首页> 外文期刊>Chemical biology and drug design >Synthesis of 4-aminoquinoline-1,2,3-triazole and 4-aminoquinoline-1,2,3-triazole-1,3,5-triazine Hybrids as Potential Antimalarial Agents
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Synthesis of 4-aminoquinoline-1,2,3-triazole and 4-aminoquinoline-1,2,3-triazole-1,3,5-triazine Hybrids as Potential Antimalarial Agents

机译:4-氨基喹啉-1,2,3-三唑和4-氨基喹啉-1,2,3-三唑-1,3,5-三嗪杂化物的合成作为潜在的抗疟剂

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摘要

We report herein synthesis of a series of 4-aminoquinoline-1,2,3-triazole and 4-aminoquinoline-1,2,3-triazole-1,3,5-triazine hybrids and evaluate their antimalarial activity against D6 and W2 strains of Plasmodium falciparum. To study the structure–activity relationship of substituted 4-aminoquinoline–based hybrids, 34 structurally diverse compounds were synthesized and tested against D6 and W2 strains of P. falciparum. Some of the compounds have shown promising antimalarial activity without toxicity against Vero cells.
机译:我们在这里报告了一系列4-氨基喹啉-1,2,3-三唑和4-氨基喹啉-1,2,3-三唑-1,3,5-三嗪杂种的合成,并评估了其对D6和W2菌株的抗疟活性。恶性疟原虫。为了研究基于取代的4-氨基喹啉的杂化物的结构-活性关系,合成了34种结构多样的化合物,并针对恶性疟原虫的D6和W2菌株进行了测试。一些化合物显示出有希望的抗疟活性,而对Vero细胞无毒性。

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