-
1
-
-
21844434930
-
Structure and Chemistry of Cytochrome P450
-
Denisov, I. G.; Makris, T. M.; Sugar, S. G.; Schlichting, I. Structure and Chemistry of Cytochrome P450. Chem. Rev. 2005, 105, 2253-2277.
-
(2005)
Chem. Rev
, vol.105
, pp. 2253-2277
-
-
Denisov, I.G.1
Makris, T.M.2
Sugar, S.G.3
Schlichting, I.4
-
2
-
-
33645809139
-
The Human Intestinal Cytochrome P450 "PIE
-
Paine, M. F.; Hart, H. L.; Ludington, S. S.; Haining, R. L.; Rettie, A. E.; Zeldin, D. C. The Human Intestinal Cytochrome P450 "PIE". Drug Metab. Dispos. 2006, 34, 880-886.
-
(2006)
Drug Metab. Dispos
, vol.34
, pp. 880-886
-
-
Paine, M.F.1
Hart, H.L.2
Ludington, S.S.3
Haining, R.L.4
Rettie, A.E.5
Zeldin, D.C.6
-
3
-
-
0028237729
-
Interindividual Variations in Human Liver Cytochrome P-450 Enzymes Involved in the Oxidation of Drugs, Carcinogens and Toxic Chemicals: Studies with Liver Microsomes of 30 Japanese and 30 Caucasians
-
Shimada, T.; Yamazaki, H.; Mimura, M.; Inui, Y.; Guengerich, F. P. Interindividual Variations in Human Liver Cytochrome P-450 Enzymes Involved in the Oxidation of Drugs, Carcinogens and Toxic Chemicals: Studies with Liver Microsomes of 30 Japanese and 30 Caucasians. J. Pharmacol. Exp. Ther. 1994, 270, 414-423.
-
(1994)
J. Pharmacol. Exp. Ther
, vol.270
, pp. 414-423
-
-
Shimada, T.1
Yamazaki, H.2
Mimura, M.3
Inui, Y.4
Guengerich, F.P.5
-
4
-
-
0031841377
-
Cytochrome P4502C9: An Enzyme of Major Importance in Human Drug Metabolism
-
Miners, J. O.; Birkett, D. J. Cytochrome P4502C9: An Enzyme of Major Importance in Human Drug Metabolism. Br. J. Clin. Pharmacol. 1998, 45, 525-538.
-
(1998)
Br. J. Clin. Pharmacol
, vol.45
, pp. 525-538
-
-
Miners, J.O.1
Birkett, D.J.2
-
5
-
-
0030857031
-
Regioselective and Stereoselective Metabolism of Ibuprofen by Human Cytochrome P450 2C
-
Hamman, M. A.; Thompson, G. A.; Hall, S. D. Regioselective and Stereoselective Metabolism of Ibuprofen by Human Cytochrome P450 2C. Biochem. Pharmacol. 1997, 54, 33-41.
-
(1997)
Biochem. Pharmacol
, vol.54
, pp. 33-41
-
-
Hamman, M.A.1
Thompson, G.A.2
Hall, S.D.3
-
6
-
-
0029916692
-
Cytochromes P450. 1A2, and 2C9 are Responsible for the Human Hepatic O-Demethylation of R- and S-Naproxen
-
Miners, J. O.; Coulter, S.; Tukey, R. H.; Veronese, M. E.; Birkett, D. J. Cytochromes P450. 1A2, and 2C9 are Responsible for the Human Hepatic O-Demethylation of R- and S-Naproxen. Biochem. Pharmacol. 1996, 51, 1003-1008.
-
(1996)
Biochem. Pharmacol
, vol.51
, pp. 1003-1008
-
-
Miners, J.O.1
Coulter, S.2
Tukey, R.H.3
Veronese, M.E.4
Birkett, D.J.5
-
7
-
-
0031757521
-
Comparative Studies on the Catalytic Roles of Cytochrome P450 2C9 and its Cys-and Leu- Variants in the Oxidation of Warfarin, Flurbiprofen, and Diclofenac by Human Liver Microsomes
-
Yamazaki, H.; Inoue, K.; Chiba, K.; Ozawa, N.; Kawai, T.; Suzuki, Y.; Goldstein, J. A.; Guengerich, F. P.; Shimada, T. Comparative Studies on the Catalytic Roles of Cytochrome P450 2C9 and its Cys-and Leu- Variants in the Oxidation of Warfarin, Flurbiprofen, and Diclofenac by Human Liver Microsomes. Biochem. Pharmacol. 1998, 56, 243-251.
