-
1
-
-
0033856082
-
Stereoselective metabolism of omeprazole by human cytochrome P450 enzymes
-
Abelo, A., T. B. Andersson, M. Antonsson, A. K. Naudot, I. Skanberg, and L. Weidolf. 2000. Stereoselective metabolism of omeprazole by human cytochrome P450 enzymes. Drug Metab. Dispos. 28:966-972.
-
(2000)
Drug Metab. Dispos
, vol.28
, pp. 966-972
-
-
Abelo, A.1
Andersson, T.B.2
Antonsson, M.3
Naudot, A.K.4
Skanberg, I.5
Weidolf, L.6
-
2
-
-
0029977698
-
Pharmacokinetics, metabolism and interactions of acid pump inhibitors. Focus on omeprazole, lansoprazole and pantoprazole
-
Andersson, T. 1996. Pharmacokinetics, metabolism and interactions of acid pump inhibitors. Focus on omeprazole, lansoprazole and pantoprazole. Clin. Pharmacokinet. 31:9-28.
-
(1996)
Clin. Pharmacokinet
, vol.31
, pp. 9-28
-
-
Andersson, T.1
-
3
-
-
0030935086
-
Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions
-
Bertz, R. J., and G. R. Granneman. 1997. Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin. Pharmacokinet. 32:210-258.
-
(1997)
Clin. Pharmacokinet
, vol.32
, pp. 210-258
-
-
Bertz, R.J.1
Granneman, G.R.2
-
4
-
-
0030430033
-
Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes
-
Bourrie, M., V. Meunier, Y. Berger, and G. Fabre. 1996. Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes. J. Pharmacol. Exp. Ther. 277:321-332.
-
(1996)
J. Pharmacol. Exp. Ther
, vol.277
, pp. 321-332
-
-
Bourrie, M.1
Meunier, V.2
Berger, Y.3
Fabre, G.4
-
5
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:248-254.
-
(1976)
Anal. Biochem
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
6
-
-
0024359553
-
Effect of quinidine on the dextromethorphan O-demethylase activity of microsomal fractions from human liver
-
Broly, F., C. Libersa, M. Lhermitte, P. Bechtel, and B. Dupuis. 1989. Effect of quinidine on the dextromethorphan O-demethylase activity of microsomal fractions from human liver. Br. J. Clin. Pharmacol. 28:29-36.
-
(1989)
Br. J. Clin. Pharmacol
, vol.28
, pp. 29-36
-
-
Broly, F.1
Libersa, C.2
Lhermitte, M.3
Bechtel, P.4
Dupuis, B.5
-
7
-
-
18844433876
-
The naturally occurring cytochrome P450 (P450) 2B6 K262R mutant of P450 2B6 exhibits alterations in substrate metabolism and inactivation
-
Bumpus, N. N., C. Sridar, U. M. Kent, and P. F. Hollenberg. 2005. The naturally occurring cytochrome P450 (P450) 2B6 K262R mutant of P450 2B6 exhibits alterations in substrate metabolism and inactivation. Drug Metab. Dispos. 33:795-802.
-
(2005)
Drug Metab. Dispos
, vol.33
, pp. 795-802
-
-
Bumpus, N.N.1
Sridar, C.2
Kent, U.M.3
Hollenberg, P.F.4
-
8
-
-
0031808548
-
Identification and characterization of human cytochrome P450 isoforms interacting with pimozide
-
Desta, Z., T. Kerbusch, N. Soukhova, E. Richard, J. W. Ko, and D. A. Flockhart. 1998. Identification and characterization of human cytochrome P450 isoforms interacting with pimozide. J. Pharmacol. Exp. Ther. 285:428-437.
-
(1998)
J. Pharmacol. Exp. Ther
, vol.285
, pp. 428-437
-
-
Desta, Z.1
Kerbusch, T.2
Soukhova, N.3
Richard, E.4
Ko, J.W.5
Flockhart, D.A.6
-
9
-
-
34250764311
-
Impact of CYP2B6 polymorphism on hepatic efavirenz metabolism in vitro
-
Desta, Z., T. Saussele, B. Ward, J. Blievernicht, L. Li, K. Klein, D. A. Flockhart, and U. M. Zanger. 2007. Impact of CYP2B6 polymorphism on hepatic efavirenz metabolism in vitro. Pharmacogenomics 8:547-558.
-
(2007)
Pharmacogenomics
, vol.8
, pp. 547-558
-
-
Desta, Z.1
Saussele, T.2
Ward, B.3
Blievernicht, J.4
Li, L.5
Klein, K.6
Flockhart, D.A.7
Zanger, U.M.8
-
10
-
-
0035144768
-
Inhibition of cytochrome P450 (CYP450) isoforms by isoniazid: Potent inhibition of CYP2C19 and CYP3A
-
Desta, Z., N. V. Soukhova, and D. A. Flockhart. 2001. Inhibition of cytochrome P450 (CYP450) isoforms by isoniazid: potent inhibition of CYP2C19 and CYP3A. Antimicrob. Agents Chemother. 45:382-392.
