A STUDY OF POTENTIAL HISTIDINE DECARBOXYLASE INHIBITORS

Abstract
A series of compounds has been examined for ability to inhibit histidine decarboxylase. Histidine analogues having substituents in the imidazole ring showed a wide variation in potency, but these were all much less active than α-methyldopa [β-(3,4-dihydroxyphenyl)-α-methylalanine], the most potent known inhibitor of histidine decarboxylase. Some tentative conclusions are drawn regarding the relationship between chemical structure and inhibitory activity.

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