Department of Chemistry, United Arab Emirates University, Al-Ain, United Arab Emirates.
Department of Chemistry, Faculty of Science, Cairo University, Gamma Street, 12613, Egypt.
Dalton Trans. 2024 Jun 10;53(23):9612-9656. doi: 10.1039/d4dt00087k.
Carbon monoxide, the "silent killer" gas, is increasingly recognised as an important signalling molecule in human physiology, which has beneficial biological properties. A particular way of achieving controlled CO administration is based on the use of biocompatible molecules that only release CO when triggered by internal or external factors. These approaches include the development of pharmacologically effective prodrugs known as CO releasing molecules (CORMs), which can supply biological systems with CO in well-regulated doses. An overview of transition metal-based CORMs with cytotoxic properties is here reported. The mechanisms at the basis of the biological activities of these molecules and their potential therapeutical applications with respect to their stability and CO releasing properties have been discussed. The activation of metal-based CORMs is determined by the type of metal and by the nature and features of the auxiliary ligands, which affect the metal core electronic density and therefore the prodrug resistance towards oxidation and CO release ability. A major role in regulating the cytotoxic properties of these CORMs is played by CO and/or CO-depleted species. However, several mysteries concerning the cytotoxicity of CORMs remain as intriguing questions for scientists.
一氧化碳,这种“沉默的杀手”气体,越来越被认为是人体生理学中一种重要的信号分子,具有有益的生物学特性。一种实现 CO 受控给药的特殊方法是基于使用生物相容性分子,这些分子只有在内部或外部因素触发时才会释放 CO。这些方法包括开发被称为一氧化碳释放分子(CORMs)的药理学有效前药,这些前药可以以良好调节的剂量向生物系统提供 CO。本文综述了具有细胞毒性的基于过渡金属的 CORMs。讨论了这些分子的生物学活性的基础机制及其在稳定性和 CO 释放特性方面的潜在治疗应用。金属基 CORMs 的激活取决于金属的类型以及辅助配体的性质和特征,这会影响金属核的电子密度,从而影响前药对氧化的抗性和 CO 释放能力。CO 和/或 CO 耗尽物种在调节这些 CORMs 的细胞毒性特性方面起着主要作用。然而,CORMs 的细胞毒性仍有一些未解之谜,这仍是科学家们感兴趣的问题。