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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.
Archives internationales de pharmacodynamie et de therapie Pub Date : 1983-02-01 A Karasawa , K Shuto , K Kubo , Y Kasuya , M Hashikami , K Shigenobu
Archives internationales de pharmacodynamie et de therapie Pub Date : 1983-02-01 A Karasawa , K Shuto , K Kubo , Y Kasuya , M Hashikami , K Shigenobu
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.
中文翻译:
新型苯并咪唑啉酮衍生物threo-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- -1-基)哌啶(KF-4942):类似于哌唑嗪的作用方式。
在一系列苯并咪唑啉酮衍生物中,检查了KF-4942的降压作用模式。发现KF-4942是有效的降压药,而低血压主要是由α-肾上腺素能阻滞引起的。KF-4942的α-肾上腺素阻断作用被认为对突触后受体具有选择性。因此,KF-4942被认为是一种具有类似于哌唑嗪性质的药物。
更新日期:2019-11-01
中文翻译:
新型苯并咪唑啉酮衍生物threo-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- -1-基)哌啶(KF-4942):类似于哌唑嗪的作用方式。
在一系列苯并咪唑啉酮衍生物中,检查了KF-4942的降压作用模式。发现KF-4942是有效的降压药,而低血压主要是由α-肾上腺素能阻滞引起的。KF-4942的α-肾上腺素阻断作用被认为对突触后受体具有选择性。因此,KF-4942被认为是一种具有类似于哌唑嗪性质的药物。