首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >In vitro and in vivo trypanocidal activity of the ethyl esters of N-allyl and N-propyl oxamates using different Trypanosoma cruzi strains.
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In vitro and in vivo trypanocidal activity of the ethyl esters of N-allyl and N-propyl oxamates using different Trypanosoma cruzi strains.

机译:使用不同的克鲁氏锥虫菌株的N-烯丙基和N-丙基草酸乙酯的体外和体内锥虫杀虫活性。

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摘要

The trypanocidal activity of N-allyl (NAOx) and N-propyl (NPOx) oxamates and that of the ethyl esters ofN-allyl (Et-NAOx) and N-propyl (Et-NPOx) oxamates were tested on cultured epimastigotes (in vitro) and murine trypanosomiasis (in vivo) using five different T. cruzi strains. NAOx and NPOx did not penetrate intact epimastigotes and therefore we were not able to detect any trypanocidal effect with these oxamates. Whereas the ethyl esters (Et-NAOx and Et-NPOx), acting as prodrugs, exhibited in vitro and in vivo trypanocidal activity on the five tested T. cruzi strains. On the contrary, when Nifurtimox and Benznidazole used as reference drugs were tested, we found that only three of the five tested T cruzi strains were affected, whereas the other two strains, Miguz and Compostela, were resistant to the in vitro and in vivo trypanocidal activity of these compounds.
机译:N-烯丙基(NAOx)和草酸N-丙基(NPOx)的锥虫杀虫活性以及N-烯丙基(Et-NAOx)和草酸N-丙基(Et-NPOx)的乙酯的体外杀虫活性)和鼠类锥虫病(体内),使用五种不同的克鲁斯锥虫菌株。 NAOx和NPOx不能穿透完整的假鞭毛动物,因此我们无法检测到这些草酸盐的锥虫作用。而作为前药的乙酯(Et-NAOx和Et-NPOx)则对五种测试的克鲁氏梭菌表现出体外和体内锥虫杀灭活性。相反,在对尼古丁酮和苯并咪唑作为参比药物进行测试时,我们发现在测试的五种T克鲁兹菌株中,只有三株受到影响,而其他两种菌株Miguz和Compostela对体外和体内的锥虫病耐药这些化合物的活性。

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