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喹啉:药物设计中的有吸引力的骨架。

Quinoline: An Attractive Scaffold in Drug Design.

机构信息

Departamento de Quimica Organica, Programa de Pos-Graduacao em Quimica, Instituto de Quimica, Universidade Federal Fluminense, Outeiro de Sao Joao Batista, s/no, Centro, Niteroi, 24020-141, Rio de Janeiro, Brazil.

出版信息

Mini Rev Med Chem. 2021;21(16):2209-2226. doi: 10.2174/1389557521666210210155908.

DOI:10.2174/1389557521666210210155908
PMID:33568032
Abstract

Quinoline and its derivatives comprise an important group of heterocyclic compounds that exhibits a wide range of pharmacological properties such as antibacterial, antiviral, anticancer, antiparasitic, anti-Alzheimer and anticholesterol. The quinoline nucleus is found in the structure of many drugs and rational design in medicinal chemistry for the discovery of novel bioactive molecules. Persistent efforts have been made over the years to develop novel congeners with superior biological activities and minimal potential for undesirable side effects. This review highlights some discoveries on the development of quinoline-based compounds in recent years (2013-2019), focusing on their biological activities, including anticancer, antitubercular, antimalarial, anti-ZIKV, anti-DENV, anti- Leishmania and anti-Alzheimer's disease.

摘要

喹啉及其衍生物是一类重要的杂环化合物,具有广泛的药理活性,如抗菌、抗病毒、抗癌、抗寄生虫、抗阿尔茨海默病和降胆固醇。喹啉核存在于许多药物的结构中,在药物化学中对其进行合理设计以发现新的生物活性分子。多年来,人们一直致力于开发具有更好生物活性和最小不良副作用潜力的新型同系物。本文综述了近年来(2013-2019 年)在喹啉类化合物开发方面的一些发现,重点介绍了它们的生物活性,包括抗癌、抗结核、抗疟疾、抗寨卡病毒、抗登革热病毒、抗利什曼原虫和抗阿尔茨海默病。

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1
Quinoline: An Attractive Scaffold in Drug Design.喹啉:药物设计中的有吸引力的骨架。
Mini Rev Med Chem. 2021;21(16):2209-2226. doi: 10.2174/1389557521666210210155908.
2
5-Oxo-hexahydroquinoline: an attractive scaffold with diverse biological activities.5-氧代己基六氢喹啉:一种具有多种生物活性的有吸引力的支架。
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A comprehensive review on the biological interest of quinoline and its derivatives.喹啉及其衍生物的生物学研究进展综述
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Quinolines, a perpetual, multipurpose scaffold in medicinal chemistry.喹啉,医药化学中永恒的多功能支架。
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Quinoline Derivatives as Promising Scaffolds for Antitubercular Activity: A Comprehensive Review.喹啉衍生物作为抗结核活性的有前景骨架:综述
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Identification of quinoline-chalcones and heterocyclic chalcone-appended quinolines as broad-spectrum pharmacological agents.鉴定喹啉查耳酮和杂环查尔酮取代喹啉作为广谱药理试剂。
Bioorg Chem. 2020 Dec;105:104419. doi: 10.1016/j.bioorg.2020.104419. Epub 2020 Oct 22.
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Synthetic Methods of Quinoline Derivatives as Potent Anticancer Agents.喹啉衍生物作为强效抗癌剂的合成方法。
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Therapeutic significance of quinolines: a patent review (2013-2015).喹啉类药物的治疗意义:专利综述(2013 - 2015年)
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Friedlӓnder's synthesis of quinolines as a pivotal step in the development of bioactive heterocyclic derivatives in the current era of medicinal chemistry.弗里德兰德喹啉合成法是当代药物化学中生物活性杂环衍生物发展的关键步骤。
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Biological activities of quinoline derivatives.喹啉衍生物的生物活性。
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Evaluating Quinolines: Molecular Dynamics Approach to Assess Their Potential as Acetylcholinesterase Inhibitors for Alzheimer's Disease.评估喹啉类化合物:采用分子动力学方法评估其作为阿尔茨海默病乙酰胆碱酯酶抑制剂的潜力
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Designing novel anti-plasmodial quinoline-furanone hybrids: computational insights, synthesis, and biological evaluation targeting lactate dehydrogenase.新型抗疟喹啉-呋喃酮杂合物的设计:基于乳酸脱氢酶的计算分析、合成及生物学评价
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Saturation Transfer Difference NMR and Molecular Docking Interaction Study of Aralkyl-Thiodigalactosides as Potential Inhibitors of the Human-Galectin-3 Protein.饱和转移差异 NMR 与烷基硫代半乳糖苷作为人半乳糖凝集素-3 蛋白潜在抑制剂的分子对接相互作用研究。
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Design, synthesis and evaluation of quinoline--carbamate derivatives as multifunctional agents for the treatment of Alzheimer's disease.设计、合成及评估喹啉-氨基甲酸酯衍生物作为治疗阿尔茨海默病的多功能药物。
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