-
(2001)
Antimicrob. Agents Chemother
, vol.45
, pp. 382-392
-
-
Desta, Z.1
Soukhova, N.V.2
Flockhart, D.A.3
-
11
-
-
0036394942
-
Clinical significance of the cytochrome P450 2C19 genetic polymorphism
-
Desta, Z., X. Zhao, J. G. Shin, and D. A. Flockhart. 2002. Clinical significance of the cytochrome P450 2C19 genetic polymorphism. Clin. Pharmacokinet. 41:913-958.
-
(2002)
Clin. Pharmacokinet
, vol.41
, pp. 913-958
-
-
Desta, Z.1
Zhao, X.2
Shin, J.G.3
Flockhart, D.A.4
-
12
-
-
27844502515
-
Safety and pharmacokinetics of coadministered voriconazole and anidulafungin
-
Dowell, J. A., J. Schranz, A. Baruch, and G. Foster. 2005. Safety and pharmacokinetics of coadministered voriconazole and anidulafungin. J. Clin. Pharmacol. 45:1373-1382.
-
(2005)
J. Clin. Pharmacol
, vol.45
, pp. 1373-1382
-
-
Dowell, J.A.1
Schranz, J.2
Baruch, A.3
Foster, G.4
-
13
-
-
0031149716
-
Inhibition of coumarin 7-hydroxylase activity in human liver microsomes
-
Draper, A. J., A. Madan, and A. Parkinson. 1997. Inhibition of coumarin 7-hydroxylase activity in human liver microsomes. Arch. Biochem. Biophys. 341:47-61.
-
(1997)
Arch. Biochem. Biophys
, vol.341
, pp. 47-61
-
-
Draper, A.J.1
Madan, A.2
Parkinson, A.3
-
14
-
-
0036439851
-
Interindividual variability of the clinical pharmacokinetics of methadone: Implications for the treatment of opioid dependence
-
Eap, C. B., T. Buclin, and P. Baumann. 2002. Interindividual variability of the clinical pharmacokinetics of methadone: implications for the treatment of opioid dependence. Clin. Pharmacokinet. 41:1153-1193.
-
(2002)
Clin. Pharmacokinet
, vol.41
, pp. 1153-1193
-
-
Eap, C.B.1
Buclin, T.2
Baumann, P.3
-
15
-
-
0033810079
-
Validation of bupropion hydroxylation as a selective marker of human cytochrome P450 2B6 catalytic activity
-
Faucette, S. R., R. L. Hawke, E. L. Lecluyse, S. S. Shord, B. Yan, R. M. Laethem, and C. M. Lindley. 2000. Validation of bupropion hydroxylation as a selective marker of human cytochrome P450 2B6 catalytic activity. Drug Metab. Dispos. 28:1222-1230.
-
(2000)
Drug Metab. Dispos
, vol.28
, pp. 1222-1230
-
-
Faucette, S.R.1
Hawke, R.L.2
Lecluyse, E.L.3
Shord, S.S.4
Yan, B.5
Laethem, R.M.6
Lindley, C.M.7
-
16
-
-
85085225411
-
-
Briefing document for Voriconazole. 4 October, FDA, Rockville, MD
-
FDA Antiviral Drugs Advisory Committee. 2001. Briefing document for Voriconazole. 4 October 2001. FDA, Rockville, MD.
-
(2001)
FDA Antiviral Drugs Advisory Committee. 2001
-
-
-
18
-
-
0028234586
-
Regioselective biotransformation of midazolam by members of the human cytochrome P450 3A (CYP3A) subfamily
-
Gorski, J. C., S. D. Hall, D. R. Jones, M. Vandenbranden, and S. A. Wrighton. 1994. Regioselective biotransformation of midazolam by members of the human cytochrome P450 3A (CYP3A) subfamily. Biochem. Pharmacol. 47:1643-1653.
-
(1994)
Biochem. Pharmacol
, vol.47
, pp. 1643-1653
-
-
Gorski, J.C.1
Hall, S.D.2
Jones, D.R.3
Vandenbranden, M.4
Wrighton, S.A.5
-
19
-
-
0042833213
-
The effect of age, sex, and rifampin administration on intestinal and hepatic cytochrome P450 3A activity
-
Gorski, J. C., S. Vannaprasaht, M. A. Hamman, W. T. Ambrosius, M. A. Bruce, B. Haehner-Daniels, and S. D. Hall. 2003. The effect of age, sex, and rifampin administration on intestinal and hepatic cytochrome P450 3A activity. Clin. Pharmacol. Ther. 74:275-287.
-
(2003)
Clin. Pharmacol. Ther
, vol.74
, pp. 275-287
-
-
Gorski, J.C.1
Vannaprasaht, S.2
Hamman, M.A.3
Ambrosius, W.T.4
Bruce, M.A.5
Haehner-Daniels, B.6
Hall, S.D.7
-
20
-
-
0017847465
-
An improved assay of 7-ethoxycoumarin O-deethylase activity: Induction of hepatic enzyme activity in C57BL/6J and DBA/2J mice by phenobarbital, 3-methylcholanthrene and 2,3,7,8-tetrachlorodibenzo-p-dioxin
-
Greenlee, W. F., and A. Poland. 1978. An improved assay of 7-ethoxycoumarin O-deethylase activity: induction of hepatic enzyme activity in C57BL/6J and DBA/2J mice by phenobarbital, 3-methylcholanthrene and 2,3,7,8-tetrachlorodibenzo-p-dioxin. J. Pharmacol. Exp. Ther. 205:596-605.
