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2,5-二酮哌嗪(DKPs):有前途的抗癌药物支架。

2,5-Diketopiperazines (DKPs): Promising Scaffolds for Anticancer Agents.

机构信息

Chemistry Department, Faculty of Science, Benha University, Benha 13518, Egypt.

Nanotechnology Research Centre (NTRC), The British University in Egypt (BUE), Suez Desert Road, El Sherouk City, Cairo 1183, Egypt.

出版信息

Curr Pharm Des. 2024;30(8):597-623. doi: 10.2174/0113816128291798240201112916.

Abstract

2,5-Diketopiperazine (2,5-DKP) derivatives represent a family of secondary metabolites widely produced by bacteria, fungi, plants, animals, and marine organisms. Many natural products with DKP scaffolds exhibited various pharmacological activities such as antiviral, antifungal, antibacterial, and antitumor. 2,5-DKPs are recognized as privileged structures in medicinal chemistry, and compounds that incorporate the 2,5-DKP scaffold have been extensively investigated for their anticancer properties. This review is a thorough update on the anti-cancer activity of natural and synthesized 2,5-DKPs from 1997 to 2022. We have explored various aspects of 2,5-DKPs modifications and summarized their structure-activity relationships (SARs) to gain insight into their anticancer activities. We have also highlighted the novel approaches to enhance the specificity and pharmacokinetics of 2,5-DKP-based anticancer agents.

摘要

2,5-二酮哌嗪(2,5-DKP)衍生物是一类广泛存在于细菌、真菌、植物、动物和海洋生物中的次生代谢产物。许多具有 DKP 支架的天然产物表现出多种药理活性,如抗病毒、抗真菌、抗菌和抗肿瘤。2,5-DKPs 被认为是药物化学中的优势结构,含有 2,5-DKP 支架的化合物因其抗癌特性而得到广泛研究。本文综述了 1997 年至 2022 年天然和合成 2,5-DKPs 的抗癌活性的最新研究进展。我们探讨了 2,5-DKPs 修饰的各个方面,并总结了它们的结构-活性关系(SARs),以深入了解它们的抗癌活性。我们还强调了提高基于 2,5-DKP 的抗癌剂的特异性和药代动力学的新方法。

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