-
1
-
-
71049130780
-
CYP2C8 activity recovers within 96 hours after gemfibrozil dosing: Estimation of CYP2C8 half-life using repaglinide as an in vivo probe
-
Backman JT, Honkalammi J, Neuvonen M, Kurkinen KJ, Tornio A, Niemi M, and Neuvonen PJ (2009) CYP2C8 activity recovers within 96 hours after gemfibrozil dosing: estimation of CYP2C8 half-life using repaglinide as an in vivo probe. Drug Metab Dispos 37:2359-2366.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 2359-2366
-
-
Backman, J.T.1
Honkalammi, J.2
Neuvonen, M.3
Kurkinen, K.J.4
Tornio, A.5
Niemi, M.6
Neuvonen, P.J.7
-
2
-
-
84872223878
-
Effect of peginterferon alfa-2a (40KD) on cytochrome P450 isoenzyme activity
-
Brennan BJ, Xu ZX, and Grippo JF (2013) Effect of peginterferon alfa-2a (40KD) on cytochrome P450 isoenzyme activity. Br J Clin Pharmacol 75:497-506.
-
(2013)
Br J Clin Pharmacol
, vol.75
, pp. 497-506
-
-
Brennan, B.J.1
Xu, Z.X.2
Grippo, J.F.3
-
3
-
-
27444445468
-
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
-
4
-
-
84888583720
-
Drug metabolites as cytochrome p450 inhibitors: A retrospective analysis and proposed algorithm for evaluation of the pharmacokinetic interaction potential of metabolites in drug discovery and development
-
Callegari E, Kalgutkar AS, Leung L, Obach RS, Plowchalk DR, and Tse S (2013) Drug metabolites as cytochrome p450 inhibitors: a retrospective analysis and proposed algorithm for evaluation of the pharmacokinetic interaction potential of metabolites in drug discovery and development. Drug Metab Dispos 41:2047-2055.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 2047-2055
-
-
Callegari, E.1
Kalgutkar, A.S.2
Leung, L.3
Obach, R.S.4
Plowchalk, D.R.5
Tse, S.6
-
5
-
-
84920114260
-
Mass balance, metabolite profile, and in vitro-in vivo comparison of clearance pathways of deleobuvir, a hepatitis C virus polymerase inhibitor
-
Chen LZ, Sabo JP, Philip E, Rowland L, Mao Y, Latli B, Ramsden D, Mandarino DA, and Sane RS (2015) Mass balance, metabolite profile, and in vitro-in vivo comparison of clearance pathways of deleobuvir, a hepatitis C virus polymerase inhibitor. Antimicrob Agents Chemother 59:25-37.
-
(2015)
Antimicrob Agents Chemother
, vol.59
, pp. 25-37
-
-
Chen, L.Z.1
Sabo, J.P.2
Philip, E.3
Rowland, L.4
Mao, Y.5
Latli, B.6
Ramsden, D.7
Mandarino, D.A.8
Sane, R.S.9
-
6
-
-
67649404709
-
In vitro and in vivo induction of cytochrome p450: A survey of the current practices and recommendations: A pharmaceutical research and manufacturers of america perspective
-
Chu V, Einolf HJ, Evers R, Kumar G, Moore D, Ripp S, Silva J, Sinha V, Sinz M, and Skerjanec A (2009) In vitro and in vivo induction of cytochrome p450: a survey of the current practices and recommendations: a pharmaceutical research and manufacturers of america perspective. Drug Metab Dispos 37:1339-1354.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 1339-1354
-
-
Chu, V.1
Einolf, H.J.2
Evers, R.3
Kumar, G.4
Moore, D.5
Ripp, S.6
Silva, J.7
Sinha, V.8
Sinz, M.9
Skerjanec, A.10
-
7
-
-
84893723325
-
Evaluation of various static and dynamic modeling methods to predict clinical CYP3A induction using in vitro CYP3A4 mRNA induction data
-
Einolf HJ, Chen L, Fahmi OA, Gibson CR, Obach RS, Shebley M, Silva J, Sinz MW, Unadkat JD, and Zhang L, et al. (2014) Evaluation of various static and dynamic modeling methods to predict clinical CYP3A induction using in vitro CYP3A4 mRNA induction data. Clin Pharmacol Ther 95:179-188.