-
(1998)
Biochem. Pharmacol
, vol.56
, pp. 243-251
-
-
Yamazaki, H.1
Inoue, K.2
Chiba, K.3
Ozawa, N.4
Kawai, T.5
Suzuki, Y.6
Goldstein, J.A.7
Guengerich, F.P.8
Shimada, T.9
-
8
-
-
17044450722
-
Prediction of In Vivo Drug-Drug Interactions Between Tolbutamide and Various Sulfonamides in Humans Based on In Vitro Experiments
-
Komatsu, K.; Ito, K.; Nakajima, Y.; Kanamitsu, S. I.; Imaoka, S.; Funae, Y.; Green, C. E.; Tyson, C. A.; Shimada, N.; Sugiyama, Y. Prediction of In Vivo Drug-Drug Interactions Between Tolbutamide and Various Sulfonamides in Humans Based on In Vitro Experiments. Drug Metab. Dispos. 2000, 28, 475-481.
-
(2000)
Drug Metab. Dispos
, vol.28
, pp. 475-481
-
-
Komatsu, K.1
Ito, K.2
Nakajima, Y.3
Kanamitsu, S.I.4
Imaoka, S.5
Funae, Y.6
Green, C.E.7
Tyson, C.A.8
Shimada, N.9
Sugiyama, Y.10
-
9
-
-
0035028935
-
Relative Contributions of CYP2C9 and 2C19 to Phenytoin 4-Hydroxylation In Vitro: Inhibition by Sulfaphenazole, Omeprazole, and Ticlopidine
-
Giancarlo, G. M.; Venkatakrislinan, K.; Granda, B. W.; Von Moltke, L. L.; Greenblatt, D. J. Relative Contributions of CYP2C9 and 2C19 to Phenytoin 4-Hydroxylation In Vitro: Inhibition by Sulfaphenazole, Omeprazole, and Ticlopidine. Eur. J. Clin. Pharmacol. 2001, 57, 31-36.
-
(2001)
Eur. J. Clin. Pharmacol
, vol.57
, pp. 31-36
-
-
Giancarlo, G.M.1
Venkatakrislinan, K.2
Granda, B.W.3
Von Moltke, L.L.4
Greenblatt, D.J.5
-
10
-
-
0028962940
-
Human Hepatic P450 2C9 Catalyses the Rate-Limiting Pathway of Torsemide Metabolism
-
Miners, J. O.; Rees, D. L. P.; Valente, L.; Veronese, M. E.; Birkett, D. J. Human Hepatic P450 2C9 Catalyses the Rate-Limiting Pathway of Torsemide Metabolism. J. Pharmacol. Exp. Ther. 1995, 272, 1076-1081.
-
(1995)
J. Pharmacol. Exp. Ther
, vol.272
, pp. 1076-1081
-
-
Miners, J.O.1
Rees, D.L.P.2
Valente, L.3
Veronese, M.E.4
Birkett, D.J.5
-
11
-
-
1342323499
-
In Vitro Sulfoxidation of Thioether Compounds by Human Cytochrome P450 and Flavin-Contaning Monooxygenase Isoforms with Particular Reference to the CYP2C Subfamily
-
Usmani, K. A.; Karoly, E. D.; Hodgson, E.; Rose, R. L. In Vitro Sulfoxidation of Thioether Compounds by Human Cytochrome P450 and Flavin-Contaning Monooxygenase Isoforms with Particular Reference to the CYP2C Subfamily. Drug Metab. Dispos. 2004, 32, 333-339.
