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rdf:type |
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lifeskim:mentions |
|
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pubmed:issue |
17
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pubmed:dateCreated |
1998-2-5
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pubmed:abstractText |
N(O,S)-Ethoxycarbonyl trifluoroethyl amino acid esters are formed by the reaction of amino acids with ethylchloroformate plus trifluoroethanol plus pyridine. The use of these derivatives for a rapid and sensitive determination of specific enrichment of stable isotopically labeled tracer amino acids in blood plasma and protein hydrolysates, by using gas chromatography/electron impact mass spectrometry, is discussed.
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pubmed:language |
eng
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pubmed:journal |
|
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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pubmed:issn |
0951-4198
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
|
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1835-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9404034-Amino Acids,
pubmed-meshheading:9404034-Apolipoproteins,
pubmed-meshheading:9404034-Calibration,
pubmed-meshheading:9404034-Carbon Isotopes,
pubmed-meshheading:9404034-Deuterium,
pubmed-meshheading:9404034-Formic Acid Esters,
pubmed-meshheading:9404034-Gas Chromatography-Mass Spectrometry,
pubmed-meshheading:9404034-Humans,
pubmed-meshheading:9404034-Kinetics,
pubmed-meshheading:9404034-Models, Biological,
pubmed-meshheading:9404034-Trifluoroethanol
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|
pubmed:year |
1997
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pubmed:articleTitle |
Stable isotope ratio analysis of amino acids: the use of N(O,S)-ethoxycarbonyl trifluoroethyl ester derivatives and gas chromatography/mass spectrometry.
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pubmed:affiliation |
Institute of Clinical Metabolic Research, Medical Faculty Carl Gustav Carus, Technical University Dresden, Germany.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't
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