Quinoxaline Moiety: A Potential Scaffold against Mycobacterium tuberculosis

被引:28
|
作者
Montana, Marc [1 ,2 ]
Montero, Vincent [1 ]
Khoumeri, Omar [1 ]
Vanelle, Patrice [1 ,3 ]
机构
[1] Aix Marseille Univ, CNRS, ICR, Equipe Pharmacochim Radicalaire,Fac Pharm, F-13005 Marseille, France
[2] Oncopharma, AP HM, F-13015 Marseille, France
[3] AP HM, Serv Cent Qualite & Informat Pharmaceut SCQIP, F-13005 Marseille, France
来源
MOLECULES | 2021年 / 26卷 / 16期
关键词
quinoxaline; Mycobacterium; tuberculosis; SAR; biological applications; chemistry; IN-VITRO; ANTIMYCOBACTERIAL ACTIVITY; 1,4-DI-N-OXIDE DERIVATIVES; AMIDE DERIVATIVES; DESIGN; 1,2-DIAMINES; RESISTANT; DISCOVERY; 3D-QSAR; GREEN;
D O I
10.3390/molecules26164742
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background. The past decades have seen numerous efforts to develop new antitubercular agents. Currently, the available regimens are lengthy, only partially effective, and associated with high rates of adverse events. The challenge is therefore to develop new agents with faster and more efficient action. The versatile quinoxaline ring possesses a broad spectrum of pharmacological activities, ensuring considerable attention to it in the field of medicinal chemistry. Objectives. In continuation of our program on the pharmacological activity of quinoxaline derivatives, this review focuses on potential antimycobacterial activity of recent quinoxaline derivatives and discusses their structure-activity relationship for designing new analogs with improved activity. Methods. The review compiles recent studies published between January 2011 and April 2021. Results. The final total of 23 studies were examined. Conclusions. Data from studies of quinoxaline and quinoxaline 1,4-di-N-oxide derivatives highlight that specific derivatives show encouraging perspectives in the treatment of Mycobacterium tuberculosis and the recent growing interest for these scaffolds. These interesting results warrant further investigation, which may allow identification of novel antitubercular candidates based on this scaffold.
引用
收藏
页数:23
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