메뉴 건너뛰기




Volumn 40, Issue 10, 2010, Pages 713-720

Sources of variability in ketoconazole inhibition of human cytochrome P450 3A in vitro

Author keywords

cytochrome P450 3A; drug interactions; Ketoconazole; metabolic inhibition

Indexed keywords

CYTOCHROME P450 3A4; CYTOCHROME P450 3A5; KETOCONAZOLE; MIDAZOLAM;

EID: 77956592952     PISSN: 00498254     EISSN: 13665928     Source Type: Journal    
DOI: 10.3109/00498254.2010.506224     Document Type: Review
Times cited : (29)

References (79)
  • 1
    • 33846461184 scopus 로고    scopus 로고
    • Inhibition of CYP3A4 and CYP3A5 catalyzed metabolism of alprazolam and quinine by ketoconazole as racemate and four diferent enanti-omers
    • Allqvist A, Miura J, Bertilsson L, Mirghani RA. (2007). Inhibition of CYP3A4 and CYP3A5 catalyzed metabolism of alprazolam and quinine by ketoconazole as racemate and four diferent enanti-omers. Eur J Clin Pharmacol 63:173-179.
    • (2007) Eur J Clin Pharmacol , vol.63 , pp. 173-179
    • Allqvist, A.1    Miura, J.2    Bertilsson, L.3    Mirghani, R.A.4
  • 2
    • 33644861762 scopus 로고    scopus 로고
    • Inhibition constants, inhibitor concentrations and the prediction of inhibitory drug drug interactions: Pitfalls, progress and promise
    • Bachmann KA. (2006). Inhibition constants, inhibitor concentrations and the prediction of inhibitory drug drug interactions: pitfalls, progress and promise. Curr Drug Metab 7:1-14.
    • (2006) Curr Drug Metab , vol.7 , pp. 1-14
    • Bachmann, K.A.1
  • 3
    • 0025949455 scopus 로고
    • Comparative efects of the antimycotic drugs ketoconazole, fuconazole, itraconazole and terbinafne on the metabolism of cyclosporin by human liver microsomes
    • Back DJ, Tjia J F. (1991). Comparative efects of the antimycotic drugs ketoconazole, fuconazole, itraconazole and terbinafne on the metabolism of cyclosporin by human liver microsomes. Br J Clin Pharmacol 32:624-626.
    • (1991) Br J Clin Pharmacol , vol.32 , pp. 624-626
    • Back, D.J.1    Tjia, J.F.2
  • 4
    • 0032929024 scopus 로고    scopus 로고
    • Efect of selected antimalarial drugs and inhibitors of cytochrome P-450 3A4 on halofantrine metabolism by human liver microsomes
    • Baune B, Furlan V, Taburet AM, Farinotti R. (1999). Efect of selected antimalarial drugs and inhibitors of cytochrome P-450 3A4 on halofantrine metabolism by human liver microsomes. Drug Metab Dispos 27:565-568.
    • (1999) Drug Metab Dispos , vol.27 , pp. 565-568
    • Baune, B.1    Furlan, V.2    Taburet, A.M.3    Farinotti, R.4
  • 5
    • 0030430033 scopus 로고    scopus 로고
    • Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes
    • Bourrié M, Meunier V, Berger Y, Fabre G. (1996). Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes. J Pharmacol Exp Ter 277:321-332.
    • (1996) J Pharmacol Exp ter , vol.277 , pp. 321-332
    • Bourrié, M.1    Meunier, V.2    Berger, Y.3    Fabre, G.4
  • 7
    • 1842779162 scopus 로고    scopus 로고
    • Prediction of in vivo drug interactions with eplerenone in man from in vitro metabolic inhibition data
    • Cook CS, Berry LM, Burton E. (2004). Prediction of in vivo drug interactions with eplerenone in man from in vitro metabolic inhibition data. Xenobiotica 34:215-228.
    • (2004) Xenobiotica , vol.34 , pp. 215-228
    • Cook, C.S.1    Berry, L.M.2    Burton, E.3
  • 8
    • 0033912432 scopus 로고    scopus 로고
    • Interaction of cisapride with the human cytochrome P450 system: Metabolism and inhibition studies
    • Desta Z, Soukhova N, Mahal SK, Flockhart DA. (2000) Interaction of cisapride with the human cytochrome P450 system: metabolism and inhibition studies. Drug Metab Dispos 28:789-800.
    • (2000) Drug Metab Dispos , vol.28 , pp. 789-800
    • Desta, Z.1    Soukhova, N.2    Mahal, S.K.3    Flockhart, D.A.4
  • 9
    • 28144461609 scopus 로고    scopus 로고
    • In vitro inhibitory efect of 1-aminobenzotriazole on drug oxidations catalyzed by human cytochrome P450 enzymes: A comparison with SKF-525A and ketoconazole
    • Emoto C, Murase S, Sawada Y, Jones BC, Iwasaki K. (2003).In vitro inhibitory efect of 1-aminobenzotriazole on drug oxidations catalyzed by human cytochrome P450 enzymes: a comparison with SKF-525A and ketoconazole. Drug Metab Pharmacokinet 18:287-295.
