Michne W F, Salsbury R L, Michalec S J
J Med Chem. 1977 May;20(5):682-6. doi: 10.1021/jm00215a013.
A general synthesis of variously substituted 2,6-methano-3-benzazocine-11-propanols is described. Nine N-CH3 derivatives and their corresponding N-cyclopropylmethyl counterparts were prepared and studied in the mouse acetylcholine induced writhing and rat phenazocine antagonism tests. The results are compared with literature information on the bridged oripavine methanols. It is concluded that the synthetic analogues have a different structure-activity profile, in general being weak agonists but potent antagonists.
描述了各种取代的2,6-亚甲基-3-苯并氮杂环辛烷-11-丙醇的一般合成方法。制备了九种N-CH₃衍生物及其相应的N-环丙基甲基类似物,并在小鼠乙酰胆碱诱导的扭体试验和大鼠非那佐辛拮抗试验中进行了研究。将结果与关于桥连阿片碱甲醇的文献信息进行了比较。得出的结论是,合成类似物具有不同的构效关系,总体上是弱激动剂但却是强效拮抗剂。