-
1
-
-
0027468346
-
Terfenadine-ketoconazole interaction. Pharmacokinetic and electrocardiographic consequences
-
Honig PK, Wortham DC, Zamani K, Conner DP, Mullin JC, et al. (1993) Terfenadine-ketoconazole interaction. Pharmacokinetic and electrocardiographic consequences. JAMA 269: 1513-1518.
-
(1993)
JAMA
, vol.269
, pp. 1513-1518
-
-
Honig, P.K.1
Wortham, D.C.2
Zamani, K.3
Conner, D.P.4
Mullin, J.C.5
-
2
-
-
78649482869
-
Drug-drug interactions in the treatment of HIV infection: focus on pharmacokinetic enhancement through CYP3A inhibition
-
Josephson F, (2010) Drug-drug interactions in the treatment of HIV infection: focus on pharmacokinetic enhancement through CYP3A inhibition. J Intern Med 268: 530-539.
-
(2010)
J Intern Med
, vol.268
, pp. 530-539
-
-
Josephson, F.1
-
3
-
-
0035041368
-
The interaction of saquinavir (soft gelatin capsule) with ketoconazole, erythromycin and rifampicin: comparison of the effect in healthy volunteers and in HIV-infected patients
-
Grub S, Bryson H, Goggin T, Lüdin E, Jorga K, (2001) The interaction of saquinavir (soft gelatin capsule) with ketoconazole, erythromycin and rifampicin: comparison of the effect in healthy volunteers and in HIV-infected patients. Eur J Clin Pharmacol 57: 115-121.
-
(2001)
Eur J Clin Pharmacol
, vol.57
, pp. 115-121
-
-
Grub, S.1
Bryson, H.2
Goggin, T.3
Lüdin, E.4
Jorga, K.5
-
4
-
-
0030484780
-
Drug interaction between cyclosporine and two antimicrobial agents, josamycin and rifampicin, in organ-transplanted patients
-
Capone D, Aiello C, Santoro GA, Gentile A, Stanziale P, et al. (1996) Drug interaction between cyclosporine and two antimicrobial agents, josamycin and rifampicin, in organ-transplanted patients. Int J Clin Pharmacol Res 16: 73-76.
-
(1996)
Int J Clin Pharmacol Res
, vol.16
, pp. 73-76
-
-
Capone, D.1
Aiello, C.2
Santoro, G.A.3
Gentile, A.4
Stanziale, P.5
-
5
-
-
0033140371
-
Tuberculosis in renal transplant recipients
-
Lattes R, Radisic M, Rial M, Argento J, Casadei D, (1999) Tuberculosis in renal transplant recipients. Transpl Infect Dis 1: 98-104.
-
(1999)
Transpl Infect Dis
, vol.1
, pp. 98-104
-
-
Lattes, R.1
Radisic, M.2
Rial, M.3
Argento, J.4
Casadei, D.5
-
6
-
-
0021941863
-
Acute rejection and massive cyclosporine requirements in heart transplant recipients treated with rifampin
-
Modry DL, Stinson EB, Oyer PE, Jamieson SW, Baldwin JC, et al. (1985) Acute rejection and massive cyclosporine requirements in heart transplant recipients treated with rifampin. Transplantation 39: 313-314.
-
(1985)
Transplantation
, vol.39
, pp. 313-314
-
-
Modry, D.L.1
Stinson, E.B.2
Oyer, P.E.3
Jamieson, S.W.4
Baldwin, J.C.5
-
7
-
-
46749154596
-
The quantitative prediction of CYP-mediated drug interaction by physiologically based pharmacokinetic modeling
-
Kato M, Shitara Y, Sato H, Yoshisue K, Hirano M, et al. (2008) The quantitative prediction of CYP-mediated drug interaction by physiologically based pharmacokinetic modeling. Pharm Res 25: 1891-1901.
-
(2008)
Pharm Res
, vol.25
, pp. 1891-1901
-
-
Kato, M.1
Shitara, Y.2
Sato, H.3
Yoshisue, K.4
Hirano, M.5
-
8
-
-
29944446485
-
Prediction of time-dependent CYP3A4 drug-drug interactions: impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition
-
Galetin A, Burt H, Gibbons L, 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
-
9
-
-
0033994866
-
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 S, Ito K, Sugiyama Y, (2000) 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 17: 336-343.
-
(2000)
Pharm Res
, vol.17
, pp. 336-343
-
-
Kanamitsu, S.1
Ito, K.2
Sugiyama, Y.3
-
10
-
-
1942455361
-
Database analyses for the prediction of in vivo drug-drug interactions from in vitro data
-
Ito K, Brown HS, Houston JB, (2004) Database analyses for the prediction of in vivo drug-drug interactions from in vitro data. Br J Clin Pharmacol 57: 473-486.
-
(2004)
Br J Clin Pharmacol
, vol.57
, pp. 473-486
-
-
Ito, K.1
Brown, H.S.2
Houston, J.B.3
-
11
-
-
33646498651
-
The quantitative prediction of in vivo enzyme-induction caused by drug exposure from in vitro information on human hepatocytes
-
Kato M, Chiba K, Horikawa M, Sugiyama Y, (2005) The quantitative prediction of in vivo enzyme-induction caused by drug exposure from in vitro information on human hepatocytes. Drug Metab Pharmacokinet 20: 236-243.
-
(2005)
Drug Metab Pharmacokinet
, vol.20
, pp. 236-243
-
-
Kato, M.1
Chiba, K.2
Horikawa, M.3
Sugiyama, Y.4
-
12
-
-
54349113314
-
Modeling, prediction, and in vitro in vivo correlation of CYP3A4 induction
-
Shou M, Hayashi M, Pan Y, Xu Y, Morrissey K, et al. (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
-
13
-
-
68349150527
-
Towards a quantitative framework for the prediction of DDIs arising from cytochrome P450 induction
-
Almond LM, Yang J, Jamei M, Tucker GT, Rostami-Hodjegan A, (2009) Towards a quantitative framework for the prediction of DDIs arising from cytochrome P450 induction. Curr Drug Metab 10: 420-432.
-
(2009)
Curr Drug Metab
, vol.10
, pp. 420-432
-
-
Almond, L.M.1
Yang, J.2
Jamei, M.3
Tucker, G.T.4
Rostami-Hodjegan, A.5
-
14
-
-
79851493460
-
The use of HepaRG and human hepatocyte data in predicting CYP induction drug-drug interactions via static equation and dynamic mechanistic modelling approaches
-
Grime K, Ferguson DD, Riley RJ, (2010) The use of HepaRG and human hepatocyte data in predicting CYP induction drug-drug interactions via static equation and dynamic mechanistic modelling approaches. Curr Drug Metab 11: 870-885.
-
(2010)
Curr Drug Metab
, vol.11
, pp. 870-885
-
-
Grime, K.1
Ferguson, D.D.2
Riley, R.J.3
-
15
-
-
47749122616
-
Cytochrome p450 turnover: regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions
-
Yang J, Liao M, Shou M, Jamei M, Yeo KR, et al. (2008) Cytochrome p450 turnover: regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions. Curr Drug Metab 9: 384-394.
-
(2008)
Curr Drug Metab
, vol.9
, pp. 384-394
-
-
Yang, J.1
Liao, M.2
Shou, M.3
Jamei, M.4
Yeo, K.R.5
-
16
-
-
67650825002
-
Comparison of different algorithms for predicting clinical drug-drug 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, et al. (2009) Comparison of different algorithms for predicting clinical drug-drug 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
-
17
-
-
78650336624
-
A multi-endpoint evaluation of cytochrome P450 1A2, 2B6 and 3A4 induction response in human hepatocyte cultures after treatment with β-naphthoflavone, phenobarbital and rifampicin
-
Zhang JG, Ho T, Callendrello AL, Crespi CL, Stresser DM, (2010) A multi-endpoint evaluation of cytochrome P450 1A2, 2B6 and 3A4 induction response in human hepatocyte cultures after treatment with β-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
-
18
-
-
85047693782
-
Possible involvement of pregnane X receptor-enhanced CYP24 expression in drug-induced osteomalacia
-
Pascussi JM, Robert A, Nguyen M, Walrant-Debray O, Garabedian M, et al. (2005) Possible involvement of pregnane X receptor-enhanced CYP24 expression in drug-induced osteomalacia. J Clin Invest 115: 177-186.
-
(2005)
J Clin Invest
, vol.115
, pp. 177-186
-
-
Pascussi, J.M.1
Robert, A.2
Nguyen, M.3
Walrant-Debray, O.4
Garabedian, M.5
-
19
-
-
4444278991
-
The effects of gender, age, ethnicity, and liver cirrhosis on cytochrome P450 enzyme activity in human liver microsomes and inducibility in cultured human hepatocytes
-
Parkinson A, Mudra DR, Johnson C, Dwyer A, Carroll KM, (2004) The effects of gender, age, ethnicity, and liver cirrhosis on cytochrome P450 enzyme activity in human liver microsomes and inducibility in cultured human hepatocytes. Toxicol Appl Pharmacol 199: 193-209.
-
(2004)
Toxicol Appl Pharmacol
, vol.199
, pp. 193-209
-
-
Parkinson, A.1
Mudra, D.R.2
Johnson, C.3
Dwyer, A.4
Carroll, K.M.5
-
20
-
-
0033655573
-
Expression and regulation of cytochrome P450 enzymes in primary cultures of human hepatocytes
-
LeCluyse E, Madan A, Hamilton G, Carroll K, DeHaan R, et al. (2000) Expression and regulation of cytochrome P450 enzymes in primary cultures of human hepatocytes. J Biochem Mol Toxicol 14: 177-188.
-
(2000)
J Biochem Mol Toxicol
, vol.14
, pp. 177-188
-
-
LeCluyse, E.1
Madan, A.2
Hamilton, G.3
Carroll, K.4
DeHaan, R.5
-
21
-
-
0021271867
-
Experience with NONMEM: analysis of routine phenytoin clinical pharmacokinetic data
-
Sheiner LB, Grasela TH, (1984) Experience with NONMEM: analysis of routine phenytoin clinical pharmacokinetic data. Drug Metab Rev 15: 293-303.
-
(1984)
Drug Metab Rev
, vol.15
, pp. 293-303
-
-
Sheiner, L.B.1
Grasela, T.H.2
-
22
-
-
0021884198
-
Pharmacokinetic parameter estimates from several least squares procedures: superiority of extended least squares
-
Sheiner LB, Beal SL, (1985) Pharmacokinetic parameter estimates from several least squares procedures: superiority of extended least squares. J Pharmacokinet Biopharm 13: 185-201.
-
(1985)
J Pharmacokinet Biopharm
, vol.13
, pp. 185-201
-
-
Sheiner, L.B.1
Beal, S.L.2
-
23
-
-
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, 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
-
24
-
-
51649098439
-
General framework for the prediction of oral drug interactions caused by CYP3A4 induction from in vivo information
-
Ohno Y, Hisaka A, Ueno M, Suzuki H, (2008) General framework for the prediction of oral drug interactions caused by CYP3A4 induction from in vivo information. Clin Pharmacokinet 47: 669-680.
-
(2008)
Clin Pharmacokinet
, vol.47
, pp. 669-680
-
-
Ohno, Y.1
Hisaka, A.2
Ueno, M.3
Suzuki, H.4
-
25
-
-
23444452547
-
Rifampin markedly decreases and gemfibrozil increases the plasma concentrations of atorvastatin and its metabolites
-
Backman JT, Luurila H, Neuvonen M, Neuvonen PJ, (2005) Rifampin markedly decreases and gemfibrozil increases the plasma concentrations of atorvastatin and its metabolites. Clin Pharmacol Ther 78: 154-167.
-
(2005)
Clin Pharmacol Ther
, vol.78
, pp. 154-167
-
-
Backman, J.T.1
Luurila, H.2
Neuvonen, M.3
Neuvonen, P.J.4
-
26
-
-
0442313672
-
Effect of rifampicin on the pharmacokinetics of imatinib mesylate (Gleevec, STI571) in healthy subjects
-
Bolton AE, Peng B, Hubert M, Krebs-Brown A, Capdeville R, et al. (2004) Effect of rifampicin on the pharmacokinetics of imatinib mesylate (Gleevec, STI571) in healthy subjects. Cancer Chemother Pharmacol 53: 102-106.
-
(2004)
Cancer Chemother Pharmacol
, vol.53
, pp. 102-106
-
-
Bolton, A.E.1
Peng, B.2
Hubert, M.3
Krebs-Brown, A.4
Capdeville, R.5
-
27
-
-
33646100099
-
Comparison of midazolam and simvastatin as cytochrome P450 3A probes
-
Chung E, Nafziger AN, Kazierad DJ, Bertino JS, (2006) Comparison of midazolam and simvastatin as cytochrome P450 3A probes. Clin Pharmacol Ther 79: 350-361.
-
(2006)
Clin Pharmacol Ther
, vol.79
, pp. 350-361
-
-
Chung, E.1
Nafziger, A.N.2
Kazierad, D.J.3
Bertino, J.S.4
-
28
-
-
0032986347
-
Interactions of buspirone with itraconazole and rifampicin: effects on the pharmacokinetics of the active 1-(2-pyrimidinyl)-piperazine metabolite of buspirone
-
Kivistö KT, Lamberg TS, Neuvonen PJ, (1999) Interactions of buspirone with itraconazole and rifampicin: effects on the pharmacokinetics of the active 1-(2-pyrimidinyl)-piperazine metabolite of buspirone. Pharmacol Toxicol 84: 94-97.
-
(1999)
Pharmacol Toxicol
, vol.84
, pp. 94-97
-
-
Kivistö, K.T.1
Lamberg, T.S.2
Neuvonen, P.J.3
-
29
-
-
0034527327
-
Rifampin greatly reduces plasma simvastatin and simvastatin acid concentrations
-
Kyrklund C, Backman JT, Kivistö KT, Neuvonen M, Laitila J, et al. (2000) Rifampin greatly reduces plasma simvastatin and simvastatin acid concentrations. Clin Pharmacol Ther 68: 592-597.
-
(2000)
Clin Pharmacol Ther
, vol.68
, pp. 592-597
-
-
Kyrklund, C.1
Backman, J.T.2
Kivistö, K.T.3
Neuvonen, M.4
Laitila, J.5
-
30
-
-
0020695718
-
Rifampicin reduces effectiveness and bioavailability of prednisolone
-
McAllister WA, Thompson PJ, Al-Habet SM, Rogers HJ, (1983) Rifampicin reduces effectiveness and bioavailability of prednisolone. Br Med J (Clin Res Ed) 286: 923-925.
-
(1983)
Br Med J (Clin Res Ed)
, vol.286
, pp. 923-925
-
-
McAllister, W.A.1
Thompson, P.J.2
Al-Habet, S.M.3
Rogers, H.J.4
-
31
-
-
25144436285
-
Pharmacokinetic drug interactions of gefitinib with rifampicin, itraconazole and metoprolol
-
Swaisland HC, Ranson M, Smith RP, Leadbetter J, Laight A, et al. (2005) Pharmacokinetic drug interactions of gefitinib with rifampicin, itraconazole and metoprolol. Clin Pharmacokinet 44: 1067-1081.
-
(2005)
Clin Pharmacokinet
, vol.44
, pp. 1067-1081
-
-
Swaisland, H.C.1
Ranson, M.2
Smith, R.P.3
Leadbetter, J.4
Laight, A.5
-
32
-
-
0030919660
-
Concentrations and effects of zopiclone are greatly reduced by rifampicin
-
Villikka K, Kivistö KT, Lamberg TS, Kantola T, Neuvonen PJ, (1997) Concentrations and effects of zopiclone are greatly reduced by rifampicin. Br J Clin Pharmacol 43: 471-474.
-
(1997)
Br J Clin Pharmacol
, vol.43
, pp. 471-474
-
-
Villikka, K.1
Kivistö, K.T.2
Lamberg, T.S.3
Kantola, T.4
Neuvonen, P.J.5
-
33
-
-
0031417357
-
Rifampin reduces plasma concentrations and effects of zolpidem
-
Villikka K, Kivistö KT, Luurila H, Neuvonen PJ, (1997) Rifampin reduces plasma concentrations and effects of zolpidem. Clin Pharmacol Ther 62: 629-634.
-
(1997)
Clin Pharmacol Ther
, vol.62
, pp. 629-634
-
-
Villikka, K.1
Kivistö, K.T.2
Luurila, H.3
Neuvonen, P.J.4
-
34
-
-
0031027350
-
Triazolam is ineffective in patients taking rifampin
-
Villikka K, Kivistö KT, Backman JT, Olkkola KT, Neuvonen PJ, (1997) Triazolam is ineffective in patients taking rifampin. Clin Pharmacol Ther 61: 8-14.
-
(1997)
Clin Pharmacol Ther
, vol.61
, pp. 8-14
-
-
Villikka, K.1
Kivistö, K.T.2
Backman, J.T.3
Olkkola, K.T.4
Neuvonen, P.J.5
-
35
-
-
0033461821
-
Simultaneous assessment of CYP3A4 and CYP1A2 activity in vivo with alprazolam and caffeine
-
Schmider J, Brockmöller J, Arold G, Bauer S, Roots I, (1999) Simultaneous assessment of CYP3A4 and CYP1A2 activity in vivo with alprazolam and caffeine. Pharmacogenetics 9: 725-734.
-
(1999)
Pharmacogenetics
, vol.9
, pp. 725-734
-
-
Schmider, J.1
Brockmöller, J.2
Arold, G.3
Bauer, S.4
Roots, I.5
-
36
-
-
0026457407
-
Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction
-
Hebert MF, Roberts JP, Prueksaritanont T, Benet LZ, (1992) Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction. Clin Pharmacol Ther 52: 453-457.
-
(1992)
Clin Pharmacol Ther
, vol.52
, pp. 453-457
-
-
Hebert, M.F.1
Roberts, J.P.2
Prueksaritanont, T.3
Benet, L.Z.4
-
37
-
-
0029972195
-
The nifedipine-rifampin interaction. Evidence for induction of gut wall metabolism
-
Holtbecker N, Fromm MF, Kroemer HK, Ohnhaus EE, Heidemann H, (1996) The nifedipine-rifampin interaction. Evidence for induction of gut wall metabolism. Drug Metab Dispos 24: 1121-1123.
