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硝唑尼特和替硝唑苯并呋喃类似物的合成:体外广谱抗原生动物活性比较研究。

Synthesis of benzologues of Nitazoxanide and Tizoxanide: a comparative study of their in vitro broad-spectrum antiprotozoal activity.

机构信息

Facultad de Farmacia, Universidad Autónoma del Estado de Morelos, Cuernavaca, Morelos 62209, Mexico.

出版信息

Bioorg Med Chem Lett. 2011 May 15;21(10):3168-71. doi: 10.1016/j.bmcl.2011.02.100. Epub 2011 Feb 26.

Abstract

We have synthesized two new benzologues of Nitazoxanide (NIT) and Tizoxanide (TIZ), using a short synthetic route. Both compounds were tested in vitro against six protozoa (Giardia intestinalis, Trichomonas vaginalis, Entamoeba histolytica, Plasmodium berghei, Leishmania mexicana and Trypanosoma cruzi). Compound 1 (benzologue of NIT) showed broad antiprotozoal effect against all parasites tested, showing IC(50)'s<5 μM. This compound was five-times more active than NIT, and 18-times more potent than metronidazole against G. intestinalis. It was 10-times more active than pentamidine against L. mexicana, and it was sevenfold more potent than benznidazole versus T. cruzi. This compound could be considered as a new broad spectrum antiprotozoal agent.

摘要

我们使用一种简短的合成路线合成了硝唑尼特(NIT)和替硝唑(TIZ)的两个新苯并呋喃衍生物。这两种化合物都在体外对六种原生动物(肠道贾第鞭毛虫、阴道毛滴虫、溶组织内阿米巴、伯氏疟原虫、墨西哥利什曼原虫和克氏锥虫)进行了测试。化合物 1(NIT 的苯并呋喃衍生物)对所有测试的寄生虫均表现出广泛的抗原生动物作用,其 IC50<5 μM。该化合物比 NIT 活性高五倍,对肠道贾第鞭毛虫的活性比甲硝唑高 18 倍。它比戊烷脒对墨西哥利什曼原虫的活性高 10 倍,比苯并硝唑对克氏锥虫的活性高 7 倍。该化合物可以被认为是一种新的广谱抗原生动物药物。

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