碳酸酐酶抑制剂;磷酰磺酰胺——一类新的高亲和力同工酶I和II抑制剂。

I Fenesan, R Popescu, A Scozzafava, V Crucin, E Mateiciuc, R Bauer, M A Ilies, C T Supuran
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引用次数: 8

摘要

以ArSO2NH2为原料,与五氯化磷进行缩合,在甲酸的存在下进行水解,制备了一系列芳香/杂环磺胺类化合物,其分子式为ArSO2NHPO3H2。新的衍生物通常作为两种碳酸酐酶(CA)同工酶,CA I和CA II,较强的抑制剂相比,从母体未取代的磺胺得到它们。本文还讨论了这类新型CA抑制剂的抑制机理,以及所研究的一系列衍生物的构效关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carbonic anhydrase inhibitors; phosphoryl-sulfonamides--a new class of high affinity inhibitors of isozymes I and II.

A series of phosphorylated aromatic/heterocyclic sulfonamides with the general formula ArSO2NHPO3H2 have been prepared by condensing ArSO2NH2 with phosphorus pentachloride, followed by controlled hydrolysis in the presence of formic acid. The new derivatives generally act as stronger inhibitors of two carbonic anhydrase (CA) isozymes, CA I and CA II, as compared to the parent unsubstituted sulfonamides from which they were obtained. The inhibition mechanism by this new class of CA inhibitors, as well as structure activity correlations for the series of investigated derivatives, are also discussed.

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