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Identification of the cytochrome P450 enzymes involved in the metabolism of cisapride: in vitro studies of potential co-medication interactions
1. Cisapride is a prokinetic drug that is widely used to facilitate gastrointestinal tract motility. 2. Structurally, cisapride is a substituted piperidinyl benzamide that interacts with 5-hydroxytryptamine-4 receptors and which is largely without central depressant or antidopaminergic side-effects....
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| Huvudupphovsmän: | , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2000
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1572003/ https://ncbi.nlm.nih.gov/pubmed/10780971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjp.0703246 |
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