    • (2003) Drug Metab Pharmacokinet , vol.18 , pp. 287-295
    • Emoto, C.1    Murase, S.2    Sawada, Y.3    Jones, B.C.4    Iwasaki, K.5
  • 10
    • 0035527719 scopus 로고    scopus 로고
    • A novel testosterone 6 beta-hydroxylase activity assay for the study of CYP3A-mediated metabolism, inhibition, and induction in vitro
    • Fayer JL, Petullo DM, Ring BJ, Wrighton SA, Ruterbories KJ. (2002). A novel testosterone 6 beta-hydroxylase activity assay for the study of CYP3A-mediated metabolism, inhibition, and induction in vitro. J Pharmacol Toxicol Methods 46:117-123.
    • (2002) J Pharmacol Toxicol Methods , vol.46 , pp. 117-123
    • Fayer, J.L.1    Petullo, D.M.2    Ring, B.J.3    Wrighton, S.A.4    Ruterbories, K.J.5
  • 11
    • 4143074861 scopus 로고    scopus 로고
    • Drug-drug interactions of Z-338, a novel gastroprokinetic agent, with terfenadine, comparison with cisapride, and involvement of UGT1A9 and 1A8 in the human metabolism of Z-338
    • Furuta S, Kamada E, Omata T, Sugimoto T, Kawabata Y, Yonezawa K, Wu XC, Kurimoto T. (2004). Drug-drug interactions of Z-338, a novel gastroprokinetic agent, with terfenadine, comparison with cisapride, and involvement of UGT1A9 and 1A8 in the human metabolism of Z-338. Eur J Pharmacol 497:223-231.
    • (2004) Eur J Pharmacol , vol.497 , pp. 223-231
    • Furuta, S.1    Kamada, E.2    Omata, T.3    Sugimoto, T.4    Kawabata, Y.5    Yonezawa, K.6    Wu, X.C.7    Kurimoto, T.8
  • 12
    • 1842866515 scopus 로고    scopus 로고
    • Quinidine and haloperidol as modifers of CYP3A4 activity: Multisite kinetic model approach
    • Galetin A, Clarke SE, Houston JB. (2002). Quinidine and haloperidol as modifers of CYP3A4 activity: multisite kinetic model approach. Drug Metab Dispos 30:1512-1522.
    • (2002) Drug Metab Dispos , vol.30 , pp. 1512-1522
    • Galetin, A.1    Clarke, S.E.2    Houston, J.B.3
  • 13
    • 0042357511 scopus 로고    scopus 로고
    • Multisite kinetic analysis of interactions between prototypical CYP3A4 subgroup substrates: Midazolam, testosterone, and nifedipine
    • Galetin A, Clarke SE, Houston JB. (2003). Multisite kinetic analysis of interactions between prototypical CYP3A4 subgroup substrates: midazolam, testosterone, and nifedipine. Drug Metab Dispos 31:1108-1116.
    • (2003) Drug Metab Dispos , vol.31 , pp. 1108-1116
    • Galetin, A.1    Clarke, S.E.2    Houston, J.B.3
  • 14
    • 23044500208 scopus 로고    scopus 로고
    • CYP3A4 substrate selection and substitution in the prediction of potential drug-drug interactions
    • Galetin A, Ito K, Hallifax D, Houston JB. (2005). CYP3A4 substrate selection and substitution in the prediction of potential drug-drug interactions. J Pharmacol Exp Ter 314:180-190.
    • (2005) J Pharmacol Exp ter , vol.314 , pp. 180-190
    • Galetin, A.1    Ito, K.2    Hallifax, D.3    Houston, J.B.4
  • 15
    • 0025999285 scopus 로고
    • In vitro forecasting of drugs which may interfere with the biotransformation of midazolam
    • Gascon MP, Dayer P. (1991). In vitro forecasting of drugs which may interfere with the biotransformation of midazolam. Eur J Clin Pharmacol 41:573-578.
    • (1991) Eur J Clin Pharmacol , vol.41 , pp. 573-578
    • Gascon, M.P.1    Dayer, P.2
  • 16
    • 0030435332 scopus 로고    scopus 로고
    • Dexamethasone metabolism by human liver in vitro. Metabolite identifcation and inhibition of 6-hydroxylation
    • Gentile DM, Tomlinson ES, Maggs JL, Park BK, Back DJ. (1996). Dexamethasone metabolism by human liver in vitro. Metabolite identifcation and inhibition of 6-hydroxylation. J Pharmacol Exp Ter 277:105-112.
    • (1996) J Pharmacol Exp ter , vol.277 , pp. 105-112
    • Gentile, D.M.1    Tomlinson, E.S.2    Maggs, J.L.3    Park, B.K.4    Back, D.J.5
  • 17
    • 33645103778 scopus 로고    scopus 로고
    • Identifcation of human liver cytochrome P450 enzymes responsible for the metabolism of lonafarnib (Sarasar)
    • Ghosal A, Chowdhury SK, Tong W, Hapangama N, Yuan Y, Su AD, Zbaida S. (2006). Identifcation of human liver cytochrome P450 enzymes responsible for the metabolism of lonafarnib (Sarasar). Drug Metab Dispos 34:628-635.
