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Merck

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

Journal of pharmaceutical sciences (1976-10-01)
W J Keller, G G Ferguson
PMID978418
RÉSUMÉ

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.

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Sigma-Aldrich
4-Methoxyphenethylamine, ≥98%