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PUBMED FOR HANDHELDS

Journal Abstract Search


314 related items for PubMed ID: 16307862

  • 1. Characterization of the cytochrome P450 enzymes and enzyme kinetic parameters for metabolism of BVT.2938 using different in vitro systems.
    Baranczewski P, Edlund PO, Postlind H.
    J Pharm Biomed Anal; 2006 Mar 18; 40(5):1121-30. PubMed ID: 16307862
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  • 2. Stereoselective metabolism of cibenzoline, an antiarrhythmic drug, by human and rat liver microsomes: possible involvement of CYP2D and CYP3A.
    Niwa T, Shiraga T, Mitani Y, Terakawa M, Tokuma Y, Kagayama A.
    Drug Metab Dispos; 2000 Sep 18; 28(9):1128-34. PubMed ID: 10950860
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  • 3. Studies on the cytochrome P450 (CYP)-mediated metabolic properties of miocamycin: evaluation of the possibility of a metabolic intermediate complex formation with CYP, and identification of the human CYP isoforms.
    Kasahara M, Suzuki H, Komiya I.
    Drug Metab Dispos; 2000 Apr 18; 28(4):409-17. PubMed ID: 10725309
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  • 5. Characterization of human cytochrome P450 enzymes involved in the in vitro metabolism of perospirone.
    Kitamura A, Mizuno Y, Natsui K, Yabuki M, Komuro S, Kanamaru H.
    Biopharm Drug Dispos; 2005 Mar 18; 26(2):59-65. PubMed ID: 15619261
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  • 10. Determination of the enzyme(s) involved in the metabolism of amiodarone in liver and intestine of rat: the contribution of cytochrome P450 3A isoforms.
    Shayeganpour A, El-Kadi AO, Brocks DR.
    Drug Metab Dispos; 2006 Jan 18; 34(1):43-50. PubMed ID: 16204463
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  • 11. Prediction of human liver microsomal oxidations of 7-ethoxycoumarin and chlorzoxazone with kinetic parameters of recombinant cytochrome P-450 enzymes.
    Shimada T, Tsumura F, Yamazaki H.
    Drug Metab Dispos; 1999 Nov 18; 27(11):1274-80. PubMed ID: 10534312
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  • 12. Characterization of metabolites and cytochrome P450 isoforms involved in the microsomal metabolism of aconitine.
    Wang Y, Wang S, Liu Y, Yan L, Dou G, Gao Y.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Dec 05; 844(2):292-300. PubMed ID: 16949890
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  • 13. Utility of intersystem extrapolation factors in early reaction phenotyping and the quantitative extrapolation of human liver microsomal intrinsic clearance using recombinant cytochromes P450.
    Chen Y, Liu L, Nguyen K, Fretland AJ.
    Drug Metab Dispos; 2011 Mar 05; 39(3):373-82. PubMed ID: 21148079
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  • 14. Imipramine-induced inactivation of a cytochrome P450 2D enzyme in rat liver microsomes: in relation to covalent binding of its reactive intermediate.
    Masubuchi Y, Igarashi S, Suzuki T, Horie T, Narimatsu S.
    J Pharmacol Exp Ther; 1996 Nov 05; 279(2):724-31. PubMed ID: 8930177
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  • 18. In vitro metabolism of carbofuran by human, mouse, and rat cytochrome P450 and interactions with chlorpyrifos, testosterone, and estradiol.
    Usmani KA, Hodgson E, Rose RL.
    Chem Biol Interact; 2004 Dec 07; 150(3):221-32. PubMed ID: 15560889
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  • 19. Evaluation of recombinant cytochrome P450 enzymes as an in vitro system for metabolic clearance predictions.
    Stringer RA, Strain-Damerell C, Nicklin P, Houston JB.
    Drug Metab Dispos; 2009 May 07; 37(5):1025-34. PubMed ID: 19196847
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  • 20. Characterization of benidipine and its enantiomers' metabolism by human liver cytochrome P450 enzymes.
    Yoon YJ, Kim KB, Kim H, Seo KA, Kim HS, Cha IJ, Kim EY, Liu KH, Shin JG.
    Drug Metab Dispos; 2007 Sep 07; 35(9):1518-24. PubMed ID: 17537876
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