Dias Catarina, Paulo Alexandra, Nascimento José, Houghton Peter, Hawkes Jane E, Gonçalves M Lurdes
CECF, Faculty of Pharmacy, University of Lisbon, Lisbon, Portugal.
Planta Med. 2003 Nov;69(11):1060-2. doi: 10.1055/s-2003-45158.
A new natural pyrimidine derivative, 2-(4'-aminobenzenamine)-pyrimidine (1), was isolated from the bulbs of Autonoë madeirensis, a Hyacinthaceae of the Madeira Archipelago (Portugal) and the structure determined on the basis of spectroscopic data. As some pyrimidine compounds are important alpha1-adrenergic antagonists, we investigated the effect of 1 on rat vas deferens contractility induced by the alpha1-agonist phenylephrine. In concentrations virtually devoid of effect on the rat vas deferens contractility, 1 shifted to the right the concentration-response curves of phenylephrine without changing the maximal effect. These results provide evidence that 1 acts as an alpha1-adrenoceptor antagonist and suggest a competitive mechanism of action.
从葡萄牙马德拉群岛风信子科植物马德拉奥托诺伊(Autonoë madeirensis)的球茎中分离出一种新的天然嘧啶衍生物2-(4'-氨基苯胺)-嘧啶(1),并根据光谱数据确定了其结构。由于一些嘧啶化合物是重要的α1-肾上腺素能拮抗剂,我们研究了化合物1对α1-激动剂去氧肾上腺素诱导的大鼠输精管收缩性的影响。在对大鼠输精管收缩性几乎无影响的浓度下,化合物1使去氧肾上腺素的浓度-反应曲线右移,而最大效应不变。这些结果证明化合物1作为α1-肾上腺素能受体拮抗剂起作用,并提示其作用机制为竞争性。