
doi: 10.1038/213802a0
pmid: 6031806
THE metabolism of dihydroxyphenylalanine (DOPA; I, R = H) may be very complex. By analogy with other amino-acids, degradation may involve decarboxylation (route A) or transamination (route B), with methylation of the 3-hydroxy group possible at any stage. The principal metabolite in normal human urine appears to be homovanillic acid (HVA; III, R = CH3), and excretion of small amounts of 3-methoxytyramine (II, R = CH3) clearly points to the operation of route A.
Flavoring Agents, Phenylpyruvic Acids, Humans, Tyramine, Dihydroxyphenylalanine, Phenylacetates
Flavoring Agents, Phenylpyruvic Acids, Humans, Tyramine, Dihydroxyphenylalanine, Phenylacetates
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