نتایج جستجو برای: ژن cyp2c9

تعداد نتایج: 17690  

Journal: :Bioscience, biotechnology, and biochemistry 2008
Muneaki Hidaka Masashi Nagata Yohei Kawano Hiroshi Sekiya Hirofumi Kai Keishi Yamasaki Manabu Okumura Kazuhiko Arimori

There is limited information on the effect of fruits on human cytochrome P450 (CYP) 2C9 activity. The objective of this study was to determine the effect of fruit juice on CYP2C9-mediated drug metabolism. Nine citrus fruits and eight tropical fruits were chosen. We investigated effects of the fruits on diclofenac 4'-hydroxylation and tolbutamide hydroxylation by human liver microsomes. Among th...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 1999
V Fischer L Johanson F Heitz R Tullman E Graham J P Baldeck W T Robinson

Fluvastatin, a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, was metabolized by human liver microsomes to 5-hydroxy-, 6-hydroxy-, and N-deisopropyl-fluvastatin. Total metabolite formation was biphasic with apparent Km values of 0.2 to 0.7 and 7.9 to 50 microM and intrinsic metabolic clearance rates of 1.4 to 4 and 0.3 to 1.5 ml/h/mg microsomal protein for the high and low Km compon...

2016
Nagendra Chaudhary Madhulika Kabra Sheffali Gulati Yogendra Kumar Gupta Ravindra Mohan Pandey Bal Dev Bhatia

BACKGROUND Phenytoin, mainly metabolized by cytochrome P450 enzyme system, has a narrow therapeutic index and may have adverse effects due to inter-individual variation in the dose requirement and genetic polymorphisms. This cross-sectional study was done to study the prevalence of cytochrome P450 CYP2C9 polymorphisms in Indian epileptic children and to see the effect of polymorphisms on serum ...

Journal: :JAMA 2002
Mitchell K Higashi David L Veenstra L Midori Kondo Ann K Wittkowsky Sengkeo L Srinouanprachanh Fred M Farin Allan E Rettie

CONTEXT Warfarin is a commonly used anticoagulant that requires careful clinical management to balance the risks of overanticoagulation and bleeding with those of underanticoagulation and clotting. The principal enzyme involved in warfarin metabolism is CYP2C9, and 2 relatively common variant forms with reduced activity have been identified, CYP2C9*2 and CYP2C9*3. Patients with these genetic va...

Journal: :Clinical pharmacology and therapeutics 2008
Y Caraco S Blotnick M Muszkat

Warfarin anticoagulation effect is characterized by marked variability, some of which has been attributed to CYP2C9 polymorphisms. This study prospectively examines whether a priori knowledge of CYP2C9 genotype may improve warfarin therapy. Patients were randomly assigned to receive warfarin by a validated algorithm ("control", 96 patients) or CYP2C9 genotype-adjusted algorithms ("study", 95 pa...

2011
Karel Berka Tereza Hendrychová Pavel Anzenbacher Michal Otyepka

Cytochrome P450 2C9 (CYP2C9) is a membrane-anchored human microsomal protein involved in the drug metabolism in liver. CYP2C9 consists of an N-terminal transmembrane anchor and a catalytic cytoplasmic domain. While the structure of the catalytic domain is well-known from X-ray experiments, the complete structure and its incorporation into the membrane remains unsolved. We constructed an atomist...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2009
Mingli Yang Jarod L Kabulski Lance Wollenberg Xinqi Chen Murali Subramanian Timothy S Tracy David Lederman Peter M Gannett Nianqiang Wu

Cytochrome P450 (P450) enzymes typically require the presence of at least cytochrome P450 reductase (CPR) and NADPH to carry out the metabolism of xenobiotics. To address whether the need for redox transfer proteins and the NADPH cofactor protein could be obviated, CYP2C9 was bonded to a gold electrode through an 11-mercaptoundecanoic acid and octanethiol self-assembled monolayer (SAM) through ...

Journal: :Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2015
Nuttawut Sermsathanasawadi Chukij Sritongsathian Nunthapol Pongrattanaman Banjerd Praditsuktavorn Kiattisak Hongku Chumpol Wongwanit Chanean Ruangsetakit Khamin Chinsakchai Pramook Mutirangura Naravat Poungvarin

BACKGROUND Polymorphisms in cytochrome P450 2C9 and vitamin K epoxide reductase complex, subunit 1 genes (CYP2C9 and VKORC1, respectively) were previously shown to affect the warfarin dose required in anticoagulant therapy of deep vein thrombosis (DVT). However, little is known about the role of these genetic variants in the Thai population. OBJECTIVE To identify the effect of CYP2C9 and VKOR...

Journal: :The Journal of pharmacology and experimental therapeutics 2001
B J Ring J A Eckstein J S Gillespie S N Binkley M VandenBranden S A Wrighton

The formation of R- and S-norfluoxetine was analyzed in vitro in human liver microsomes. Low apparent K(m) values for R-norfluoxetine formation of < or =8 microM and S-norfluoxetine of <0.2 microM were determined. R-Norfluoxetine formation rates in a characterized microsomal bank correlated with the catalytic activities for cytochrome P450 (CYP) 2D6, CYP2C9, and CYP2C8. Expressed CYP2C9, CYP2C1...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2010
Kaori Yasuda Shinichi Ikushiro Masaki Kamakura Miho Ohta Toshiyuki Sakaki

Metabolism of sesamin by cytochrome P450 (P450) was examined using yeast expression system and human liver microsomes. Saccharomyces cerevisiae cells expressing each of human P450 isoforms (CYP1A1, 1A2, 2A6, 2B6, 2C8, 2C9, 2C18, 2C19, 2D6, 2E1, and 3A4) were cultivated with sesamin, and monocatechol metabolite was observed in most of P450s. Kinetic analysis using the microsomal fractions of the...

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