-
(2014)
Clin Pharmacol Ther
, vol.95
, pp. 179-188
-
-
Einolf, H.J.1
Chen, L.2
Fahmi, O.A.3
Gibson, C.R.4
Obach, R.S.5
Shebley, M.6
Silva, J.7
Sinz, M.W.8
Unadkat, J.D.9
Zhang, L.10
-
8
-
-
85019294956
-
European Medicines Agency; Committee for Human Medicinal Products (CHMP); Guideline on the investigation of drug interactions. 6-21-2012. 9-13-0013. Online source Faber MS and Fuhr U (2004) Time response of cytochrome P450 1A2 activity on cessation of heavy smoking
-
EMA (2012) European Medicines Agency; Committee for Human Medicinal Products (CHMP); Guideline on the investigation of drug interactions. 6-21-2012. 9-13-0013. Online source Faber MS and Fuhr U (2004) Time response of cytochrome P450 1A2 activity on cessation of heavy smoking. Clin Pharmacol Ther 76:178-184.
-
(2012)
Clin Pharmacol Ther
, vol.76
, pp. 178-184
-
-
EMA1
-
9
-
-
50049091411
-
Prediction of drug-drug interactions from in vitro induction data: Application of the relative induction score approach using cryopreserved human hepatocytes
-
Fahmi OA, Boldt S, Kish M, Obach RS, and Tremaine LM (2008a) Prediction of drug-drug interactions from in vitro induction data: application of the relative induction score approach using cryopreserved human hepatocytes. Drug Metab Dispos 36:1971-1974.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 1971-1974
-
-
Fahmi, O.A.1
Boldt, S.2
Kish, M.3
Obach, R.S.4
Tremaine, L.M.5
-
10
-
-
67650825002
-
Comparison of different algorithms for predicting clinical drugdrug interactions, based on the use of CYP3A4 in vitro data: Predictions of compounds as precipitants of interaction
-
Fahmi OA, Hurst S, Plowchalk D, Cook J, Guo F, Youdim K, Dickins M, Phipps A, Darekar A, and Hyland R, et al. (2009) Comparison of different algorithms for predicting clinical drugdrug interactions, based on the use of CYP3A4 in vitro data: predictions of compounds as precipitants of interaction. Drug Metab Dispos 37:1658-1666.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 1658-1666
-
-
Fahmi, O.A.1
Hurst, S.2
Plowchalk, D.3
Cook, J.4
Guo, F.5
Youdim, K.6
Dickins, M.7
Phipps, A.8
Darekar, A.9
Hyland, R.10
-
11
-
-
77955999532
-
Cytochrome P450 3A4 mRNA is a more reliable marker than CYP3A4 activity for detecting pregnane X receptor-activated induction of drug-metabolizing enzymes
-
Fahmi OA, Kish M, Boldt S, and Obach RS (2010) Cytochrome P450 3A4 mRNA is a more reliable marker than CYP3A4 activity for detecting pregnane X receptor-activated induction of drug-metabolizing enzymes. Drug Metab Dispos 38:1605-1611.
-
(2010)
Drug Metab Dispos
, vol.38
, pp. 1605-1611
-
-
Fahmi, O.A.1
Kish, M.2
Boldt, S.3
Obach, R.S.4
-
12
-
-
47949115175
-
A combined model for predicting CYP3A4 clinical net drug-drug interaction based on CYP3A4 inhibition, inactivation, and induction determined in vitro
-
Fahmi OA, Maurer TS, Kish M, Cardenas E, Boldt S, and Nettleton D (2008b) A combined model for predicting CYP3A4 clinical net drug-drug interaction based on CYP3A4 inhibition, inactivation, and induction determined in vitro. Drug Metab Dispos 36:1698-1708.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 1698-1708
-
-
Fahmi, O.A.1
Maurer, T.S.2
Kish, M.3
Cardenas, E.4
Boldt, S.5
Nettleton, D.6
-
14
-
-
33846607427
-
Appropriate phenotyping procedures for drug metabolizing enzymes and transporters in humans and their simultaneous use in the "cocktail" approach
-
Fuhr U, Jetter A, and Kirchheiner J (2007) Appropriate phenotyping procedures for drug metabolizing enzymes and transporters in humans and their simultaneous use in the "cocktail" approach. Clin Pharmacol Ther 81:270-283.