    • (2006) Drug Metab Dispos , vol.34 , pp. 628-635
    • Ghosal, A.1    Chowdhury, S.K.2    Tong, W.3    Hapangama, N.4    Yuan, Y.5    Su, A.D.6    Zbaida, S.7
  • 18
    • 0032904865 scopus 로고    scopus 로고
    • Efect of inhibitor depletion on inhibitory potency: Tight binding inhibition of CYP3A by clotrimazole
    • Gibbs MA, Kunze KL, Howald WN, Tummel KE. (1999a). Efect of inhibitor depletion on inhibitory potency: tight binding inhibition of CYP3A by clotrimazole. Drug Metab Dispos 27:596-599.
    • (1999) Drug Metab Dispos , vol.27 , pp. 596-599
    • Ma, G.1    Kunze, K.L.2    Howald, W.N.3    Tummel, K.E.4
  • 19
    • 0032956839 scopus 로고    scopus 로고
    • Inhibition of cytochrome P-450 3A (CYP3A) in human intestinal and liver microsomes: Comparison of Ki values and impact of CYP3A5 expression
    • Gibbs MA, Tummel KE, Shen DD, Kunze KL. (1999b). Inhibition of cytochrome P-450 3A (CYP3A) in human intestinal and liver microsomes: comparison of Ki values and impact of CYP3A5 expression. Drug Metab Dispos 27:180-187.
    • (1999) Drug Metab Dispos , vol.27 , pp. 180-187
    • Ma, G.1    Tummel, K.E.2    Shen, D.D.3    Kunze, K.L.4
  • 20
    • 0032778975 scopus 로고    scopus 로고
    • Metabolism of artelinic acid to dihydroqinqhaosu by human liver cytochrome P4503A
    • Grace JM, Skanchy DJ, Aguilar AJ. (1999). Metabolism of artelinic acid to dihydroqinqhaosu by human liver cytochrome P4503A. Xenobiotica 29:703-717.
    • (1999) Xenobiotica , vol.29 , pp. 703-717
    • Grace, J.M.1    Skanchy, D.J.2    Aguilar, A.J.3
  • 24
    • 33846577441 scopus 로고    scopus 로고
    • Drug interaction studies: Study design, data analysis, and implications for dosing and labeling
    • Huang SM, Temple R, Trockmorton DC, Lesko LJ. (2007). Drug interaction studies: study design, data analysis, and implications for dosing and labeling. Clin Pharmacol Ter 81:298-304.
    • (2007) Clin Pharmacol ter , vol.81 , pp. 298-304
    • Huang, S.M.1    Temple, R.2    Trockmorton, D.C.3    Lesko, L.J.4
  • 26
    • 1942455361 scopus 로고    scopus 로고
    • 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
  • 27
    • 9444257635 scopus 로고    scopus 로고
    • Identifcation and characterization of potent CYP3A4 inhibitors in Schisandra fruit extract
    • Iwata H, Tezuka Y, Kadota S, Hiratsuka A, Watabe T. (2004). Identifcation and characterization of potent CYP3A4 inhibitors in Schisandra fruit extract. Drug Metab Dispos 32:1351-1358.
    • (2004) Drug Metab Dispos , vol.32 , pp. 1351-1358
    • Iwata, H.1    Tezuka, Y.2    Kadota, S.3    Hiratsuka, A.4    Watabe, T.5
  • 28
    • 0032911163 scopus 로고    scopus 로고
    • Comparison of cytochrome P-450-dependent metabolism and drug interactions of the 3-hydroxy-3-methylglutaryl-CoA reduct-ase inhibitors lovastatin and pravastatin in the liver
    • Jacobsen W, Kirchner G, Hallensleben K, Mancinelli L, Deters M, Hackbarth I, Benet LZ, Sewing KF, Christians U. (1999). Comparison of cytochrome P-450-dependent metabolism and drug interactions of the 3-hydroxy-3- methylglutaryl-CoA reduct-ase inhibitors lovastatin and pravastatin in the liver. Drug Metab Dispos 27:173-179.
    • (1999) Drug Metab Dispos , vol.27 , pp. 173-179
    • Jacobsen, W.1    Kirchner, G.2    Hallensleben, K.3    Mancinelli, L.4    Deters, M.5    Hackbarth, I.6    Benet, L.Z.7    Sewing, K.F.8    Christians, U.9
  • 29
    • 0027996327 scopus 로고
    • Terfenadine metabolism in human liver: In vitro inhibition by macrolide antibiotics and azole antifungals
    • Jurima-Romet M, Crawford K, Cyr T, Inaba T. (1994). Terfenadine metabolism in human liver: in vitro inhibition by macrolide antibiotics and azole antifungals. Drug Metabolism and Disposition 22:849-857.
