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pyrogallol and Alkaptonuria

pyrogallol has been researched along with Alkaptonuria in 1 studies

benzenetriol : A triol in which three hydroxy groups are substituted onto a benzene ring.

Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.

Research Excerpts

ExcerptRelevanceReference
"The metabolic disorder, alkaptonuria, is distinguished by elevated serum levels of 2,5-dihydroxyphenylacetic acid (homogentisic acid), pigmentation of cartilage and connective tissue and, ultimately, the development of inflammatory arthritis."7.67Homogentisic acid autoxidation and oxygen radical generation: implications for the etiology of alkaptonuric arthritis. ( Batkoff, B; Martin, JP, 1987)
"The metabolic disorder, alkaptonuria, is distinguished by elevated serum levels of 2,5-dihydroxyphenylacetic acid (homogentisic acid), pigmentation of cartilage and connective tissue and, ultimately, the development of inflammatory arthritis."3.67Homogentisic acid autoxidation and oxygen radical generation: implications for the etiology of alkaptonuric arthritis. ( Batkoff, B; Martin, JP, 1987)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (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
Martin, JP1
Batkoff, B1

Other Studies

1 other study available for pyrogallol and Alkaptonuria

ArticleYear
Homogentisic acid autoxidation and oxygen radical generation: implications for the etiology of alkaptonuric arthritis.
    Free radical biology & medicine, 1987, Volume: 3, Issue:4

    Topics: Alkaptonuria; Animals; Arthritis; Ascorbic Acid; Edetic Acid; Free Radicals; Homogentisic Acid; Hyal

1987