Source:http://linkedlifedata.com/resource/pubmed/id/10805063
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11-12
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pubmed:dateCreated |
2000-7-14
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pubmed:abstractText |
1,4-Dihydropyridine calcium antagonists such as nifedipine are potent vasodilators. It is now commonly agreed that the oxidation of 1,4-dihydropyridine into pyridine, which is one of the main metabolic pathways, is catalysed by the cytochrome P450 (CYP) 3A4 isoform. In the present study, the inhibitory effects of 13 kinds of 1,4-dihydropyridine calcium antagonists clinically used in Japan on human CYP-isoform-dependent reactions were investigated to predict the drug interactions using microsomes from human B-lymphoblast cells expressing CYP.
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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 |
0031-6970
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
55
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
843-52
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10805063-B-Lymphocytes,
pubmed-meshheading:10805063-Calcium Channel Blockers,
pubmed-meshheading:10805063-Cytochrome P-450 Enzyme System,
pubmed-meshheading:10805063-Dihydropyridines,
pubmed-meshheading:10805063-Drug Interactions,
pubmed-meshheading:10805063-Humans,
pubmed-meshheading:10805063-Kinetics,
pubmed-meshheading:10805063-Liver,
pubmed-meshheading:10805063-Microsomes
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pubmed:articleTitle |
Inhibition of human cytochrome P450 enzymes by 1,4-dihydropyridine calcium antagonists: prediction of in vivo drug-drug interactions.
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pubmed:affiliation |
Division of Drug Metabolism, Faculty of Pharmaceutical Sciences, Kanazawa University, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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