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加兰他敏类似物对大鼠主动脉条的α-肾上腺素能阻断及抗血清素活性

Alpha-adrenolytic and anti-serotonin activities of apogalanthamine analogs on the rat aortic strips.

作者信息

Ishida Y, Sadamune K, Kobayashi S, Kihara M

出版信息

J Pharmacobiodyn. 1983 Jun;6(6):391-6. doi: 10.1248/bpb1978.6.391.

Abstract

Most of apogalanthamine analogs were more specific in alpha-adrenolytic activity than in anti-serotonin activity. In this report, 1,2,11-trimethoxy-N-methyl-5,6,7,8-tetrahydrodibenz[c,e]azocine(abbreviated as K-35) was found to be stronger in activity against serotonin (pA2 = 7.11 +/- 0.08) than against adrenaline (pA2 = 6.24 +/- 0.06). Apogalanthamine analogs have a tetrahydrodibenz[c,e]azocine structure, in which one benzene can be regarded as a part of benzylamine and other as a part of phenethylamine. From the pharmacological point of view, various azocine compounds were tested, the phenethylamine in the azocine structure is demonstrated to contribute toward the alpha-adrenolytic activity and the benzylamine having two methoxy groups contributes toward the anti-serotonin activity.

摘要

大多数加兰他敏类似物在α-肾上腺素能阻断活性方面比抗血清素活性更具特异性。在本报告中,发现1,2,11-三甲氧基-N-甲基-5,6,7,8-四氢二苯并[c,e]氮杂环辛烷(简称为K-35)对血清素的活性(pA2 = 7.11±0.08)比对肾上腺素的活性(pA2 = 6.24±0.06)更强。加兰他敏类似物具有四氢二苯并[c,e]氮杂环辛烷结构,其中一个苯可视为苄胺的一部分,另一个苯可视为苯乙胺的一部分。从药理学角度来看,测试了各种氮杂环辛烷化合物,结果表明氮杂环辛烷结构中的苯乙胺有助于α-肾上腺素能阻断活性,而具有两个甲氧基的苄胺有助于抗血清素活性。

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