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环亚烷基羧酸作为Ras/Raf相互作用新效应物的合成及生物学评价

Synthesis and biological evaluation of cycloalkylidene carboxylic acids as novel effectors of Ras/Raf interaction.

作者信息

Friese Anke, Hell-Momeni Katja, Zündorf Ilse, Winckler Thomas, Dingermann Theodor, Dannhardt Gerd

机构信息

Institut für Pharmazeutische Biologie, Universität Frankfurt/M. (Biozentrum), D-60439 Frankfurt am Main, Germany.

出版信息

J Med Chem. 2002 Mar 28;45(7):1535-42. doi: 10.1021/jm011101q.

Abstract

The protooncogenes Ras and Raf play important roles in signal transduction pathways regulated by mitogen-activated protein kinases. Mutations of Ras that arrest the protein in its active state are frequently implicated in tumor formation. We used Ras and Raf proteins in the yeast two-hybrid system to search for natural or synthesized substances capable of modulating Ras/Raf interaction by specifically binding to one of the interacting partners. We found that cycloalkylidene carboxylic acids enhanced Ras/Raf interaction by acting on the cysteine-rich domain of Raf. Several analogues of the active substance 2-cyclohexylidene propanoic acid were synthesized and the importance of the semicyclic double bond in the stabilization of Ras/Raf interaction was demonstrated. Variation of the size and the substituents of the cyclic system as well as the length of the carboxylic acid resulted in enhanced Ras/Raf interaction.

摘要

原癌基因Ras和Raf在丝裂原活化蛋白激酶调控的信号转导途径中发挥重要作用。使蛋白质停滞于活性状态的Ras突变常与肿瘤形成有关。我们在酵母双杂交系统中使用Ras和Raf蛋白,以寻找能够通过特异性结合其中一个相互作用伙伴来调节Ras/Raf相互作用的天然或合成物质。我们发现亚环烷基羧酸通过作用于Raf的富含半胱氨酸结构域增强了Ras/Raf相互作用。合成了活性物质2-环己叉基丙酸的几种类似物,并证明了半环状双键在稳定Ras/Raf相互作用中的重要性。环状系统的大小和取代基以及羧酸长度的变化导致Ras/Raf相互作用增强。

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