-
(1978)
J. Pharmacol. Exp. Ther
, vol.205
, pp. 596-605
-
-
Greenlee, W.F.1
Poland, A.2
-
21
-
-
19944428456
-
Pharmacogenetics of efavirenz and central nervous system side effects: An Adult AIDS Clinical Trials Group study
-
Haas, D. W., H. J. Ribaudo, R. B. Kim, C. Tierney, G. R. Wilkinson, R. M. Gulick, D. B. Clifford, T. Hulgan, C. Marzolini, and E. P. Acosta. 2004. Pharmacogenetics of efavirenz and central nervous system side effects: an Adult AIDS Clinical Trials Group study. AIDS 18:2391-2400.
-
(2004)
AIDS
, vol.18
, pp. 2391-2400
-
-
Haas, D.W.1
Ribaudo, H.J.2
Kim, R.B.3
Tierney, C.4
Wilkinson, G.R.5
Gulick, R.M.6
Clifford, D.B.7
Hulgan, T.8
Marzolini, C.9
Acosta, E.P.10
-
22
-
-
85085226149
-
-
Hagelberg, N. M., T. H. Nieminen, T. I. Saari, M. Neuvonen, P. J. Neuvonen, K. Laine, and K. T. Olkkola. 3 October 2008. Voriconazole drastically increases exposure to oral oxycodone. Eur. J. Clin. Pharmacol. [Epub ahead of print.]
-
Hagelberg, N. M., T. H. Nieminen, T. I. Saari, M. Neuvonen, P. J. Neuvonen, K. Laine, and K. T. Olkkola. 3 October 2008. Voriconazole drastically increases exposure to oral oxycodone. Eur. J. Clin. Pharmacol. [Epub ahead of print.]
-
-
-
-
23
-
-
33749339075
-
Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects
-
Hulot, J. S., A. Bura, E. Villard, M. Azizi, V. Remones, C. Goyenvalle, M. Aiach, P. Lechat, and P. Gaussem. 2006. Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects. Blood 108:2244-2247.
-
(2006)
Blood
, vol.108
, pp. 2244-2247
-
-
Hulot, J.S.1
Bura, A.2
Villard, E.3
Azizi, M.4
Remones, V.5
Goyenvalle, C.6
Aiach, M.7
Lechat, P.8
Gaussem, P.9
-
24
-
-
0037403687
-
Identification of the cytochrome P450 enzymes involved in the N-oxidation of voriconazole
-
Hyland, R., B. C. Jones, and D. A. Smith. 2003. Identification of the cytochrome P450 enzymes involved in the N-oxidation of voriconazole. Drug Metab. Dispos. 31:540-547.
-
(2003)
Drug Metab. Dispos
, vol.31
, pp. 540-547
-
-
Hyland, R.1
Jones, B.C.2
Smith, D.A.3
-
25
-
-
38349116038
-
Effect of terbinafine and voriconazole on the pharmacokinetics of the antidepressant venlafaxine
-
Hynninen, V. V., K. T. Olkkola, L. Bertilsson, K. Kurkinen, P. J. Neuvonen, and K. Laine. 2008. Effect of terbinafine and voriconazole on the pharmacokinetics of the antidepressant venlafaxine. Clin. Pharmacol. Ther. 83:342-348.
-
(2008)
Clin. Pharmacol. Ther
, vol.83
, pp. 342-348
-
-
Hynninen, V.V.1
Olkkola, K.T.2
Bertilsson, L.3
Kurkinen, K.4
Neuvonen, P.J.5
Laine, K.6
-
26
-
-
36348940960
-
Effect of voriconazole on the pharmacokinetics of diclofenac
-
Hynninen, V. V., K. T. Olkkola, K. Leino, S. Lundgren, P. J. Neuvonen, A. Rane, M. Valtonen, and K. Laine. 2007. Effect of voriconazole on the pharmacokinetics of diclofenac. Fundam. Clin. Pharmacol. 21:651-656.
-
(2007)
Fundam. Clin. Pharmacol
, vol.21
, pp. 651-656
-
-
Hynninen, V.V.1
Olkkola, K.T.2
Leino, K.3
Lundgren, S.4
Neuvonen, P.J.5
Rane, A.6
Valtonen, M.7
Laine, K.8
-
27
-
-
33744500482
-
Effects of the antifungals voriconazole and fluconazole on the pharmacokinetics of S-(+)-and R-(-)-ibuprofen
-
Hynninen, V. V., K. T. Olkkola, K. Leino, S. Lundgren, P. J. Neuvonen, A. Rane, M. Valtonen, H. Vyyrylainen, and K. Laine. 2006. Effects of the antifungals voriconazole and fluconazole on the pharmacokinetics of S-(+)-and R-(-)-ibuprofen. Antimicrob. Agents Chemother. 50:1967-1972.
-
(2006)
Antimicrob. Agents Chemother
, vol.50
, pp. 1967-1972
-
-
Hynninen, V.V.1
Olkkola, K.T.2
Leino, K.3
Lundgren, S.4
Neuvonen, P.J.5
Rane, A.6
Valtonen, M.7
Vyyrylainen, H.8
Laine, K.9
-
28
-
-
85085220536
-
-
Hynninen, V. V., K. T. Olkkola, P. J. Neuvonen, and K. Laine. 9 September 2008. Oral voriconazole and miconazole oral gel produce comparable effects on the pharmacokinetics and pharmacodynamics of etoricoxib. Eur. J. Clin. Pharmacol. [Epub ahead of print.]