-
(2007)
Clin Pharmacol Ther
, vol.81
, pp. 270-283
-
-
Fuhr, U.1
Jetter, A.2
Kirchheiner, J.3
-
15
-
-
49649116162
-
Potential role of intestinal first-pass metabolism in the prediction of drug-drug interactions
-
Galetin A, Gertz M, and Houston JB (2008) Potential role of intestinal first-pass metabolism in the prediction of drug-drug interactions. Expert Opin Drug Metab Toxicol 4:909-922.
-
(2008)
Expert Opin Drug Metab Toxicol
, vol.4
, pp. 909-922
-
-
Galetin, A.1
Gertz, M.2
Houston, J.B.3
-
16
-
-
79959741711
-
Effects of multiple-dose pegylated interferon alfa-2b on the activity of drug-metabolizing enzymes in persons with chronic hepatitis C
-
Gupta SK, Kolz K, and Cutler DL (2011) Effects of multiple-dose pegylated interferon alfa-2b on the activity of drug-metabolizing enzymes in persons with chronic hepatitis C. Eur J Clin Pharmacol 67:591-599.
-
(2011)
Eur J Clin Pharmacol
, vol.67
, pp. 591-599
-
-
Gupta, S.K.1
Kolz, K.2
Cutler, D.L.3
-
17
-
-
42049097101
-
Multiple inhibition mechanisms and prediction of drug-drug interactions: Status of metabolism and transporter models as exemplified by gemfibrozil-drug interactions
-
Hinton LK, Galetin A, and Houston JB (2008) Multiple inhibition mechanisms and prediction of drug-drug interactions: status of metabolism and transporter models as exemplified by gemfibrozil-drug interactions. Pharm Res 25:1063-1074.
-
(2008)
Pharm Res
, vol.25
, pp. 1063-1074
-
-
Hinton, L.K.1
Galetin, A.2
Houston, J.B.3
-
18
-
-
33745395225
-
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 23:1089-1116.
-
(2006)
Pharm Res
, vol.23
, pp. 1089-1116
-
-
Lin, J.H.1
-
19
-
-
84888580865
-
Stereoselective inhibition of CYP2C19 and CYP3A4 by fluoxetine and its metabolite: Implications for risk assessment of multiple time-dependent inhibitor systems
-
Lutz JD, VandenBrink BM, Babu KN, Nelson WL, Kunze KL, and Isoherranen N (2013) Stereoselective inhibition of CYP2C19 and CYP3A4 by fluoxetine and its metabolite: implications for risk assessment of multiple time-dependent inhibitor systems. Drug Metab Dispos 41:2056-2065.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 2056-2065
-
-
Lutz, J.D.1
VandenBrink, B.M.2
Babu, K.N.3
Nelson, W.L.4
Kunze, K.L.5
Isoherranen, N.6
-
20
-
-
84946219236
-
Defining the role of gut bacteria in the metabolism of deleobuvir: In vitro and in vivo studies
-
McCabe M, Sane RS, Keith-Luzzi M, Xu J, King I, Whitcher-Johnstone A, Johnstone N, Tweedie DJ, and Li Y (2015) Defining the role of gut bacteria in the metabolism of deleobuvir: in vitro and in vivo studies. Drug Metab Dispos 43:1612-1618 10.1124/dmd.115.064477.
-
(2015)
Drug Metab Dispos
, vol.43
, pp. 1612-1618
-
-
McCabe, M.1
Sane, R.S.2
Keith-Luzzi, M.3
Xu, J.4
King, I.5
Whitcher-Johnstone, A.6
Johnstone, N.7
Tweedie, D.J.8
Li, Y.9
-
21
-
-
68949209308
-
Arsenite and its metabolites, MMA(III) and DMA(III), modify CYP3A4, PXR and RXR alpha expression in the small intestine of CYP3A4 transgenic mice
-
Medina-Díaz IM, Estrada-Muñiz E, Reyes-Hernández OD, Ramírez P, Vega L, and Elizondo G (2009) Arsenite and its metabolites, MMA(III) and DMA(III), modify CYP3A4, PXR and RXR alpha expression in the small intestine of CYP3A4 transgenic mice. Toxicol Appl Pharmacol 239:162-168.
-
(2009)
Toxicol Appl Pharmacol
, vol.239
, pp. 162-168
-
-
Medina-Díaz, I.M.1
Estrada-Muñiz, E.2
Reyes-Hernández, O.D.3
Ramírez, P.4
Vega, L.5
Elizondo, G.6
-
22
-
-
33846449874
-
Mechanism-based inactivation of human cytochrome p450 enzymes and the prediction of drug-drug interactions
-
Obach RS, Walsky RL, and Venkatakrishnan K (2007) Mechanism-based inactivation of human cytochrome p450 enzymes and the prediction of drug-drug interactions. Drug Metab Dispos 35:246-255.
