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Volumn 35, Issue 2, 2007, Pages 246-255

Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions

Author keywords

[No Author keywords available]

Indexed keywords

3,4 METHYLENEDIOXYMETHAMPHETAMINE; ALPRAZOLAM; AMFEBUTAMONE; AMODIAQUINE; BUSPIRONE; CAFFEINE; CYTOCHROME P450; DEETHYLAMIODARONE; DESIPRAMINE; DEXTROMETHORPHAN; DICLOFENAC; DILTIAZEM; ERYTHROMYCIN; FURAFYLLINE; MEPHENYTOIN; MIDAZOLAM; MONTELUKAST; OMEPRAZOLE; PAROXETINE; PHENACETIN; RITONAVIR; TESTOSTERONE; THEOPHYLLINE; THIOTEPA; TICLOPIDINE; TIENILIC ACID; TRIAZOLAM; UNINDEXED DRUG; VERAPAMIL; ZILEUTON;

EID: 33846449874     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.106.012633     Document Type: Article
Times cited : (404)

References (53)
  • 3
    • 0037369622 scopus 로고    scopus 로고
    • Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine : Comparison with fluoxetine and quinidine
    • Bertelsen KM, Venkatakrishnan K, Von Moltke LL, Obach RS, and Greenblatt DJ (2003) Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine : Comparison with fluoxetine and quinidine. Drug Metab Dispos 31:289-293.
    • (2003) Drug Metab Dispos , vol.31 , pp. 289-293
    • Bertelsen, K.M.1    Venkatakrishnan, K.2    Von Moltke, L.L.3    Obach, R.S.4    Greenblatt, D.J.5
  • 4
    • 27444445468 scopus 로고    scopus 로고
    • Prediction of in vivo drug-drug interactions from in vitro data: Impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant
    • Brown HS, Ito K, Galetin A, and Houston JB (2005) Prediction of in vivo drug-drug interactions from in vitro data: impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant. Br J Clin Pharmacol 60:508-518.
    • (2005) Br J Clin Pharmacol , vol.60 , pp. 508-518
    • Brown, H.S.1    Ito, K.2    Galetin, A.3    Houston, J.B.4
  • 5
    • 2442711592 scopus 로고    scopus 로고
    • Lack of pharmacologic interaction between paroxetine and alprazolam at steady state in healthy volunteers
    • Calvo G, Garcia-Gea C, Luque A, Morte A, Dal-Re R, and Barbanoj M (2004) Lack of pharmacologic interaction between paroxetine and alprazolam at steady state in healthy volunteers. J Clin Psychopharmacol 24:268-276.
    • (2004) J Clin Psychopharmacol , vol.24 , pp. 268-276
    • Calvo, G.1    Garcia-Gea, C.2    Luque, A.3    Morte, A.4    Dal-Re, R.5    Barbanoj, M.6
  • 6
    • 0033861911 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochromes P450 2B1 and P450 2B6 by 2-phenyl-2-(1-piperidinyl)propane
    • Chun J, Kent UM, Moss RM, Sayre LM, and Hollenberg PF (2000) Mechanism-based inactivation of cytochromes P450 2B1 and P450 2B6 by 2-phenyl-2-(1-piperidinyl)propane. Drug Metab Dispos 28:905-911.
    • (2000) Drug Metab Dispos , vol.28 , pp. 905-911
    • Chun, J.1    Kent, U.M.2    Moss, R.M.3    Sayre, L.M.4    Hollenberg, P.F.5
  • 8
    • 13244299150 scopus 로고    scopus 로고
    • Mechanism-based inactivation of CYP3A by HIV protease inhibitors
    • Ernest CS, Hall SD, and Jones DR (2005) Mechanism-based inactivation of CYP3A by HIV protease inhibitors. J Pharmacol Exp Ther 312:583-591.
    • (2005) J Pharmacol Exp Ther , vol.312 , pp. 583-591
    • Ernest, C.S.1    Hall, S.D.2    Jones, D.R.3
  • 9
    • 3543019165 scopus 로고    scopus 로고
    • Time response of cytochrome P450 1A2 activity on cessation of heavy smoking
    • Faber MS and Fuhr U (2004) Time response of cytochrome P450 1A2 activity on cessation of heavy smoking. Clin Pharmacol Ther 76:178-184.
