2-Aminothiazoles as Therapeutic Leads for Prion Diseases

被引:127
作者
Gallardo-Godoy, Alejandra [1 ]
Gever, Joel [2 ]
Fife, Kimberly L. [2 ]
Silber, B. Michael [2 ,4 ]
Prusiner, Stanley B. [2 ,4 ]
Renslo, Adam R. [1 ,3 ]
机构
[1] Univ Calif San Francisco, Small Mol Discovery Ctr, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Inst Neurodegenerat Dis, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
[4] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94158 USA
关键词
NEUROBLASTOMA-CELLS; ANTIPRION COMPOUNDS; DERIVATIVES; INHIBITION; REPLICATION; ACRIDINE; DESIGN;
D O I
10.1021/jm101250y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
2-Aminothiazoles are a new class of small molecules with antiprion activity in prion-infected neuroblastoma cell lines (J. Virol. 2010, 84, 3408). We report here structure-activity studies undertaken to improve the potency and physiochemical properties of 2-aminothiazoles, with a particular emphasis on achieving and sustaining high drug concentrations in the brain. The results of this effort include the generation of informative structure-activity relationships (SAR) and the identification of lead compounds that are orally absorbed and achieve high brain concentrations in animals. The new aminothiazole analogue (5-methylpyridin-2-yl)-[4-(3-phenylisoxazol-5-yl)-thiazol-2-yl]-amine (27), for example, exhibited an EC50 of 0.94 mu M in prion-infected neuroblastoma cells (ScN2a-cl3) and reached a concentration of similar to 25 mu M in the brains of mice following three days of oral administration in a rodent liquid diet. The studies described herein suggest 2-aminothiazoles as promising new leads in the search for effective therapeutics for prion diseases.
引用
收藏
页码:1010 / 1021
页数:12
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