喹恶啉衍生物的合成及其生物活性的最新方法。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Thoraya A Farghaly, Raghad M Alqurashi, Ghada S Masaret, Hanan Gaber Abdulwahab
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引用次数: 0

摘要

喹恶啉衍生物已被纳入许多用于治疗各种疾病的上市药物中。实例包括glecaprevir(Mavyret)、voxilaprevir(Vosevi)、Balversa(L01EX16)(erdafitinib)、卡巴多克斯、XK469R(NSC698215)和becompanel(AMP397)。这些喹喔啉衍生物具有多种药理活性,包括抗菌、抗结核、抗病毒、抗HIV、抗炎、抗真菌、抗癌、抗增殖、抗肿瘤、激酶抑制、抗菌、抗氧化和镇痛作用。认识到这些具有生物活性的喹喔啉衍生物的重要性,研究人员致力于开发各种生产方法。本综述旨在汇编2015年至2023年喹喔啉衍生物的合成和生物特性的最新发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent Methods for the Synthesis of Quinoxaline Derivatives and their Biological Activities.

Quinoxaline derivatives have been incorporated into numerous marketed drugs used for the treatment of various diseases. Examples include glecaprevir (Mavyret), voxilaprevir (Vosevi), Balversa (L01EX16) (erdafitinib), carbadox, XK469R (NSC698215), and becampanel (AMP397). These quinoxaline derivatives exhibit a diverse range of pharmacological activities, including antibacterial, antitubercular, antiviral, anti-HIV, anti-inflammatory, antifungal, anticancer, antiproliferative, antitumor, kinase inhibition, antimicrobial, antioxidant, and analgesic effects. Recognizing the significance of these bioactive quinoxaline derivatives, researchers have dedicated their efforts to developing various synthetic methods for their production. This review aimed to compile the most recent findings on the synthesis and biological properties of quinoxaline derivatives from 2015 to 2023.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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