New 4-iminohydantoin sulfamide derivatives with antiviral and anticancer activity

Y. Kornii, O. Shablykin, O. Shablykina, V. Brovarets
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引用次数: 1

Abstract

A number of sulfamides were obtained by reaction of (5-(dichloromethylene)-2-oxoimidazolidin-4-ylidene)sulfamoyl chloride with anilines, benzylamines, Boc-protected piperazine, methylalylamine, and amino acids methyl esters with primary and secondary amino group. The antiviral and anticancer activity of new derivatives was evaluated. The most effective compounds against Human cytomegalovirus were sulfamides based on anisidine (1b), N-Boc-piperazine (1h), and the derivatives 1n,o with fragments of nipecotic and azetidine-3-carboxylic acids, respectively. Anticancer activity was most significant for sulfamides based on p-methoxybenzylamine (compound 1d), benzylmethylamine (compound 1f), and allylmethylamine (compound 1g).
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新的具有抗病毒和抗癌活性的4-亚胺酰脲胺衍生物
以(5-(二氯乙烯)-2-氧咪唑烷-4-酰基)磺胺酰氯与苯胺、苄胺、boc保护哌嗪、甲基乙胺、氨基酸甲酯与叔胺基和仲胺基反应得到了多种磺胺。评价了新衍生物的抗病毒和抗癌活性。对人巨细胞病毒最有效的化合物分别是以茴香胺(1b)、n - boc -哌嗪(1h)为基础的磺胺类化合物,以及以硝基苯胺和氮杂啶-3-羧酸片段为基础的衍生物1n、0。以对甲氧基苄胺(化合物1d)、苄基甲胺(化合物1f)和烯丙基甲胺(化合物1g)为基础的磺胺类化合物的抗癌活性最为显著。
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