-
Hynninen, V. V., K. T. Olkkola, P. J. Neuvonen, and K. Laine. 9 September 2008. Oral voriconazole and miconazole oral gel produce comparable effects on the pharmacokinetics and pharmacodynamics of etoricoxib. Eur. J. Clin. Pharmacol. [Epub ahead of print.]
-
-
-
-
29
-
-
0032735988
-
CYP3A4 drug interactions: Correlation of 10 in vitro probe substrates
-
Kenworthy, K. E., J. C. Bloomer, S. E. Clarke, and J. B. Houston. 1999. CYP3A4 drug interactions: correlation of 10 in vitro probe substrates. Br. J. Clin. Pharmacol. 48:716-727.
-
(1999)
Br. J. Clin. Pharmacol
, vol.48
, pp. 716-727
-
-
Kenworthy, K.E.1
Bloomer, J.C.2
Clarke, S.E.3
Houston, J.B.4
-
30
-
-
11844304376
-
Clinical consequences of cytochrome P450 2C9 polymorphisms
-
Kirchheiner, J., and J. Brockmoller. 2005. Clinical consequences of cytochrome P450 2C9 polymorphisms. Clin. Pharmacol. Ther. 77:1-16.
-
(2005)
Clin. Pharmacol. Ther
, vol.77
, pp. 1-16
-
-
Kirchheiner, J.1
Brockmoller, J.2
-
31
-
-
0034128040
-
In vitro inhibition of the cytochrome P450 (CYP450) system by the antiplatelet drug ticlopidine: Potent effect on CYP2C19 and CYP2D6
-
Ko, J. W., Z. Desta, N. V. Soukhova, T. Tracy, and D. A. Flockhart. 2000. In vitro inhibition of the cytochrome P450 (CYP450) system by the antiplatelet drug ticlopidine: potent effect on CYP2C19 and CYP2D6. Br. J. Clin. Pharmacol. 49:343-351.
-
(2000)
Br. J. Clin. Pharmacol
, vol.49
, pp. 343-351
-
-
Ko, J.W.1
Desta, Z.2
Soukhova, N.V.3
Tracy, T.4
Flockhart, D.A.5
-
32
-
-
0030811096
-
Evaluation of omeprazole and lansoprazole as inhibitors of cytochrome P450 isoforms
-
Ko, J. W., N. Sukhova, D. Thacker, P. Chen, and D. A. Flockhart. 1997. Evaluation of omeprazole and lansoprazole as inhibitors of cytochrome P450 isoforms. Drug Metab. Dispos. 25:853-862.
-
(1997)
Drug Metab. Dispos
, vol.25
, pp. 853-862
-
-
Ko, J.W.1
Sukhova, N.2
Thacker, D.3
Chen, P.4
Flockhart, D.A.5
-
33
-
-
0024373348
-
Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4
-
Kronbach, T., D. Mathys, M. Umeno, F. J. Gonzalez, and U. A. Meyer. 1989. Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4. Mol. Pharmacol. 36:89-96.
-
(1989)
Mol. Pharmacol
, vol.36
, pp. 89-96
-
-
Kronbach, T.1
Mathys, D.2
Umeno, M.3
Gonzalez, F.J.4
Meyer, U.A.5
-
34
-
-
0036154008
-
Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: A new high affinity and turnover enzyme-specific probe substrate
-
Li, X. Q., A. Bjorkman, T. B. Andersson, M. Ridderstrom, and C. M. Masimirembwa. 2002. Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: a new high affinity and turnover enzyme-specific probe substrate. J. Pharmacol. Exp. Ther. 300:399-407.
-
(2002)
J. Pharmacol. Exp. Ther
, vol.300
, pp. 399-407
-
-
Li, X.Q.1
Bjorkman, A.2
Andersson, T.B.3
Ridderstrom, M.4
Masimirembwa, C.M.5
-
35
-
-
36348965389
-
Polymorphisms of CYP2C19 gene are associated with the efficacy of thalidomide based regimens in multiple myeloma
-
Li, Y., J. Hou, H. Jiang, D. Wang, W. Fu, Z. Yuan, Y. Chen, and L. Zhou. 2007. Polymorphisms of CYP2C19 gene are associated with the efficacy of thalidomide based regimens in multiple myeloma. Haematologica 92:1246-1249.
-
(2007)
Haematologica
, vol.92
, pp. 1246-1249
-
-
Li, Y.1
Hou, J.2
Jiang, H.3
Wang, D.4
Fu, W.5
Yuan, Z.6
Chen, Y.7
Zhou, L.8
-
36
-
-
33845980611
-
Pharmacokinetic interaction between voriconazole and methadone at steady state in patients on methadone therapy
-
Liu, P., G. Foster, R. Labadie, E. Somoza, and A. Sharma. 2007. Pharmacokinetic interaction between voriconazole and methadone at steady state in patients on methadone therapy. Antimicrob. Agents Chemother. 51:110-118.
