Salicylanilide Inhibitors of Toxoplasma gondii

被引:37
作者
Fomovska, Alina [1 ,2 ,3 ]
Wood, Richard D. [4 ]
Mui, Ernest [1 ,2 ,3 ]
Dubey, Jitenter P. [5 ]
Ferreira, Leandra R. [5 ]
Hickman, Mark R. [6 ]
Lee, Patricia J. [6 ]
Leed, Susan E. [6 ]
Auschwitz, Jennifer M. [6 ]
Welsh, William J. [4 ,7 ]
Sommerville, Caroline [8 ]
Woods, Stuart [8 ]
Roberts, Craig [8 ]
McLeod, Rima [1 ,2 ,3 ]
机构
[1] Univ Chicago, Dept Ophthalmol & Visual Sci, Comm Genet, Inst Genom & Syst Biol,The Coll, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Ophthalmol & Visual Sci, Comm Immunol, Inst Genom & Syst Biol,The Coll, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Ophthalmol & Visual Sci, Comm Mol Med, Inst Genom & Syst Biol,The Coll, Chicago, IL 60637 USA
[4] Snowdon Inc, Monmouth Jct, NJ USA
[5] ARS, USDA, Anim Nat Resources Inst, Anim Parasit Dis Lab,BARC E, Beltsville, MD 20705 USA
[6] Walter Reed Army Inst Res, Div Expt Therapeut, Dept Discovery, Silver Spring, MD 20910 USA
[7] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pharmacol, Piscataway, NJ 08854 USA
[8] Strathclyde Inst Pharm & Biomed Sci, Glasgow G4 0RE, Lanark, Scotland
关键词
CONGENITAL TOXOPLASMOSIS; MECHANISM; OOCYSTS;
D O I
10.1021/jm3007596
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Toxoplasma gondii (T. gondii) is an apicomplexan parasite that can cause eye disease, brain disease, and death, especially in congenitally infected and immune-compromised people. Novel medicines effective against both active and latent forms of the parasite are greatly needed. The current study focused on the discovery of such medicines by exploring a family of potential inhibitors whose antiapicomplexan activity has not been previously reported. Initial screening efforts revealed that niclosamide, a drug approved for anthelmintic use, possessed promising activity in vitro against T. gondii. This observation inspired the evaluation of the activity of a series of salicylanilides and derivatives. Several inhibitors with activities in the nanomolar range with no appreciable in vitro toxicity to human cells were identified. An initial structure activity relationship was explored. Four compounds were selected for evaluation in an in vivo model of infection, and two derivatives with potentially enhanced pharmacological parameters demonstrated the best activity profiles.
引用
收藏
页码:8375 / 8391
页数:17
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