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Chemistry and Biology of the Aeruginosin Family of Serine Protease Inhibitors

机译:丝氨酸蛋白酶抑制剂铜绿素家族的化学和生物学

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摘要

The aeruginosins have been isolated from marine sponges and cyanobacterial waterblooms,sources that are phylo genetically distinct and the bodies of water are geographically well-separated.The aeruginosins comprise a central hydroxy-(ordihydroxy-) octahydroindole carboxamide core unit,onto which are appended uhusuaiammo adds on the carboxy and amino termini as part of the linear peptide array.Potent inhibitory activity of serine proteases in vitro is exhibited by some of the aeruginosins as a result of the presence and proper deployment of three important pharmacophoric subunits:a PI argi-nine mimetic,and two hydrophobic residues with interaction sites designated as P2 and P3.In this article,we provide the first comprehensive review on the chemistry and biology of the aeruginosins,with an emphasis on their sources,structural revisions,and total syntheses.
机译:铜绿素是从海洋海绵和蓝藻水华中分离出来的,其来源是系统遗传学上独特的,水体在地理上是分开的。铜绿素包括一个中央羟基-(二羟基-)八氢吲哚羧酰胺核心单元,其上附加了uhusuaiammomo由于三个重要药效基团亚基的存在和正确部署,一些铜绿素酶在体外具有丝氨酸蛋白酶的强抑制活性,这是线性肽阵列的一部分。模拟,以及两个疏水残基,它们的相互作用位点分别为P2和P3。在本文中,我们对铜绿素酶的化学和生物学特性进行了首次全面综述,重点介绍了它们的来源,结构修饰和总合成。

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