-
(2007)
Drug Metab Dispos
, vol.35
, pp. 246-255
-
-
Obach, R.S.1
Walsky, R.L.2
Venkatakrishnan, K.3
-
23
-
-
77953756056
-
Efavirenz primary and secondary metabolism in vitro and in vivo: Identification of novel metabolic pathways and cytochrome P450 2A6 as the principal catalyst of efavirenz 7-hydroxylation
-
Ogburn ET, Jones DR, Masters AR, Xu C, Guo Y, and Desta Z (2010) Efavirenz primary and secondary metabolism in vitro and in vivo: identification of novel metabolic pathways and cytochrome P450 2A6 as the principal catalyst of efavirenz 7-hydroxylation. Drug Metab Dispos 38:1218-1229.
-
(2010)
Drug Metab Dispos
, vol.38
, pp. 1218-1229
-
-
Ogburn, E.T.1
Jones, D.R.2
Masters, A.R.3
Xu, C.4
Guo, Y.5
Desta, Z.6
-
24
-
-
29944446317
-
Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: Implications for drug-drug interactions
-
Ogilvie BW, Zhang D, Li W, Rodrigues AD, Gipson AE, Holsapple J, Toren P, and Parkinson A (2006) Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: implications for drug-drug interactions. Drug Metab Dispos 34:191-197.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 191-197
-
-
Ogilvie, B.W.1
Zhang, D.2
Li, W.3
Rodrigues, A.D.4
Gipson, A.E.5
Holsapple, J.6
Toren, P.7
Parkinson, A.8
-
25
-
-
34547641389
-
General framework for the quantitative prediction of CYP3A4-mediated oral drug interactions based on the AUC increase by coadministration of standard drugs
-
Ohno Y, Hisaka A, and Suzuki H (2007) General framework for the quantitative prediction of CYP3A4-mediated oral drug interactions based on the AUC increase by coadministration of standard drugs. Clin Pharmacokinet 46:681-696.
-
(2007)
Clin Pharmacokinet
, vol.46
, pp. 681-696
-
-
Ohno, Y.1
Hisaka, A.2
Suzuki, H.3
-
26
-
-
0344420328
-
Phase 2 enzyme induction by the major metabolite of oltipraz
-
Petzer JP, Navamal M, Johnson JK, Kwak MK, Kensler TW, and Fishbein JC (2003) Phase 2 enzyme induction by the major metabolite of oltipraz. Chem Res Toxicol 16:1463-1469.
-
(2003)
Chem Res Toxicol
, vol.16
, pp. 1463-1469
-
-
Petzer, J.P.1
Navamal, M.2
Johnson, J.K.3
Kwak, M.K.4
Kensler, T.W.5
Fishbein, J.C.6
-
27
-
-
84920110967
-
Carboxymefloquine, the major metabolite of the antimalarial drug mefloquine, induces drug-metabolizing enzyme and transporter expression by activation of pregnane X receptor
-
Piedade R, Traub S, Bitter A, Nüssler AK, Gil JP, Schwab M, and Burk O (2015) Carboxymefloquine, the major metabolite of the antimalarial drug mefloquine, induces drug-metabolizing enzyme and transporter expression by activation of pregnane X receptor. Antimicrob Agents Chemother 59:96-104.
-
(2015)
Antimicrob Agents Chemother
, vol.59
, pp. 96-104
-
-
Piedade, R.1
Traub, S.2
Bitter, A.3
Nüssler, A.K.4
Gil, J.P.5
Schwab, M.6
Burk, O.7
-
28
-
-
0033815032
-
Differential maintenance of cytochrome P450 enzymes in cultured precision-cut human liver slices
-
Renwick AB, Watts PS, Edwards RJ, Barton PT, Guyonnet I, Price RJ, Tredger JM, Pelkonen O, Boobis AR, and Lake BG (2000) Differential maintenance of cytochrome P450 enzymes in cultured precision-cut human liver slices. Drug Metab Dispos 28:1202-1209.