    • (1994) Drug Metabolism and Disposition , vol.22 , pp. 849-857
    • Jurima-Romet, M.1    Crawford, K.2    Cyr, T.3    Inaba, T.4
  • 31
    • 0032811807 scopus 로고    scopus 로고
    • Potent inhibition of the cytochrome P-450 3A-mediated human liver micro-somal metabolism of a novel HIV protease inhibitor by ritonavir: A positive drug-drug interaction
    • Kumar GN, Dykstra J, Roberts EM, Jayanti VK, Hickman D, Uchic J, Yao Y, Surber B, Tomas S, Granneman GR. (1999). Potent inhibition of the cytochrome P-450 3A-mediated human liver micro-somal metabolism of a novel HIV protease inhibitor by ritonavir: A positive drug-drug interaction. Drug Metab Dispos 27:902-908.
    • (1999) Drug Metab Dispos , vol.27 , pp. 902-908
    • Kumar, G.N.1    Dykstra, J.2    Roberts, E.M.3    Jayanti, V.K.4    Hickman, D.5    Uchic, J.6    Yao, Y.7    Surber, B.8    Tomas, S.9    Granneman, G.R.10
  • 32
    • 1842536807 scopus 로고    scopus 로고
    • Quantitative contribution of CYP2D6 and CYP3A to oxycodone metabolism in human liver and intestinal microsomes
    • Lalovic B, Phillips B, Risler LL, Howald W, Shen DD. (2004). Quantitative contribution of CYP2D6 and CYP3A to oxycodone metabolism in human liver and intestinal microsomes. Drug Metab Dispos 32:447-454.
    • (2004) Drug Metab Dispos , vol.32 , pp. 447-454
    • Lalovic, B.1    Phillips, B.2    Risler, L.L.3    Howald, W.4    Shen, D.D.5
  • 33
    • 0029960192 scopus 로고    scopus 로고
    • Drug interactions and interindividual variability of ciclosporin metabolism in the small intestine
    • Lampen A, Christians U, Bader A, Hackbarth I, Sewing KF. (1996). Drug interactions and interindividual variability of ciclosporin metabolism in the small intestine. Pharmacology 52:159-168.
    • (1996) Pharmacology , vol.52 , pp. 159-168
    • Lampen, A.1    Christians, U.2    Bader, A.3    Hackbarth, I.4    Sewing, K.F.5
  • 36
    • 3242676832 scopus 로고    scopus 로고
    • Comparison of inhibitory efects of the proton pump-inhibiting drugs omepra-zole, esomeprazole, lansoprazole, pantoprazole, and rabepra-zole on human cytochrome P450 activities
    • Li XQ, Andersson TB, Ahlström M, Weidolf L. (2004). Comparison of inhibitory efects of the proton pump-inhibiting drugs omepra-zole, esomeprazole, lansoprazole, pantoprazole, and rabepra-zole on human cytochrome P450 activities. Drug Metab Dispos 32:821-827.
    • (2004) Drug Metab Dispos , vol.32 , pp. 821-827
    • Li, X.Q.1    Andersson, T.B.2    Ahlström, M.3    Weidolf, L.4
  • 37
    • 0344765487 scopus 로고    scopus 로고
    • Characterization of the selectivity and mechanism of human cytochrome P450 inhibition by the human immu-nodefciency virus-protease inhibitor nelfnavir mesylate
    • Lillibridge JH, Liang BH, Kerr BM, Webber S, Quart B, Shetty BV, Lee CA. (1998). Characterization of the selectivity and mechanism of human cytochrome P450 inhibition by the human immu-nodefciency virus-protease inhibitor nelfnavir mesylate. Drug Metab Dispos 26:609-616.
    • (1998) Drug Metab Dispos , vol.26 , pp. 609-616
    • Lillibridge, J.H.1    Liang, B.H.2    Kerr, B.M.3    Webber, S.4    Quart, B.5    Shetty, B.V.6    Lee, C.A.7
  • 38
    • 33748676891 scopus 로고    scopus 로고
    • Metabolic activation of pradefovir by CYP3A4 and its potential as an inhibitor or inducer
    • Lin CC, Fang C, Benetton S, Xu GF, Yeh LT. (2006). Metabolic activation of pradefovir by CYP3A4 and its potential as an inhibitor or inducer. Antimicrob Agents Chemother 50:2926-2931.
    • (2006) Antimicrob Agents Chemother , vol.50 , pp. 2926-2931
    • Lin, C.C.1    Fang, C.2    Benetton, S.3    Xu, G.F.4    Yeh, L.T.5
  • 39
    • 0033870265 scopus 로고    scopus 로고
    • Enzyme kinetics and inhibition of nimodipine metabolism in human liver microsomes
    • Liu XQ, Ren YL, Qian ZY, Wang GJ. (2000). Enzyme kinetics and inhibition of nimodipine metabolism in human liver microsomes. Acta Pharmacol Sin 21:690-694.