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 110-118
-
-
Liu, P.1
Foster, G.2
Labadie, R.3
Somoza, E.4
Sharma, A.5
-
37
-
-
37349046483
-
Pharmacokinetic interaction between voriconazole and efavirenz at steady state in healthy male subjects
-
Liu, P., G. Foster, R. R. LaBadie, M. J. Gutierrez, and A. Sharma. 2008. Pharmacokinetic interaction between voriconazole and efavirenz at steady state in healthy male subjects. J. Clin. Pharmacol. 48:73-84.
-
(2008)
J. Clin. Pharmacol
, vol.48
, pp. 73-84
-
-
Liu, P.1
Foster, G.2
LaBadie, R.R.3
Gutierrez, M.J.4
Sharma, A.5
-
38
-
-
0036335573
-
Hepatic but not intestinal CYP3A4 displays dose-dependent induction by efavirenz in humans
-
Mouly, S., K. S. Lown, D. Kornhauser, J. L. Joseph, W. D. Fiske, I. H. Benedek, and P. B. Watkins. 2002. Hepatic but not intestinal CYP3A4 displays dose-dependent induction by efavirenz in humans. Clin. Pharmacol. Ther. 72:1-9.
-
(2002)
Clin. Pharmacol. Ther
, vol.72
, pp. 1-9
-
-
Mouly, S.1
Lown, K.S.2
Kornhauser, D.3
Joseph, J.L.4
Fiske, W.D.5
Benedek, I.H.6
Watkins, P.B.7
-
39
-
-
0036957299
-
Voriconazole: In the treatment of invasive aspergillosis
-
Muijsers, R. B., K. L. Goa, and L. J. Scott. 2002. Voriconazole: in the treatment of invasive aspergillosis. Drugs 62:2655-2664.
-
(2002)
Drugs
, vol.62
, pp. 2655-2664
-
-
Muijsers, R.B.1
Goa, K.L.2
Scott, L.J.3
-
40
-
-
34247558084
-
Roles of CYP3A4 and CYP2C19 in methyl hydroxylated and N-oxidized metabolite formation from voriconazole, a new anti-fungal agent, in human liver microsomes
-
Murayama, N., N. Imai, T. Nakane, M. Shimizu, and H. Yamazaki. 2007. Roles of CYP3A4 and CYP2C19 in methyl hydroxylated and N-oxidized metabolite formation from voriconazole, a new anti-fungal agent, in human liver microsomes. Biochem. Pharmacol. 73:2020-2026.
-
(2007)
Biochem. Pharmacol
, vol.73
, pp. 2020-2026
-
-
Murayama, N.1
Imai, N.2
Nakane, T.3
Shimizu, M.4
Yamazaki, H.5
-
41
-
-
24944458055
-
Effect of antifungal drugs on cytochrome P450 (CYP) 1A2, CYP2D6, and CYP2E1 activities in human liver microsomes
-
Niwa, T., S. Inoue-Yamamoto, T. Shiraga, and A. Takagi. 2005. Effect of antifungal drugs on cytochrome P450 (CYP) 1A2, CYP2D6, and CYP2E1 activities in human liver microsomes. Biol. Pharm. Bull. 28:1813-1816.
-
(2005)
Biol. Pharm. Bull
, vol.28
, pp. 1813-1816
-
-
Niwa, T.1
Inoue-Yamamoto, S.2
Shiraga, T.3
Takagi, A.4
-
42
-
-
24944576037
-
Effect of antifungal drugs on cytochrome P450 (CYP) 2C9, CYP2C19, and CYP3A4 activities in human liver microsomes
-
Niwa, T., T. Shiraga, and A. Takagi. 2005. Effect of antifungal drugs on cytochrome P450 (CYP) 2C9, CYP2C19, and CYP3A4 activities in human liver microsomes. Biol. Pharm. Bull. 28:1805-1808.
-
(2005)
Biol. Pharm. Bull
, vol.28
, pp. 1805-1808
-
-
Niwa, T.1
Shiraga, T.2
Takagi, A.3
-
43
-
-
25844456585
-
Drug-drug interaction of antifungal drugs
-
In Japanese
-
Niwa, T., T. Shiraga, and A. Takagi. 2005. Drug-drug interaction of antifungal drugs. Yakugaku Zasshi 125:795-805. (In Japanese.)
-
(2005)
Yakugaku Zasshi
, vol.125
, pp. 795-805
-
-
Niwa, T.1
Shiraga, T.2
Takagi, A.3
-
44
-
-
34447569316
-
Amodiaquine metabolism is impaired by common polymorphisms in CYP2C8: Implications for malaria treatment in Africa
-
Parikh, S., J. B. Ouedraogo, J. A. Goldstein, P. J. Rosenthal, and D. L. Kroetz. 2007. Amodiaquine metabolism is impaired by common polymorphisms in CYP2C8: implications for malaria treatment in Africa. Clin. Pharmacol. Ther. 82:197-203.
-
(2007)
Clin. Pharmacol. Ther
, vol.82
, pp. 197-203
-
-
Parikh, S.1
Ouedraogo, J.B.2
Goldstein, J.A.3
Rosenthal, P.J.4
Kroetz, D.L.5
-
45
-
-
0026781890
-
Species differences and interindividual variation in liver microsomal cytochrome P450 2A enzymes: Effects on coumarin, dicumarol, and testosterone oxidation
-
Pearce, R., D. Greenway, and A. Parkinson. 1992. Species differences and interindividual variation in liver microsomal cytochrome P450 2A enzymes: effects on coumarin, dicumarol, and testosterone oxidation. Arch. Biochem. Biophys. 298:211-225.
