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含希夫碱配体的 Pt(II)和 Au(III) 配合物:抗肿瘤治疗的有前途的来源。

Pt(II) and Au(III) complexes containing Schiff-base ligands: A promising source for antitumor treatment.

机构信息

Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, School of Pharmacy, School of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing, 210023, China.

Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, School of Pharmacy, School of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing, 210023, China; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China; State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing, 210023, China.

出版信息

Eur J Med Chem. 2021 Feb 5;211:113098. doi: 10.1016/j.ejmech.2020.113098. Epub 2020 Dec 11.

Abstract

The effective application of cisplatin in the clinic as an antitumor treatment has stimulated widespread interest in inorganic metal drugs. In particular, complexes containing the transition metals platinum and gold have attracted considerable attention due to their antitumor effects. The Pt(II) and Au(III) Schiff-base complexes are potential antitumor agents because of their remarkable biological activities and good stability, lipophilicity, and electroluminescent properties. These complexes act via various antitumor mechanisms that are unlike those of the classic platinum drugs, providing a feasible solution for improving the serious side effects caused by metal chemotherapy. In this review, promising antitumor agents based on Pt(II) and Au(III) complexes containing Schiff-base ligands, and their biological targets, including G-quadruplex DNA and thioredoxin reductase, are comprehensively summarized.

摘要

顺铂在临床上作为抗肿瘤治疗药物的有效应用激发了人们对无机金属药物的广泛兴趣。特别是,含有过渡金属铂和金的配合物由于其抗肿瘤作用而引起了相当大的关注。Pt(II)和 Au(III)席夫碱配合物是潜在的抗肿瘤剂,因为它们具有显著的生物活性和良好的稳定性、亲脂性和电致发光性能。这些配合物通过不同于经典铂类药物的各种抗肿瘤机制发挥作用,为改善金属化疗引起的严重副作用提供了可行的解决方案。在这篇综述中,全面总结了基于含席夫碱配体的 Pt(II)和 Au(III)配合物的有前途的抗肿瘤剂及其生物靶标,包括 G-四链体 DNA 和硫氧还蛋白还原酶。

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