摘要
结核病(TB)是一种由分枝杆菌属的细菌结核如分枝杆菌(MTB)引起的传染病。世界卫生组织想在未来几年内使结核病患病率大幅减少;然而,多药耐药(MDR)数量和细菌耐药(XDR)形式的增加以及潜伏性结核的治疗手段的缺乏是需要克服的难题本文证实了近年来文献中描述的MIC值<7µm、毒性低和高选择性最有效的化合物。此外,结核分枝杆菌的新靶点为新的抗结核药物的发现提供了新的视角。本文旨在总结抗结核药物的研究进展并促进抗结核药物的发现。更多内容请访问:
关键词: 抗结核药物,药物发现,结核分枝杆菌耐药结核,肺结核,肺结核靶点。
Current Medicinal Chemistry
Title:Current Advances in Antitubercular Drug Discovery: Potent Prototypes and New Targets
Volume: 22 Issue: 27
Author(s): Guilherme Felipe dos Santos Fernandes, Daniela Hartmann Jornada, Paula, Carolina de Souza, Chung Man Chin and Fernando Rogerio Pavan and Jean Leandro dos Santos
Affiliation:
关键词: 抗结核药物,药物发现,结核分枝杆菌耐药结核,肺结核,肺结核靶点。
摘要: Tuberculosis (TB) is an infectious disease caused by bacterium of the Mycobacterium genus, mainly by Mycobacterium tuberculosis (MTB). The World Health Organization aims to substantially reduce the number of cases in the coming years; however, the increased number of multidrug-resistant (MDR) and extremely drug-resistant (XDR) forms of the bacterium and the lack of treatment for latent tuberculosis are challenges to be overcome. In this review, we have identified the most potent compounds described in the literature during recent years with MIC values < 7 µM, low toxicity and a high selective index. In addition, emerging targets in MTB are presented to provide new perspectives for the discovery of new antitubercular drugs. This review aims to summarize the current advances in and promote insights into antitubercular drug discovery.
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Guilherme Felipe dos Santos Fernandes, Daniela Hartmann Jornada, Paula, Carolina de Souza, Chung Man Chin and Fernando Rogerio Pavan and Jean Leandro dos Santos , Current Advances in Antitubercular Drug Discovery: Potent Prototypes and New Targets, Current Medicinal Chemistry 2015; 22 (27) . https://dx.doi.org/10.2174/0929867322666150818103836
DOI https://dx.doi.org/10.2174/0929867322666150818103836 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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