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基于羟基吡啶酮的金属螯合剂的生态毒性:修复及生物机制。

Hydroxypyridinone-Based Metal Chelators towards Ecotoxicity: Remediation and Biological Mechanisms.

机构信息

Centro de Química Estrutural and Departamento de Engenharia Química, Institute of Molecular Sciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais 1, 1049-001 Lisboa, Portugal.

Dipartimento di Scienze Chimiche, Biologiche, Farmaceutiche ed Ambientali, Università di Messina, Viale F. Stagno d'Alcontres, 31, I-98166 Messina, Italy.

出版信息

Molecules. 2022 Mar 18;27(6):1966. doi: 10.3390/molecules27061966.

Abstract

Hydroxypyridinones (HPs) are recognized as excellent chemical tools for engineering a diversity of metal chelating agents, with high affinity for metal ions, exhibiting a broad range of activities and applications, namely in medical, biological and environmental contexts. They are easily made and functionalizable towards the tuning of their pharmacokinetic properties or the improving of their metal complex thermodynamic stabilities. In this review, an analysis of the recently published works on hydroxypyridinone-based ligands, that have been mostly addressed for environmental applications, namely for remediation of metal ion ecotoxicity in living beings and other biological matrices is carried out. In particular, herein the most recent developments in the design of new chelating systems, from bidentate mono-HP to polydentate multi-HP derivatives, with a structural diversity of soluble or solid-supported backbones are outlined. Along with the ligand design, an analysis of the relationship between their structures and activities is presented and discussed, namely associated with the metal affinity and the thermodynamic stability of the corresponding metal complexes.

摘要

羟基吡啶酮 (HPs) 被认为是工程化多种金属螯合剂的优秀化学工具,对金属离子具有高亲和力,表现出广泛的活性和应用,即在医学、生物和环境方面。它们易于制备并且可官能化,以调整其药代动力学性质或提高其金属配合物热力学稳定性。在这篇综述中,对最近发表的基于羟基吡啶酮配体的研究工作进行了分析,这些工作主要针对环境应用,即用于修复生物体内和其他生物基质中金属离子的生态毒性。特别是,本文概述了新型螯合系统的最新设计进展,从双齿单-HP 到多齿多-HP 衍生物,具有可溶性或固载骨架的结构多样性。除了配体设计外,还分析并讨论了它们的结构与活性之间的关系,特别是与金属亲和力和相应金属配合物的热力学稳定性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e89/8950932/803776771388/molecules-27-01966-g001.jpg

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