PubMed · 576809
Structure-anorectic activity relationships in substituted phenethylamines.
Abstract
A series of phenylisopropylamine derivatives are compared with the correspondent beta-methoxy- and beta-hydroxy-phenethylamine compounds. Unlike amphetamine, the beta-methoxy phenethylamine has no anorectic activity. This property appears only with the introduction of a CF3 group on the benzene nucleus. The racemic N-alkyl derivatives are more active than the racemic or even the levorotatory N-benzyl compound. The beta-hydroxy-phenethylamines are devoid of anorectic activity.
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S L Beregi, J Duhault. 1977. Structure-anorectic activity relationships in substituted phenethylamines.. https://pubmed.ncbi.nlm.nih.gov/576809/
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