In vitro and in vivo anti-Trypanosoma cruzi activity of a novel nitro-derivative

被引:18
|
作者
Muelas-Serrano, S
Le-Senne, A
Fernández-Portillo, C
Nogal, JJ
Ochoa, C
Gómez-Barrio, A
机构
[1] Univ Complutense Madrid, Fac Farm, Dept Parasitol, E-28040 Madrid, Spain
[2] CSIC, Inst Quim Med, E-28006 Madrid, Spain
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2002年 / 97卷 / 04期
关键词
Trypanosoma cruzi; nitroarylidene; malononitriles; in vitro assays; cytotoxicity assays; in vivo experiments;
D O I
10.1590/S0074-02762002000400019
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Nitroarylidenemalononitriles and their cyanoacetamide derivatives with remarkable anti-epimastigote properties, were synthesized attempting to obtain new 3,5-diamino-4-(5'-nitroarylidene)-4H-thiadiazine 1,1-dioxide derivatives, which in previous reports had shown anti-Trypanosoma cruzi activity Tests to evaluate the cytotoxicity of compounds were performed on J774 macrophages. 5-nitro-2-thienyl-malononitrile (5NO(2)TM), was the only product which maintained a high anti-epimastigote activity at concentrations in which it was no longer cytotoxic, thus it was assayed against intracellular amastigotes. Its anti-amastigote activity was similar to that of nifurtimox. Afterwards in vivo toxicity and anti-chagasic activity were determined. A reduction in parasitemia was observed.
引用
收藏
页码:553 / 557
页数:5
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