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An interesting paper on the use of integrated model to predict clinical net drug-drug interactions due to CYP3A4 inhibition and induction
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Fahmi OA, Maurer TS, Kish M, et al. A combined model for predicting CYP3A4 clinical net drug-drug interaction based on CYP3A4 inhibition, inactivation, and induction determined in vitro. Drug Metab Dispos 2008;36:1698-1708 •• An interesting paper on the use of integrated model to predict clinical net drug-drug interactions due to CYP3A4 inhibition and induction.
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(2008)
Drug Metab Dispos
, vol.36
, pp. 1698-1708
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Fahmi, O.A.1
Maurer, T.S.2
Kish, M.3
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86
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0034824312
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Optimizing drug development: Strategies to assess drug metabolism/transporter interaction potential - Towards a consensus
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DOI 10.1046/j.0306-5251.2001.Temp.1441.x
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Tucker GT, Houston JB, Huang SM. Optimizing drug development: strategies to assess drug metabolism/transporter interaction potential - Towards a consensus. Br J Clin Pharmacol 2001;52:107-117 •• An excellent paper discussing the importance of evaluating drug-drug interactions in drug development. (Pubitemid 32862777)
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(2001)
British Journal of Clinical Pharmacology
, vol.52
, Issue.1
, pp. 107-117
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Tucker, G.T.1
Houston, J.B.2
Huang, S.-M.3
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87
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10744232330
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The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective
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DOI 10.1124/dmd.31.7.815
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Bjornsson TD, Callaghan JT, Einolf HJ, et al. The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab Dispos 2003;31:815-832 (Pubitemid 36759050)
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(2003)
Drug Metabolism and Disposition
, vol.31
, Issue.7
, pp. 815-832
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Bjornsson, T.D.1
Callaghan, J.T.2
Einolf, H.J.3
Fischer, V.4
Gan, L.5
Grimm, S.6
Kao, J.7
King, S.P.8
Miwa, G.9
Ni, L.10
Kumar, G.11
McLeod, J.12
Obach, R.S.13
Roberts, S.14
Roe, A.15
Shah, A.16
Snikeris, F.17
Sullivan, J.T.18
Tweedie, D.19
Vega, J.M.20
Walsh, J.21
Wrighton, S.A.22
more..
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88
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0036219979
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Differential time course of cytochrome P450 2D6 enzyme inhibition by fluoxetine, sertraline, and paroxetine in healthy volunteers
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An excellent report showing the time-dependent inhibition of CYP2D6 by several selective serotonin reuptake inhibitors in vivo
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Liston HL, DeVane CL, Boulton DW, et al. Differential time course of cytochrome P450 2D6 enzyme inhibition by fluoxetine, sertraline, and paroxetine in healthy volunteers. J Clin Psychopharmacol 2002;22:169-73 •• An excellent report showing the time-dependent inhibition of CYP2D6 by several selective serotonin reuptake inhibitors in vivo.
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(2002)
J Clin Psychopharmacol
, vol.22
, pp. 169-173
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Liston, H.L.1
DeVane, C.L.2
Boulton, D.W.3
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89
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49949093994
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The effect of gemfibrozil on repaglinide pharmacokinetics persists for at least 12 h after the dose: Evidence for mechanism-based inhibition of CYP2C8 in vivo
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Another report showing evidence that CYP2C8 is inhibited in a time-dependent manner in vivo
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Tornio A, Niemi M, Neuvonen M, et al. The effect of gemfibrozil on repaglinide pharmacokinetics persists for at least 12 h after the dose: evidence for mechanism-based inhibition of CYP2C8 in vivo. Clin Pharmacol Ther 2008;84:403-11 • Another report showing evidence that CYP2C8 is inhibited in a time-dependent manner in vivo.
