Title : Coadministration of cyclosporine strongly enhances the oral bioavailability of docetaxel.

Pub. Date : 2001 Feb 15

PMID : 11181682






5 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 PURPOSE: Oral bioavailability of docetaxel is very low, which is, at least in part, due to its affinity for the intestinal drug efflux pump P-glycoprotein (P-gp). Docetaxel ATP binding cassette subfamily B member 1 Homo sapiens
2 PURPOSE: Oral bioavailability of docetaxel is very low, which is, at least in part, due to its affinity for the intestinal drug efflux pump P-glycoprotein (P-gp). Docetaxel ATP binding cassette subfamily B member 1 Homo sapiens
3 In addition, metabolism of docetaxel by cytochrome P450 (CYP) 3A4 in gut and liver may also contribute. Docetaxel cytochrome P450 family 3 subfamily A member 4 Homo sapiens
4 The purpose of this study was to enhance the systemic exposure to oral docetaxel on coadministration of cyclosporine (CsA), an efficacious inhibitor of P-gp and substrate for CYP 3A4. Docetaxel ATP binding cassette subfamily B member 1 Homo sapiens
5 The purpose of this study was to enhance the systemic exposure to oral docetaxel on coadministration of cyclosporine (CsA), an efficacious inhibitor of P-gp and substrate for CYP 3A4. Docetaxel cytochrome P450 family 3 subfamily A member 4 Homo sapiens