-
(1992)
Arch. Biochem. Biophys
, vol.298
, pp. 211-225
-
-
Pearce, R.1
Greenway, D.2
Parkinson, A.3
-
46
-
-
0037371098
-
Voriconazole: A new triazole antifungal agent
-
Pearson, M. M., P. D. Rogers, J. D. Cleary, and S. W. Chapman. 2003. Voriconazole: a new triazole antifungal agent. Ann. Pharmacother. 37:420-432.
-
(2003)
Ann. Pharmacother
, vol.37
, pp. 420-432
-
-
Pearson, M.M.1
Rogers, P.D.2
Cleary, J.D.3
Chapman, S.W.4
-
48
-
-
0344943289
-
Coadministration of voriconazole and phenytoin: Pharmacokinetic interaction, safety, and toleration
-
Purkins, L., N. Wood, P. Ghahramani, E. R. Love, M. D. Eve, and A. Fielding. 2003. Coadministration of voriconazole and phenytoin: pharmacokinetic interaction, safety, and toleration. Br. J. Clin. Pharmacol. 56(Suppl. 1):37-44.
-
(2003)
Br. J. Clin. Pharmacol
, vol.56
, Issue.SUPPL. 1
, pp. 37-44
-
-
Purkins, L.1
Wood, N.2
Ghahramani, P.3
Love, E.R.4
Eve, M.D.5
Fielding, A.6
-
49
-
-
0344943294
-
Voriconazole potentiates warfarin-induced prothrombin time prolongation
-
Purkins, L., N. Wood, D. Kleinermans, and D. Nichols. 2003. Voriconazole potentiates warfarin-induced prothrombin time prolongation. Br. J. Clin. Pharmacol. 56(Suppl. 1):24-29.
-
(2003)
Br. J. Clin. Pharmacol
, vol.56
, Issue.SUPPL. 1
, pp. 24-29
-
-
Purkins, L.1
Wood, N.2
Kleinermans, D.3
Nichols, D.4
-
50
-
-
0025014594
-
Tolbutamide and mephenytoin hydroxylation by human cytochrome P450s in the CYP2C subfamily
-
Relling, M. V., T. Aoyama, F. J. Gonzalez, and U. A. Meyer. 1990. Tolbutamide and mephenytoin hydroxylation by human cytochrome P450s in the CYP2C subfamily. J. Pharmacol. Exp. Ther. 252:442-447.
-
(1990)
J. Pharmacol. Exp. Ther
, vol.252
, pp. 442-447
-
-
Relling, M.V.1
Aoyama, T.2
Gonzalez, F.J.3
Meyer, U.A.4
-
51
-
-
0037855889
-
-
Roffey, S. J., S. Cole, P. Comby, D. Gibson, S. G. Jezequel, A. N. Nedderman, D. A. Smith, D. K. Walker, and N. Wood. 2003. The disposition of voriconazole in mouse, rat, rabbit, guinea pig, dog, and human. Drug Metab. Dispos. 31:731-741.
-
Roffey, S. J., S. Cole, P. Comby, D. Gibson, S. G. Jezequel, A. N. Nedderman, D. A. Smith, D. K. Walker, and N. Wood. 2003. The disposition of voriconazole in mouse, rat, rabbit, guinea pig, dog, and human. Drug Metab. Dispos. 31:731-741.
-
-
-
-
52
-
-
34548590645
-
Voriconazole and fluconazole increase the exposure to oral diazepam
-
Saari, T. I., K. Laine, L. Bertilsson, P. J. Neuvonen, and K. T. Olkkola. 2007. Voriconazole and fluconazole increase the exposure to oral diazepam. Eur. J. Clin. Pharmacol. 63:941-949.
-
(2007)
Eur. J. Clin. Pharmacol
, vol.63
, pp. 941-949
-
-
Saari, T.I.1
Laine, K.2
Bertilsson, L.3
Neuvonen, P.J.4
Olkkola, K.T.5
-
53
-
-
33645847236
-
Effect of voriconazole on the pharmacokinetics and pharmacodynamics of intravenous and oral midazolam
-
Saari, T. I., K. Laine, K. Leino, M. Valtonen, P. J. Neuvonen, and K. T. Olkkola. 2006. Effect of voriconazole on the pharmacokinetics and pharmacodynamics of intravenous and oral midazolam. Clin. Pharmacol. Ther. 79: 362-370.
-
(2006)
Clin. Pharmacol. Ther
, vol.79
, pp. 362-370
-
-
Saari, T.I.1
Laine, K.2
Leino, K.3
Valtonen, M.4
Neuvonen, P.J.5
Olkkola, K.T.6
-
54
-
-
33751111707
-
Voriconazole, but not terbinafine, markedly reduces alfentanil clearance and prolongs its half-life
-
Saari, T. I., K. Laine, K. Leino, M. Valtonen, P. J. Neuvonen, and K. T. Olkkola. 2006. Voriconazole, but not terbinafine, markedly reduces alfentanil clearance and prolongs its half-life. Clin. Pharmacol. Ther. 80:502-508.