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(2008)
Clin Pharmacol Ther
, vol.84
, pp. 403-411
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Tornio, A.1
Niemi, M.2
Neuvonen, M.3
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90
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60349085250
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Irreversible CYP3A inhibition accompanied by plasma protein-binding displacement: A comparative analysis in subjects with normal and impaired liver function
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First paper to investigate the impact of liver function on quinine-erythromycin interaction in vivo
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Orlando R, De Martin S, Pegoraro P, et al. Irreversible CYP3A inhibition accompanied by plasma protein-binding displacement: a comparative analysis in subjects with normal and impaired liver function. Clin Pharmacol Ther 2009;85:319-26 • First paper to investigate the impact of liver function on quinine-erythromycin interaction in vivo.
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(2009)
Clin Pharmacol Ther
, vol.85
, pp. 319-326
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Orlando, R.1
De Martin, S.2
Pegoraro, P.3
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91
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61449202932
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An inhibitory metabolite leads to dose- and time-dependent pharmacokinetics of (R)-N-{1-[3-(4-ethoxy-phenyl)-4-oxo-3,4-dihydro-pyrido[2,3- d]pyrimidin-2-y l]-ethyl}-N-pyridin-3-yl-methyl-2-(4-trifluoromethoxy-phenyl)- acetamide (AMG 487) in human subjects after multiple dosing
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A recent report showing evidence for in vivo mechanism-based CYP inhibition in humans
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Tonn GR, Wong SG, Wong SC, et al. An inhibitory metabolite leads to dose- and time-dependent pharmacokinetics of (R)-N-{1-[3-(4-ethoxy-phenyl)-4-oxo-3,4- dihydro-pyrido[2,3-d]pyrimidin-2-y l]-ethyl}-N-pyridin-3-yl-methyl-2-(4- trifluoromethoxy-phenyl)-acetamide (AMG 487) in human subjects after multiple dosing. Drug Metab Dispos 2009;37:502-13 • A recent report showing evidence for in vivo mechanism-based CYP inhibition in humans.
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(2009)
Drug Metab Dispos
, vol.37
, pp. 502-513
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Tonn, G.R.1
Wong, S.G.2
Wong, S.C.3
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92
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0025236599
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Metabolite inhibition of parent drug biotransformation. Studies of diltiazem
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Tsao S-C, Dickinson TH, Abernethy DR. Metabolite inhibition of parent drug biotransformation. Studies of diltiazem. Drug Metab Dispos 1990;18:180-182
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(1990)
Drug Metab Dispos
, vol.18
, pp. 180-182
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Tsao, S.-C.1
Dickinson, T.H.2
Abernethy, D.R.3
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93
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0024359587
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Inhibition of alfentanil metabolism by erythromycin
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Bartkowski RR, Goldberg ME, Larijani GE, et al. Inhibition of alfentanil metabolism by erythromycin. Clin Pharmacol Ther 1989;46:99-102 (Pubitemid 19195780)
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(1989)
Clinical Pharmacology and Therapeutics
, vol.46
, Issue.1
, pp. 99-102
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Bartkowski, R.R.1
Goldberg, M.E.2
Larijani, G.E.3
Boerner, T.4
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94
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0032496879
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Life-threatening interaction of mibefradil and β-blockers with dihydropyridine calcium channel blockers
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DOI 10.1001/jama.280.2.157
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Mullins ME, Horowitz Z, Linden DHJ, et al. Life-threatening interaction of mibefradil and beta-blockers with dihydropyridine calcium channel blockers. JAMA 1998;280:157-158 • First report on life-threatening interaction of mibefradil (withdrawn in 1998) and β-blockers with dihydropyridine calcium channel inhibitors in patients. (Pubitemid 28498388)
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(1998)
Journal of the American Medical Association
, vol.280
, Issue.2
, pp. 157-158
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Mullins, M.E.1
Horowitz, B.Z.2
Linden, D.H.J.3
Smith, G.W.4
Norton, R.L.5
Stump, J.6
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95
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0033026601
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Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: An in vitro investigation with human liver preperations
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DOI 10.1046/j.1365-2125.1999.00903.x
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Prueksaritanont T, Ma B, Tang C, et al. Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: an in vitro investigation with human liver preparations. Br J Clin Pharmacol 1999;47:291-298 (Pubitemid 29131344)
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(1999)
British Journal of Clinical Pharmacology
, vol.47
, Issue.3
, pp. 291-298
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Prueksaritanont, T.1
Ma, B.2
Tang, C.3
Meng, Y.4
Assang, C.5
Lu, P.6
Reider, P.J.7
Lin, J.H.8
Baillie, T.A.9
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96
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44449112267
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Potential strategies for minimizing mechanism-based inhibition of cytochrome P450 3A4
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An excellent paper discussing the potential for reducing the impact of mechanism-based CYP inhibition in drug development
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Zhou SF. Potential strategies for minimizing mechanism-based inhibition of cytochrome P450 3A4. Curr Pharm Des 2008;14:990-1000 •• An excellent paper discussing the potential for reducing the impact of mechanism-based CYP inhibition in drug development.
