首页> 外文期刊>Indian Journal of Chemistry. Section B, Organic Including Medicinal >Studies in antiparasitic agents: Part 24-Synthesis of 5-(2-furyl)-2-substituted-amino-1,3,4-triazoles and substituted 1,3,4-triazolo[1,5-a]-pyrimidines as potential antifilarial and leishmanicidal agents
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Studies in antiparasitic agents: Part 24-Synthesis of 5-(2-furyl)-2-substituted-amino-1,3,4-triazoles and substituted 1,3,4-triazolo[1,5-a]-pyrimidines as potential antifilarial and leishmanicidal agents

机译:抗寄生虫药的研究:第24部分:5-(2-呋喃基)-2-取代的氨基-1,3,4-三唑和取代的1,3,4-三唑并[1,5-a]-嘧啶的合成潜在的抗孝顺和杀菌剂

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摘要

A series of 5-(2-furyl)-2-substituted-amino-1,3,4-triazoles (3-5) and 2-(2-furyl)-1,3,4-triazolo[1,5-a]pyrimidines (6, 9-19) have been synthesized as possible inhibitors of antioxidant enzymes in filarii-ds and leishmanial parasites. All the compounds have been evaluated for their antifilarial and anti-leishmanial activities. The antifilarial activity has been evaluated against Litomosoides carinii infection in cotton rats while the in vitro leishmanicidal activity determined using macrophage amastigote culture isolated from cotton rats infected with Leishmania donovani. In both the tests none of the compounds exhibits any noteworthy antiparasitic activity.
机译:一系列5-(2-呋喃基)-2-取代的氨基-1,3,4-三唑(3-5)和2-(2-呋喃基)-1,3,4-三唑[1,5-已合成α]嘧啶(6、9-19),作为可能的丝虫和利什曼寄生虫中抗氧化酶的抑制剂。已经评估了所有化合物的抗丝和抗利什曼活性。已经评估了棉鼠抗线粒体卡美丝虫感染的抗丝活性,而体外巨噬细胞杀线虫活性是用巨噬细胞鞭毛体培养物测定的,该培养物是从感染了利什曼原虫的棉鼠中分离得到的。在两种测试中,没有一种化合物表现出任何值得注意的抗寄生虫活性。

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