Tuberculosis Drug Discovery: Challenges and New Horizons

被引:70
|
作者
Fernandes, Guilherme F. S. [1 ]
Thompson, Andrew M. [2 ]
Castagnolo, Daniele [1 ]
Denny, William A. [2 ]
Dos Santos, Jean L. [3 ]
机构
[1] UCL, Dept Chem, London WC1H 0AJ, England
[2] Univ Auckland, Auckland Canc Soc Res Ctr, Fac Med & Hlth Sci, Auckland 1142, New Zealand
[3] Sa Paulo State Univ UNESP, Sch Pharmaceut Sci, BR-14800903 Araraquara, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
KILL MYCOBACTERIUM-TUBERCULOSIS; MYCOLIC ACID BIOSYNTHESIS; CELL-WALL CORE; IN-VIVO; RESISTANT TUBERCULOSIS; SMALL-MOLECULE; ANTITUBERCULOSIS DRUGS; ANTIBACTERIAL ACTIVITY; DISEASE PROGRESSION; MMPL3; INHIBITORS;
D O I
10.1021/acs.jmedchem.2c00227
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Over the past 2000 years, tuberculosis (TB) has claimed more lives than any other infectious disease. In 2020 alone, TB was responsible for 1.5 million deaths worldwide, comparable to the 1.8 million deaths caused by COVID-19. The World Health Organization has stated that new TB drugs must be developed to end this pandemic. After decades of neglect in this field, a renaissance era of TB drug discovery has arrived, in which many novel candidates have entered clinical trials. However, while hundreds of molecules are reported annually as promising anti-TB agents, very few successfully progress to clinical development. In this Perspective, we critically review those anti-TB compounds published in the last 6 years that demonstrate good in vivo efficacy against Mycobacterium tuberculosis. Additionally, we highlight the main challenges and strategies for developing new TB drugs and the current global pipeline of drug candidates in clinical studies to foment fresh research perspectives.
引用
收藏
页码:7489 / 7531
页数:43
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