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(2008)
Curr Pharm Des
, vol.14
, pp. 990-1000
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Zhou, S.F.1
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97
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55549119262
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Assessing and minimizing time-dependent inhibition of cytochrome P450 3A in drug discovery: A case study with melanocortin-4 receptor agonists
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This paper reported the incorporation of minimizing mechanism-based CYP3A inhibition by new drug candidates in drug development of novel melanocortin-4 receptor agonists
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Tang W, Stearns RA, Wang RW, et al. Assessing and minimizing time-dependent inhibition of cytochrome P450 3A in drug discovery: a case study with melanocortin-4 receptor agonists. Xenobiotica 2008;38:1437-1451 • This paper reported the incorporation of minimizing mechanism-based CYP3A inhibition by new drug candidates in drug development of novel melanocortin-4 receptor agonists.
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(2008)
Xenobiotica
, vol.38
, pp. 1437-1451
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Tang, W.1
Stearns, R.A.2
Wang, R.W.3
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98
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34548070044
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Computational approaches that predict metabolic intermediate complex formation with CYP3A4 (+b5)
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An excellent paper reporting the use of in silico approaches to predict potential for metabolic intermediate complex formation with CYP3A4
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Jones DR, Ekins S, Li L, et al. Computational approaches that predict metabolic intermediate complex formation with CYP3A4 (+b5). Drug Metab Dispos 2007;35:1466-75 • An excellent paper reporting the use of in silico approaches to predict potential for metabolic intermediate complex formation with CYP3A4.
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(2007)
Drug Metab Dispos
, vol.35
, pp. 1466-1475
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Jones, D.R.1
Ekins, S.2
Li, L.3
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99
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70149110672
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Polymorphism of human cytochrome P450 2D6 and its clinical significance
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(accepted) An excellent paper summarizing our knowledge on the genetic polymorphisms of CYP2D6 and the clinical impact
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Zhou SF. Polymorphism of human cytochrome P450 2D6 and its clinical significance. Drug Metab Rev 2009 (accepted) •• An excellent paper summarizing our knowledge on the genetic polymorphisms of CYP2D6 and the clinical impact.
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(2009)
Drug Metab Rev
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Zhou, S.F.1
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100
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47749122616
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Cytochrome P450 turnover: Regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions
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DOI 10.2174/138920008784746382
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Yang J, Liao M, Shou M, et al. Cytochrome p450 turnover: regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions. Curr Drug Metab 2008;9:384-394 •• An excellent paper highlights the importance of accurate estimation of CYP turnover half-lives in the prediction for drug-drug interactions due to mechanism-based CYP inhibition. (Pubitemid 352025193)
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(2008)
Current Drug Metabolism
, vol.9
, Issue.5
, pp. 384-393
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Yang, J.1
Liao, M.2
Shou, M.3
Jamei, M.4
Yeo, K.R.5
Tucker, G.T.6
Rostami-Hodjegan, A.7
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