硝唑烷
结核分枝杆菌
体外
肺结核
微生物学
病毒学
医学
化学
生物
免疫学
生物化学
病理
作者
Joshua Odingo,Mai A. Bailey,Megan Files,Julie V. Early,Torey Alling,Devon Dennison,Julie Bowman,Suryakanta Dalai,Naresh Kumar,Jeffrey W. Cramer,Thierry Masquelin,Philip A. Hipskind,Tanya Parish
出处
期刊:ACS omega
[American Chemical Society]
日期:2017-09-18
卷期号:2 (9): 5873-5890
被引量:24
标识
DOI:10.1021/acsomega.7b00892
摘要
Nitazoxanide has antiparasitic and antibiotic activities including activity against Mycobacterium tuberculosis. We prepared and evaluated a set of its analogues to determine the structure–activity relationship, and identified several amide- and urea-based analogues with low micromolar activity against M. tuberculosis in vitro. Pharmacokinetics in the rat suggested a path forward to obtain bioavailable compounds. The series had a good microbiological profile with bactericidal activity in vitro against replicating and nonreplicating M. tuberculosis. Analogues had limited activity against other Gram-positive bacteria but no activity against Gram-negative bacteria. Our studies identified the key liability in this series as cytotoxicity. Future work concentrating on identifying the target(s) could assist in removing activity against eukaryotic cells.
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