-
(1996)
Drug Metab Dispos
, vol.24
, pp. 1121-1123
-
-
Holtbecker, N.1
Fromm, M.F.2
Kroemer, H.K.3
Ohnhaus, E.E.4
Heidemann, H.5
-
38
-
-
0033751972
-
Effect of rifampin on plasma concentrations of mefloquine in healthy volunteers
-
Ridtitid W, Wongnawa M, Mahatthanatrakul W, Chaipol P, Sunbhanich M, (2000) Effect of rifampin on plasma concentrations of mefloquine in healthy volunteers. J Pharm Pharmacol 52: 1265-1269.
-
(2000)
J Pharm Pharmacol
, vol.52
, pp. 1265-1269
-
-
Ridtitid, W.1
Wongnawa, M.2
Mahatthanatrakul, W.3
Chaipol, P.4
Sunbhanich, M.5
-
39
-
-
24344466640
-
Clinical pharmacokinetics of telithromycin, the first ketolide antibacterial
-
Shi J, Montay G, Bhargava VO, (2005) Clinical pharmacokinetics of telithromycin, the first ketolide antibacterial. Clin Pharmacokinet 44: 915-934.
-
(2005)
Clin Pharmacokinet
, vol.44
, pp. 915-934
-
-
Shi, J.1
Montay, G.2
Bhargava, V.O.3
-
40
-
-
0030068752
-
Rifampin drastically reduces plasma concentrations and effects of oral midazolam
-
Backman JT, Olkkola KT, Neuvonen PJ, (1996) Rifampin drastically reduces plasma concentrations and effects of oral midazolam. Clin Pharmacol Ther 59: 7-13.
-
(1996)
Clin Pharmacol Ther
, vol.59
, pp. 7-13
-
-
Backman, J.T.1
Olkkola, K.T.2
Neuvonen, P.J.3
-
41
-
-
0015169660
-
Kinetic studies on rifampicin. I. Serum concentration analysis in subjects treated with different oral doses over a period of two weeks
-
Acocella G, Pagani V, Marchetti M, Baroni GC, Nicolis FB, (1971) Kinetic studies on rifampicin. I. Serum concentration analysis in subjects treated with different oral doses over a period of two weeks. Chemotherapy 16: 356-370.
-
(1971)
Chemotherapy
, vol.16
, pp. 356-370
-
-
Acocella, G.1
Pagani, V.2
Marchetti, M.3
Baroni, G.C.4
Nicolis, F.B.5
-
42
-
-
1042265446
-
Cryopreserved human hepatocytes as alternative in vitro model for cytochrome p450 induction studies
-
Garcia M, Rager J, Wang Q, Strab R, Hidalgo IJ, et al. (2003) Cryopreserved human hepatocytes as alternative in vitro model for cytochrome p450 induction studies. In Vitro Cell Dev Biol Anim 39: 283-287.
-
(2003)
In Vitro Cell Dev Biol Anim
, vol.39
, pp. 283-287
-
-
Garcia, M.1
Rager, J.2
Wang, Q.3
Strab, R.4
Hidalgo, I.J.5
-
43
-
-
6344240478
-
Induction of CYP3A4 by efavirenz in primary human hepatocytes: comparison with rifampin and phenobarbital
-
Hariparsad N, Nallani SC, Sane RS, Buckley DJ, Buckley AR, et al. (2004) Induction of CYP3A4 by efavirenz in primary human hepatocytes: comparison with rifampin and phenobarbital. J Clin Pharmacol 44: 1273-1281.
-
(2004)
J Clin Pharmacol
, vol.44
, pp. 1273-1281
-
-
Hariparsad, N.1
Nallani, S.C.2
Sane, R.S.3
Buckley, D.J.4
Buckley, A.R.5
-
44
-
-
44149104931
-
Comparison of immortalized Fa2N-4 cells and human hepatocytes as in vitro models for cytochrome P450 induction
-
Hariparsad N, Carr BA, Evers R, Chu X, (2008) Comparison of immortalized Fa2N-4 cells and human hepatocytes as in vitro models for cytochrome P450 induction. Drug Metab Dispos 36: 1046-1055.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 1046-1055
-
-
Hariparsad, N.1
Carr, B.A.2
Evers, R.3
Chu, X.4
-
45
-
-
0030803654
-
Applications of primary human hepatocytes in the evaluation of pharmacokinetic drug-drug interactions: evaluation of model drugs terfenadine and rifampin
-
Li AP, Jurima-Romet M, (1997) Applications of primary human hepatocytes in the evaluation of pharmacokinetic drug-drug interactions: evaluation of model drugs terfenadine and rifampin. Cell Biol Toxicol 13: 365-374.
-
(1997)
Cell Biol Toxicol
, vol.13
, pp. 365-374
-
-
Li, A.P.1
Jurima-Romet, M.2
-
46
-
-
17644426320
-
Comparative effects of fibrates on drug metabolizing enzymes in human hepatocytes
-
Prueksaritanont T, Richards KM, Qiu Y, Strong-Basalyga K, Miller A, et al. (2005) Comparative effects of fibrates on drug metabolizing enzymes in human hepatocytes. Pharm Res 22: 71-78.
-
(2005)
Pharm Res
, vol.22
, pp. 71-78
-
-
Prueksaritanont, T.1
Richards, K.M.2
Qiu, Y.3
Strong-Basalyga, K.4
Miller, A.5
-
47
-
-
0017944237
-
Clinical pharmacokinetics of rifampicin
-
Acocella G, (1978) Clinical pharmacokinetics of rifampicin. Clin Pharmacokinet 3: 108-127.
-
(1978)
Clin Pharmacokinet
, vol.3
, pp. 108-127
-
-
Acocella, G.1
-
48
-
-
0037342537
-
The systems biology markup language (SBML): a medium for representation and exchange of biochemical network models
-
Hucka M, Finney A, Sauro HM, Bolouri H, Doyle JC, et al. (2003) The systems biology markup language (SBML): a medium for representation and exchange of biochemical network models. Bioinformatics 19: 524-531.
-
(2003)
Bioinformatics
, vol.19
, pp. 524-531
-
-
Hucka, M.1
Finney, A.2
Sauro, H.M.3
Bolouri, H.4
Doyle, J.C.5
-
49
-
-
81355123249
-
Software for systems biology: from tools to integrated platforms
-
Ghosh S, Matsuoka Y, Asai Y, Hsin KY, Kitano H, (2011) Software for systems biology: from tools to integrated platforms. Nat Rev Genet 12: 821-832.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 821-832
-
-
Ghosh, S.1
Matsuoka, Y.2
Asai, Y.3
Hsin, K.Y.4
Kitano, H.5
-
50
-
-
23444439817
-
Using process diagrams for the graphical representation of biological networks
-
Kitano H, Funahashi A, Matsuoka Y, Oda K, (2005) Using process diagrams for the graphical representation of biological networks. Nat Biotechnol 23: 961-966.
-
(2005)
Nat Biotechnol
, vol.23
, pp. 961-966
-
-
Kitano, H.1
Funahashi, A.2
Matsuoka, Y.3
Oda, K.4
-
51
-
-
77953787344
-
Confidence assessment of the Simcyp time-based approach and a static mathematical model in predicting clinical drug-drug interactions for mechanism-based CYP3A inhibitors
-
Wang YH, (2010) Confidence assessment of the Simcyp time-based approach and a static mathematical model in predicting clinical drug-drug interactions for mechanism-based CYP3A inhibitors. Drug Metab Dispos 38: 1094-1104.
-
(2010)
Drug Metab Dispos
, vol.38
, pp. 1094-1104
-
-
Wang, Y.H.1
-
52
-
-
80054751099
-
Effect of different durations and formulations of diltiazem on the single-dose pharmacokinetics of midazolam: how long do we go?
-
Friedman EJ, Fraser IP, Wang YH, Bergman AJ, Li CC, et al. (2011) Effect of different durations and formulations of diltiazem on the single-dose pharmacokinetics of midazolam: how long do we go? J Clin Pharmacol 51: 1561-1570.
-
(2011)
J Clin Pharmacol
, vol.51
, pp. 1561-1570
-
-
Friedman, E.J.1
Fraser, I.P.2
Wang, Y.H.3
Bergman, A.J.4
Li, C.C.5
-
53
-
-
0042787016
-
The small heterodimer partner interacts with the pregnane X receptor and represses its transcriptional activity
-
Ourlin JC, Lasserre F, Pineau T, Fabre JM, Sa-Cunha A, et al. (2003) The small heterodimer partner interacts with the pregnane X receptor and represses its transcriptional activity. Mol Endocrinol 17: 1693-1703.
