Buspirone

cytochrome P450, family 3, subfamily a, polypeptide 62 ; Rattus norvegicus







9 Article(s)
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1 31317804 Bergamottin can be used to assess CYP3A-mediated intestinal first-pass metabolism without affecting P-glycoprotein-mediated efflux in rats. 2020 Apr 1
2 32078103 Evaluation of the Role of P-glycoprotein (P-gp)-Mediated Efflux in the Intestinal Absorption of Common Substrates with Elacridar, a P-gp Inhibitor, in Rats. 2020 Jun 1
3 30537097 Differential regulation of intestinal and hepatic CYP3A by 1α,25-dihydroxyvitamin D3 : Effects on in vivo oral absorption and disposition of buspirone in rats. 2019 May 5
4 25574821 Pinelliae rhizoma, a toxic chinese herb, can significantly inhibit CYP3A activity in rats. 2015 Jan 7 1
5 27013798 Modulation of Hepatic Cytochrome P450 Enzymes by Curcumin and its Pharmacokinetic Consequences in Sprague-dawley Rats. 2015 Oct 1
6 24710899 In vitro and in vivo evaluation of the effect of puerarin on hepatic cytochrome p450-mediated drug metabolism. 2014 May 1
7 25434398 The influences of aconitine, an active/toxic alkaloid from aconitum, on the oral pharmacokinetics of CYP3A probe drug buspirone in rats. 2014 4
8 23085095 The exposure of highly toxic aconitine does not significantly impact the activity and expression of cytochrome P450 3A in rats determined by a novel ultra performance liquid chromatography-tandem mass spectrometric method of a specific probe buspirone. 2013 Jan 1
9 23873286 Assessment of CYP3A-mediated drug-drug interaction potential for victim drugs using an in vivo rat model. 2013 Oct 1