Title : Interaction with P-glycoprotein and transport of erythromycin, midazolam and ketoconazole in Caco-2 cells.

Pub. Date : 1998 Oct 9

PMID : 9822896






5 Functional Relationships(s)
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1 Interaction with P-glycoprotein and transport of erythromycin, midazolam and ketoconazole in Caco-2 cells. Erythromycin ATP binding cassette subfamily B member 1 Homo sapiens
2 The basal-to-apical transport of rhodamine 123, a P-glycoprotein substrate, was inhibited by erythromycin, midazolam and ketoconazole, as well as by P-glycoprotein inhibitors such as verapamil. Erythromycin ATP binding cassette subfamily B member 1 Homo sapiens
3 In conclusion, erythromycin, midazolam and ketoconazole could interact with P-glycoprotein-mediated transport, and P-glycoprotein could be, at least in part, involved in the transport of erythromycin, but not of midazolam and ketoconazole, in the intestinal epithelia. Erythromycin ATP binding cassette subfamily B member 1 Homo sapiens
4 In conclusion, erythromycin, midazolam and ketoconazole could interact with P-glycoprotein-mediated transport, and P-glycoprotein could be, at least in part, involved in the transport of erythromycin, but not of midazolam and ketoconazole, in the intestinal epithelia. Erythromycin ATP binding cassette subfamily B member 1 Homo sapiens
5 In conclusion, erythromycin, midazolam and ketoconazole could interact with P-glycoprotein-mediated transport, and P-glycoprotein could be, at least in part, involved in the transport of erythromycin, but not of midazolam and ketoconazole, in the intestinal epithelia. Erythromycin ATP binding cassette subfamily B member 1 Homo sapiens