    • (2004) Clin Pharmacol Ther , vol.76 , pp. 178-184
    • Faber, M.S.1    Fuhr, U.2
  • 10
    • 0029786432 scopus 로고    scopus 로고
    • Differential induction of prehepatic and hepatic metabolism of verapamil by rifampin
    • Fromm MF, Busse D, Kroemer HK, and Eichelbaum M (1996) Differential induction of prehepatic and hepatic metabolism of verapamil by rifampin. Hepatology 24:796-801.
    • (1996) Hepatology , vol.24 , pp. 796-801
    • Fromm, M.F.1    Busse, D.2    Kroemer, H.K.3    Eichelbaum, M.4
  • 11
    • 29944446485 scopus 로고    scopus 로고
    • Prediction of time-dependent CYP3A4 drug-drug interactions: Impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition
    • Galetin A, Burt H, Gibbons L, and Houston JB (2006) Prediction of time-dependent CYP3A4 drug-drug interactions: impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition. Drug Metab Dispos 34:166-175.
    • (2006) Drug Metab Dispos , vol.34 , pp. 166-175
    • Galetin, A.1    Burt, H.2    Gibbons, L.3    Houston, J.B.4
  • 12
    • 33645980647 scopus 로고    scopus 로고
    • A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation
    • Ghanbari F, Rowland-Yeo K, Bloomer JC, Clarke SE, Lennard MS, Tucker GT, and Rostami-Hodjegan A (2006) A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation. Curr Drug Metab 7:315-334.
    • (2006) Curr Drug Metab , vol.7 , pp. 315-334
    • Ghanbari, F.1    Rowland-Yeo, K.2    Bloomer, J.C.3    Clarke, S.E.4    Lennard, M.S.5    Tucker, G.T.6    Rostami-Hodjegan, A.7
  • 16
    • 0030057725 scopus 로고    scopus 로고
    • Biotransformation of caffeine by cDNAexpressed human cytochromes P-450
    • Ha HR, Chen J, Krahenbuhl S, Follath F (1996) Biotransformation of caffeine by cDNAexpressed human cytochromes P-450. Eur J Clin Pharmacol 49:309-315.
    • (1996) Eur J Clin Pharmacol , vol.49 , pp. 309-315
    • Ha, H.R.1    Chen, J.2    Krahenbuhl, S.3    Follath, F.4
  • 19
    • 18844369894 scopus 로고    scopus 로고
    • Impact of parallel pathways of drug elimination and multiple cytochrome P450 involvement on drug-drug interactions: CYP2D6 paradigm
    • Ito K, Hallifax D, Obach RS, and Houston JB (2005) Impact of parallel pathways of drug elimination and multiple cytochrome P450 involvement on drug-drug interactions: CYP2D6 paradigm. Drug Metab Dispos 33:837-844.
    • (2005) Drug Metab Dispos , vol.33 , pp. 837-844
    • Ito, K.1    Hallifax, D.2    Obach, R.S.3    Houston, J.B.4
  • 20
    • 0038311984 scopus 로고    scopus 로고
    • Prediction of the in vivo interaction between midazolam and macrolides based on in vitro studies using human liver microsomes
    • Ito K, Ogihara K, Kanamitsu SI, and Itoh T (2003) Prediction of the in vivo interaction between midazolam and macrolides based on in vitro studies using human liver microsomes. Drug Metab Dispos 31:945-954.
    • (2003) Drug Metab Dispos , vol.31 , pp. 945-954
    • Ito, K.1    Ogihara, K.2    Kanamitsu, S.I.3    Itoh, T.4
  • 21
    • 0034089555 scopus 로고    scopus 로고
    • Prediction of in vivo interaction between triazolam and erythromycin based on in vitro studies using human liver microsomes and recombinant human CYP3A4
    • Kanamitsu SI, Ito K, Green CE, Tyson CA, Shimada N, and Sugiyama Y (2000a) Prediction of in vivo interaction between triazolam and erythromycin based on in vitro studies using human liver microsomes and recombinant human CYP3A4. Pharm Res (NY) 17:419-426.