-
(2003)
Mol Endocrinol
, vol.17
, pp. 1693-1703
-
-
Ourlin, J.C.1
Lasserre, F.2
Pineau, T.3
Fabre, J.M.4
Sa-Cunha, A.5
-
54
-
-
33645808917
-
Rifampicin induction of CYP3A4 requires pregnane X receptor cross talk with hepatocyte nuclear factor 4alpha and coactivators, and suppression of small heterodimer partner gene expression
-
Li T, Chiang JY, (2006) Rifampicin induction of CYP3A4 requires pregnane X receptor cross talk with hepatocyte nuclear factor 4alpha and coactivators, and suppression of small heterodimer partner gene expression. Drug Metab Dispos 34: 756-764.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 756-764
-
-
Li, T.1
Chiang, J.Y.2
-
55
-
-
33845626633
-
Photochemotherapeutic agent 8-methoxypsoralen induces cytochrome P450 3A4 and carboxylesterase HCE2: evidence on an involvement of the pregnane X receptor
-
Yang J, Yan B, (2007) Photochemotherapeutic agent 8-methoxypsoralen induces cytochrome P450 3A4 and carboxylesterase HCE2: evidence on an involvement of the pregnane X receptor. Toxicol Sci 95: 13-22.
-
(2007)
Toxicol Sci
, vol.95
, pp. 13-22
-
-
Yang, J.1
Yan, B.2
-
56
-
-
0037386735
-
Control of steroid, heme, and carcinogen metabolism by nuclear pregnane X receptor and constitutive androstane receptor
-
Xie W, Yeuh MF, Radominska-Pandya A, Saini SP, Negishi Y, et al. (2003) Control of steroid, heme, and carcinogen metabolism by nuclear pregnane X receptor and constitutive androstane receptor. Proc Natl Acad Sci U S A 100: 4150-4155.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 4150-4155
-
-
Xie, W.1
Yeuh, M.F.2
Radominska-Pandya, A.3
Saini, S.P.4
Negishi, Y.5
-
57
-
-
1642498178
-
Induction of human CYP2C9 by rifampicin, hyperforin, and phenobarbital is mediated by the pregnane X receptor
-
Chen Y, Ferguson SS, Negishi M, Goldstein JA, (2004) Induction of human CYP2C9 by rifampicin, hyperforin, and phenobarbital is mediated by the pregnane X receptor. J Pharmacol Exp Ther 308: 495-501.
-
(2004)
J Pharmacol Exp Ther
, vol.308
, pp. 495-501
-
-
Chen, Y.1
Ferguson, S.S.2
Negishi, M.3
Goldstein, J.A.4
-
58
-
-
80255130599
-
Human arylacetamide deacetylase is responsible for deacetylation of rifamycins: rifampicin, rifabutin, and rifapentine
-
Nakajima A, Fukami T, Kobayashi Y, Watanabe A, Nakajima M, et al. (2011) Human arylacetamide deacetylase is responsible for deacetylation of rifamycins: rifampicin, rifabutin, and rifapentine. Biochem Pharmacol 82: 1747-1756.
-
(2011)
Biochem Pharmacol
, vol.82
, pp. 1747-1756
-
-
Nakajima, A.1
Fukami, T.2
Kobayashi, Y.3
Watanabe, A.4
Nakajima, M.5
-
59
-
-
0014092325
-
Rifampicin: a new rifamycin. 3. Absorption, distribution, and elimination in man
-
Furesz S, Scotti R, Pallanza R, Mapelli E, (1967) Rifampicin: a new rifamycin. 3. Absorption, distribution, and elimination in man. Arzneimittelforschung 17: 534-537.
-
(1967)
Arzneimittelforschung
, vol.17
, pp. 534-537
-
-
Furesz, S.1
Scotti, R.2
Pallanza, R.3
Mapelli, E.4
-
60
-
-
0036144815
-
Prediction of pharmacokinetics prior to in vivo studies. 1. Mechanism-based prediction of volume of distribution
-
Poulin P, Theil FP, (2002) Prediction of pharmacokinetics prior to in vivo studies. 1. Mechanism-based prediction of volume of distribution. J Pharm Sci 91: 129-156.
-
(2002)
J Pharm Sci
, vol.91
, pp. 129-156
-
-
Poulin, P.1
Theil, F.P.2
-
61
-
-
47749122616
-
Cytochrome P450 turnover: regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions
-
Yang J, Liao M, Shou M, Jamei M, Yeo KR, et al. (2008) Cytochrome P450 turnover: regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions. Curr Drug Metab 9: 384-393.
