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α-氨基-α'-卤代甲基酮:作为丝氨酸和半胱氨酸蛋白酶抑制剂的合成方法和药物应用。

α-Amino-α'-halomethylketones: synthetic methodologies and pharmaceutical applications as serine and cysteine protease inhibitors.

机构信息

Department of Drug and Natural Product Synthesis, University of Vienna, Althanstrasse, 14-A-1090 Vienna, Austria.

出版信息

Mini Rev Med Chem. 2013 Jun;13(7):988-96. doi: 10.2174/1389557511313070004.

Abstract

α-Amino-α'-halomethylketones are interesting scaffolds bearing (at least) two sequential electrophilic carbons that by interacting with the nucleophilic moieties of several enzymes, represent the ideal candidates for in vivo and in vitro inhibition studies. In this work a summary of their use as optimal inhibitors of physiologically relevant serine and cysteine proteases is given with a particular emphasis on recently established SAR studies. A brief survey of the most relevant synthetic processes for their obtainment and the importance they possess in synthetic medicinal chemistry is reported.

摘要

α-氨基-α'-卤代甲基酮是一类有趣的结构骨架,含有(至少)两个连续的亲电碳原子,通过与几种酶的亲核部分相互作用,它们成为体内和体外抑制研究的理想候选物。本文总结了它们作为生理相关丝氨酸和半胱氨酸蛋白酶的最佳抑制剂的应用,特别强调了最近建立的 SAR 研究。本文还简要综述了获得它们的最相关的合成方法以及它们在合成药物化学中的重要性。

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