نتایج جستجو برای: cyp2a6

تعداد نتایج: 638  

2016
Dong-sheng Ouyang Wei-hua Huang Dan Chen Wei Zhang Zhi-rong Tan Jing-bo Peng Yi-cheng Wang Ying Guo Dong-li Hu Jian Xiao Yao Chen

BACKGROUND Sodium tanshinone IIA sulfonate (STS) is a water-soluble derivative of tanshinone IIA for treating cardiovascular disorders. The roles of cytochrome P450 enzymes (CYPs) in the metabolism of STS have remained unclear. This study aims to screen the main CYPs for metabolism of STS and study their interactions in vitro. METHODS Seven major CYPs were screened for metabolism of STS by hu...

2017
Ju-Hyun Kim Soon-Sang Kwon Hyeon-Uk Jeong Hye Suk Lee

Magnolin, epimagnolin A, dimethyllirioresinol, eudesmin, and fargesin are pharmacologically active tetrahydrofurofuranoid lignans found in Flos Magnoliae. The inhibitory potentials of dimethyllirioresinol, epimagnolin A, eudesmin, fargesin, and magnolin on eight major human cytochrome P450 (CYP) enzyme activities in human liver microsomes were evaluated using liquid chromatography-tandem mass s...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2016
David M Stresser Elke S Perloff Andrew K Mason Andrew P Blanchard Shangara S Dehal Timothy P Creegan Ritu Singh Eric T Gangl

The sedative clomethiazole (CMZ) has been used in Europe since the mid-1960s to treat insomnia and alcoholism. It has been previously demonstrated in clinical studies to reversibly inhibit human CYP2E1 in vitro and decrease CYP2E1-mediated elimination of chlorzoxazone. We have investigated the selectivity of CMZ inhibition of CYP2E1 in pooled human liver microsomes (HLMs). In a reversible inhib...

Journal: :African journal of traditional, complementary, and alternative medicines : AJTCAM 2013
Showande Segun Johnson Fakeye Titilayo Oyelola Tolonen Ari Hokkanen Juho

Literature is scanty on the interaction potential of Hibiscus sabdariffa L., plant extract with other drugs and the affected targets. This study was conducted to investigate the cytochrome P450 (CYP) isoforms that are inhibited by the extract of Hibiscus sabdariffa L. in vitro. The inhibition towards the major drug metabolizing CYP isoforms by the plant extract were estimated in human liver mic...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2001
L M Hesse K Venkatakrishnan L L von Moltke R I Shader D J Greenblatt

The kinetics of flunitrazepam (FNTZ) N-demethylation to desmethylflunitrazepam (DM FNTZ), and 3-hydroxylation to 3-hydroxyflunitrazepam (3-OH FNTZ), were studied in human liver microsomes and in microsomes containing heterologously expressed individual human CYPs. FNTZ was N-demethylated by cDNA-expressed CYP2A6 (K(m) = 1921 microM), CYP2B6 (K(m) = 101 microM), CYP2C9 (K(m) = 50 microM), CYP2C1...

Journal: :Environmental Health Perspectives 1994
A K Daly S Cholerton M Armstrong J R Idle

Polymorphisms in many xenobiotic metabolizing enzymes occur leading to variation in the level of enzyme expression in vivo. Enzymes showing such polymorphisms include the cytochrome P450 enzymes CYP1A1, CYP1A2, CYP2A6, CYP2D6, and CYP2E1 and the phase two metabolism enzymes glutathione S-transferase MI (GSTMI) and arylamine N-acetyltransferase 2 (NAT2). In the past, these polymorphisms have bee...

Journal: :Clinical pharmacology and therapeutics 2015
L Dickinson J Amin L Else M Boffito D Egan A Owen S Khoo D Back C Orrell A Clarke M Losso P Phanuphak D Carey D A Cooper S Emery R Puls

Daily efavirenz 400 mg (EFV400) was virologically noninferior to 600 mg (EFV600) at 48 weeks in treatment-naïve patients. We evaluated EFV400 and EFV600 pharmacokinetics (NONMEM v. 7.2), assessing patient demographics and genetic polymorphisms (CYP2B6, CYP2A6, CYP3A4, NR1I3) as covariates and explored relationships with efficacy (plasma HIV-RNA (pVL) <200 copies/mL) and safety outcomes at 48 we...

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