    • (2000) Acta Pharmacol Sin , vol.21 , pp. 690-694
    • Liu, X.Q.1    Ren, Y.L.2    Qian, Z.Y.3    Wang, G.J.4
  • 40
    • 0037336297 scopus 로고    scopus 로고
    • Metabolism and metabolic inhibition of cilnidipine in human liver microsomes
    • Liu XQ, Zhao Y, Li D, Qian ZY, Wang GJ. (2003). Metabolism and metabolic inhibition of cilnidipine in human liver microsomes. Acta Pharmacol Sin 24:263-268.
    • (2003) Acta Pharmacol Sin , vol.24 , pp. 263-268
    • Liu, X.Q.1    Zhao, Y.2    Li, D.3    Qian, Z.Y.4    Wang, G.J.5
  • 41
    • 0029937721 scopus 로고    scopus 로고
    • Hepatic biotransformation of docetaxel (Taxotere) in vitro: Involvement of the CYP3A subfamily in humans
    • Marre F, Sanderink GJ, de Sousa G, Gaillard C, Martinet M, Rahmani R. (1996). Hepatic biotransformation of docetaxel (Taxotere) in vitro: involvement of the CYP3A subfamily in humans. Cancer Res 56:1296-1302.
    • (1996) Cancer Res , vol.56 , pp. 1296-1302
    • Marre, F.1    Sanderink, G.J.2    De Sousa, G.3    Gaillard, C.4    Martinet, M.5    Rahmani, R.6
  • 42
    • 0037048285 scopus 로고    scopus 로고
    • Expression of paclitaxel-inactivating CYP3A activity in human colorectal cancer: Implications for drug therapy
    • Martínez C, García-Martín E, Pizarro RM, García-Gamito FJ, Agúndez JA. (2002). Expression of paclitaxel-inactivating CYP3A activity in human colorectal cancer: implications for drug therapy. Br J Cancer 87:681-686.
    • (2002) Br J Cancer , vol.87 , pp. 681-686
    • Martínez, C.1    García-Martín, E.2    Pizarro, R.M.3    García-Gamito, F.J.4    Agúndez, J.A.5
  • 43
    • 0026595179 scopus 로고
    • Efects of imidazole derivatives on cytochromes P450 from human hepatocytes in primary culture
    • Maurice M, Pichard L, Daujat M, Fabre I, Joyeux H, Domergue J, Maurel P. (1992). Efects of imidazole derivatives on cytochromes P450 from human hepatocytes in primary culture. FASEB J 6:752-758.
    • (1992) FASEB J , vol.6 , pp. 752-758
    • Maurice, M.1    Pichard, L.2    Daujat, M.3    Fabre, I.4    Joyeux, H.5    Domergue, J.6    Maurel, P.7
  • 44
    • 0032947029 scopus 로고    scopus 로고
    • In vitro metabolism of quinidine: The (3S)-3-hydroxylation of quinidine is a specifc marker reaction for cytochrome P-4503A4 activity in human liver microsomes
    • Nielsen TL, Rasmussen BB, Flinois JP, Beaune P, Brosen K. (1999). In vitro metabolism of quinidine: the (3S)-3-hydroxylation of quinidine is a specifc marker reaction for cytochrome P-4503A4 activity in human liver microsomes. J Pharmacol Exp Ter 289:31-37.
    • (1999) J Pharmacol Exp ter , vol.289 , pp. 31-37
    • Nielsen, T.L.1    Rasmussen, B.B.2    Flinois, J.P.3    Beaune, P.4    Brosen, K.5
  • 45
    • 38849106780 scopus 로고    scopus 로고
    • Comparison of kinetic parameters for drug oxidation rates and substrate inhibition potential mediated by cytochrome P450 3A4 and 3A5
    • Niwa T, Murayama N, Emoto C, Yamazaki H. (2008). Comparison of kinetic parameters for drug oxidation rates and substrate inhibition potential mediated by cytochrome P450 3A4 and 3A5. Curr Drug Metab 9:20-33.
    • (2008) Curr Drug Metab , vol.9 , pp. 20-33
    • Niwa, T.1    Murayama, N.2    Emoto, C.3    Yamazaki, H.4
  • 46
    • 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 JB, 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 Ter 78:582-592.
    • (2005) Clin Pharmacol ter , vol.78 , pp. 582-592
    • Obach, R.S.1    Walsky, R.L.2    Venkatakrishnan, K.3    Houston, J.B.4    Tremaine, L.M.5
  • 47
    • 0031423883 scopus 로고    scopus 로고
    • Ketoconazole and fuconazole inhibition of the metabolism of cyclosporin A by human liver in vitro
    • Omar G, Whiting PH, Hawksworth GM, Humphrey MJ, Burke MD. (1997). Ketoconazole and fuconazole inhibition of the metabolism of cyclosporin A by human liver in vitro. Ter Drug Monit 19:436-445.
    • (1997) Ter Drug Monit , vol.19 , pp. 436-445
    • Omar, G.1    Whiting, P.H.2    Hawksworth, G.M.3    Humphrey, M.J.4    Burke, M.D.5
  • 48
    • 0030716846 scopus 로고    scopus 로고
    • Characterization of the cytochrome P450 isoenzymes involved in the in vitro N-dealkylation of haloperidol
    • Pan L P, Wijnant P, De Vriendt C, Rosseel MT, Belpaire FM. (1997). Characterization of the cytochrome P450 isoenzymes involved in the in vitro N-dealkylation of haloperidol. Br J Clin Pharmacol 44:557-564.
