SAR Analysis of Small Molecules Interfering with Energy-Metabolism in Mycobacterium tuberculosis

被引:14
作者
Appetecchia, Federico [1 ]
Consalvi, Sara [1 ]
Scarpecci, Cristina [1 ]
Biava, Mariangela [1 ]
Poce, Giovanna [1 ]
机构
[1] Sapienza Univ Rome, Dept Chem & Technol Drug, Piazzale A Moro 5, I-00185 Rome, Italy
关键词
tuberculosis; drug discovery; antimicrobials; antimycobacterials; energy-metabolism; ATP SYNTHASE INHIBITORS; BIOLOGICAL EVALUATION; POTENT INHIBITORS; RESPIRATORY-CHAIN; ISOCITRATE LYASE; RIMINOPHENAZINE DERIVATIVES; DRUG BEDAQUILINE; MALATE SYNTHASE; DISCOVERY; ANALOGS;
D O I
10.3390/ph13090227
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tuberculosis remains the world's top infectious killer: it caused a total of 1.5 million deaths and 10 million people fell ill with TB in 2018. Thanks to TB diagnosis and treatment, mortality has been falling in recent years, with an estimated 58 million saved lives between 2000 and 2018. However, the emergence of multidrug-resistant (MDR) and extensively drug-resistant (XDR)Mtbstrains is a major concern that might reverse this progress. Therefore, the development of new drugs acting upon novel mechanisms of action is a high priority in the global health agenda. With the approval of bedaquiline, which targets mycobacterial energy production, and delamanid, which targets cell wall synthesis and energy production, the energy-metabolism inMtbhas received much attention in the last decade as a potential target to investigate and develop new antimycobacterial drugs. In this review, we describe potent anti-mycobacterial agents targeting the energy-metabolism at different steps with a special focus on structure-activity relationship (SAR) studies of the most advanced compound classes.
引用
收藏
页码:1 / 33
页数:33
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