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喹啉作为一种优势结构:合成与生物活性的最新研究进展。

Quinoline as a Privileged Structure: A Recent Update on Synthesis and Biological Activities.

机构信息

Department of Chemistry, University of Lucknow, Lucknow-226007, UP, India.

出版信息

Curr Top Med Chem. 2024;24(27):2377-2419. doi: 10.2174/0115680266314303240830074056.

DOI:10.2174/0115680266314303240830074056
PMID:39313876
Abstract

Among heterocyclic compounds, quinoline is one of the best ubiquitous heterocyclic rings for medicinal chemistry purposes. Quinoline appears to be a powerful chemical structure to develop new drug entities. The quinoline derivatives own a wide array of biological activities such as anticancer, antimalarial, antimicrobial, anti-inflammatory, anti-leishmanial, etc. Because of the wide spectrum of bioactivities, the scientific communities are still looking for more efficient synthetic routes to form quinoline derivatives. Therefore, the primary focus of this review is to provide a thorough and inclusive, updated report on quinoline analogs that may pave the way for more efficient drug development.

摘要

在杂环化合物中,喹啉是医药化学中用途最广泛的杂环之一。喹啉似乎是开发新药物实体的强大化学结构。喹啉衍生物具有广泛的生物活性,如抗癌、抗疟、抗菌、抗炎、抗利什曼原虫等。由于其广泛的生物活性,科学界仍在寻找更有效的合成途径来合成喹啉衍生物。因此,本综述的主要重点是提供关于喹啉类似物的全面、综合和最新报告,为更有效的药物开发铺平道路。

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本文引用的文献

1
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
RSC Adv. 2024 Jun 12;14(26):18764-18776. doi: 10.1039/d4ra01804d. eCollection 2024 Jun 6.
2
Synthesis,Antidiabetic and Antitubercular Evaluation of Quinoline-pyrazolopyrimidine hybrids and Quinoline-4-Arylamines.喹啉-吡唑并嘧啶杂合体和喹啉-4-芳胺的合成、抗糖尿病和抗结核评估。
ChemistryOpen. 2024 Sep;13(9):e202400014. doi: 10.1002/open.202400014. Epub 2024 Mar 20.
3
Developing a new multi-featured chitosan-quinoline Schiff base with potent antibacterial, antioxidant, and antidiabetic activities: design and molecular modeling simulation.
开发一种具有强大抗菌、抗氧化和抗糖尿病活性的新型多功能壳聚糖-喹啉席夫碱:设计与分子模拟仿真。
Sci Rep. 2023 Dec 21;13(1):22792. doi: 10.1038/s41598-023-50130-3.
4
Visible-Light-Mediated Annulation/Thiolation of 2-Isocyanobiaryls with Disulfides to Organoylthiophenanthridines Derivatives.可见光介导的2-异氰基联芳基与二硫化物环化/硫醇化反应合成有机硫代菲啶衍生物
J Org Chem. 2023 Dec 15;88(24):17322-17329. doi: 10.1021/acs.joc.3c02152. Epub 2023 Dec 3.
5
Design, synthesis, and biological evaluation of quinoline-piperazine/pyrrolidine derivatives as possible antileishmanial agents.设计、合成及喹啉-哌嗪/吡咯烷衍生物的生物评价作为可能的抗利什曼原虫药物。
Eur J Med Chem. 2023 Dec 5;261:115863. doi: 10.1016/j.ejmech.2023.115863. Epub 2023 Oct 7.
6
Quinoline- and Isoindoline-Integrated Polycyclic Compounds as Antioxidant, and Antidiabetic Agents Targeting the Dual Inhibition of α-Glycosidase and α-Amylase Enzymes.喹啉和异吲哚啉整合的多环化合物作为抗氧化剂和抗糖尿病药物,靶向α-糖苷酶和α-淀粉酶的双重抑制作用。
Pharmaceuticals (Basel). 2023 Aug 30;16(9):1222. doi: 10.3390/ph16091222.
7
Discovery and Structural Optimization of Novel Quinolone Derivatives as Potent Irreversible Pan-Fibroblast Growth Factor Receptor Inhibitors for Treating Solid Tumors.新型喹诺酮衍生物的发现和结构优化,作为治疗实体瘤的有效、不可逆的泛成纤维细胞生长因子受体抑制剂。
J Med Chem. 2023 Jul 13;66(13):8858-8875. doi: 10.1021/acs.jmedchem.3c00455. Epub 2023 Jun 19.
8
Versatile applications of transition metal incorporating quinoline Schiff base metal complexes: An overview.过渡金属整合喹啉席夫碱金属配合物的多功能应用:概述。
Eur J Med Chem. 2023 Oct 5;258:115549. doi: 10.1016/j.ejmech.2023.115549. Epub 2023 Jun 8.
9
A Pummerer Reaction-Enabled Modular Synthesis of Alkyl Quinoline-3-carboxylates and 3-Arylquinolines from Amino Acids.氨基酸促进的 Pummerer 反应模块化合成烷基喹啉-3-羧酸酯和 3-芳基喹啉
J Org Chem. 2023 Mar 17;88(6):3760-3771. doi: 10.1021/acs.joc.2c03034. Epub 2023 Feb 23.
10
Cu-Catalyzed Decarboxylative Annulation of -Phenylglycines with Maleimides: Synthesis of 1-Pyrrolo[3,4-]quinoline-1,3(2)-diones.铜催化的 - 苯甘氨酸与马来酰亚胺的脱羧环化反应:1-吡咯并[3,4-]喹啉-1,3(2)-二酮的合成。
J Org Chem. 2023 Feb 17;88(4):2358-2366. doi: 10.1021/acs.joc.2c02757. Epub 2023 Feb 8.