    • (2000) Pharm Res (NY) , vol.17 , pp. 419-426
    • Kanamitsu, S.I.1    Ito, K.2    Green, C.E.3    Tyson, C.A.4    Shimada, N.5    Sugiyama, Y.6
  • 22
    • 0033994866 scopus 로고    scopus 로고
    • Quantitative prediction of in vivo drug-drug interactions from in vitro data based on physiological pharmacokinetics: Use of maximum unbound concentration of inhibitor at the inlet to the liver
    • Kanamitsu SI, Ito K, and Sugiyama Y (2000b) Quantitative prediction of in vivo drug-drug interactions from in vitro data based on physiological pharmacokinetics: use of maximum unbound concentration of inhibitor at the inlet to the liver. Pharm Res (NY) 17:336-343.
    • (2000) Pharm Res (NY) , vol.17 , pp. 336-343
    • Kanamitsu, S.I.1    Ito, K.2    Sugiyama, Y.3
  • 23
    • 0030882158 scopus 로고    scopus 로고
    • Plasma buspirone concentrations are greatly increased by erythromycin and itraconazole
    • Kivisto KT, Lamberg TS, Kantola T, and Neuvonen PJ (1997) Plasma buspirone concentrations are greatly increased by erythromycin and itraconazole. Clin Pharmacol Ther 62:348-354.
    • (1997) Clin Pharmacol Ther , vol.62 , pp. 348-354
    • Kivisto, K.T.1    Lamberg, T.S.2    Kantola, T.3    Neuvonen, P.J.4
  • 24
    • 0031844932 scopus 로고    scopus 로고
    • Lamberg TS, Kivisto KT, and Neuvonen PJ (1998) of verapamil and diltiazem on the pharmacokinetics and pharmacodynamics of buspirone. Clin Pharmacol Ther 63:640-645.
    • Lamberg TS, Kivisto KT, and Neuvonen PJ (1998) of verapamil and diltiazem on the pharmacokinetics and pharmacodynamics of buspirone. Clin Pharmacol Ther 63:640-645.
  • 25
    • 33745395225 scopus 로고    scopus 로고
    • CYP induction-mediated drug interactions: In vitro assessment and clinical implications
    • Lin JH (2006) CYP induction-mediated drug interactions: in vitro assessment and clinical implications. Pharm Res (NY) 23:1089-1116.
    • (2006) Pharm Res (NY) , vol.23 , pp. 1089-1116
    • Lin, J.H.1
  • 26
    • 0036219979 scopus 로고    scopus 로고
    • Differential time course of cytochrome P450 2D6 enzyme inhibition by fluoxetine, sertraline, and paroxetine in healthy volunteers
    • Liston HL, DeVane CL, Boulton DW, Risch SC, Markowitz JS, and Goldman J (2002) Differential time course of cytochrome P450 2D6 enzyme inhibition by fluoxetine, sertraline, and paroxetine in healthy volunteers. J Clin Psychopharmacol 22:169-173.
    • (2002) J Clin Psychopharmacol , vol.22 , pp. 169-173
    • Liston, H.L.1    DeVane, C.L.2    Boulton, D.W.3    Risch, S.C.4    Markowitz, J.S.5    Goldman, J.6
  • 27
    • 0142243111 scopus 로고    scopus 로고
    • Mechanism-based inhibition of human liver microsomal cytochrome P450 1A2 by zileuton, a 5-lipoxygenase inhibitor
    • Lu P, Schrag ML, Slaughter DE, Raab CE, Shou M, and Rodrigues AD (2003) Mechanism-based inhibition of human liver microsomal cytochrome P450 1A2 by zileuton, a 5-lipoxygenase inhibitor. Drug Metab Dispos 31:1352-1360.
