Perez F, Rosell G, Mauleon D, Carganico G
Departament de Farmacologia I Quimica Terapeutica, Facultat de Farmacia, Universitat de Barcelona, Spain.
Farmaco. 1991 Oct;46(10):1155-66.
New duplicated analogs of the alpha 1-selective agonist methoxamine and of its cyclic derivative 5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthylamine have been synthesized and tested for their adrenergic properties. All the compounds prepared, presenting a polymethylene spacer of varying length between two units of the active structure, turned out to be completely devoid of any alpha-stimulating activity. Surprisingly, some of them showed a marked beta-adrenergic agonistic effect, being the most interesting compound active at nanomolar concentration.
已合成了α1选择性激动剂甲氧明及其环状衍生物5,8-二甲氧基-1,2,3,4-四氢-2-萘胺的新型重复类似物,并对其肾上腺素能特性进行了测试。所制备的所有化合物在活性结构的两个单元之间具有不同长度的聚亚甲基间隔基,结果表明它们完全没有任何α刺激活性。令人惊讶的是,其中一些化合物表现出明显的β肾上腺素能激动作用,最有趣的化合物在纳摩尔浓度下具有活性。