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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1989-5-30
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pubmed:abstractText |
1. Like 2- and 4-dimethylaminophenol, 4-aminophenol in the presence of oxyhaemoglobin forms numerous adducts with glutathione (GSH). Using 14C-4-aminophenol and 3H-glutathione, ten different thioethers were isolated, by h.p.l.c., with isotope ratios of 1:1, 1:2, 1:3, respectively. The structural identification of the different thioethers is under current investigation. 2. In erythrocytes of human and dog, and in dog blood, in vivo, the same pattern of 4-aminophenol conjugates with GSH was found. 3. In vivo, 5% of administered 4-aminophenol is converted into thioethers within erythrocytes, accompanied by a 60% decrease in the cellular GSH, indicating the role of erythrocytes in the biotransformation of xenobiotics.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/4-aminophenol,
http://linkedlifedata.com/resource/pubmed/chemical/Aminophenols,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione,
http://linkedlifedata.com/resource/pubmed/chemical/Methemoglobin,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfides
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0049-8254
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1319-26
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3245228-Aminophenols,
pubmed-meshheading:3245228-Animals,
pubmed-meshheading:3245228-Biotransformation,
pubmed-meshheading:3245228-Dogs,
pubmed-meshheading:3245228-Erythrocytes,
pubmed-meshheading:3245228-Glutathione,
pubmed-meshheading:3245228-Humans,
pubmed-meshheading:3245228-Kinetics,
pubmed-meshheading:3245228-Male,
pubmed-meshheading:3245228-Methemoglobin,
pubmed-meshheading:3245228-Sulfides
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pubmed:year |
1988
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pubmed:articleTitle |
The metabolism of aminophenols in erythrocytes.
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pubmed:affiliation |
Walther-Straub-Institut für Pharmakologie und Toxikologie, Ludwig-Maximilians-Universität München, F.R. Germany.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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