    • (2003) Drug Metab Dispos , vol.31 , pp. 1352-1360
    • Lu, P.1    Schrag, M.L.2    Slaughter, D.E.3    Raab, C.E.4    Shou, M.5    Rodrigues, A.D.6
  • 28
    • 0033831197 scopus 로고    scopus 로고
    • An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation
    • Mayhew BS, Jones DR, and Hall SD (2000) An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation. Drug Metab Dispos 28:1031-1037.
    • (2000) Drug Metab Dispos , vol.28 , pp. 1031-1037
    • Mayhew, B.S.1    Jones, D.R.2    Hall, S.D.3
  • 29
    • 4644331461 scopus 로고    scopus 로고
    • Differences in the inhibition of cytochromes P450 3A4 and 3A5 by metabolite-inhibitor complex-forming drugs
    • McConn DJ, Lin YS, Allen K, Kunze KL, and Thummel KE (2004) Differences in the inhibition of cytochromes P450 3A4 and 3A5 by metabolite-inhibitor complex-forming drugs. Drug Metab Dispos 32:1083-1091.
    • (2004) Drug Metab Dispos , vol.32 , pp. 1083-1091
    • McConn, D.J.1    Lin, Y.S.2    Allen, K.3    Kunze, K.L.4    Thummel, K.E.5
  • 30
    • 0037228099 scopus 로고    scopus 로고
    • Melet A, Assrir N, Jean P, Pilar Lopez-Garcia M, Marques-Soares C, Jaouen M, Dansette PM, Sari MA, and Mansuy D (2003) Substrate selectivity of human cytochrome P450 2C9: importance of residues 476, 365, and 114 in recognition of diclofenac and sulfaphenazole and in mechanism-based inactivation by tienilic acid. Arch Biochem Biophys 409:80-91.
    • Melet A, Assrir N, Jean P, Pilar Lopez-Garcia M, Marques-Soares C, Jaouen M, Dansette PM, Sari MA, and Mansuy D (2003) Substrate selectivity of human cytochrome P450 2C9: importance of residues 476, 365, and 114 in recognition of diclofenac and sulfaphenazole and in mechanism-based inactivation by tienilic acid. Arch Biochem Biophys 409:80-91.
  • 32
    • 28844476587 scopus 로고    scopus 로고
    • In vitro cytochrome P450 inhibition data and the prediction of drug-drug interactions: Qualitative relationships, quantitative predictions, and the rank-order approach
    • Obach RS, Walsky RL, Venkatakrishnan K, Houston BJ, and Tremaine LM (2005) In vitro cytochrome P450 inhibition data and the prediction of drug-drug interactions: qualitative relationships, quantitative predictions, and the rank-order approach. Clin Pharmacol Ther 78:582-592.
    • (2005) Clin Pharmacol Ther , vol.78 , pp. 582-592
    • Obach, R.S.1    Walsky, R.L.2    Venkatakrishnan, K.3    Houston, B.J.4    Tremaine, L.M.5
  • 33
    • 0020261689 scopus 로고
    • Ticrynafen-racemic warfarin interaction: Hepatotoxic or stereoselective?
    • O'Reilly RA (1982) Ticrynafen-racemic warfarin interaction: hepatotoxic or stereoselective? Clin Pharmacol Ther 32:356-361.
    • (1982) Clin Pharmacol Ther , vol.32 , pp. 356-361
    • O'Reilly, R.A.1
  • 34
    • 0027050416 scopus 로고
    • Effect of corticosteroids on the expression of cytochromes P450 and on cyclosporin A oxidase activity in primary cultures of human hepatocytes
    • Pichard L, Fabre I, Daujat M, Domergue J, Joyeux H, and Maurel P (1992) Effect of corticosteroids on the expression of cytochromes P450 and on cyclosporin A oxidase activity in primary cultures of human hepatocytes. Mol Pharmacol 41:1047-1055.
    • (1992) Mol Pharmacol , vol.41 , pp. 1047-1055
    • Pichard, L.1    Fabre, I.2    Daujat, M.3    Domergue, J.4    Joyeux, H.5    Maurel, P.6
  • 35
    • 10044257558 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human cytochrome P4502C8 by drugs in vitro
    • Polasek TM, Elliot DJ, Lewis BC, and Miners JO (2004) Mechanism-based inactivation of human cytochrome P4502C8 by drugs in vitro. J Pharmacol Exp Ther 311:996-1007.