-
(2004)
Drug Metab. Dispos
, vol.32
, pp. 333-339
-
-
Usmani, K.A.1
Karoly, E.D.2
Hodgson, E.3
Rose, R.L.4
-
12
-
-
0035065393
-
Competitive CYP2C9 Inhibitors: Enzyme Inhibition Studies, Protein Homology Modeling, and Three-Dimensional Quantitative Structure-Activity Relationship Analysis
-
Afzelius, L.; Zamora, I.; Ridderström, M.; Andersson, T. B.; Karlén, A.; Masimirembwa, C. M. Competitive CYP2C9 Inhibitors: Enzyme Inhibition Studies, Protein Homology Modeling, and Three-Dimensional Quantitative Structure-Activity Relationship Analysis. Mol. Pharmacol. 2001, 59, 909-919.
-
(2001)
Mol. Pharmacol
, vol.59
, pp. 909-919
-
-
Afzelius, L.1
Zamora, I.2
Ridderström, M.3
Andersson, T.B.4
Karlén, A.5
Masimirembwa, C.M.6
-
13
-
-
0037204549
-
Pharmacophore Modeling of Cytochromes P450
-
De Groot, M. J.; Ekins, S. Pharmacophore Modeling of Cytochromes P450. Adv. Drug Delivery Rev. 2002, 54, 367-383.
-
(2002)
Adv. Drug Delivery Rev
, vol.54
, pp. 367-383
-
-
De Groot, M.J.1
Ekins, S.2
-
14
-
-
33745216665
-
Designing Better Drugs: Predicting Cytochrome P450 Metabolism
-
De Groot, M. J. Designing Better Drugs: Predicting Cytochrome P450 Metabolism. Drug Discovery Today 2006, 11, 601-606.
-
(2006)
Drug Discovery Today
, vol.11
, pp. 601-606
-
-
De Groot, M.J.1
-
15
-
-
0034721138
-
A Refined 3-Dimensional QSAR of Cytochrome P450 2C9: Computational Predictions of Drug Interactions
-
Rao. S.; Aoyama, R.; Schrag, M.; Trager, W. F.; Rettie, A.; Jones, J. P. A Refined 3-Dimensional QSAR of Cytochrome P450 2C9: Computational Predictions of Drug Interactions. J. Med. Chem. 2000, 43, 2789-2796.
-
(2000)
J. Med. Chem
, vol.43
, pp. 2789-2796
-
-
Rao, S.1
Aoyama, R.2
Schrag, M.3
Trager, W.F.4
Rettie, A.5
Jones, J.P.6
-
16
-
-
0037046521
-
Development of a Combined Protein and Pharmacophore Model for Cytochrome P450 2C9
-
De Groot, M. J.; Alex, A. A.; Jones, B. C. Development of a Combined Protein and Pharmacophore Model for Cytochrome P450 2C9. J. Med. Chem. 2002, 45, 1983-1993.
-
(2002)
J. Med. Chem
, vol.45
, pp. 1983-1993
-
-
De Groot, M.J.1
Alex, A.A.2
Jones, B.C.3
-
17
-
-
0038440502
-
Predicting Drug Metabolism: A Site of Metabolism Prediction Tool Applied to the Cytochrome P450 2C9
-
Zamora, I.; Afzelius, L.; Cruciani, G. Predicting Drug Metabolism: A Site of Metabolism Prediction Tool Applied to the Cytochrome P450 2C9. J. Med. Chem. 2003, 46, 2313-2324.
-
(2003)
J. Med. Chem
, vol.46
, pp. 2313-2324
-
-
Zamora, I.1
Afzelius, L.2
Cruciani, G.3
-
18
-
-
0042265520
-
Crystal Structure of Human Cytochrome P450 2C9 with Bound Warfarin
-
Williams, P. A.; Cosme, J.; Ward, A.; Angove, H. C.; Vinkovic, D. M.; Jhoti, H. Crystal Structure of Human Cytochrome P450 2C9 with Bound Warfarin. Nature 2003, 424, 464-468.
