Reifenrath W G, Fries D S
J Med Chem. 1979 Feb;22(2):204-6. doi: 10.1021/jm00188a017.
The synthesis and the opiate agonist and antagonist activities of three derivatives of cis-2-[methyl(cyclopropanemethyl)amino]-1-phenyltetralin are reported. The compounds were obtained by synthetic modification from 2-amino-1-tetralone. The 1-propionoxy derivative 4c shows analgetic activity (ED50 = 17.8 mg/kg) one-half that of codeine, and the 1-methoxy derivative 4b has weak antagonist activity (AD50 = 33.5 mg/kg). The compounds showed no other significant opiate-related activity.
报道了顺式-2-[甲基(环丙基甲基)氨基]-1-苯基四氢萘三种衍生物的合成及其阿片激动剂和拮抗剂活性。这些化合物是通过对2-氨基-1-四氢萘酮进行合成修饰得到的。1-丙酰氧基衍生物4c显示出镇痛活性(ED50 = 17.8 mg/kg),为可待因的一半,而1-甲氧基衍生物4b具有弱拮抗剂活性(AD50 = 33.5 mg/kg)。这些化合物没有表现出其他显著的阿片相关活性。