    • (2004) J Pharmacol Exp Ther , vol.311 , pp. 996-1007
    • Polasek, T.M.1    Elliot, D.J.2    Lewis, B.C.3    Miners, J.O.4
  • 36
    • 0032546575 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human cytochrome P450 1A2 by furafylline: Detection of a 1:1 adduct to protein and evidence for the formation of a novel imidazomethide intermediate
    • Racha JK, Rettie AE, and Kunze KL (1998) Mechanism-based inactivation of human cytochrome P450 1A2 by furafylline: detection of a 1:1 adduct to protein and evidence for the formation of a novel imidazomethide intermediate. Biochemistry 37:7407-7419.
    • (1998) Biochemistry , vol.37 , pp. 7407-7419
    • Racha, J.K.1    Rettie, A.E.2    Kunze, K.L.3
  • 38
    • 11844283327 scopus 로고    scopus 로고
    • Inhibition of human CYP2B6 by N,N′,N″-triethylenethiophosphoramide is irreversible and mechanism-based
    • Richter T, Schwab M, Eichelbaum M, and Zanger UM (2005) Inhibition of human CYP2B6 by N,N′,N″-triethylenethiophosphoramide is irreversible and mechanism-based. Biochem Pharmacol 69:517-524.
    • (2005) Biochem Pharmacol , vol.69 , pp. 517-524
    • Richter, T.1    Schwab, M.2    Eichelbaum, M.3    Zanger, U.M.4
  • 39
    • 33748905486 scopus 로고    scopus 로고
    • Use of immortalized human hepatocytes to predict the magnitude of clinical drug-drug interactions caused by CYP3A4 induction
    • Ripp SL, Mills JB, Fahmi OA, Trevena KA, Liras JL, Maurer TS, and de Morais SM (2006) Use of immortalized human hepatocytes to predict the magnitude of clinical drug-drug interactions caused by CYP3A4 induction. Drug Metab Dispos 34:1742-1748.
    • (2006) Drug Metab Dispos , vol.34 , pp. 1742-1748
    • Ripp, S.L.1    Mills, J.B.2    Fahmi, O.A.3    Trevena, K.A.4    Liras, J.L.5    Maurer, T.S.6    de Morais, S.M.7
  • 40
    • 0029040042 scopus 로고
    • Caffeine metabolism in patients with chronic liver disease
    • Rodopoulos N, Wisen O, and Norman A (1995) Caffeine metabolism in patients with chronic liver disease. Scand J Clin Lab Investig 55:229-242.
    • (1995) Scand J Clin Lab Investig , vol.55 , pp. 229-242
    • Rodopoulos, N.1    Wisen, O.2    Norman, A.3
  • 41
    • 13244287685 scopus 로고    scopus 로고
    • In silico' simulations to assess the 'in vivo' consequences of 'in vitro' metabolic drug-drug interactions
    • Rostami-Hodjegan A and Tucker GT (2004) 'In silico' simulations to assess the 'in vivo' consequences of 'in vitro' metabolic drug-drug interactions. Drug Discov Today Tech 1:441-448.
    • (2004) Drug Discov Today Tech , vol.1 , pp. 441-448
    • Rostami-Hodjegan, A.1    Tucker, G.T.2
  • 42
    • 84889354966 scopus 로고    scopus 로고
    • In vitro models for studying induction of cytochrome P450 enzymes
    • Rodrigues AD ed pp, Marcel Dekker, Inc, New York
    • Silva JM and Nicholl-Griffith DA (2002) In vitro models for studying induction of cytochrome P450 enzymes, in Drug-Drug Interactions (Rodrigues AD ed) pp 189-216, Marcel Dekker, Inc., New York.
    • (2002) Drug-Drug Interactions , pp. 189-216
    • Silva, J.M.1    Nicholl-Griffith, D.A.2
  • 45
  • 46
    • 0002106247 scopus 로고    scopus 로고
    • Metabolically based drug-drug interactions: Principles and mechanisms
    • Levy RH et al. ed pp, Lippincott Williams & Wilkins, Philadelphia
    • Thummel KE, Kunze KL, and Shen DD (2000) Metabolically based drug-drug interactions: principles and mechanisms, in Metabolic Drug Interactions (Levy RH et al. ed) pp 3-19, Lippincott Williams & Wilkins, Philadelphia.