-
(2003)
Nature
, vol.424
, pp. 464-468
-
-
Williams, P.A.1
Cosme, J.2
Ward, A.3
Angove, H.C.4
Vinkovic, D.M.5
Jhoti, H.6
-
19
-
-
4143143372
-
The Structure of Human Cytochrome P450 2C9 Complexed with Flurbiprofen at 2.0 Å Resolution
-
Wester, M. R.; Yano, J. K.; Schoch, G. A.; Yang, C.; Griffin, K. J.; Stout, C. D.; Johnson, E. F. The Structure of Human Cytochrome P450 2C9 Complexed with Flurbiprofen at 2.0 Å Resolution. J. Biol. Chem. 2004, 279, 35630-35637.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 35630-35637
-
-
Wester, M.R.1
Yano, J.K.2
Schoch, G.A.3
Yang, C.4
Griffin, K.J.5
Stout, C.D.6
Johnson, E.F.7
-
20
-
-
33947196753
-
Ensemble Modeling of Substrate Binding to Cytochromes P450: Analysis of Catalytic Differences between CYP1A Orthologs
-
Prasad, J. C.; Goldstone, J. V.; Camacho, C. J.; Vajda, S.; Stegeman, J. J. Ensemble Modeling of Substrate Binding to Cytochromes P450: Analysis of Catalytic Differences between CYP1A Orthologs. Biochemistry 2007, 46, 2640-2654.
-
(2007)
Biochemistry
, vol.46
, pp. 2640-2654
-
-
Prasad, J.C.1
Goldstone, J.V.2
Camacho, C.J.3
Vajda, S.4
Stegeman, J.J.5
-
21
-
-
0023873591
-
Tolbutamide Hydroxylation by Human Liver Microsomes: Kinetic Characterisation and Relationship to Other Cytochrome P-450 Dependent Xenobiotic Oxidations
-
Miners, J. O.; Smith, K. J.; Robson, R. A.; McManus, M. E.; Veronese, M. E.; Birkett, D. J. Tolbutamide Hydroxylation by Human Liver Microsomes: Kinetic Characterisation and Relationship to Other Cytochrome P-450 Dependent Xenobiotic Oxidations. Biochem. Pharmacol. 1988, 37, 1137-1144.
-
(1988)
Biochem. Pharmacol
, vol.37
, pp. 1137-1144
-
-
Miners, J.O.1
Smith, K.J.2
Robson, R.A.3
McManus, M.E.4
Veronese, M.E.5
Birkett, D.J.6
-
22
-
-
23844460948
-
Prediction of Cytochrome P450 3A4, 2D6, and 2C9 Inhibitors and Substrates by Using Support Vector Machines
-
Yap, C. W.; Chen, Y. Z. Prediction of Cytochrome P450 3A4, 2D6, and 2C9 Inhibitors and Substrates by Using Support Vector Machines. J. Chem. Inf. Model. 2005, 45, 982-992.
-
(2005)
J. Chem. Inf. Model
, vol.45
, pp. 982-992
-
-
Yap, C.W.1
Chen, Y.Z.2
-
23
-
-
39749107077
-
-
Omega, version 2.1; Openeye Scientific Software: Santa Fe, NM, 2006
-
Omega, version 2.1; Openeye Scientific Software: Santa Fe, NM, 2006.
-
-
-
-
24
-
-
0347296066
-
Assessing the Performance of Omega with Respect to Retrieving Bioactive Conformations
-
Böstrom, J.; Greenwood, J. R.; Gottfries, J. Assessing the Performance of Omega with Respect to Retrieving Bioactive Conformations. J. Mol. Graphics Modell. 2003, 21, 449-462.
-
(2003)
J. Mol. Graphics Modell
, vol.21
, pp. 449-462
-
-
Böstrom, J.1
Greenwood, J.R.2
Gottfries, J.3
-
25
-
-
33746921247
-
Comparative Performance Assessment of the Conformational Model Generators Omega and Catalyst: A Large-Scale Survey on the Retrieval of Protein-Bound Ligand Conformations
-
Kirchmair, J.; Wolber, G.; Laggner, C.; Langer, T. Comparative Performance Assessment of the Conformational Model Generators Omega and Catalyst: A Large-Scale Survey on the Retrieval of Protein-Bound Ligand Conformations. J. Chem. Inf. Model. 2006, 46, 1848-1861.
