Title : Effects of naringin on the pharmacokinetics of intravenous paclitaxel in rats.

Pub. Date : 2006 Dec

PMID : 17009338






6 Functional Relationships(s)
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1 It was reported that paclitaxel is an inhibitor of hepatic P-glycoprotein (P-gp) and hepatic microsomal cytochrome P450 (CYP) 3A1/2, and that naringin is an inhibitor of biliary P-gp and CYP3A1/2 in rats. naringin ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
2 It was reported that paclitaxel is an inhibitor of hepatic P-glycoprotein (P-gp) and hepatic microsomal cytochrome P450 (CYP) 3A1/2, and that naringin is an inhibitor of biliary P-gp and CYP3A1/2 in rats. naringin ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
3 It was reported that paclitaxel is an inhibitor of hepatic P-glycoprotein (P-gp) and hepatic microsomal cytochrome P450 (CYP) 3A1/2, and that naringin is an inhibitor of biliary P-gp and CYP3A1/2 in rats. naringin cytochrome P450, family 3, subfamily a, polypeptide 23-polypeptide 1 Rattus norvegicus
4 The significantly greater AUC could be due mainly to an inhibition of metabolism of paclitaxel via CYP3A1/2 by oral naringin. naringin cytochrome P450, family 3, subfamily a, polypeptide 23-polypeptide 1 Rattus norvegicus
5 The inhibition of hepatic P-gp by oral naringin could also contribute to the significantly greater AUC of intravenous paclitaxel by oral naringin. naringin ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
6 The inhibition of hepatic P-gp by oral naringin could also contribute to the significantly greater AUC of intravenous paclitaxel by oral naringin. naringin ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus