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Selectivity of 4-methoxyphenethylamine derivatives as inhibitors of monoamine oxidase.

It has been established that the oxidative deamination of tyramine by monoamine xodase is inhibited by (+/-)-4-methoxy-beta-hydroxyphenethylamine and its N-methylated derivatives. This particular series of compounds does not inhibit the action of monoamine oxidase when tryptamine is used as the substrate. In contrast, 4-methoxyphenethylamine and its N-methylated homologs inhibit the monoamine oxidase-catalyzed deamination of both tyramine and tryptamine.[1]

References

  1. Selectivity of 4-methoxyphenethylamine derivatives as inhibitors of monoamine oxidase. Keller, W.J., Ferguson, G.G. Journal of pharmaceutical sciences. (1976) [Pubmed]
 
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