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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1986-5-28
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pubmed:abstractText |
p-Nitrophenyl pent-1-yl ether was metabolized (65-70%) in the presence of liver microsomes from phenobarbital-treated rats to give the 4-(major), 3-(minor), and 2-hydroxypent-1-yl (minor) derivatives which were characterized by g.l.c.-mass spectrometry; O-dealkylation (reflecting 1-hydroxylation) and 5-hydroxylation did not occur to a significant extent. 5,5,5-Trifluorination of the pent-1-yl group markedly reduced the extent of metabolism (to approximately 10%). p-Nitrophenyl 2,2,2-trifluoroethyl ether was virtually completely resistant to microsomal metabolism under conditions where the ethyl analogue was extensively O-dealkylated.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0049-8254
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
16
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
195-203
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:3705616-Animals,
pubmed-meshheading:3705616-Biotransformation,
pubmed-meshheading:3705616-Fluorine,
pubmed-meshheading:3705616-Gas Chromatography-Mass Spectrometry,
pubmed-meshheading:3705616-Hydroxylation,
pubmed-meshheading:3705616-Male,
pubmed-meshheading:3705616-Microsomes, Liver,
pubmed-meshheading:3705616-Nitrobenzenes,
pubmed-meshheading:3705616-Rats,
pubmed-meshheading:3705616-Rats, Inbred Strains,
pubmed-meshheading:3705616-Structure-Activity Relationship
|
pubmed:year |
1986
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pubmed:articleTitle |
Effect of omega-trifluorination on the microsomal metabolism of ethyl and pent-1-yl p-nitrophenyl ether.
|
pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
|