    • (2000) Metabolic Drug Interactions , pp. 3-19
    • Thummel, K.E.1    Kunze, K.L.2    Shen, D.D.3
  • 47
    • 20444458419 scopus 로고    scopus 로고
    • Effect of clopidogrel and ticlopidine on cytochrome P450 2B6 activity as measured by bupropion hydroxylation
    • Turpeinen M, Tolonen A, Uusitalo J, Jalonen J, Pelkonen O, and Laine K (2005) Effect of clopidogrel and ticlopidine on cytochrome P450 2B6 activity as measured by bupropion hydroxylation. Clin Pharmacol Ther 77:553-559.
    • (2005) Clin Pharmacol Ther , vol.77 , pp. 553-559
    • Turpeinen, M.1    Tolonen, A.2    Uusitalo, J.3    Jalonen, J.4    Pelkonen, O.5    Laine, K.6
  • 48
    • 18844426008 scopus 로고    scopus 로고
    • In vitro-in vivo extrapolation of CYP2D6 inactivation by paroxetine: Prediction of nonstationary pharmacokinetics and drug interaction magnitude
    • Venkatakrishnan K and Obach RS (2005) In vitro-in vivo extrapolation of CYP2D6 inactivation by paroxetine: prediction of nonstationary pharmacokinetics and drug interaction magnitude. Drug Metab Dispos 33:845-852.
    • (2005) Drug Metab Dispos , vol.33 , pp. 845-852
    • Venkatakrishnan, K.1    Obach, R.S.2
  • 49
    • 2442690439 scopus 로고    scopus 로고
    • Validated assays for human cytochrome P450 activities
    • Walsky RL and Obach RS (2004) Validated assays for human cytochrome P450 activities. Drug Metab Dispos 32:647-660.
    • (2004) Drug Metab Dispos , vol.32 , pp. 647-660
    • Walsky, R.L.1    Obach, R.S.2
  • 51
    • 0842282550 scopus 로고    scopus 로고
    • Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites
    • Wang YH, Jones DR, and Hall SD (2004) Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites. Drug Metab Dispos 32:259-266.
    • (2004) Drug Metab Dispos , vol.32 , pp. 259-266
    • Wang, Y.H.1    Jones, D.R.2    Hall, S.D.3
  • 52
    • 0035064595 scopus 로고    scopus 로고
    • Prediction of midazolam-CYP3A inhibitors interaction in the human liver from in vivo/in vitro absorption, distribution, and metabolism data
    • Yamano K, Yamamoto K, Katashima M, Kotaki H, Takedomi S, Matsuo H, Ohtani H, Sawada Y, and Iga T (2001) Prediction of midazolam-CYP3A inhibitors interaction in the human liver from in vivo/in vitro absorption, distribution, and metabolism data. Drug Metab Dispos 29:443-452.
    • (2001) Drug Metab Dispos , vol.29 , pp. 443-452
    • Yamano, K.1    Yamamoto, K.2    Katashima, M.3    Kotaki, H.4    Takedomi, S.5    Matsuo, H.6    Ohtani, H.7    Sawada, Y.8    Iga, T.9
  • 53
    • 24644441043 scopus 로고    scopus 로고
    • Kinetic values for mechanism-based enzyme inhibition: Assessing the bias introduced by the conventional experimental protocol
    • Yang J, Jamei M, Yeo KR, Tucker GT, and Rostami-Hodjegan A (2005) Kinetic values for mechanism-based enzyme inhibition: assessing the bias introduced by the conventional experimental protocol. Eur J Pharm Sci 26:334-340.
    • (2005) Eur J Pharm Sci , vol.26 , pp. 334-340
    • Yang, J.1    Jamei, M.2    Yeo, K.R.3    Tucker, G.T.4    Rostami-Hodjegan, A.5


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