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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
1995-9-18
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pubmed:abstractText |
Racemic trans-anethole epoxide [1-(4'-methoxyphenyl)-propane-1,2-oxide] was incubated with water, buffers, and rat liver microsomes and cytosol and the stereochemistry of the diols produced was determined by HPLC as their dicamphanyl esters. The diol metabolites were isolated by HPLC from the urine of rats administered [1'-14C] trans-anethole and their stereochemistry determined after derivatization to their camphanyl esters. The stereochemical course of the metabolism of trans-anethole by rat liver microsomes and cytosol 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 |
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pubmed:status |
MEDLINE
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pubmed:issn |
0899-0042
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
278-84
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7640171-Animals,
pubmed-meshheading:7640171-Anisoles,
pubmed-meshheading:7640171-Biotransformation,
pubmed-meshheading:7640171-Chromatography, High Pressure Liquid,
pubmed-meshheading:7640171-Cytosol,
pubmed-meshheading:7640171-Flavoring Agents,
pubmed-meshheading:7640171-Gas Chromatography-Mass Spectrometry,
pubmed-meshheading:7640171-Male,
pubmed-meshheading:7640171-Microsomes, Liver,
pubmed-meshheading:7640171-Oxygen Radioisotopes,
pubmed-meshheading:7640171-Rats,
pubmed-meshheading:7640171-Rats, Sprague-Dawley,
pubmed-meshheading:7640171-Stereoisomerism,
pubmed-meshheading:7640171-Water
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pubmed:year |
1995
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pubmed:articleTitle |
Stereochemical aspects of the hydration of trans-anethole epoxide in the rat.
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pubmed:affiliation |
Department of Pharmacology and Toxicology, St. Mary's Hospital Medical School, Imperial College of Science, Technology and Medicine, London, England.
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pubmed:publicationType |
Journal Article,
In Vitro
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