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M2 毒蕈碱变构调节剂的构效关系。

Structure/activity relationships of M2 muscarinic allosteric modulators.

作者信息

Mohr K, Tränkle C, Holzgrabe U

机构信息

Pharmacology and Toxicology, Institute of Pharmacy, University of Bonn, Bonn, Germany.

出版信息

Recept Channels. 2003;9(4):229-40.

Abstract

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.

摘要

G蛋白偶联受体的变构调节在毒蕈碱型乙酰胆碱受体方面已得到深入研究。使用典型变构剂(如加拉明、阿库氯铵和双(铵)烷烃类试剂)的研究结果表明,附着于乙酰胆碱位点的正构配体的结合可通过变构作用以亚型选择性方式减少、增加或保持不变。结构/活性关系(SAR)分析有助于阐明变构作用背后的分子事件,并且可能指导开发具有改进特性和治疗前景的新型变构剂。本综述聚焦于SAR,阐述了毒蕈碱型变构相互作用的原理,概述了典型变构剂同系物中的SAR,并探讨了以不同结合模式为特征的M(2)毒蕈碱型变构相互作用的拓扑结构。

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