抗细菌
肺结核
药理学
硝基咪唑
化学
体内
结核分枝杆菌
医学
生物技术
生物
病理
有机化学
作者
Wei Luo,Zhigang Huang,Deming Xu,Yang Meng,Yusong Zhu,Liang Shen,Shu‐Hui Chen,Xin Tao,Bin Wang,Yinghu Hu,Scott G. Franzblau,Ning Jiang,Yuquan Wei,Xiawei Wei,Charles Z. Ding
标识
DOI:10.1016/j.bmcl.2022.128871
摘要
Multidrug-resistant pulmonary tuberculosis (MDR-TB) is a major health problem worldwide. The treatment for MDR-TB requires medications for a long duration (up to 20-24 months) with second-line drugs resulting in unfavorable outcomes. Nitroimidazoles are promising antimycobacterial agents known to inhibit both aerobic and anaerobic mycobacterial activity. Delamanid and pretomanid are two nitroimidazoles approved by the regulatory agencies for MDR-TB treatment. However, both agents possess unsatisfactory absorption and QTc prolongation. In our search for a safer nitroimidazole, we discovered JBD0131 (2). It exhibited excellent anti-mycobacterial activity against M. tuberculosis H37Rv in vitro and in vivo, improved PK and absorption, reduced QT prolongation potential of delamanid. JBD0131 is currently in clinical development in China for pulmonary tuberculosis (CTR20202308).
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