Page last updated: 2024-10-17

hippuric acid and Inborn Urea Cycle Disorder

hippuric acid has been researched along with Inborn Urea Cycle Disorder in 1 studies

hippuric acid: RN given refers to parent cpd; structure in Merck Index, 9th ed, #4591
N-benzoylglycine : An N-acylglycine in which the acyl group is specified as benzoyl.

Research Excerpts

ExcerptRelevanceReference
"Available medications for treating urea cycle disorders include sodium benzoate (BA), sodium phenylacetate (PAA), and sodium phenylbutyrate (PBA) and are given to provide alternate routes for disposition of waste nitrogen excretion."1.36Simultaneous LC-MS/MS determination of phenylbutyrate, phenylacetate benzoate and their corresponding metabolites phenylacetylglutamine and hippurate in blood and urine. ( Herebian, D; Laryea, MD; Mayatepek, E; Meissner, T, 2010)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Laryea, MD1
Herebian, D1
Meissner, T1
Mayatepek, E1

Other Studies

1 other study available for hippuric acid and Inborn Urea Cycle Disorder

ArticleYear
Simultaneous LC-MS/MS determination of phenylbutyrate, phenylacetate benzoate and their corresponding metabolites phenylacetylglutamine and hippurate in blood and urine.
    Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3

    Topics: Benzoates; Biomarkers; Biotransformation; Calibration; Chromatography, Reverse-Phase; Glutamine; Hip

2010