-
(2006)
Clin. Pharmacol. Ther
, vol.80
, pp. 502-508
-
-
Saari, T.I.1
Laine, K.2
Leino, K.3
Valtonen, M.4
Neuvonen, P.J.5
Olkkola, K.T.6
-
55
-
-
38049041555
-
Effect of voriconazole and fluconazole on the pharmacokinetics of intravenous fentanyl
-
Saari, T. I., K. Laine, M. Neuvonen, P. J. Neuvonen, and K. T. Olkkola. 2008. Effect of voriconazole and fluconazole on the pharmacokinetics of intravenous fentanyl. Eur. J. Clin. Pharmacol. 64:25-30.
-
(2008)
Eur. J. Clin. Pharmacol
, vol.64
, pp. 25-30
-
-
Saari, T.I.1
Laine, K.2
Neuvonen, M.3
Neuvonen, P.J.4
Olkkola, K.T.5
-
56
-
-
33847042702
-
Voriconazole: A review of its use in the management of invasive fungal infections
-
Scott, L. J., and D. Simpson. 2007. Voriconazole: a review of its use in the management of invasive fungal infections. Drugs 67:269-298.
-
(2007)
Drugs
, vol.67
, pp. 269-298
-
-
Scott, L.J.1
Simpson, D.2
-
57
-
-
3142760835
-
Cytochrome P450 pharmacogenetics as a predictor of toxicity and clinical response to pulse cyclophosphamide in lupus nephritis
-
Takada, K., M. Arefayene, Z. Desta, C. H. Yarboro, D. T. Boumpas, J. E. Balow, D. A. Flockhart, and G. G. Illei. 2004. Cytochrome P450 pharmacogenetics as a predictor of toxicity and clinical response to pulse cyclophosphamide in lupus nephritis. Arthritis Rheum. 50:2202-2210.
-
(2004)
Arthritis Rheum
, vol.50
, pp. 2202-2210
-
-
Takada, K.1
Arefayene, M.2
Desta, Z.3
Yarboro, C.H.4
Boumpas, D.T.5
Balow, J.E.6
Flockhart, D.A.7
Illei, G.G.8
-
58
-
-
0027364928
-
Specificity of substrate and inhibitor probes for human cytochromes P450 1A1 and 1A2
-
Tassaneeyakul, W., D. J. Birkett, M. E. Veronese, M. E. McManus, R. H. Tukey, L. C. Quattrochi, H. V. Gelboin, and J. O. Miners. 1993. Specificity of substrate and inhibitor probes for human cytochromes P450 1A1 and 1A2. J. Pharmacol. Exp. Ther. 265:401-407.
-
(1993)
J. Pharmacol. Exp. Ther
, vol.265
, pp. 401-407
-
-
Tassaneeyakul, W.1
Birkett, D.J.2
Veronese, M.E.3
McManus, M.E.4
Tukey, R.H.5
Quattrochi, L.C.6
Gelboin, H.V.7
Miners, J.O.8
-
59
-
-
33745632766
-
Pharmacokinetic/pharmacodynamic profile of voriconazole
-
Theuretzbacher, U., F. Ihle, and H. Derendorf. 2006. Pharmacokinetic/pharmacodynamic profile of voriconazole. Clin. Pharmacokinet. 45:649-663.
-
(2006)
Clin. Pharmacokinet
, vol.45
, pp. 649-663
-
-
Theuretzbacher, U.1
Ihle, F.2
Derendorf, H.3
-
60
-
-
0030015297
-
Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism
-
Thummel, K. E., D. O'Shea, M. F. Paine, D. D. Shen, K. L. Kunze, J. D. Perkins, and G. R. Wilkinson. 1996. Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism. Clin. Pharmacol. Ther. 59:491-502.
-
(1996)
Clin. Pharmacol. Ther
, vol.59
, pp. 491-502
-
-
Thummel, K.E.1
O'Shea, D.2
Paine, M.F.3
Shen, D.D.4
Kunze, K.L.5
Perkins, J.D.6
Wilkinson, G.R.7
-
61
-
-
0027985506
-
Use of midazolam as a human cytochrome P450 3A probe. II. Characterization of inter- and intraindividual hepatic CYP3A variability after liver transplantation
-
Thummel, K. E., D. D. Shen, T. D. Podoll, K. L. Kunze, W. F. Trager, C. E. Bacchi, C. L. Marsh, J. P. McVicar, D. M. Barr, and J. D. Perkins. 1994. Use of midazolam as a human cytochrome P450 3A probe. II. Characterization of inter- and intraindividual hepatic CYP3A variability after liver transplantation. J. Pharmacol. Exp. Ther. 271:557-566.
-
(1994)
J. Pharmacol. Exp. Ther
, vol.271
, pp. 557-566
-
-
Thummel, K.E.1
Shen, D.D.2
Podoll, T.D.3
Kunze, K.L.4
Trager, W.F.5
Bacchi, C.E.6
Marsh, C.L.7
McVicar, J.P.8
Barr, D.M.9
Perkins, J.D.10
-
62
-
-
0028114619
-
Use of midazolam as a human cytochrome P450 3A probe. I. In vitro-in vivo correlations in liver transplant patients
-
Thummel, K. E., D. D. Shen, T. D. Podoll, K. L. Kunze, W. F. Trager, P. S. Hartwell, V. A. Raisys, C. L. Marsh, J. P. McVicar, and D. M. Barr. 1994. Use of midazolam as a human cytochrome P450 3A probe. I. In vitro-in vivo correlations in liver transplant patients. J. Pharmacol. Exp. Ther. 271:549-556.