-
(2006)
J. Chem. Inf. Model
, vol.46
, pp. 1848-1861
-
-
Kirchmair, J.1
Wolber, G.2
Laggner, C.3
Langer, T.4
-
26
-
-
39749165492
-
-
ROCS, version 2.2; Openeye Scientific Software: Santa Fe, NM, 2006
-
ROCS, version 2.2; Openeye Scientific Software: Santa Fe, NM, 2006.
-
-
-
-
27
-
-
39749150806
-
-
FRED, version 2.1.2; Openeye Scientific Software: Santa Fe, NM, 2005
-
FRED, version 2.1.2; Openeye Scientific Software: Santa Fe, NM, 2005.
-
-
-
-
28
-
-
33845763471
-
Molecular Modelling Approaches for the Prediction of the Nonspecific Binding of Drugs to Hepatic Microsomes
-
Sykes, M. J.; Sorich, M. J.; Miners, J. O. Molecular Modelling Approaches for the Prediction of the Nonspecific Binding of Drugs to Hepatic Microsomes. J. Chem. Inf. Model. 2006, 46, 2661-2673.
-
(2006)
J. Chem. Inf. Model
, vol.46
, pp. 2661-2673
-
-
Sykes, M.J.1
Sorich, M.J.2
Miners, J.O.3
-
29
-
-
0029010518
-
Role of the Cytochrome P450 2C9 and an Allelic Variant in the 4′-Hydroxylation of (R)- and (S)-Flurbiprofen
-
Tracy, T. S.; Rosenbluth, B. W.; Wrighton, S. A.; Gonzalez, F. J.; Korzekwa, K. R. Role of the Cytochrome P450 2C9 and an Allelic Variant in the 4′-Hydroxylation of (R)- and (S)-Flurbiprofen. Biochem. Pharmacol. 1995, 49, 1269-1275.
-
(1995)
Biochem. Pharmacol
, vol.49
, pp. 1269-1275
-
-
Tracy, T.S.1
Rosenbluth, B.W.2
Wrighton, S.A.3
Gonzalez, F.J.4
Korzekwa, K.R.5
-
30
-
-
39749166109
-
-
VIDA, version 2.1.2; Openeye Scientific Software: Santa Fe, NM, 2006
-
VIDA, version 2.1.2; Openeye Scientific Software: Santa Fe, NM, 2006.
-
-
-
-
31
-
-
0032878955
-
Identification of Human Cytochrome P450 Isoforms Involved in the Metabolism of S-2-[4-(3-Methyl-2-Thienyl)Phenyl]Propionic Acid
-
Taguchi, K.; Konishi, T.; Nishikawa, H.; Kitamura, S. Identification of Human Cytochrome P450 Isoforms Involved in the Metabolism of S-2-[4-(3-Methyl-2-Thienyl)Phenyl]Propionic Acid. Xenobiotica 1999, 29, 899-907.
-
(1999)
Xenobiotica
, vol.29
, pp. 899-907
-
-
Taguchi, K.1
Konishi, T.2
Nishikawa, H.3
Kitamura, S.4
-
32
-
-
0029128881
-
The Substrate Binding Site of Human Liver Cytochrome P450 2C9: An Approach Using Designed Tienilic Acid Derivatives and Molecular Modeling
-
Mancy, A.; Broto, P.; Dijols, S.; Dansette, P. M.; Mansuy, D. The Substrate Binding Site of Human Liver Cytochrome P450 2C9: An Approach Using Designed Tienilic Acid Derivatives and Molecular Modeling. Biochemistry 1995, 34, 10365-10375.
-
(1995)
Biochemistry
, vol.34
, pp. 10365-10375
-
-
Mancy, A.1
Broto, P.2
Dijols, S.3
Dansette, P.M.4
Mansuy, D.5
-
33
-
-
0027468338
-
Human-Liver Cytochromes P-450 Expressed in Yeast as Tools for Reactive-Metabolite Formation Studies. Oxidative Activation of Tienilic Acid by Cytochromes P-450 2C9 and 2C10
-
Lopez Garcia, M. P.; Dansette, P. M.; Valadon, P.; Amar, C.; Beaune, P. H.; Guengerich, F. P.; Mansuy, D. Human-Liver Cytochromes P-450 Expressed in Yeast as Tools for Reactive-Metabolite Formation Studies. Oxidative Activation of Tienilic Acid by Cytochromes P-450 2C9 and 2C10. Eur. J. Biochem. 1993, 213, 223-232.