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 1202-1209
-
-
Renwick, A.B.1
Watts, P.S.2
Edwards, R.J.3
Barton, P.T.4
Guyonnet, I.5
Price, R.J.6
Tredger, J.M.7
Pelkonen, O.8
Boobis, A.R.9
Lake, B.G.10
-
29
-
-
77549084821
-
Physiologically based mechanistic modelling to predict complex drug-drug interactions involving simultaneous competitive and time-dependent enzyme inhibition by parent compound and its metabolite in both liver and gut - The effect of diltiazem on the time-course of exposure to triazolam
-
Rowland Yeo K, Jamei M, Yang J, Tucker GT, and Rostami-Hodjegan A (2010) Physiologically based mechanistic modelling to predict complex drug-drug interactions involving simultaneous competitive and time-dependent enzyme inhibition by parent compound and its metabolite in both liver and gut-the effect of diltiazem on the time-course of exposure to triazolam. Eur J Pharm Sci 39:298-309.
-
(2010)
Eur J Pharm Sci
, vol.39
, pp. 298-309
-
-
Rowland Yeo, K.1
Jamei, M.2
Yang, J.3
Tucker, G.T.4
Rostami-Hodjegan, A.5
-
30
-
-
84924353003
-
Interactions of the hepatitis C virus protease inhibitor faldaprevir with cytochrome P450 enzymes: In vitro and in vivo correlation
-
Sabo JP, Kort J, Ballow C, Kashuba AD, Haschke M, Battegay M, Girlich B, Ting N, Lang B, and Zhang W, et al. (2015) Interactions of the hepatitis C virus protease inhibitor faldaprevir with cytochrome P450 enzymes: in vitro and in vivo correlation. J Clin Pharmacol 55: 467-477.
-
(2015)
J Clin Pharmacol
, vol.55
, pp. 467-477
-
-
Sabo, J.P.1
Kort, J.2
Ballow, C.3
Kashuba, A.D.4
Haschke, M.5
Battegay, M.6
Girlich, B.7
Ting, N.8
Lang, B.9
Zhang, W.10
-
31
-
-
84862658556
-
A comprehensive assessment of repaglinide metabolic pathways: Impact of choice of in vitro system and relative enzyme contribution to in vitro clearance
-
Säll C, Houston JB, and Galetin A (2012) A comprehensive assessment of repaglinide metabolic pathways: impact of choice of in vitro system and relative enzyme contribution to in vitro clearance. Drug Metab Dispos 40:1279-1289.
-
(2012)
Drug Metab Dispos
, vol.40
, pp. 1279-1289
-
-
Säll, C.1
Houston, J.B.2
Galetin, A.3
-
32
-
-
54349113314
-
Modeling, prediction, and in vitro in vivo correlation of CYP3A4 induction
-
Shou M, Hayashi M, Pan Y, Xu Y, Morrissey K, Xu L, and Skiles GL (2008) Modeling, prediction, and in vitro in vivo correlation of CYP3A4 induction. Drug Metab Dispos 36: 2355-2370.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 2355-2370
-
-
Shou, M.1
Hayashi, M.2
Pan, Y.3
Xu, Y.4
Morrissey, K.5
Xu, L.6
Skiles, G.L.7
-
33
-
-
53849093733
-
Current industrial practices in assessing CYP450 enzyme induction: Preclinical and clinical
-
Sinz M, Wallace G, and Sahi J (2008) Current industrial practices in assessing CYP450 enzyme induction: preclinical and clinical. AAPS J 10:391-400.
-
(2008)
AAPS J
, vol.10
, pp. 391-400
-
-
Sinz, M.1
Wallace, G.2
Sahi, J.3
-
34
-
-
84921630257
-
Glucuronidation converts clopidogrel to a strong timedependent inhibitor of CYP2C8: A phase II metabolite as a perpetrator of drug-drug interactions
-
Tornio A, Filppula AM, Kailari O, Neuvonen M, Nyrönen TH, Tapaninen T, Neuvonen PJ, Niemi M, and Backman JT (2014) Glucuronidation converts clopidogrel to a strong timedependent inhibitor of CYP2C8: a phase II metabolite as a perpetrator of drug-drug interactions. Clin Pharmacol Ther 96:498-507.
-
(2014)
Clin Pharmacol Ther
, vol.96
, pp. 498-507
-
-
Tornio, A.1
Filppula, A.M.2
Kailari, O.3
Neuvonen, M.4
Nyrönen, T.H.5
Tapaninen, T.6
Neuvonen, P.J.7
Niemi, M.8
Backman, J.T.9
-
35
-
-
84876483882
-
Mechanistic modeling to predict the transporter-and enzyme-mediated drug-drug interactions of repaglinide
-
Varma MV, Lai Y, Kimoto E, Goosen TC, El-Kattan AF, and Kumar V (2013a) Mechanistic modeling to predict the transporter-and enzyme-mediated drug-drug interactions of repaglinide. Pharm Res 30:1188-1199.
