M2毒蕈碱变构调节剂的构效关系。

K. Mohr, C. Tränkle, U. Holzgrabe
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引用次数: 36

摘要

G蛋白偶联受体的变构调节已经在毒蕈碱乙酰胆碱受体中得到了深入的研究。对典型变构剂如胆碱胺、铝库溴铵和双(氨)烷烃型药物的研究结果表明,与乙酰胆碱位点结合的正构配体可以变构减少或增加,或以亚型选择性方式保持不变。结构/活性关系(sar)的分析有助于阐明变构作用背后的分子事件,并可能引导具有改进性能和治疗前景的新变构剂的开发。本文重点阐述了毒蕈碱变构相互作用的原理,概述了典型变构剂同系物中的毒蕈碱变构相互作用,并考虑了以不同结合模式为特征的M(2)毒蕈碱变构相互作用的拓扑结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure/activity relationships of M2 muscarinic allosteric modulators.
Allosteric modulation of G protein-coupled receptors has been intensively studied at muscarinic acetylcholine receptors. Findings made with archetypal allosteric agents such as gallamine, alcuronium, and bis(ammonio)alkane-type agents revealed that binding of orthosteric ligands that attach to the acetylcholine site can be allosterically decreased or increased or left unaltered in a subtype-selective fashion. Analyses of structure/activity relationships (SARs) help to elucidate the molecular events underlying the allosteric action and they may pilot the development of new allosteric agents with improved properties and therapeutic perspectives. With a focus on SARs, this review illustrates the principles of muscarinic allosteric interactions, gives an overview of SARs in congeners of archetypal allosteric agents, and considers the topology of M(2) muscarinic allosteric interactions that are characterized by divergent binding modes.
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