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The 4-amino 5-alkyl-sulfone substituted orthoanisamides can be distinguished from their non-aminated homologues (sultopride) or sulfamoyl homologues (sulpride) mainly by the intensity of their anti-emetic effects with regard to apomorphine and their mode of action, either on hippocampic rhythms or on locomotor rhythms in the Cat.
The substituted orthoveratramides, derived from the orthopramides by the addition of a second methoxy radical at position 3 in the benzene ring, possess strong endocrinological effects. In particular the N[(allyl-1 pyrrolidinyl-2) methyl] dimethoxy-2-3 sulfamoyl-5 benzamide blocks oestrus in the Rat at doses considerably lower than sultopride and inhibits… (More)