-
(2013)
Pharm Res
, vol.30
, pp. 1188-1199
-
-
Varma, M.V.1
Lai, Y.2
Kimoto, E.3
Goosen, T.C.4
El-Kattan, A.F.5
Kumar, V.6
-
36
-
-
84876752739
-
Quantitative prediction of repaglinide-rifampicin complex drug interactions using dynamic and static mechanistic models: Delineating differential CYP3A4 induction and OATP1B1 inhibition potential of rifampicin
-
Varma MV, Lin J, Bi YA, Rotter CJ, Fahmi OA, Lam JL, El-Kattan AF, Goosen TC, and Lai Y (2013b) Quantitative prediction of repaglinide-rifampicin complex drug interactions using dynamic and static mechanistic models: delineating differential CYP3A4 induction and OATP1B1 inhibition potential of rifampicin. Drug Metab Dispos 41:966-974.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 966-974
-
-
Varma, M.V.1
Lin, J.2
Bi, Y.A.3
Rotter, C.J.4
Fahmi, O.A.5
Lam, J.L.6
El-Kattan, A.F.7
Goosen, T.C.8
Lai, Y.9
-
37
-
-
34548738229
-
Drug-drug interactions via mechanism-based cytochrome P450 inactivation: Points to consider for risk assessment from in vitro data and clinical pharmacologic evaluation
-
Venkatakrishnan K and Obach RS (2007) Drug-drug interactions via mechanism-based cytochrome P450 inactivation: points to consider for risk assessment from in vitro data and clinical pharmacologic evaluation. Curr Drug Metab 8:449-462.
-
(2007)
Curr Drug Metab
, vol.8
, pp. 449-462
-
-
Venkatakrishnan, K.1
Obach, R.S.2
-
38
-
-
35648987166
-
Mechanism-based inactivation of human cytochrome P450 enzymes: Strategies for diagnosis and drug-drug interaction risk assessment
-
Venkatakrishnan K, Obach RS, and Rostami-Hodjegan A (2007) Mechanism-based inactivation of human cytochrome P450 enzymes: strategies for diagnosis and drug-drug interaction risk assessment. Xenobiotica 37:1225-1256.
-
(2007)
Xenobiotica
, vol.37
, pp. 1225-1256
-
-
Venkatakrishnan, K.1
Obach, R.S.2
Rostami-Hodjegan, A.3
-
39
-
-
0036892714
-
Gemfibrozil inhibits CYP2C8-mediated cerivastatin metabolism in human liver microsomes
-
Wang JS, Neuvonen M, Wen X, Backman JT, and Neuvonen PJ (2002) Gemfibrozil inhibits CYP2C8-mediated cerivastatin metabolism in human liver microsomes. Drug Metab Dispos 30:1352-1356.
-
(2002)
Drug Metab Dispos
, vol.30
, pp. 1352-1356
-
-
Wang, J.S.1
Neuvonen, M.2
Wen, X.3
Backman, J.T.4
Neuvonen, P.J.5
-
40
-
-
84874038558
-
A perspective on the contribution of metabolites to drug-drug interaction potential: The need to consider both circulating levels and inhibition potency
-
Yu H and Tweedie D (2013) A perspective on the contribution of metabolites to drug-drug interaction potential: the need to consider both circulating levels and inhibition potency. Drug Metab Dispos 41:536-540.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 536-540
-
-
Yu, H.1
Tweedie, D.2
-
41
-
-
84940394361
-
Contribution of metabolites to P450 inhibition-based drug-drug interactions: Scholarship from the drug metabolism leadership group of the innovation and quality consortium metabolite group
-
Yu H, Balani SK, Chen W, Cui D, He L, Humphreys WG, Mao J, Lai WG, Lee AJ, and Lim HK, et al. (2015) Contribution of metabolites to P450 inhibition-based drug-drug interactions: scholarship from the drug metabolism leadership group of the innovation and quality consortium metabolite group. Drug Metab Dispos 43:620-630.
