1-(SUBSTITUTED)BENZYL-5-AMINOIMIDAZOLE-4-CARBOXAMIDES ARE POTENT ORALLY ACTIVE INHIBITORS OF TRYPANOSOMA-CRUZI IN MICE

被引:12
作者
CHABALA, JC [1 ]
WAITS, VB [1 ]
IKELER, T [1 ]
PATCHETT, AA [1 ]
PAYNE, L [1 ]
PETERSON, LH [1 ]
REAMER, RA [1 ]
HOOGSTEEN, K [1 ]
WYVRATT, M [1 ]
HANSON, WL [1 ]
FISHER, MH [1 ]
机构
[1] UNIV GEORGIA,COLL VET MED,ATHENS,GA 30602
来源
EXPERIENTIA | 1991年 / 47卷 / 01期
关键词
1-(SUBSTITUTED)-BENZYL-5-AMINOIMIDAZOLE-4-CARBOXAMIDE; TRYPANOSOMA-CRUZI; CHAGAS DISEASE;
D O I
10.1007/BF02041250
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
1-(Substituted)benzyl-5-aminoimidazole-4-carboxamides are potent orally active inhibitors of Trypanosoma cruzi infections in mice. The most active compounds are the 1-(4-chlorobenzyl)- and 1-(3,4-dichlorobenzyl)-analogs (L-153,094 [2] and L-153,153 [4], resp.) which are approximately 7-fold more potent upon oral administration than nifurtimox (Lampit) in suppressing parasite levels in the blood of mice with acute Trypanosoma cruzi infections.
引用
收藏
页码:51 / 53
页数:3
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