Paper
Potential resperine analogues. Part II. 3,4,5-Trimethoxybenzoic acid derivatives.
Published 1960 · M. A. Karim, W. H. Linnel, L. K. Sharp
The Journal of pharmacy and pharmacology
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Abstract
Seven derivatives of 3,4,5‐trimethoxybenzoic acid have been prepared and tested for their ability to potentiate barbiturate hypnosis in mice, to deplete the 5‐hydroxytryptamine content of rat brain, and to exert a hypotensive action on the cat blood pressure. The only derivative to exert all three actions is the simple anilide, 3,4,5‐trimethoxybenzanilide, which is about 8 times less active than reserpine. The anilide, N‐(3,4‐dimethoxyphenethyl)‐3,4,5‐trimethoxybenzamide, is also about 8 times less active than reserpine in the first two tests but it raises the blood pressure.
3,4,5-trimethoxybenzanilide effectively potentiates barbiturate hypnosis, depletes 5hydroxytryptamine, and reduces cat blood pressure, while N-(3,4-dimethoxyphenethyl)-3,4,5-trimethoxybenzamide
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