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铁-亚硝酰配合物在药物研发中的应用:当代进展。

Iron-Imine Cocktail in Drug Development: A Contemporary Update.

机构信息

School of Integrative Biological and Chemical Sciences (SIBCS), University of Texas Rio Grande Valley, Edinburg, TX 78539, USA.

Laboratorio de Biotecnología Farmacéutica, Centro de Biotecnología Genómica, Instituto Politécnico Nacional, Reynosa 88710, Mexico.

出版信息

Int J Mol Sci. 2024 Feb 13;25(4):2263. doi: 10.3390/ijms25042263.

DOI:10.3390/ijms25042263
PMID:38396940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10888693/
Abstract

Organometallic drug development is still in its early stage, but recent studies show that organometallics having iron as the central atom have the possibility of becoming good drug candidates because iron is an important micro-nutrient, and it is compatible with many biological systems, including the human body. Being an eco-friendly Lewis acid, iron can accept the lone pair of electrons from imino(sp)-nitrogen, and the resultant iron-imine complexes with iron as a central atom have the possibility of interacting with several proteins and enzymes in humans. Iron-imine complexes have demonstrated significant potential with anticancer, bactericidal, fungicidal, and other medicinal activities in recent years. This article systematically discusses major synthetic methods and pharmacological potentials of iron-imine complexes having in vitro activity to significant clinical performance from 2016 to date. In a nutshell, this manuscript offers a simplistic view of iron complexes in medicinal inorganic chemistry: for instance, iron is presented as an "eco-friendly non-toxic" metal (as opposed to platinum) that will lead to non-toxic pharmaceuticals. The abundant literature on iron chelators shows that many iron complexes, particularly if redox-active in cells, can be quite cytotoxic, which can be beneficial for future targeted therapies. While we made every effort to include all the related papers, any omission is purely unintentional.

摘要

金属有机药物研发仍处于起步阶段,但最近的研究表明,以铁为中心原子的金属有机化合物有可能成为良好的药物候选物,因为铁是一种重要的微量营养素,它与许多生物系统(包括人体)兼容。作为一种环保型路易斯酸,铁可以接受亚氨基(sp)-氮的孤对电子,所得的铁-亚胺配合物以铁为中心原子,有可能与人体中的几种蛋白质和酶相互作用。近年来,铁-亚胺配合物在抗癌、杀菌、杀菌等药物活性方面表现出了显著的潜力。本文系统地讨论了从 2016 年至今具有体外活性的铁-亚胺配合物的主要合成方法和药理学潜力,以期达到显著的临床效果。简而言之,本文为药物无机化学中的铁配合物提供了一个简单的观点:例如,铁被呈现为一种“环保无毒”的金属(与铂相反),这将导致无毒的药物。丰富的铁螯合剂文献表明,许多铁配合物,特别是在细胞中具有氧化还原活性的铁配合物,可能具有相当的细胞毒性,这对未来的靶向治疗可能是有益的。虽然我们尽力包括了所有相关的论文,但任何遗漏纯粹是无意的。

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