Mouillé P, Dabiré H, Joly G, Schmitt H
Arzneimittelforschung. 1984;34(12):1749-52.
Peripheral postsynaptic alpha-adrenoceptor blocking properties of six new dihydrobenzofurane and imidazoline derivatives have been investigated in pithed rat against the pressor effects of phenylephrine and cirazoline (alpha 1-agonists) and clonidine and azepexole (alpha 2-agonists). Except for (N-methylimidazolinyl-2)-2 dihydro-2,3 benzofurane (II) that acted neither on alpha 1- nor alpha 2-adrenoceptors, all the compounds revealed blocking effects - plus or minor - on both alpha 1- and alpha 2-adrenoceptors. (Imidazolinyl-2)-2-chloro-7 dihydro-2,3-benzofurane (IV) is equipotent in blocking both alpha 1- and alpha 2-adrenoceptors. 7-Methoxy-(imidazolinyl-2)-2 dihydro-2,3-benzofurane (III) and (imidazolinyl-2)-2-fluoro-7-dihydro-2,3-benzofurane (V) block more effectively alpha 1- than alpha 2-adrenoceptors whereas (imidazolinyl-2)-2-benzocyclobutane (VI) is more potent in blocking alpha 2- than alpha 1-adrenoceptors. (Imidazolinyl-2)-2-dihydro-2,3-benzofurane (I) is a preferential alpha 2-adrenoceptor blocking agent. The most effective agents on alpha 2-adrenoceptors are under further pharmacological investigations.
研究了六种新型二氢苯并呋喃和咪唑啉衍生物对去脑大鼠外周突触后α-肾上腺素能受体的阻断特性,以对抗去氧肾上腺素和可乐唑啉(α1-激动剂)以及可乐定和阿泽哌唑(α2-激动剂)的升压作用。除了(N-甲基咪唑啉基-2)-2-二氢-2,3-苯并呋喃(II)对α1-和α2-肾上腺素能受体均无作用外,所有化合物均显示出对α1-和α2-肾上腺素能受体的阻断作用——或强或弱。(咪唑啉基-2)-2-氯-7-二氢-2,3-苯并呋喃(IV)对α1-和α2-肾上腺素能受体的阻断作用相当。7-甲氧基-(咪唑啉基-2)-2-二氢-2,3-苯并呋喃(III)和(咪唑啉基-2)-2-氟-7-二氢-2,3-苯并呋喃(V)对α1-肾上腺素能受体的阻断作用比对α2-肾上腺素能受体更有效,而(咪唑啉基-2)-2-苯环丁烷(VI)对α2-肾上腺素能受体的阻断作用比对α1-肾上腺素能受体更强。(咪唑啉基-2)-2-二氢-2,3-苯并呋喃(I)是一种选择性α2-肾上腺素能受体阻断剂。对α2-肾上腺素能受体最有效的药物正在进行进一步的药理学研究。