Abstract
Benzodioxan derivatives active on the alpha-adrenergic receptor are considered. The half-chair equilibrium of the dioxane ring was studied by 1H-NMR spectroscopy for piperoxan X and quiloflex XII. The preferred conformation was also obtained by PCILO calculations for X. The results were evaluated in order to obtain information about the mechanism of the alpha-adrenergic drug-receptor interaction.
- Copyright © 1981 by The American Society for Pharmacology and Experimental Therapeutics
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