-
(1994)
J. Pharmacol. Exp. Ther
, vol.271
, pp. 549-556
-
-
Thummel, K.E.1
Shen, D.D.2
Podoll, T.D.3
Kunze, K.L.4
Trager, W.F.5
Hartwell, P.S.6
Raisys, V.A.7
Marsh, C.L.8
McVicar, J.P.9
Barr, D.M.10
-
63
-
-
39749195431
-
Role of CYP2B6 in stereoselective human methadone metabolism
-
Totah, R. A., P. Sheffels, T. Roberts, D. Whittington, K. Thummel, and E. D. Kharasch. 2008. Role of CYP2B6 in stereoselective human methadone metabolism. Anesthesiology 108:363-374.
-
(2008)
Anesthesiology
, vol.108
, pp. 363-374
-
-
Totah, R.A.1
Sheffels, P.2
Roberts, T.3
Whittington, D.4
Thummel, K.5
Kharasch, E.D.6
-
64
-
-
33749453826
-
The functional role of CYP2B6 in human drug metabolism: Substrates and inhibitors in vitro, in vivo and in silico
-
Turpeinen, M., H. Raunio, and O. Pelkonen. 2006. The functional role of CYP2B6 in human drug metabolism: substrates and inhibitors in vitro, in vivo and in silico. Curr. Drug Metab. 7:705-714.
-
(2006)
Curr. Drug Metab
, vol.7
, pp. 705-714
-
-
Turpeinen, M.1
Raunio, H.2
Pelkonen, O.3
-
65
-
-
17844387084
-
Differential mechanism-based inhibition of CYP3A4 and CYP3A5 by verapamil
-
Wang, Y. H., D. R. Jones, and S. D. Hall. 2005. Differential mechanism-based inhibition of CYP3A4 and CYP3A5 by verapamil. Drug Metab. Dispos. 33:664-671.
-
(2005)
Drug Metab. Dispos
, vol.33
, pp. 664-671
-
-
Wang, Y.H.1
Jones, D.R.2
Hall, S.D.3
-
66
-
-
0038002981
-
The cytochrome P4502B6 (CYP2B6) is the main catalyst of efavirenz primary and secondary metabolism: Implication for HIV/AIDS therapy and utility of efavirenz as a substrate marker of CYP2B6 catalytic activity
-
Ward, B. A., J. C. Gorski, D. R. Jones, S. D. Hall, D. A. Flockhart, and Z. Desta. 2003. The cytochrome P4502B6 (CYP2B6) is the main catalyst of efavirenz primary and secondary metabolism: implication for HIV/AIDS therapy and utility of efavirenz as a substrate marker of CYP2B6 catalytic activity. J. Pharmacol. Exp. Ther. 306:287-300.
-
(2003)
J. Pharmacol. Exp. Ther
, vol.306
, pp. 287-300
-
-
Ward, B.A.1
Gorski, J.C.2
Jones, D.R.3
Hall, S.D.4
Flockhart, D.A.5
Desta, Z.6
-
67
-
-
19444376971
-
Drug metabolism and variability among patients in drug response
-
Wilkinson, G. R. 2005. Drug metabolism and variability among patients in drug response. N. Engl. J. Med. 352:2211-2221.
-
(2005)
N. Engl. J. Med
, vol.352
, pp. 2211-2221
-
-
Wilkinson, G.R.1
-
68
-
-
0027445449
-
Isolation and characterization of human liver cytochrome P450 2C19: Correlation between 2C19 and S-mephenytoin 4′-hydroxylation
-
Wrighton, S. A., J. C. Stevens, G. W. Becker, and M. Vandenbranden. 1993. Isolation and characterization of human liver cytochrome P450 2C19: correlation between 2C19 and S-mephenytoin 4′-hydroxylation. Arch. Biochem. Biophys. 306:240-245.
-
(1993)
Arch. Biochem. Biophys
, vol.306
, pp. 240-245
-
-
Wrighton, S.A.1
Stevens, J.C.2
Becker, G.W.3
Vandenbranden, M.4
-
69
-
-
34548105118
-
Polymorphic CYP2B6: Molecular mechanisms and emerging clinical significance
-
Zanger, U. M., K. Klein, T. Saussele, J. Blievernicht, H. Hofmann, and M. Schwab. 2007. Polymorphic CYP2B6: molecular mechanisms and emerging clinical significance. Pharmacogenomics 8:743-759.
-
(2007)
Pharmacogenomics
, vol.8
, pp. 743-759
-
-
Zanger, U.M.1
Klein, K.2
Saussele, T.3
Blievernicht, J.4
Hofmann, H.5
Schwab, M.6
-
70
-
-
54949144309
-
Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation
-
Zanger, U. M., M. Turpeinen, K. Klein, and M. Schwab. 2008. Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation. Anal. Bioanal. Chem. 392:1093-1108.
-
(2008)
Anal. Bioanal. Chem
, vol.392
, pp. 1093-1108
-
-
Zanger, U.M.1
Turpeinen, M.2
Klein, K.3
Schwab, M.4
|