by a promising scaffold with great potential for the development of new drugs.

摘要

苯乙烯基色酮(SC)是一类含氧杂环化合物,其特征在于苯乙烯基与色酮核心相连。SC 可以在自然界中找到,也可以在实验室中通过化学合成得到。由于自然界中 SC 的存在较为稀少,因此其合成来源最为常见。已知有两种类型的 SC:2-苯乙烯基色酮和 3-苯乙烯基色酮。然而,2-苯乙烯基色酮更为常见,在自然界中更为常见,且其化学合成也更为常见。文献中描述了各种各样的 SC,其不同位置具有不同的取代基,其中大多数分布在 A-和/或 B-环上。多年来,人们已经将多种生物活性归因于 SC。本综述基于已发表的文献检索,自 1989 年以来,对 SC 的生物活性及其构效关系进行了全面综述。在本综述中,对以下生物活性进行了深入的综述和讨论:抗氧化、抗过敏、抗病毒、抗菌、抗真菌、抗炎和抗肿瘤、对 A 腺苷受体的亲和力和选择性、神经保护和β-葡萄糖苷酶抑制。总的来说,SC 是一种很有前途的支架,具有开发新药的巨大潜力。

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