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Journal Abstract Search

381 related items for PubMed ID: 11236840

  • 1. Azide inhibits human cytochrome P -4502E1, 1A2, and 3A4.
    Salmela KS, Tsyrlov IB, Lieber CS.
    Alcohol Clin Exp Res; 2001 Feb; 25(2):253-60. PubMed ID: 11236840
    [Abstract] [Full Text] [Related]

  • 2. Respective roles of human cytochrome P-4502E1, 1A2, and 3A4 in the hepatic microsomal ethanol oxidizing system.
    Salmela KS, Kessova IG, Tsyrlov IB, Lieber CS.
    Alcohol Clin Exp Res; 1998 Dec; 22(9):2125-32. PubMed ID: 9884161
    [Abstract] [Full Text] [Related]

  • 3. Biotransformation of parathion in human liver: participation of CYP3A4 and its inactivation during microsomal parathion oxidation.
    Butler AM, Murray M.
    J Pharmacol Exp Ther; 1997 Feb; 280(2):966-73. PubMed ID: 9023313
    [Abstract] [Full Text] [Related]

  • 4. The inhibitory effect of polyunsaturated fatty acids on human CYP enzymes.
    Yao HT, Chang YW, Lan SJ, Chen CT, Hsu JT, Yeh TK.
    Life Sci; 2006 Nov 25; 79(26):2432-40. PubMed ID: 16978661
    [Abstract] [Full Text] [Related]

  • 5. Gemfibrozil is a potent inhibitor of human cytochrome P450 2C9.
    Wen X, Wang JS, Backman JT, Kivistö KT, Neuvonen PJ.
    Drug Metab Dispos; 2001 Nov 25; 29(11):1359-61. PubMed ID: 11602509
    [Abstract] [Full Text] [Related]

  • 6. Inhibition of human cytochrome P450 enzymes by the natural hepatotoxin safrole.
    Ueng YF, Hsieh CH, Don MJ.
    Food Chem Toxicol; 2005 May 25; 43(5):707-12. PubMed ID: 15778010
    [Abstract] [Full Text] [Related]

  • 7. Isoniazid is a mechanism-based inhibitor of cytochrome P450 1A2, 2A6, 2C19 and 3A4 isoforms in human liver microsomes.
    Wen X, Wang JS, Neuvonen PJ, Backman JT.
    Eur J Clin Pharmacol; 2002 Jan 25; 57(11):799-804. PubMed ID: 11868802
    [Abstract] [Full Text] [Related]

  • 8. In vitro metabolism of the calmodulin antagonist DY-9760e (3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride 3.5 hydrate) by human liver microsomes: involvement of cytochromes p450 in atypical kinetics and potential drug interactions.
    Tachibana S, Fujimaki Y, Yokoyama H, Okazaki O, Sudo K.
    Drug Metab Dispos; 2005 Nov 25; 33(11):1628-36. PubMed ID: 16049129
    [Abstract] [Full Text] [Related]

  • 9. Polysaccharide peptides from Coriolus versicolor competitively inhibit model cytochrome P450 enzyme probe substrates metabolism in human liver microsomes.
    Yeung JH, Or PM.
    Phytomedicine; 2012 Mar 15; 19(5):457-63. PubMed ID: 22305191
    [Abstract] [Full Text] [Related]

  • 10. The involvement of CYP1A2 and CYP3A4 in the metabolism of clozapine.
    Eiermann B, Engel G, Johansson I, Zanger UM, Bertilsson L.
    Br J Clin Pharmacol; 1997 Nov 15; 44(5):439-46. PubMed ID: 9384460
    [Abstract] [Full Text] [Related]

  • 11. Interindividual variation in relative CYP1A2/3A4 phenotype influences susceptibility of clozapine oxidation to cytochrome P450-specific inhibition in human hepatic microsomes.
    Zhang WV, D'Esposito F, Edwards RJ, Ramzan I, Murray M.
    Drug Metab Dispos; 2008 Dec 15; 36(12):2547-55. PubMed ID: 18809730
    [Abstract] [Full Text] [Related]

