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一种新型苯并咪唑啉酮衍生物苏式-1-(2-羟基-2-(3,4,5-三甲氧基苯基)-1-甲基乙基)-4-(1,3-二氢-2H-苯并咪唑-2-酮-1-基)哌啶(KF-4942)的降压作用:类似哌唑嗪的作用模式。

Hypotensive action of a new benzimidazolinone derivative, threo-1-(2-hydroxy-2-(3,4,5-trimethoxyphenyl)-1-methylethyl)-4-(1,3-dihydro-2H-benzimidazol-2-one-1-yl)piperidine (KF-4942): prazosin-like mode of action.

作者信息

Karasawa A, Shuto K, Kubo K, Kasuya Y, Hashikami M, Shigenobu K

出版信息

Arch Int Pharmacodyn Ther. 1983 Feb;261(2):278-90.

PMID:6132590
Abstract

Among a series of benzimidazolinone derivatives, KF-4942 was examined on its mode of hypotensive action. It was found that KF-4942 was a potent hypotensive agent, and that the hypotension was produced mostly by alpha-adrenergic blockade. Alpha-adrenergic blocking action of KF-4942 was suggested to be selective to the postsynaptic receptor. Thus, KF-4942 was concluded to be an agent with properties similar to prazosin.

摘要

在一系列苯并咪唑啉酮衍生物中,对KF - 4942的降压作用方式进行了研究。发现KF - 4942是一种强效降压剂,其降压作用主要是由α - 肾上腺素能阻断引起的。KF - 4942的α - 肾上腺素能阻断作用被认为对突触后受体具有选择性。因此,得出结论,KF - 4942是一种具有与哌唑嗪相似性质的药物。

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