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含亚氨基脲部分的席夫碱对碳酸酐酶同工酶I、II、IX和XII的抑制作用

Inhibition of carbonic anhydrase isoforms I, II, IX and XII with Schiff's bases incorporating iminoureido moieties.

作者信息

Singasane Namrata, Kharkar Prashant S, Ceruso Mariangela, Supuran Claudiu T, Toraskar Mrunmayee P

机构信息

a Department of Pharmaceutical Chemistry , Bharati Vidyapeeth's College of Pharmacy , Navi Mumbai , India .

b Department of Pharmaceutical Chemistry , SPP School of Pharmacy and Technology Management, SVKM's NMIMS , Mumbai , India .

出版信息

J Enzyme Inhib Med Chem. 2015 Dec;30(6):901-7. doi: 10.3109/14756366.2014.986118. Epub 2015 Sep 4.

Abstract

A series of new Schiff's bases was obtained from the sulfanilamide semicarbazone (4-aminosulfonylphenyl semicarbazide) and aromatic/heterocyclic aldehydes. The new compounds were designed to incorporate moieties known to induce effective inhibitory activity against carbonic anhydrase (CA, EC 4.2.1.1) isoforms involved in crucial physiologic or pathologic processes such as the cytosolic CA I and II or the transmembrane, tumor-associated CA IX and XII: the compounds were medium potency - weak CA I inhibitors, highly effective, low nanomolar CA II inhibitors, but few of them inhibited effectively CA IX and XII. This may probably due to the long spacer between the sulfamoylphenyl and imine fragments of the molecules, which probably induces a highly flexible conformation of the inhibitor bound to the active site of the enzyme, with destabilizing effects for the adduct. The detailed structure activity relationship for this class of inhibitors is discussed.

摘要

通过磺胺半卡巴腙(4-氨基磺酰基苯基半卡巴腙)与芳香族/杂环醛反应得到了一系列新的席夫碱。设计这些新化合物是为了引入已知对参与关键生理或病理过程的碳酸酐酶(CA,EC 4.2.1.1)同工型具有有效抑制活性的部分,例如胞质CA I和II或跨膜的、与肿瘤相关的CA IX和XII:这些化合物是中等效力的——弱CA I抑制剂,高效、低纳摩尔CA II抑制剂,但其中很少能有效抑制CA IX和XII。这可能是由于分子中氨磺酰苯基和亚胺片段之间的间隔较长,这可能导致与酶活性位点结合的抑制剂具有高度灵活的构象,对加合物产生不稳定作用。讨论了这类抑制剂的详细构效关系。

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