Ginsenosides

cytochrome P450 family 3 subfamily A member 4 ; Homo sapiens







9 Article(s)
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1 30342195 Reversing effects of ginsenosides on LPS-induced hepatic CYP3A11/3A4 dysfunction through the pregnane X receptor. 2019 Jan 30 2
2 31358899 Intravenous formulation of Panax notoginseng root extract: human pharmacokinetics of ginsenosides and potential for perpetrating drug interactions. 2019 Oct 1
3 24486455 Ginsenoside-mediated blockade of 1α,25-dihydroxyvitamin D3 inactivation in human liver and intestine in vitro. 2014 May 1
4 21178302 Deglycosylated ginsenosides are more potent inducers of CYP1A1, CYP1A2 and CYP3A4 expression in HepG2 cells than glycosylated ginsenosides. 2011 4
5 20580705 Induction of CYP3A4 and MDR1 gene expression by baicalin, baicalein, chlorogenic acid, and ginsenoside Rf through constitutive androstane receptor- and pregnane X receptor-mediated pathways. 2010 Aug 25 4
6 20639434 Microsomal cytochrome p450-mediated metabolism of protopanaxatriol ginsenosides: metabolite profile, reaction phenotyping, and structure-metabolism relationship. 2010 Oct 2
7 18628990 Structure-activity relationship and substrate-dependent phenomena in effects of ginsenosides on activities of drug-metabolizing P450 enzymes. 2008 Jul 16 2
8 15133536 The inhibitory effects of herbal components on CYP2C9 and CYP3A4 catalytic activities in human liver microsomes. 2004 May-Jun 2
9 10574228 Effects of ginseng components on c-DNA-expressed cytochrome P450 enzyme catalytic activity. 1999 1