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吲哚植物抗毒素及其类似物的抗癌潜力。

Anticancer Potential of Indole Phytoalexins and Their Analogues.

机构信息

Department of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University, 040 01 Košice, Slovakia.

出版信息

Molecules. 2024 May 19;29(10):2388. doi: 10.3390/molecules29102388.

Abstract

Indole phytoalexins, found in economically significant family plants, are synthesized in response to pathogen attacks or stress, serving as crucial components of plant defense mechanisms against bacterial and fungal infections. Furthermore, recent research indicates that these compounds hold promise for improving human health, particularly in terms of potential anticancer effects that have been observed in various studies. Since our last comprehensive overview in 2016 focusing on the antiproliferative effects of these substances, brassinin and camalexin have been the most extensively studied. This review analyses the multifaceted pharmacological effects of brassinin and camalexin, highlighting their anticancer potential. In this article, we also provide an overview of the antiproliferative activity of new synthetic analogs of indole phytoalexins, which were synthesized and tested at our university with the aim of enhancing efficacy compared to the parent compound.

摘要

植物吲哚类抗毒素,存在于具有经济重要性的植物家族中,是植物对病原体攻击或胁迫的反应合成的,作为植物防御机制的关键组成部分,可抵抗细菌和真菌感染。此外,最近的研究表明,这些化合物有望改善人类健康,特别是在各种研究中观察到的潜在抗癌作用方面。自我们 2016 年最后一次全面综述关注这些物质的抗增殖作用以来,藜芦硫素和开马毒素一直是研究最多的。本综述分析了藜芦硫素和开马毒素的多方面药理作用,强调了它们的抗癌潜力。在本文中,我们还概述了新合成的吲哚植物抗毒素类似物的抗增殖活性,这些类似物是在我们的大学合成并进行测试的,目的是提高与母体化合物相比的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b313/11124384/3fe296e0d755/molecules-29-02388-g001.jpg

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