Compounds > phenylpyruvic acid
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phenylpyruvic acid and Amino Acid Metabolism Disorders, Inborn

phenylpyruvic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 5 studies

phenylpyruvic acid: RN given refers to parent cpd
phenylpyruvate : A 2-oxo monocarboxylic acid anion resulting from deprotonation of the carboxy group of either keto- or enol-phenylpyruvic acid.
keto-phenylpyruvic acid : A 2-oxo monocarboxylic acid that is 3-phenylpropanoic acid substituted by an oxo group at position 2. It is an intermediate metabolite in the phenylalanine pathway.

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19905 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
HENNING, U1
AMMON, R1
ZETTERSTROEM, R1
HALVORSEN, S1
GJESSING, LR1
HUMBEL, R1
ALAGILLE, D1
GENTIL, C1

Other Studies

5 other studies available for phenylpyruvic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
[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].
    Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 1957, Feb-05, Volume: 306, Issue:4-6

    Topics: Amino Acid Metabolism, Inborn Errors; Humans; Keto Acids; Ketones; Phenylpyruvic Acids; Tyrosine

1957
TYROSINOSIS.
    Annals of the New York Academy of Sciences, 1963, Dec-30, Volume: 111

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Child; Genetics, Medical; Gl

1963
STUDIES ON TYROSINOSIS: 1, EFFECT OF LOW-TYROSINE AND LOW-PHENYLALANINE DIET.
    British medical journal, 1964, Nov-07, Volume: 2, Issue:5418

    Topics: Acetates; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Diet; Diet Therapy; Hepatomegaly

1964
[IDENTIFICATION AND DETERMINATION OF P-HYDROXYPHENYLPYRUVIC ACID AND ITS DERIVATIVES IN URINE].
    Das Medizinische Laboratorium, 1964, Volume: 17

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Humans; Lactates; Phenylacetates;

1964
[CONGENITAL CIRRHOSIS WITH COMPLEX RENAL TUBULE DISEASE DUE TO AN ANOMALY OF TYROSINE METABOLISM].
    Revue medico-chirurgicale des maladies du foie, 1964, Volume: 39

    Topics: Amino Acid Metabolism, Inborn Errors; Carcinoma, Hepatocellular; Chronic Kidney Disease-Mineral and

1964