Advances in Drug Discovery of New Antitubercular Multidrug-Resistant Compounds

被引:40
|
作者
dos Santos Fernandes, Guilherme Felipe [1 ,2 ]
Chin, Chung Man [2 ]
Dos Santos, Jean Leandro [1 ,2 ]
机构
[1] Sao Paulo State Univ UNESP, Inst Chem, BR-14800060 Araraquara, Brazil
[2] Sao Paulo State Univ UNESP, Sch Pharmaceut Sci, BR-14800903 Araraquara, Brazil
基金
巴西圣保罗研究基金会;
关键词
tuberculosis; drug discovery; antitubercular compounds; multidrug-resistant tuberculosis; KILL MYCOBACTERIUM-TUBERCULOSIS; BIOLOGICAL EVALUATION; BACTERICIDAL ACTIVITY; ESTIMATE SOLUBILITY; 2-COMPONENT SYSTEM; AGENTS; POTENT; DERIVATIVES; INHIBITORS; DESIGN;
D O I
10.3390/ph10020051
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tuberculosis (TB), a disease caused mainly by the Mycobacterium tuberculosis (Mtb), is according to the World Health Organization (WHO) the infectious disease responsible for the highest number of deaths worldwide. The increased number of multidrug-resistant (MDR-TB) and extensively drug-resistant (XDR-TB) strains, and the ineffectiveness of the current treatment against latent tuberculosis are challenges to be overcome in the coming years. The scenario of drug discovery becomes alarming when it is considered that the number of new drugs does not increase proportionally to the emergence of drug resistance. In this review, we will demonstrate the current advances in antitubercular drug discovery, focusing on the research of compounds with potent antituberculosis activity against MDR-TB strains. Herein, active compounds against MDR-TB with minimum inhibitory concentrations (MICs) less than 11 mu M and low toxicity published in the last 4 years in the databases PubMed, Web of Science and Scopus will be presented and discussed.
引用
收藏
页数:17
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