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Publikováno v:
Archives of pharmacal research. 34(10)
Docetaxel is a P-glycoprotein (P-gp) substrate and metabolized via cytochrome P450 (CYP) 3A subfamily in rats. Morin is an inhibitor of both CYPs and P-gp. Hence, the effects of morin on the intravenous and oral pharmacokinetics of docetaxel were inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb4d733a0d14731d12b346d30bb01ecc
https://pubmed.ncbi.nlm.nih.gov/22076773
https://pubmed.ncbi.nlm.nih.gov/22076773
