[Fermentative oxidation of rho-hydroxyphenylpyruvic acid to homogentisic acid].
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Homogentisic Acid↗
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Results for “PHENYLPYRUVIC ACID/related compounds”
Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.
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The metabolism of p-methoxyphenylalanine and p-methoxyphenylpyruvate.
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Liver↗
The tyrosine oxidation system of liver. IV. Studies on the inhibition of p-hydroxyphenylpyruvic acid oxidase by excess substrate.
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Ascorbic Acid↗
Phenylpyruvic acid as a possible precursor of o-hydroxyphenylacetic acid in man.
The oral administration of phenylpyruvic acid to human subjects results in increased urinary excretion of o-hydroxyphenylacetic acid. This demonstrates that phenylpyruvic acid may act as a precursor for o-hydroxy derivatives of phenylalanine and suggests that the formation of o-tyrosine is not necessary to account for the excretion of o-hydroxyphenylacetic acid in phenylketonuria.
Administration, Oral↗
Isolation of prephenic acid from Neurospora.
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Cyclohexanecarboxylic Acids↗
Identification of p-hydroxyphenlpyruvic acid-O-sulphate as a metabolite of tyrosine-O-sulphate in the rat.
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Animals↗
Aromatic biosynthesis. XVI. Aromatization of prephenic acid to p-hydroxyphenylpyruvic acid, a step in tyrosine biosynthesis in Escherichia coli.
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Cyclohexanecarboxylic Acids↗
Alkaline conversion of 4-hydroxyphenylpyruvic acid to 4-hydroxybenzaldehyde.
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Aldehydes↗
Effects of L-phenylalanine and sodium phenylpyruvate on the formation of melanin from L-tyrosine in melanoma.
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Melanins↗
[Appearance of p-hydroxyphenylpyruvic acid and other alpha-ketone acids in the urine of healthy rabbits and with liver cirrhosis].
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Animals↗
[Excretion of p-hydroxyphenylpyruvic acid, phenylpyruvic acid & other alpha-ketone acids in the urine of healthy humans, also a contribution to the problem of tyrosinosis].
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Amino Acid Metabolism, Inborn Errors↗
p-Hydroxyphenylpyruvate oxidase of liver.
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4-Hydroxyphenylpyruvate Dioxygenase↗
[Functional diagnosis of liver diseases with the p-hydroxyphenylpyruvic acid test].
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Humans↗
Metabolism of 3-hydroxy- and 3,4-dihydroxyphenylpyruvic acids in vivo.
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Phenylpyruvic Acids↗
Tyrosyluria resulting from inhibition of p-hydroxyphenylpyruvic acid oxidase in vitamin C-deficient guinea pigs.
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Ascorbic Acid↗
[Alcaptogenesis: unsolved biochemical problem].
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Alkaptonuria↗
The mechanism of p-hydroxy-phenylpyruvate accumulation in guinea pigs fed tyrosine.
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Animals↗
o-Hydroxyphenylacetic acid excretion in the phenylalanine tolerance test for carriers of phenylketonuria.
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Humans↗