-
(2015)
Drug Metab Dispos
, vol.43
, pp. 620-630
-
-
Yu, H.1
Balani, S.K.2
Chen, W.3
Cui, D.4
He, L.5
Humphreys, W.G.6
Mao, J.7
Lai, W.G.8
Lee, A.J.9
Lim, H.K.10
-
42
-
-
84886573871
-
Faldaprevir (BI 201335), deleobuvir (BI 207127) and ribavirin oral therapy for treatment-naive HCV genotype 1: SOUND-C1 final results
-
Zeuzem S, Asselah T, Angus P, Zarski JP, Larrey D, Müllhaupt B, Gane E, Schuchmann M, Lohse AW, and Pol S, et al. (2013) Faldaprevir (BI 201335), deleobuvir (BI 207127) and ribavirin oral therapy for treatment-naive HCV genotype 1: SOUND-C1 final results. Antivir Ther 18:1015-1019.
-
(2013)
Antivir Ther
, vol.18
, pp. 1015-1019
-
-
Zeuzem, S.1
Asselah, T.2
Angus, P.3
Zarski, J.P.4
Larrey, D.5
Müllhaupt, B.6
Gane, E.7
Schuchmann, M.8
Lohse, A.W.9
Pol, S.10
-
43
-
-
84881405876
-
Faldaprevir and deleobuvir for HCV genotype 1 infection
-
Zeuzem S, Soriano V, Asselah T, Bronowicki JP, Lohse AW, Müllhaupt B, Schuchmann M, Bourlière M, Buti M, Roberts SK, Gane EJ, Stern JO, Vinisko R, Kukolj G, Gallivan JP, Böcher WO, and Mensa FJ. (2013) Faldaprevir and deleobuvir for HCV genotype 1 infection. N Engl J Med 369(7):630-9.
-
(2013)
N Engl J Med
, vol.369
, Issue.7
, pp. 630-639
-
-
Zeuzem, S.1
Soriano, V.2
Asselah, T.3
Bronowicki, J.P.4
Lohse, A.W.5
Müllhaupt, B.6
Schuchmann, M.7
Bourlière, M.8
Buti, M.9
Roberts, S.K.10
Gane, E.J.11
Stern, J.O.12
Vinisko, R.13
Kukolj, G.14
Gallivan, J.P.15
Böcher, W.O.16
Mensa, F.J.17
-
44
-
-
78650336624
-
A multi-endpoint evaluation of cytochrome P450 1A2, 2B6 and 3A4 induction response in human hepatocyte cultures after treatment with b-naphthoflavone, phenobarbital and rifampicin
-
Zhang JG, Ho T, Callendrello AL, Crespi CL, and Stresser DM (2010) A multi-endpoint evaluation of cytochrome P450 1A2, 2B6 and 3A4 induction response in human hepatocyte cultures after treatment with b-naphthoflavone, phenobarbital and rifampicin. Drug Metab Lett 4: 185-194.
-
(2010)
Drug Metab Lett
, vol.4
, pp. 185-194
-
-
Zhang, J.G.1
Ho, T.2
Callendrello, A.L.3
Crespi, C.L.4
Stresser, D.M.5
-
45
-
-
78951482203
-
Applications of physiologically based pharmacokinetic (PBPK) modeling and simulation during regulatory review
-
Zhao P, Zhang L, Grillo JA, Liu Q, Bullock JM, Moon YJ, Song P, Brar SS, Madabushi R, and Wu TC, et al. (2011) Applications of physiologically based pharmacokinetic (PBPK) modeling and simulation during regulatory review. Clin Pharmacol Ther 89: 259-267.
-
(2011)
Clin Pharmacol Ther
, vol.89
, pp. 259-267
-
-
Zhao, P.1
Zhang, L.2
Grillo, J.A.3
Liu, Q.4
Bullock, J.M.5
Moon, Y.J.6
Song, P.7
Brar, S.S.8
Madabushi, R.9
Wu, T.C.10
-
46
-
-
66449111462
-
Insights into the structure, function, and regulation of human cytochrome P450 1A2
-
Zhou SF, Chan E, Zhou ZW, Xue CC, Lai X, and Duan W (2009) Insights into the structure, function, and regulation of human cytochrome P450 1A2. Curr Drug Metab 10:713-729.
-
(2009)
Curr Drug Metab
, vol.10
, pp. 713-729
-
-
Zhou, S.F.1
Chan, E.2
Zhou, Z.W.3
Xue, C.C.4
Lai, X.5
Duan, W.6
|