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N-caproylglycine

Known as: Hexanoylglycine, glycine, N-(1-oxohexyl)- 
National Institutes of Health

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2 relations

Broader (1)

Glycine
analogs & derivatives

Papers overview

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Highly Cited
2013
Highly Cited
2013
Development of Urinary Biomarkers for Internal Exposure by Cesium-137 Using a Metabolomics Approach in Mice
Cesium-137 is a fission product of uranium and plutonium in nuclear reactors and is released in large quantities during nuclear… 
2008
2008
Detection of urinary hexanoylglycine in the diagnosis of MCAD deficiency from newborn screening
We strongly support Piero Rinaldo_s and Kevin Carpenter_s comments regarding the importance of accurate and reliable… 
2007
2007
Refractory seizures associated with an organic aciduria in a dog.
A 6-month-old, female Cavalier King Charles spaniel exhibited seizures that were difficult to control with standard… 
2006
2006
Na+, K+ ATPase activity is markedly reduced by cis-4-decenoic acid in synaptic plasma membranes from cerebral cortex of rats
1995
1995
Anaphylactoid reaction to BCG vaccine containing high molecular weight dextran
particularly in newborns with hypoglycaemia [2, 5]. We report the first case of MCAD deficiency from Italy in a patient who is… 
1994
1994
Population Screening for Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Analysis of Medium-Chain Fatty Acids and Acylglyeines in Blood Spots
We have developed methods for the measurement of the medium-chain fatty acids octanoate, decanoate and cis-4-decenoate and the… 
1991
1991
Screening Newborns for Multiple Organic Acidurias in Dried Filter Paper Urine Samples: Method Development
Screening urine for inherited and acquired organic acidurias in newborns has the potential of preventing severe disease, mental… 
1990
1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency
SummaryIn order to determine which are useful early diagnostic markers for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency… 
1985
1985
Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids.
1983
1983
DICARBOXYLIC ACIDURIA DUE TO MEDIUM CHAIN ACYL CoA DEHYDROGENASE DEFECT
ABSTRACT. Dicarboxylic aciduria was found during hypoglycemic episode in a 14 months old girl. Her brother had died at the age of… 
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