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具有β-阻断活性的环己基酚类碱性醚:艾司洛尔的合成与药理学研究

Basic ethers of cyclohexylphenols with beta-blocking activity: synthesis and pharmacological study of exaprolol.

作者信息

Carissimi M, Gentili P, Grumelli E, Milla E, Picciola G, Ravenna F

出版信息

Arzneimittelforschung. 1976 Apr;26(4):506-16. doi: 10.1002/chin.197629170.

Abstract

The paper describes the preparation and study of the pharmacological properties of a series of derivatives with the general formula. (see article) where R is a cyclohexyl or cyclohexenyl radical and R1 is a hydrogen, methyl or cyclohexyl. The compounds with a single cycloaliphatic radical ortho to the basic chain, and in particular the one with a cyclohexyl (exaprolol), were found to be particularly active in blocking the beta-adrenergic receptors, as antiarrhythmics and local anesthetics, while the introduction of a second radical or the shift of the cycloaliphatic radical to meta or para position caused the said pharmacological activities to disappear almost entirely, with the exception of the local anesthetic action.

摘要

该论文描述了一系列通式衍生物(见文章)的制备及其药理性质研究,其中R为环己基或环己烯基,R1为氢、甲基或环己基。发现与碱性链邻位带有单个脂环族基团的化合物,特别是带有环己基的化合物(心得舒),在阻断β-肾上腺素能受体方面、作为抗心律失常药和局部麻醉药时具有特别的活性,而引入第二个基团或将脂环族基团移至间位或对位会使上述药理活性几乎完全消失,但局部麻醉作用除外。

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