Carnmalm B, Rämsby S, Renyi A L, Ross S B, Ogren S O
J Med Chem. 1978 Jan;21(1):78-82. doi: 10.1021/jm00199a014.
3,3-Diphenylcyclobutylamine (4), N-methyl-3,3-diphenylcyclobutylamine (6), and N,N-dimethyl-3,3-diphenyl-cyclobutylamine (7) have been prepared and tested as potential antidepressant agents. The secondary (6) and tertiary (7) amines strongly decrease the accumulation of NA and 5-HT in brain slices in vitro and in vivo. The cyclobutylamines also cause motor stimulation. The most potent compound in this respect is the tertiary amine 7. The increase in locomotion is not blocked by pretreatment with phenoxybenzamine, methergoline, or alpha-methyltyrosine. Pretreatment with pimozide or reserpine reduces the hyperactivity induced by 7. This hyperstimulation seems to be caused by a mechanism of action which differs from that of amphetamine. 7 may cause increase in locomotion by release of dopamine from granular stores.
已制备出3,3 - 二苯基环丁胺(4)、N - 甲基 - 3,3 - 二苯基环丁胺(6)和N,N - 二甲基 - 3,3 - 二苯基环丁胺(7),并作为潜在的抗抑郁药进行了测试。仲胺(6)和叔胺(7)在体外和体内均能强烈降低脑切片中去甲肾上腺素(NA)和5 - 羟色胺(5 - HT)的积累。环丁胺还会引起运动兴奋。在这方面最有效的化合物是叔胺7。用酚苄明、麦角新碱或α - 甲基酪氨酸预处理不会阻止运动增加。用匹莫齐特或利血平预处理可降低7诱导的多动。这种过度刺激似乎是由一种与苯丙胺不同的作用机制引起的。7可能通过从颗粒储存中释放多巴胺而导致运动增加。