Design, synthesis, and in vitro antiprotozoal, antimycobacterial activities of N-{2-[(7-chloroquinolin-4-yl)amino]ethyl}ureas
作者:Carlos Nava-Zuazo、Samuel Estrada-Soto、Jorge Guerrero-Álvarez、Ismael León-Rivera、Gloria María Molina-Salinas、Salvador Said-Fernández、Manuel Jesús Chan-Bacab、Roberto Cedillo-Rivera、Rosa Moo-Puc、Gumersindo Mirón-López、Gabriel Navarrete-Vazquez
DOI:10.1016/j.bmc.2010.07.008
日期:2010.9
vitro against five protozoa (Giardia intestinalis, Trichomonas vaginalis, Entamoeba histolytica, Leishmania mexicana and Trypanosoma cruzi) and Mycobacterium tuberculosis. N-(4-Butoxyphenyl)-N′-2-[(7-chloroquinolin-4-yl)amino]ethyl}urea (6) was the most active compound against all parasites tested. Compound 6 was 670 times more active than metronidazole, against G. intestinalis. It was as active as pentamidine
我们使用较短的合成路线,从氯喹,乙胺丁醇和异氧基药物合成了一系列新的喹啉三方杂化物。化合物1 - 8在体外测试对五种原生动物(贾第虫肠,阴道毛滴虫, 内阿米巴histolytic一个,墨西哥利什曼原虫和克氏锥虫)和结核分枝杆菌。N-(4-丁氧基苯基)-N '-2-[((7-氯喹啉-4-基)氨基]乙基]脲(6)是对抗所有测试寄生虫的活性最高的化合物。化合物6对肠杆菌的活性是甲硝唑的670倍。它对墨西哥乳杆菌的活性与喷他as一样,比乙胺丁醇和异氧基的效力比结核分枝杆菌高两倍。该化合物可以被认为是一种新型的广谱抗菌剂。