恰加斯病
克鲁兹锥虫
加药
体内
药理学
化学
体外
疾病
不利影响
原生动物寄生虫
寄生虫寄主
免疫学
医学
内科学
生物
生物化学
生物技术
万维网
计算机科学
作者
Martine Keenan,Jason H. Chaplin,Paul W. Alexander,Michael J. Abbott,Wayne M. Best,Andrea Khong,Adriana Botero,Catherine Perez,Scott Cornwall,RC Andrew Thompson,Karen L. White,David M. Shackleford,Maria Koltun,Francis C. K. Chiu,Julia Morizzi,Eileen Ryan,Michael G. Campbell,Thomas W von Geldern,Ivan Scandale,Eric Chatelain
摘要
Chagas disease, caused by the protozoan parasite Trypanosoma cruzi (T. cruzi), is an increasing threat to global health. Available medicines were introduced over 40 years ago, have undesirable side effects, and give equivocal results of cure in the chronic stage of the disease. We report the development of two compounds, 6 and (S)-7, with PCR-confirmed curative activity in a mouse model of established T. cruzi infection after once daily oral dosing for 20 days at 20 mg/kg 6 and 10 mg/kg (S)-7. Compounds 6 and (S)-7 have potent in vitro activity, are noncytotoxic, show no adverse effects in vivo following repeat dosing, are prepared by a short synthetic route, and have druglike properties suitable for preclinical development.
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