-
(2008)
Curr Drug Metab
, vol.9
, pp. 384-393
-
-
Yang, J.1
Liao, M.2
Shou, M.3
Jamei, M.4
Yeo, K.R.5
-
63
-
-
78650737749
-
Effects of pregnane X receptor (NR1I2) and CYP2B6 genetic polymorphisms on the induction of bupropion hydroxylation by rifampin
-
Chung JY, Cho JY, Lim HS, Kim JR, Yu KS, et al. (2011) Effects of pregnane X receptor (NR1I2) and CYP2B6 genetic polymorphisms on the induction of bupropion hydroxylation by rifampin. Drug Metab Dispos 39: 92-97.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 92-97
-
-
Chung, J.Y.1
Cho, J.Y.2
Lim, H.S.3
Kim, J.R.4
Yu, K.S.5
-
64
-
-
0033711566
-
Rifampin decreases the plasma concentrations and effects of repaglinide
-
Niemi M, Backman JT, Neuvonen M, Neuvonen PJ, Kivistö KT, (2000) Rifampin decreases the plasma concentrations and effects of repaglinide. Clin Pharmacol Ther 68: 495-500.
-
(2000)
Clin Pharmacol Ther
, vol.68
, pp. 495-500
-
-
Niemi, M.1
Backman, J.T.2
Neuvonen, M.3
Neuvonen, P.J.4
Kivistö, K.T.5
-
65
-
-
0016245363
-
Interaction of sodium warfarin and rifampicin. studies in man
-
O'Reilly RA, (1974) Interaction of sodium warfarin and rifampicin. studies in man. Ann Intern Med 81: 337-340.
-
(1974)
Ann Intern Med
, vol.81
, pp. 337-340
-
-
O'Reilly, R.A.1
-
66
-
-
0023619704
-
The mechanism of the warfarin-rifampin drug interaction in humans
-
Heimark LD, Gibaldi M, Trager WF, O'Reilly RA, Goulart DA, (1987) The mechanism of the warfarin-rifampin drug interaction in humans. Clin Pharmacol Ther 42: 388-394.
-
(1987)
Clin Pharmacol Ther
, vol.42
, pp. 388-394
-
-
Heimark, L.D.1
Gibaldi, M.2
Trager, W.F.3
O'Reilly, R.A.4
Goulart, D.A.5
-
67
-
-
33644843888
-
Roles of rifampicin in drug-drug interactions: underlying molecular mechanisms involving the nuclear pregnane X receptor
-
Chen J, Raymond K, (2006) Roles of rifampicin in drug-drug interactions: underlying molecular mechanisms involving the nuclear pregnane X receptor. Ann Clin Microb Antimicrob 5: 3.
-
(2006)
Ann Clin Microb Antimicrob
, vol.5
, pp. 3
-
-
Chen, J.1
Raymond, K.2
-
68
-
-
34250694236
-
Differential metabolism of gefitinib and erlotinib by human cytochrome P450 enzymes
-
Li J, Zhao M, He P, Hidalgo M, Baker SD, (2007) Differential metabolism of gefitinib and erlotinib by human cytochrome P450 enzymes. Clin Cancer Res 13: 3731-3737.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 3731-3737
-
-
Li, J.1
Zhao, M.2
He, P.3
Hidalgo, M.4
Baker, S.D.5
-
69
-
-
77958523673
-
Participation of CYP2C8 and CYP3A4 in the N-demethylation of imatinib in human hepatic microsomes
-
Nebot N, Crettol S, d'Esposito F, Tattam B, Hibbs DE, et al. (2010) Participation of CYP2C8 and CYP3A4 in the N-demethylation of imatinib in human hepatic microsomes. Br J Pharmacol 161: 1059-1069.
-
(2010)
Br J Pharmacol
, vol.161
, pp. 1059-1069
-
-
Nebot, N.1
Crettol, S.2
d'Esposito, F.3
Tattam, B.4
Hibbs, D.E.5
-
70
-
-
66049147027
-
Biotransformation and in vitro assessment of metabolism-associated drug-drug interaction for CRx-102, a novel combination drug candidate
-
Zhang ZY, Chen M, Chen J, Padval MV, Kansra VV, (2009) Biotransformation and in vitro assessment of metabolism-associated drug-drug interaction for CRx-102, a novel combination drug candidate. J Pharm Biomed Anal 50: 200-209.
-
(2009)
J Pharm Biomed Anal
, vol.50
, pp. 200-209
-
-
Zhang, Z.Y.1
Chen, M.2
Chen, J.3
Padval, M.V.4
Kansra, V.V.5
-
71
-
-
58149310478
-
Specifications of insilicoML 1.0: a multilevel biophysical model description language
-
Asai Y, Suzuki Y, Kido Y, Oka H, Heien E, et al. (2008) Specifications of insilicoML 1.0: a multilevel biophysical model description language. J Physiol Sci 58: 447-458.
-
(2008)
J Physiol Sci
, vol.58
, pp. 447-458
-
-
Asai, Y.1
Suzuki, Y.2
Kido, Y.3
Oka, H.4
Heien, E.5
|