| Literature DB >> 12112740 |
Blandine Comte1, Takhar Kasumov, Bradley A Pierce, Michelle A Puchowicz, Mary-Ellen Scott, Williams Dahms, Douglas Kerr, Itzhak Nissim, Henri Brunengraber.
Abstract
Phenylbutyrate is used in humans for treating inborn errors of ureagenesis, certain forms of cancer, cystic fibrosis and thalassemia. The known metabolism of phenylbutyrate leads to phenylacetylglutamine, which is excreted in urine. We have identified phenylbutyrylglutamine as a new metabolite of phenylbutyrate in human plasma and urine. We describe the synthesis of phenylbutyrylglutamine and its assay by gas chromatography/mass spectrometry as a tert-butyldimethylsilyl or methyl derivative, using standards of [(2)H(5)]phenylbutyrylglutamine and phenylpropionylglutamine. After administration of phenylbutyrate to normal humans, the cumulative urinary excretion of phenylacetate, phenylbutyrate, phenylacetylglutamine and phenylbutyrylglutamine amounts to about half of the dose of phenylbutyrate. Thus, additional metabolites of phenylbutyrate are yet to be identified. Copyright 2002 John Wiley & Sons, Ltd.Entities:
Mesh:
Substances:
Year: 2002 PMID: 12112740 DOI: 10.1002/jms.316
Source DB: PubMed Journal: J Mass Spectrom ISSN: 1076-5174 Impact factor: 1.982