Synthesis and antiprotozoal activity of novel 2-{[2-(1H-imidazol-1-yl)ethyl] sulfanyl}-1H-benzimidazole derivatives

被引:51
|
作者
Perez-Villanueva, Jaime [1 ]
Hernandez-Campos, Alicia [1 ]
Yepez-Mulia, Lilian [2 ]
Mendez-Cuesta, Carlos [1 ]
Mendez-Lucio, Oscar [1 ]
Hernandez-Luis, Francisco [1 ]
Castillo, Rafael [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Quim, Dept Farm, Mexico City 04510, DF, Mexico
[2] IMSS, Unidad Invest Med Enfermedades Infecciosas & Para, Mexico City 06720, DF, Mexico
关键词
Benzimidazole; Entamoeba histolytica; Giardia intestinalis; Trichomonas vaginalis; MOLECULAR-FIELD ANALYSIS; ANTIPARASITIC ACTIVITY; 1H-BENZIMIDAZOLE DERIVATIVES; BIOLOGICAL-ACTIVITY; PROTOZOA;
D O I
10.1016/j.bmcl.2013.05.012
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 19 new 2-{[2-(1H-imidazol-1-yl)ethyl]sulfanyl}-1H-benzimidazole derivatives was synthesized starting from the properly substituted 1,2-phenylendiamine. These compounds have hydrogen or methyl at position 1; while hydrogen, chlorine, ethoxy or methoxycarbonyl group is at position 5 and/or 6. The novel compounds were tested against protozoa Trichomonas vaginalis, Giardia intestinalis and Entamoeba histolytica. Experimental evaluations revealed strong activity for all tested compounds, having IC50 values in the nanomolar range, which were even better than metronidazole, the drug of choice for these parasites. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4221 / 4224
页数:4
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