Florvall L, Fagervall I, Ask A L, Ross S B
J Med Chem. 1986 Nov;29(11):2250-6. doi: 10.1021/jm00161a020.
Nine 4-aminophenethylamine derivatives were synthesized and tested for monoamine oxidase (MAO) inhibitory effects with particular attention to their selectivity for MAO within monoaminergic neurons in the rat brain. All compounds selectively inhibited the A form of MAO in vitro. Some of the compounds inhibited the MAO within the monoaminergic neurons at much lower doses than those required for inhibition of MAO within other cells in vivo. The most potent compounds in this respect were 4-amino-2-fluoro-alpha-methylphenethylamine (5) and 4-amino-2-chloro-alpha-methylphenethylamine (4).
合成了九种4-氨基苯乙胺衍生物,并测试了它们对单胺氧化酶(MAO)的抑制作用,特别关注它们对大鼠脑内单胺能神经元中MAO的选择性。所有化合物在体外均选择性抑制MAO的A形式。一些化合物在体内抑制单胺能神经元内的MAO所需剂量远低于抑制其他细胞内MAO所需的剂量。在这方面最有效的化合物是4-氨基-2-氟-α-甲基苯乙胺(5)和4-氨基-2-氯-α-甲基苯乙胺(4)。