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Journal Abstract Search

167 related items for PubMed ID: 15155554

  • 1. Selective inhibition of CYP2B6-catalyzed bupropion hydroxylation in human liver microsomes in vitro.
    Turpeinen M, Nieminen R, Juntunen T, Taavitsainen P, Raunio H, Pelkonen O.
    Drug Metab Dispos; 2004 Jun; 32(6):626-31. PubMed ID: 15155554
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  • 2. Potent mechanism-based inhibition of human CYP2B6 by clopidogrel and ticlopidine.
    Richter T, Mürdter TE, Heinkele G, Pleiss J, Tatzel S, Schwab M, Eichelbaum M, Zanger UM.
    J Pharmacol Exp Ther; 2004 Jan; 308(1):189-97. PubMed ID: 14563790
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  • 4. Inhibition of human CYP2B6-catalyzed bupropion hydroxylation by Ginkgo biloba extract: effect of terpene trilactones and flavonols.
    Lau AJ, Chang TK.
    Drug Metab Dispos; 2009 Sep; 37(9):1931-7. PubMed ID: 19487249
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  • 5. Potent inhibition of cytochrome P450 2B6 by sibutramine in human liver microsomes.
    Bae SH, Kwon MJ, Choi EJ, Zheng YF, Yoon KD, Liu KH, Bae SK.
    Chem Biol Interact; 2013 Sep 05; 205(1):11-9. PubMed ID: 23777987
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  • 6. A comparison of 2-phenyl-2-(1-piperidinyl)propane (ppp), 1,1',1''-phosphinothioylidynetrisaziridine (thioTEPA), clopidogrel, and ticlopidine as selective inactivators of human cytochrome P450 2B6.
    Walsky RL, Obach RS.
    Drug Metab Dispos; 2007 Nov 05; 35(11):2053-9. PubMed ID: 17682072
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  • 7. CYP2B6 mediates the in vitro hydroxylation of bupropion: potential drug interactions with other antidepressants.
    Hesse LM, Venkatakrishnan K, Court MH, von Moltke LL, Duan SX, Shader RI, Greenblatt DJ.
    Drug Metab Dispos; 2000 Oct 05; 28(10):1176-83. PubMed ID: 10997936
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  • 9. Triethylenethiophosphoramide is a specific inhibitor of cytochrome P450 2B6: implications for cyclophosphamide metabolism.
    Rae JM, Soukhova NV, Flockhart DA, Desta Z.
    Drug Metab Dispos; 2002 May 05; 30(5):525-30. PubMed ID: 11950782
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  • 13. Metabolism of endosulfan-alpha by human liver microsomes and its utility as a simultaneous in vitro probe for CYP2B6 and CYP3A4.
    Casabar RC, Wallace AD, Hodgson E, Rose RL.
    Drug Metab Dispos; 2006 Oct 05; 34(10):1779-85. PubMed ID: 16855053
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  • 14. The monoterpenoids citral and geraniol are moderate inhibitors of CYP2B6 hydroxylase activity.
    Seo KA, Kim H, Ku HY, Ahn HJ, Park SJ, Bae SK, Shin JG, Liu KH.
    Chem Biol Interact; 2008 Aug 11; 174(3):141-6. PubMed ID: 18611395
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  • 15. Mechanism-based inhibition of human cytochrome P450 2B6 by ticlopidine, clopidogrel, and the thiolactone metabolite of prasugrel.
    Nishiya Y, Hagihara K, Ito T, Tajima M, Miura S, Kurihara A, Farid NA, Ikeda T.
    Drug Metab Dispos; 2009 Mar 11; 37(3):589-93. PubMed ID: 19047469
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  • 16. Measurement of in vitro cytochrome P450 2B6 activity.
    Walsky RL, Obach RS.
    Curr Protoc Toxicol; 2009 Mar 11; Chapter 4():Unit4.27. PubMed ID: 23045012
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  • 17. Stereoselective metabolism of endosulfan by human liver microsomes and human cytochrome P450 isoforms.
    Lee HK, Moon JK, Chang CH, Choi H, Park HW, Park BS, Lee HS, Hwang EC, Lee YD, Liu KH, Kim JH.
    Drug Metab Dispos; 2006 Jul 11; 34(7):1090-5. PubMed ID: 16581944
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  • 18. Further assessment of 17alpha-ethinyl estradiol as an inhibitor of different human cytochrome P450 forms in vitro.
    Chang SY, Chen C, Yang Z, Rodrigues AD.
    Drug Metab Dispos; 2009 Aug 11; 37(8):1667-75. PubMed ID: 19454483
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  • 19. Effects of the CYP2B6*6 allele on catalytic properties and inhibition of CYP2B6 in vitro: implication for the mechanism of reduced efavirenz metabolism and other CYP2B6 substrates in vivo.
    Xu C, Ogburn ET, Guo Y, Desta Z.
    Drug Metab Dispos; 2012 Apr 11; 40(4):717-25. PubMed ID: 22232427
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  • 20. Metabolism of N,N',N"-triethylenethiophosphoramide by CYP2B1 and CYP2B6 results in the inactivation of both isoforms by two distinct mechanisms.
    Harleton E, Webster M, Bumpus NN, Kent UM, Rae JM, Hollenberg PF.
    J Pharmacol Exp Ther; 2004 Sep 11; 310(3):1011-9. PubMed ID: 15121764
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