Cannon J G, Perez Z, Long J P, Rusterholz D B, Flynn J R, Costall B, Fortune D H, Naylor R J
J Med Chem. 1979 Aug;22(8):901-7. doi: 10.1021/jm00194a003.
A series of N-alkylated alpha-methyldopamine derivatives has been prepared for comparison of their biological effects with those of semirigid dopamine congeners derived from 2-aminotetralin systems. All of the alpha-methyldopamine derivatives were inert as dopaminergic agonists in a variety of animal assays, both centrally and peripherally, although certain compounds produced powerful and prolonged locomotor hyperactivity on intra-accumbens injection in mice, by indirect mechanism(s). A rationalization, based upon conformational analysis, is presented for the lack of direct dopaminergic agonist activity of alpha-methyldopamine derivatives.
已经制备了一系列N-烷基化的α-甲基多巴胺衍生物,以便将它们的生物学效应与源自2-氨基四氢萘系统的半刚性多巴胺类似物的生物学效应进行比较。所有的α-甲基多巴胺衍生物在各种动物实验中,无论是在中枢还是外周,作为多巴胺能激动剂都是无活性的,尽管某些化合物通过间接机制在小鼠伏隔核内注射后产生强大且持久的运动性多动。基于构象分析,对α-甲基多巴胺衍生物缺乏直接多巴胺能激动剂活性给出了一种解释。