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与氧化震颤素相关的一些炔类化合物的中枢及外周毒蕈碱能和抗毒蕈碱能活性的立体化学要求

Stereochemical requirements for central and peripheral muscarinic and antimuscarinic activity of some acetylenic compounds related to oxotremorine.

作者信息

Dahlbom R, Jenden D J, Resul B, Ringdahl B

出版信息

Br J Pharmacol. 1982 Jun;76(2):299-304. doi: 10.1111/j.1476-5381.1982.tb09220.x.

Abstract

1 The enantiomers of some analogues of the central muscarinic agent, oxotremorine, were prepared and investigated for tremorogenic and tremorolytic activity in intact mice and for muscarinic and antimuscarinic activity on the isolated ileum of the guinea-pig. 2 The R-isomers were more potent than the S-isomers both in vivo and in vitro regardless of whether the compounds are agonists, partial agonists or competitive antagonists. 3 It is suggested that in the oxotremorine series, agonists and antagonists interact with a common receptor site, in contrast to classical muscarinic antagonists which are believed to bind also to accessory receptor areas, located close to the agonist binding site.

摘要
  1. 制备了中枢毒蕈碱样药物氧化震颤素某些类似物的对映体,并在完整小鼠中研究其致震颤和抗震颤活性,以及在豚鼠离体回肠上研究其毒蕈碱样和抗毒蕈碱样活性。2. 无论这些化合物是激动剂、部分激动剂还是竞争性拮抗剂,R - 异构体在体内和体外均比S - 异构体更有效。3. 有人提出,在氧化震颤素系列中,激动剂和拮抗剂与共同的受体位点相互作用,这与经典的毒蕈碱样拮抗剂不同,后者被认为还与位于激动剂结合位点附近的辅助受体区域结合。

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本文引用的文献

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AN IMPROVED SYNTHESIS OF OXOTREMORINE.氧化震颤素的改进合成法
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A comparison of the pharmacological activities of tertiary bases and their quaternary ammonium derivatives.
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