Cannon J G, Pease J P, Long J P, Flynn J
J Med Chem. 1984 Jul;27(7):922-3. doi: 10.1021/jm00373a019.
The title compounds were prepared as congeners of the dopaminergically potent 2-amino-5,6-dihydroxytetralin series ("A-5,6-DTN"). None of the variously nitrogen-substituted benzocycloheptenes demonstrated any dopamine-like effects in a variety of assays. The primary amine had alpha 1-adrenoceptor stimulant effects. This lack of dopaminergic effect parallels the inactivity found in 6-aminobenzocycloheptenes bearing no oxygen substitutents, those bearing a single phenolic group, and those bearing a resorcinol 1,3-diphenolic substitution pattern.
标题化合物作为多巴胺能活性的2-氨基-5,6-二羟基四氢萘系列(“A-5,6-DTN”)的同系物被制备出来。在各种测定中,各种氮取代的苯并环庚烯均未表现出任何多巴胺样效应。伯胺具有α1-肾上腺素能受体刺激作用。这种缺乏多巴胺能效应与在无氧取代基的6-氨基苯并环庚烯、带有单个酚基的那些以及带有间苯二酚1,3-二酚取代模式的那些化合物中发现的无活性情况相似。