  • 12. Effect of chronic disulfiram administration on the activities of CYP1A2, CYP2C19, CYP2D6, CYP2E1, and N-acetyltransferase in healthy human subjects.
    Frye RF, Branch RA.
    Br J Clin Pharmacol; 2002 Feb 15; 53(2):155-62. PubMed ID: 11851639
    [Abstract] [Full Text] [Related]

  • 13. Involvement of CYP2E1 as A low-affinity enzyme in phenacetin O-deethylation in human liver microsomes.
    Kobayashi K, Nakajima M, Oshima K, Shimada N, Yokoi T, Chiba K.
    Drug Metab Dispos; 1999 Aug 15; 27(8):860-5. PubMed ID: 10421611
    [Abstract] [Full Text] [Related]

  • 14. Role of CYP3A4 in human hepatic diltiazem N-demethylation: inhibition of CYP3A4 activity by oxidized diltiazem metabolites.
    Sutton D, Butler AM, Nadin L, Murray M.
    J Pharmacol Exp Ther; 1997 Jul 15; 282(1):294-300. PubMed ID: 9223567
    [Abstract] [Full Text] [Related]

  • 15. Effect of diclofenac, disulfiram, itraconazole, grapefruit juice and erythromycin on the pharmacokinetics of quinidine.
    Damkier P, Hansen LL, Brosen K.
    Br J Clin Pharmacol; 1999 Dec 15; 48(6):829-38. PubMed ID: 10594487
    [Abstract] [Full Text] [Related]

  • 16. The kinetics of aflatoxin B1 oxidation by human cDNA-expressed and human liver microsomal cytochromes P450 1A2 and 3A4.
    Gallagher EP, Kunze KL, Stapleton PL, Eaton DL.
    Toxicol Appl Pharmacol; 1996 Dec 15; 141(2):595-606. PubMed ID: 8975785
    [Abstract] [Full Text] [Related]

  • 17. In vitro metabolism of quinidine: the (3S)-3-hydroxylation of quinidine is a specific marker reaction for cytochrome P-4503A4 activity in human liver microsomes.
    Nielsen TL, Rasmussen BB, Flinois JP, Beaune P, Brosen K.
    J Pharmacol Exp Ther; 1999 Apr 15; 289(1):31-7. PubMed ID: 10086984
    [Abstract] [Full Text] [Related]

  • 18. Automated screening with confirmation of mechanism-based inactivation of CYP3A4, CYP2C9, CYP2C19, CYP2D6, and CYP1A2 in pooled human liver microsomes.
    Lim HK, Duczak N, Brougham L, Elliot M, Patel K, Chan K.
    Drug Metab Dispos; 2005 Aug 15; 33(8):1211-9. PubMed ID: 15860655
    [Abstract] [Full Text] [Related]

  • 19. Identification of human liver cytochrome P-450 3A4 as the enzyme responsible for fentanyl and sufentanil N-dealkylation.
    Tateishi T, Krivoruk Y, Ueng YF, Wood AJ, Guengerich FP, Wood M.
    Anesth Analg; 1996 Jan 15; 82(1):167-72. PubMed ID: 8712396
    [Abstract] [Full Text] [Related]

  • 20. Metabolic activation of o-phenylphenol to a major cytotoxic metabolite, phenylhydroquinone: role of human CYP1A2 and rat CYP2C11/CYP2E1.
    Ozawa S, Ohta K, Miyajima A, Kurebayashi H, Sunouchi M, Shimizu M, Murayama N, Matsumoto Y, Fukuoka M, Ohno Y.
    Xenobiotica; 2000 Oct 15; 30(10):1005-17. PubMed ID: 11315102
    [Abstract] [Full Text] [Related]

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