非洲锥虫病
布氏锥虫
化学
铅化合物
效力
药品
药物发现
药理学
选择性
药物开发
候选药物
流出
体外
组合化学
生物化学
锥虫病
病毒学
生物
基因
催化作用
作者
Baljinder Singh,Amrita Sharma,Naresh Gunaganti,Mitch Rivers,Pradip K. Gadekar,Brady Greene,Michael Chichioco,Carlos E. Sanz-Rodriguez,Courtney Fu,Catherine LeBlanc,Erin Burchfield,Nyle Sharif,Benjamin Hoffman,Gaurav Kumar,Andrei Purmal,Kojo Mensa-Wilmot,Michael P. Pollastri
标识
DOI:10.1021/acs.jmedchem.2c01767
摘要
The carbazole CBL0137 (1) is a lead for drug development against human African trypanosomiasis (HAT), a disease caused by Trypanosoma brucei. To advance 1 as a candidate drug, we synthesized new analogs that were evaluated for the physicochemical properties, antitrypanosome potency, selectivity against human cells, metabolism in microsomes or hepatocytes, and efflux ratios. Structure-activity/property analyses of analogs revealed eight new compounds with higher or equivalent selectivity indices (5j, 5t, 5v, 5w, 5y, 8d, 13i, and 22e). Based on the overall compound profiles, compounds 5v and 5w were selected for assessment in a mouse model of HAT; while 5v demonstrated a lead-like profile for HAT drug development, 5w showed a lack of efficacy. Lessons from these studies will inform further optimization of carbazoles for HAT and other indications.
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