铂(iv)配合物作为抗癌前药的发展:迄今为止的故事

Daniel Yuan Qiang Wong, W. Ang
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引用次数: 4

摘要

大约四十年前,Barnett Rosenberg偶然发现了顺铂的抗肿瘤特性,这给药物化学领域带来了范式转变,并挑战了关于药物中潜在有毒重金属作用的传统思维。基于铂(II)的抗癌药物已经成为临床医生武器库中最有效和最广泛使用的药物之一,并挽救了无数人的生命。然而,它们受到高毒性、严重副作用和耐药发生率的限制。近年来,人们的注意力已经转移到稳定的铂(IV)配合物作为抗癌前药。通过利用其支架的独特化学和结构属性,这些铂(IV)前药提供了靶向和杀死癌细胞的新策略。本文综述了迄今为止抗癌铂(IV)前体药物的发展,以及利用铂(IV)结构作为靶向化疗药物的一些令人兴奋的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DEVELOPMENT OF PLATINUM(IV) COMPLEXES AS ANTICANCER PRODRUGS: THE STORY SO FAR
The serendipitous discovery of the antitumor properties of cisplatin by Barnett Rosenberg some forty years ago brought about a paradigm shift in the field of medicinal chemistry and challenged conventional thinking regarding the role of potentially toxic heavy metals in drugs. Platinum(II)-based anticancer drugs have since become some of the most effective and widely-used drugs in a clinician's arsenal and have saved countless lives. However, they are limited by high toxicity, severe side-effects and the incidence of drug resistance. In recent years, attention has shifted to stable platinum(IV) complexes as anticancer prodrugs. By exploiting the unique chemical and structural attributes of their scaffolds, these platinum(IV) prodrugs offer new strategies of targeting and killing cancer cells. This review summarizes the development of anticancer platinum(IV) prodrugs to date and some of the exciting strategies that utilise the platinum(IV) construct as targeted chemotherapeutic agents against cancer.
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