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2023 年之前报道的椭圆酮衍生物的生物活性和作用机制。

Bioactivities and Action Mechanisms of Ellipticine Derivatives Reported Prior to 2023.

机构信息

College of Pharmacy, Gannan Medical University, Ganzhou, 341000, P. R. China.

Department of Pharmacy, Xingguo People's Hospital, Xingguo Hospital Affiliated to Gannan Medical University, Ganzhou, 342400, P. R. China.

出版信息

Chem Biodivers. 2024 May;21(5):e202400210. doi: 10.1002/cbdv.202400210. Epub 2024 Apr 17.

Abstract

Currently, natural products are one of the priceless options for finding novel chemical pharmaceutical entities. Ellipticine is a naturally occurring alkaloid isolated from the leaves of Ochrosia elliptica Labill. Ellipticine and its derivatives are characterized by multiple biological activities. The purpose of this review was to provide a critical and systematic assessment of ellipticine and its derivatives as bioactive molecules over the last 60 years. Publications focused mainly on the total synthesis of alkaloids of this type without any evaluation of bioactivity have been excluded. We have reviewed papers dealing with the synthesis, bioactivity evaluation and mechanism of action of ellipticine and its derivatives. It was found that ellipticine and its derivatives showed cytotoxicity, antimicrobial ability, and anti-inflammatory activity, among which cytotoxicity toward cancer cell lines was the most investigated aspect. The inhibition of DNA topoisomerase II was the most relevant mechanism for cytotoxicity. The PI3K/AKT pathway, p53 pathway, and MAPK pathway were also closely related to the antiproliferative ability of these compounds. In addition, the structure-activity relationship was deduced, and future prospects were outlined. We are confident that these findings will lay a scientific foundation for ellipticine-based drug development, especially for anticancer agents.

摘要

目前,天然产物是寻找新型化学药物实体的无价选择之一。野百合碱是从野百合的叶子中分离出来的一种天然存在的生物碱。野百合碱及其衍生物具有多种生物活性。本综述的目的是对过去 60 年来作为生物活性分子的野百合碱及其衍生物进行批判性和系统的评估。本文排除了主要关注该类型生物碱的全合成而不评估生物活性的出版物。我们回顾了关于野百合碱及其衍生物的合成、生物活性评价和作用机制的论文。结果发现,野百合碱及其衍生物具有细胞毒性、抗菌能力和抗炎活性,其中对癌细胞系的细胞毒性是研究最多的方面。抑制 DNA 拓扑异构酶 II 是细胞毒性的最相关机制。PI3K/AKT 通路、p53 通路和 MAPK 通路也与这些化合物的抗增殖能力密切相关。此外,还推导出了构效关系,并概述了未来的前景。我们相信这些发现将为以野百合碱为基础的药物开发,特别是抗癌药物的开发奠定科学基础。

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