    • (1997) Br J Clin Pharmacol , vol.44 , pp. 557-564
    • Pan, L.P.1    Wijnant, P.2    De Vriendt, C.3    Rosseel, M.T.4    Belpaire, F.M.5
  • 49
    • 0037974573 scopus 로고    scopus 로고
    • In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes p450: Role of cyp3a4 and cyp3a5
    • Patki KC, Von Moltke LL, Greenblatt DJ. (2003). In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes p450: role of cyp3a4 and cyp3a5. Drug Metab Dispos 31:938-944.
    • (2003) Drug Metab Dispos , vol.31 , pp. 938-944
    • Patki, K.C.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 51
    • 0033979574 scopus 로고    scopus 로고
    • Midazolam and triazolam biotransfor-mation in mouse and human liver microsomes: Relative contribution of CYP3A and CYP2C isoforms
    • Perlof MD, von Moltke LL, Court MH, Kotegawa T, Shader RI, Greenblatt DJ. (2000). Midazolam and triazolam biotransfor-mation in mouse and human liver microsomes: relative contribution of CYP3A and CYP2C isoforms. J Pharmacol Exp Ter 292:618-628.
    • (2000) J Pharmacol Exp ter , vol.292 , pp. 618-628
    • Perlof, M.D.1    Von Moltke, L.L.2    Court, M.H.3    Kotegawa, T.4    Shader, R.I.5    Greenblatt, D.J.6
  • 52
    • 0025134337 scopus 로고
    • Cyclosporin A drug interactions. Screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A oxidase) in primary cultures of human hepatocytes and in liver microsomes
    • Pichard L, Fabre I, Fabre G, Domergue J, Saint Aubert B, Mourad G, Maurel P. (1990). Cyclosporin A drug interactions. Screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A oxidase) in primary cultures of human hepatocytes and in liver microsomes. Drug Metab Dispos 18:595-606.
    • (1990) Drug Metab Dispos , vol.18 , pp. 595-606
    • Pichard, L.1    Fabre, I.2    Fabre, G.3    Domergue, J.4    Saint Aubert, B.5    Mourad, G.6    Maurel, P.7
  • 53
    • 0030812885 scopus 로고    scopus 로고
    • In vitro metabolism of simvastatin in humans [SBT]identifcation of metabolizing enzymes and efect of the drug on hepatic P450s
    • Prueksaritanont T, Gorham LM, Ma B, Liu L, Yu X, Zhao JJ, Slaughter DE, Arison BH, Vyas KP. (1997). In vitro metabolism of simvastatin in humans [SBT]identifcation of metabolizing enzymes and efect of the drug on hepatic P450s. Drug Metab Dispos 25:1191-1199.
    • (1997) Drug Metab Dispos , vol.25 , pp. 1191-1199
    • Prueksaritanont, T.1    Gorham, L.M.2    Ma, B.3    Liu, L.4    Yu, X.5    Zhao, J.J.6    De, S.7    Arison, B.H.8    Kp, V.9
  • 54
    • 1542649526 scopus 로고    scopus 로고
    • Studies on the interactions between drug and estrogen. II. on the inhibitory efect of 29 drugs reported to induce gyneco-mastia on the oxidation of estradiol at C-2 or C-17
    • Satoh T, Munakata H, Fujita K, Itoh S, Itoh S, Kamataki T, Yoshizawa I. (2003). Studies on the interactions between drug and estrogen. II. On the inhibitory efect of 29 drugs reported to induce gyneco-mastia on the oxidation of estradiol at C-2 or C-17. Biol Pharm Bull 26:695-700.
    • (2003) Biol Pharm Bull , vol.26 , pp. 695-700
    • Satoh, T.1    Munakata, H.2    Fujita, K.3    Itoh, S.4    Itoh, S.5    Kamataki, T.6    Yoshizawa, I.7
  • 55
    • 73349103803 scopus 로고    scopus 로고
    • Prediction of drug-drug interactions based on time-dependent inhibition from high throughput screening of cytochrome P450 3A4 inhibition
    • Sekiguchi N, Higashida A, Kato M, Nabuchi Y, Mitsui T, Takanashi K, Aso Y, Ishigai M. (2009). Prediction of drug-drug interactions based on time-dependent inhibition from high throughput screening of cytochrome P450 3A4 inhibition. Drug Metab Pharmacokinet 24:500-510.
    • (2009) Drug Metab Pharmacokinet , vol.24 , pp. 500-510
    • Sekiguchi, N.1    Higashida, A.2    Kato, M.3    Nabuchi, Y.4    Mitsui, T.5    Takanashi, K.6    Aso, Y.7    Ishigai, M.8
  • 56
    • 0030762312 scopus 로고    scopus 로고
    • Identifcation of human cytochrome P450 isoforms involved in the metabolism of brotizolam
    • Senda C, Kishimoto W, Sakai K, Nagakura A, Igarashi T. (1997). Identifcation of human cytochrome P450 isoforms involved in the metabolism of brotizolam. Xenobiotica 27:913-922.
