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A study of potential histidine decarboxylase inhibitors

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 k...

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Hlavní autoři: Mackay, D., Shepherd, D. M.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1960
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1482398/
https://ncbi.nlm.nih.gov/pubmed/13764874
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