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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
1981-1-26
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pubmed:abstractText |
The main metabolite of 2-phenyl-4-p-chlorophenylthiazol-5-ylacetic acid (fentiazac) is represented by a p-hydroxylated compound which is formed rapidly and that, still 72 later, can be detected in the general circulation. The p-hydroxylated metabolite is much less toxic than the original molecule from which it derives, being still active from an anti-inflammatory standpoint (its activity being equal to 70--75% of that of fentiazac). The metabolite, which possesses a therapeutic index much higher than that of fentiazac, represents quite an important step in the detoxication processes of the drug and enhances the therapeutic activity of the drug itself.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0004-4172
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1253-6
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7192138-Acetic Acids,
pubmed-meshheading:7192138-Animals,
pubmed-meshheading:7192138-Anti-Inflammatory Agents,
pubmed-meshheading:7192138-Biotransformation,
pubmed-meshheading:7192138-Chemistry, Physical,
pubmed-meshheading:7192138-Dogs,
pubmed-meshheading:7192138-Female,
pubmed-meshheading:7192138-Macaca fascicularis,
pubmed-meshheading:7192138-Male,
pubmed-meshheading:7192138-Physicochemical Phenomena,
pubmed-meshheading:7192138-Rats,
pubmed-meshheading:7192138-Thiazoles
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pubmed:year |
1980
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pubmed:articleTitle |
Metabolism of fentiazac.
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pubmed:publicationType |
Journal Article,
Comparative Study
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