    • (1997) Xenobiotica , vol.27 , pp. 913-922
    • Senda, C.1    Kishimoto, W.2    Sakai, K.3    Nagakura, A.4    Igarashi, T.5
  • 57
    • 33646814927 scopus 로고    scopus 로고
    • Comparative analysis of substrate and inhibitor interactions with CYP3A4 and CYP3A5
    • Soars MG, Grime K, Riley RJ. (2006). Comparative analysis of substrate and inhibitor interactions with CYP3A4 and CYP3A5. Xenobiotica 36:287-299.
    • (2006) Xenobiotica , vol.36 , pp. 287-299
    • Soars, M.G.1    Grime, K.2    Riley, R.J.3
  • 59
    • 0031748173 scopus 로고    scopus 로고
    • In vitro and in vivo drug interactions involving human CYP3A
    • Tummel KE, Wilkinson GR. (1998). In vitro and in vivo drug interactions involving human CYP3A. Annu Rev Pharmacol Toxicol 38:389-430.
    • (1998) Annu Rev Pharmacol Toxicol , vol.38 , pp. 389-430
    • Tummel, K.E.1    Wilkinson, G.R.2
  • 61
    • 0034004083 scopus 로고    scopus 로고
    • Efects of the antifungal agents on oxidative drug metabolism: Clinical relevance
    • Venkatakrishnan K, von Moltke LL, Greenblatt DJ. (2000). Efects of the antifungal agents on oxidative drug metabolism: clinical relevance. Clin Pharmacokinet 38:111-180.
    • (2000) Clin Pharmacokinet , vol.38 , pp. 111-180
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 62
    • 0034770465 scopus 로고    scopus 로고
    • Human drug metabolism and the cytochromes P450: Application and relevance of in vitro models
    • Venkatakrishnan K, von Moltke LL, Greenblatt DJ. (2001). Human drug metabolism and the cytochromes P450: application and relevance of in vitro models. J Clin Pharmacol 41:1149-1179.
    • (2001) J Clin Pharmacol , vol.41 , pp. 1149-1179
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 63
    • 0142010701 scopus 로고    scopus 로고
    • Drug metabolism and drug interactions: Application and clinical value of in vitro models
    • Venkatakrishnan K, von Moltke LL, Obach RS, Greenblatt DJ. (2003). Drug metabolism and drug interactions: application and clinical value of in vitro models. Curr Drug Metab 4:423-459.
    • (2003) Curr Drug Metab , vol.4 , pp. 423-459
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Obach, R.S.3    Greenblatt, D.J.4
  • 65
    • 0033948964 scopus 로고    scopus 로고
    • Potent mechanism-based inhibition of human CYP3A in vitro by ampre-navir and ritonavir: Comparison with ketoconazole
    • Von Moltke LL, Durol AL, Duan SX, Greenblatt DJ. (2000). Potent mechanism-based inhibition of human CYP3A in vitro by ampre-navir and ritonavir: comparison with ketoconazole. Eur J Clin Pharmacol 56:259-261.
    • (2000) Eur J Clin Pharmacol , vol.56 , pp. 259-261
    • Von Moltke, L.L.1    Durol, A.L.2    Duan, S.X.3    Greenblatt, D.J.4
  • 66
    • 0028279667 scopus 로고
    • Inhibitors of alprazolam metabolism in vitro: Efect of serotonin-reuptake-inhibitor antidepressants, ketoconazole and quinidine
    • Von Moltke LL, Greenblatt DJ, Cotreau-Bibbo MM, Harmatz JS, Shader RI. (1994a). Inhibitors of alprazolam metabolism in vitro: efect of serotonin-reuptake-inhibitor antidepressants, ketoconazole and quinidine. Br J Clin Pharmacol 38:23-31.
    • (1994) Br J Clin Pharmacol , vol.38 , pp. 23-31
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Cotreau-Bibbo, M.M.3    Harmatz, J.S.4    Shader, R.I.5
  • 69
    • 0029743080 scopus 로고    scopus 로고
    • Midazolam hydroxylation by human liver microsomes in vitro: Inhibition by fuoxetine, nor-fuoxetine, and by azole antifungal agents
    • Von Moltke LL, Greenblatt DJ, Schmider J, Duan SX, Wright CE, Harmatz JS, Shader RI. (1996b). Midazolam hydroxylation by human liver microsomes in vitro: inhibition by fuoxetine, nor-fuoxetine, and by azole antifungal agents. J Clin Pharmacol 36:783-791.
