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N-杂环配体的选定金属(金、银和铜)配合物作为潜在抗癌剂的综述

Selected Metal (Au, Ag, and Cu) Complexes of N-heterocyclic Ligands as Potential Anticancer Agents: A Review.

作者信息

Alshamrani Meshal

机构信息

Department of Pharmaceutics, College of Pharmacy, Jazan University, Jazan, Saudi Arabia.

出版信息

Anticancer Agents Med Chem. 2025;25(11):729-740. doi: 10.2174/0118715206331002241119145651.

Abstract

Nitrogen-based organic heterocyclic compounds are an important source of therapeutic agents. About 75% of drugs approved by the FDA and currently available in the market are N-heterocyclic organic compounds. The N-heterocyclic organic compounds like pyridine, indole, triazoles, triazine, imidazoles, benzimidazoles, quinazolines, pyrazoles, quinolines, pyrimidines, porphyrin, etc. have demonstrated significant biological activities. These heterocyclic organic compounds also coordinate with various metal ions and form coordination compounds. Most of them have shown improved biological activities. The research on the metal complexes of these compounds reported their significant biological activities. N-heterocyclic-based metal complexes showed outstanding anticancer activities against different cancer cell lines, including VEGFR-2, HT-29, MDA-MB-231, MCF-7 K562, A549, HepG2, HL60, A2780, WI-38, Colo-205, PC-3, and other cancer cell lines. Some of these compounds showed better anticancer activity than cisplatin. In this review, we summarized the anticancer properties of N-heterocyclic-based gold (Au), silver (Ag), and copper (Cu) complexes and explored the mechanisms of action and potential structure-activity relationships (SAR) of these complexes. Our goal is to assist researchers in designing highly potent N-heterocyclic-based Au, Ag, and Cu complexes for the potential treatment of various cancers.

摘要

氮基有机杂环化合物是治疗药物的重要来源。美国食品药品监督管理局(FDA)批准并在市场上销售的药物中,约75%是N-杂环有机化合物。吡啶、吲哚、三唑、三嗪、咪唑、苯并咪唑、喹唑啉、吡唑、喹啉、嘧啶、卟啉等N-杂环有机化合物已显示出显著的生物活性。这些杂环有机化合物还能与各种金属离子配位并形成配位化合物。其中大多数已显示出增强的生物活性。对这些化合物的金属配合物的研究报道了它们显著的生物活性。基于N-杂环的金属配合物对包括VEGFR-2、HT-29、MDA-MB-231、MCF-7、K562、A549、HepG2、HL60、A2780、WI-38、Colo-205、PC-3等不同癌细胞系显示出出色的抗癌活性。其中一些化合物的抗癌活性比顺铂更好。在本综述中,我们总结了基于N-杂环的金(Au)、银(Ag)和铜(Cu)配合物的抗癌特性,并探讨了这些配合物的作用机制和潜在的构效关系(SAR)。我们的目标是帮助研究人员设计出高效的基于N-杂环的Au、Ag和Cu配合物,用于潜在治疗各种癌症。

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