Selepe Mamoalosi A
Department of Chemistry, Faculty of Natural and Agricultural Sciences, University of Pretoria, Private bag X 20, Hatfield, 0028, South Africa.
ChemMedChem. 2024 Dec 2;19(23):e202400420. doi: 10.1002/cmdc.202400420. Epub 2024 Oct 22.
Isoflavones are phenolic natural compounds with a CCC framework. They possess a plethora of biological activities that are associated with putative benefits to human health. In particular, the cancer chemopreventive and chemotherapeutic potential of isoflavones has attracted the interest of researchers. Several isoflavone derivatives have been synthesised and probed for their anticancer activities. The isoflavone analogues are mainly synthesised by molecular hybridisation and other strategies that enable diversification through early or late-stage functionalisation of A-, B- and C-rings of the isoflavones. This has resulted in the discovery of isoflavone analogues with improved antiproliferative activities against several cancer cells and different mechanisms of action. In this review, the synthesis of isoflavone derivatives and their anticancer activity studies are discussed.
异黄酮是具有CCC骨架的酚类天然化合物。它们具有大量的生物活性,这些活性与对人类健康的假定益处相关。特别是,异黄酮的癌症化学预防和化学治疗潜力引起了研究人员的兴趣。已经合成了几种异黄酮衍生物并对其抗癌活性进行了探究。异黄酮类似物主要通过分子杂交和其他策略合成,这些策略能够通过异黄酮A、B和C环的早期或晚期功能化实现多样化。这导致发现了对几种癌细胞具有改善的抗增殖活性和不同作用机制的异黄酮类似物。在这篇综述中,将讨论异黄酮衍生物的合成及其抗癌活性研究。