    • (1996) J Clin Pharmacol , vol.36 , pp. 783-791
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Schmider, J.3    Duan, S.X.4    Wright, C.E.5    Harmatz, J.S.6    Shader, R.I.7
  • 70
    • 0030009690 scopus 로고    scopus 로고
    • Inhibition of terfenadine metabolism in vitro by azole antifungal agents and by selective serotonin reuptake inhibitor antidepressants: Relation to pharmacokinetic interactions in vivo
    • Von Moltke LL, Greenblatt DJ, Duan SX, Harmatz JS, Wright CE, Shader RI. (1996c). Inhibition of terfenadine metabolism in vitro by azole antifungal agents and by selective serotonin reuptake inhibitor antidepressants: relation to pharmacokinetic interactions in vivo. J Clin Psychopharmacol 16:104-112.
    • J Clin Psychopharmacol , vol.16 , pp. 104-112
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Duan, S.X.3    Harmatz, J.S.4    Wright, C.E.5
  • 71
    • 0033863264 scopus 로고    scopus 로고
    • Mibefradil is a P-glycoprotein substrate and a potent inhibitor of both P-glycoprotein and CYP3A in vitro
    • Wandel C, Kim RB, Guengerich FP, Wood AJ. (2000). Mibefradil is a P-glycoprotein substrate and a potent inhibitor of both P-glycoprotein and CYP3A in vitro. Drug Metab Dispos 28:895-898.
    • (2000) Drug Metab Dispos , vol.28 , pp. 895-898
    • Wandel, C.1    Kim, R.B.2    Guengerich, F.P.3    Wood, A.J.4
  • 72
    • 0032859247 scopus 로고    scopus 로고
    • Midazolam alpha-hydroxylation by human liver micro-somes in vitro: Inhibition by calcium channel blockers, itracona-zole and ketoconazole
    • Wang JS, Wen X, Backman JT, Taavitsainen P, Neuvonen PJ, Kivistö KT. (1999). Midazolam alpha-hydroxylation by human liver micro-somes in vitro: inhibition by calcium channel blockers, itracona-zole and ketoconazole. Pharmacol Toxicol 85:157-161.
    • (1999) Pharmacol Toxicol , vol.85 , pp. 157-161
    • Wang, J.S.1    Wen, X.2    Backman, J.T.3    Taavitsainen, P.4    Neuvonen, P.J.5    Kivistö, K.T.6
  • 73
    • 4444366342 scopus 로고    scopus 로고
    • Characterization of human cytochrome P450 enzymes catalyzing domperidone N-dealkylation and hydroxylation in vitro
    • Ward BA, Morocho A, Kandil A, Galinsky RE, Flockhart DA, Desta Z. (2004). Characterization of human cytochrome P450 enzymes catalyzing domperidone N-dealkylation and hydroxylation in vitro. Br J Clin Pharmacol 58:277-287.
    • (2004) Br J Clin Pharmacol , vol.58 , pp. 277-287
    • Ward, B.A.1    Morocho, A.2    Kandil, A.3    Galinsky, R.E.4    Flockhart, D.A.5    Desta, Z.6
  • 75
    • 0028361593 scopus 로고
    • Inhibition of human CYP3A catalyzed 1'-hydroxy midazolam formation by ketoconazole, nifed-ipine, erythromycin, cimetidine, and nizatidine
    • Wrighton SA, Ring BJ. (1994). Inhibition of human CYP3A catalyzed 1'-hydroxy midazolam formation by ketoconazole, nifed-ipine, erythromycin, cimetidine, and nizatidine. Pharm Res 11:921-924.
    • (1994) Pharm Res , vol.11 , pp. 921-924
    • Wrighton, S.A.1    Ring, B.J.2
  • 76
    • 0034177465 scopus 로고    scopus 로고
    • In vitro metabolism of trazodone by CYP3A: Inhibition by ketoconazole and human immunodefciency viral protease inhibitors
    • Zalma A, von Moltke LL, Granda BW, Harmatz JS, Shader RI, Greenblatt DJ. (2000). In vitro metabolism of trazodone by CYP3A: inhibition by ketoconazole and human immunodefciency viral protease inhibitors. Biol Psychiatry 47:655-661.
    • (2000) Biol Psychiatry , vol.47 , pp. 655-661
    • Zalma, A.1    Von Moltke, L.L.2    Granda, B.W.3    Harmatz, J.S.4    Shader, R.I.5    Greenblatt, D.J.6
  • 77
    • 0033392753 scopus 로고    scopus 로고
    • A further interaction study of quinine with clinically important drugs by human liver microsomes: Determinations of inhibition constant (Ki) and type of inhibition
    • Zhao XJ, Ishizaki T. (1999). A further interaction study of quinine with clinically important drugs by human liver microsomes: determinations of inhibition constant (Ki) and type of inhibition. Eur J Drug Metab Pharmacokinet 24:272-278.
    • (1999) Eur J Drug Metab Pharmacokinet , vol.24 , pp. 272-278
    • Zhao, X.J.1    Ishizaki, T.2
  • 78
    • 45249121177 scopus 로고    scopus 로고
    • Drugs behave as substrates, inhibitors and inducers of human cytochrome P450 3A4
    • Zhou SF. (2008). Drugs behave as substrates, inhibitors and inducers of human cytochrome P450 3A4. Curr Drug Metab 9:310-322.
    • (2008) Curr Drug Metab , vol.9 , pp. 310-322
    • Zhou, S.F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.