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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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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
1960
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1482398/ https://ncbi.nlm.nih.gov/pubmed/13764874 |
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