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吲哚类化合物在抗疟疾、锥虫病和利什曼病方面的研究进展。

Recent Progress in the Development of Indole-Based Compounds Active against Malaria, Trypanosomiasis and Leishmaniasis.

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, 1649-003 Lisbon, Portugal.

出版信息

Molecules. 2022 Jan 5;27(1):319. doi: 10.3390/molecules27010319.

Abstract

Human protozoan diseases represent a serious health problem worldwide, affecting mainly people in social and economic vulnerability. These diseases have attracted little investment in drug discovery, which is reflected in the limited available therapeutic arsenal. Authorized drugs present problems such as low efficacy in some stages of the disease or toxicity, which result in undesirable side effects and treatment abandonment. Moreover, the emergence of drug-resistant parasite strains makes necessary an even greater effort to develop safe and effective antiparasitic agents. Among the chemotypes investigated for parasitic diseases, the indole nucleus has emerged as a privileged molecular scaffold for the generation of new drug candidates. In this review, the authors provide an overview of the indole-based compounds developed against important parasitic diseases, namely malaria, trypanosomiasis and leishmaniasis, by focusing on the design, optimization and synthesis of the most relevant synthetic indole scaffolds recently reported.

摘要

人体原生动物疾病是一个全球性的严重健康问题,主要影响社会和经济弱势群体中的人群。这些疾病在药物发现方面的投资很少,这反映在可用的治疗武器库非常有限。已授权的药物存在一些问题,例如在疾病的某些阶段疗效低或毒性,这会导致不良的副作用和治疗中断。此外,寄生虫耐药株的出现使得开发安全有效的抗寄生虫药物变得更加必要。在针对寄生虫病的化学类型中,吲哚核已成为生成新候选药物的优势分子支架。在这篇综述中,作者通过重点介绍最近报道的最相关的合成吲哚支架的设计、优化和合成,提供了针对疟疾、锥虫病和利什曼病等重要寄生虫病开发的基于吲哚的化合物的概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7d/8746838/41e5799df064/molecules-27-00319-g001.jpg

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