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阿马瑞利氏科小生物碱类中的细胞毒素剂。

Cytotoxic Agents in the Minor Alkaloid Groups of the Amaryllidaceae.

机构信息

Research Centre for Plant Growth and Development, University of KwaZulu-Natal Pietermaritzburg, Scottsville, South Africa.

出版信息

Planta Med. 2021 Oct;87(12-13):916-936. doi: 10.1055/a-1380-1888. Epub 2021 Mar 11.

DOI:10.1055/a-1380-1888
PMID:33706400
Abstract

Over 600 alkaloids have to date been identified in the plant family Amaryllidaceae. These have been arranged into as many as 15 different groups based on their characteristic structural features. The vast majority of studies on the biological properties of Amaryllidaceae alkaloids have probed their anticancer potential. While most efforts have focused on the major alkaloid groups, the volume and diversity afforded by the minor alkaloid groups have promoted their usefulness as targets for cancer cell line screening purposes. This survey is an in-depth review of such activities described for around 90 representatives from 10 minor alkaloid groups of the Amaryllidaceae. These have been evaluated against over 60 cell lines categorized into 18 different types of cancer. The montanine and cripowellin groups were identified as the most potent, with some in the latter demonstrating low nanomolar level antiproliferative activities. Despite their challenging molecular architectures, the minor alkaloid groups have allowed for facile adjustments to be made to their structures, thereby altering the size, geometry, and electronics of the targets available for structure-activity relationship studies. Nevertheless, it was seen with a regular frequency that the parent alkaloids were better cytotoxic agents than the corresponding semisynthetic derivatives. There has also been significant interest in how the minor alkaloid groups manifest their effects in cancer cells. Among the various targets and pathways in which they were seen to mediate, their ability to induce apoptosis in cancer cells is most appealing.

摘要

迄今为止,在石蒜科植物家族中已鉴定出超过 600 种生物碱。根据其特征结构特征,这些生物碱已被排列成多达 15 个不同的组。对石蒜科生物碱的生物特性的绝大多数研究都探讨了它们的抗癌潜力。虽然大多数努力都集中在主要的生物碱群体上,但由于次要生物碱群体的数量和多样性,它们已成为癌细胞系筛选目的的有用目标。本调查是对大约 90 种来自石蒜科的 10 种次要生物碱组的代表性研究的深入回顾。这些已针对超过 60 种细胞系进行了评估,这些细胞系分为 18 种不同类型的癌症。蒙坦宁和克里波韦林组被认为是最有效的,其中一些在后一组中表现出低纳摩尔水平的抗增殖活性。尽管它们具有挑战性的分子结构,但次要生物碱群体允许对其结构进行易于调整,从而改变用于结构-活性关系研究的目标的大小、几何形状和电子性质。然而,经常看到母生物碱比相应的半合成衍生物具有更好的细胞毒性。人们也对次要生物碱群体如何在癌细胞中发挥作用产生了浓厚的兴趣。在它们被认为介导的各种靶标和途径中,它们诱导癌细胞凋亡的能力最具吸引力。

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