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Journal Abstract Search

142 related items for PubMed ID: 6135572

  • 21. Metabolic activation of norethisterone (norethindrone) to an irreversibly protein-bound derivative by rat liver microsomes.
    Kappus H, Remmer H.
    Drug Metab Dispos; 1975; 3(5):338-44. PubMed ID: 241614
    [Abstract] [Full Text] [Related]

  • 22. Metabolism and covalent binding of [14C]toluene by human and rat liver microsomal fractions and liver slices.
    Chapman DE, Moore TJ, Michener SR, Powis G.
    Drug Metab Dispos; 1990; 18(6):929-36. PubMed ID: 1981539
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  • 23. The inhibition of rat hepatic microsomal propranolol metabolism by a covalently bound reactive metabolite.
    Pritchard JF, Schneck DW, Hayes AH.
    Res Commun Chem Pathol Pharmacol; 1980 Feb; 27(2):211-22. PubMed ID: 6768117
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  • 24. NADPH-dependent covalent binding of [3H]paroxetine to human liver microsomes and S-9 fractions: identification of an electrophilic quinone metabolite of paroxetine.
    Zhao SX, Dalvie DK, Kelly JM, Soglia JR, Frederick KS, Smith EB, Obach RS, Kalgutkar AS.
    Chem Res Toxicol; 2007 Nov; 20(11):1649-57. PubMed ID: 17907785
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  • 25. DT-diaphorase and peroxidase influence the covalent binding of the metabolites of phenol, the major metabolite of benzene.
    Smart RC, Zannoni VG.
    Mol Pharmacol; 1984 Jul; 26(1):105-11. PubMed ID: 6749127
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  • 26. 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; 279(2):724-31. PubMed ID: 8930177
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  • 31. In vitro studies on the metabolic activation of the furanopyridine L-754,394, a highly potent and selective mechanism-based inhibitor of cytochrome P450 3A4.
    Sahali-Sahly Y, Balani SK, Lin JH, Baillie TA.
    Chem Res Toxicol; 1996 Sep; 9(6):1007-12. PubMed ID: 8870989
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  • 32. Metabolism of the cytochrome P450 mechanism-based inhibitor N-benzyl-1-aminobenzotriazole to products that covalently bind with protein in guinea pig liver and lung microsomes: comparative study with 1-aminobenzotriazole.
    Woodcroft KJ, Webb CD, Yao M, Weedon AC, Bend JR.
    Chem Res Toxicol; 1997 May; 10(5):589-99. PubMed ID: 9168258
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  • 33. Microsomal oxidation of N,N-diethylformamide and its effect on P450-dependent monooxygenases in rat liver.
    Amato G, Longo V, Mazzaccaro A, Gervasi PG.
    Chem Res Toxicol; 1996 May; 9(5):882-90. PubMed ID: 8828925
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  • 34. Formation of nontoxic reactive metabolites of p-bromophenol. Identification of a new glutathione conjugate.
    Monks TJ, Lau SS, Highet RJ.
    Drug Metab Dispos; 1984 May; 12(4):432-7. PubMed ID: 6148209
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  • 35. Metabolic activation of the nitroaromatic antiandrogen flutamide by rat and human cytochromes P-450, including forms belonging to the 3A and 1A subfamilies.
    Berson A, Wolf C, Chachaty C, Fisch C, Fau D, Eugene D, Loeper J, Gauthier JC, Beaune P, Pompon D.
    J Pharmacol Exp Ther; 1993 Apr; 265(1):366-72. PubMed ID: 8386241
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  • 36. In vitro studies on irreversible binding of halothane metabolite to microsomes.
    Van Dyke RA, Wood CL.
    Drug Metab Dispos; 1975 Apr; 3(1):51-7. PubMed ID: 234835
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  • 38. The formation of procainamide hydroxylamine by rat and human liver microsomes.
    Budinsky RA, Roberts SM, Coats EA, Adams L, Hess EV.
    Drug Metab Dispos; 1987 Apr; 15(1):37-43. PubMed ID: 2881757
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  • 40. Metabolic activation of 2-methylfuran by rat microsomal systems.
    Ravindranath V, Boyd MR.
    Toxicol Appl Pharmacol; 1985 May; 78(3):370-6. PubMed ID: 4049387
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