-
(1993)
Eur. J. Biochem
, vol.213
, pp. 223-232
-
-
Lopez Garcia, M.P.1
Dansette, P.M.2
Valadon, P.3
Amar, C.4
Beaune, P.H.5
Guengerich, F.P.6
Mansuy, D.7
-
34
-
-
0031920705
-
Cytochrome P450 2C9 Catalyzes Indomethacin O-Demethylation in Human Liver Microsomes
-
Nakajima, M.; Inoue, T.; Shimada, N.; Tokudome, S.; Yamamoto, T.; Kuroiwa, Y. Cytochrome P450 2C9 Catalyzes Indomethacin O-Demethylation in Human Liver Microsomes. Drug Metab. Dispos. 1998, 26, 261-266.
-
(1998)
Drug Metab. Dispos
, vol.26
, pp. 261-266
-
-
Nakajima, M.1
Inoue, T.2
Shimada, N.3
Tokudome, S.4
Yamamoto, T.5
Kuroiwa, Y.6
-
35
-
-
18544377505
-
Involvement of CYP2C9 and UGT2B7 in the Metabolism of Zaltoprofen, a Nonsteroidal Anti-Inflammatory Drug, and its Lack of Clinically Significant CYP Inhibition Potential
-
Furuta, S.; Akagawa, N.; Kamada, E.; Hiyama, A.; Kawabata, Y.; Kowata, N.; Inaba, A.; Matthews, A.; Hall, M.; Kurimoto, T. Involvement of CYP2C9 and UGT2B7 in the Metabolism of Zaltoprofen, a Nonsteroidal Anti-Inflammatory Drug, and its Lack of Clinically Significant CYP Inhibition Potential. Br. J. Clin. Pharmacol. 2002, 54, 295-303.
-
(2002)
Br. J. Clin. Pharmacol
, vol.54
, pp. 295-303
-
-
Furuta, S.1
Akagawa, N.2
Kamada, E.3
Hiyama, A.4
Kawabata, Y.5
Kowata, N.6
Inaba, A.7
Matthews, A.8
Hall, M.9
Kurimoto, T.10
-
37
-
-
0032239288
-
The Role of CYP2C in the In Vitro Bioactivation of the Contraceptive Steroid Desogestrel
-
Gentile, D. M.; Verhoeven, C. H. J.; Shimada, T.; Back, D. J. The Role of CYP2C in the In Vitro Bioactivation of the Contraceptive Steroid Desogestrel. J. Pharmacol. Exp. Ther. 1998, 287, 975-982.
-
(1998)
J. Pharmacol. Exp. Ther
, vol.287
, pp. 975-982
-
-
Gentile, D.M.1
Verhoeven, C.H.J.2
Shimada, T.3
Back, D.J.4
-
38
-
-
6944229545
-
The Involvement of CYP3A4 and CYP2C9 in the Metabolism of 17α- Ethinylestradiol
-
Wang, B.; Sanchez, R. I.; Franklin, R. B.; Evans, D. C.; Huskey, S-E. W. The Involvement of CYP3A4 and CYP2C9 in the Metabolism of 17α- Ethinylestradiol. Drug Metab. Dispos. 2004, 32, 1209-1212.
-
(2004)
Drug Metab. Dispos
, vol.32
, pp. 1209-1212
-
-
Wang, B.1
Sanchez, R.I.2
Franklin, R.B.3
Evans, D.C.4
Huskey, S.-E.W.5
-
39
-
-
0034951038
-
Role of CYP2C9 Polymorphism in Losartan Oxidation
-
Yasar, Ü.; Tybring, G.; Hidestrand, M.; Oscarson, M.; Ingelman-Sundberg, M.; Dahl, M-L.; Eliasson, E. Role of CYP2C9 Polymorphism in Losartan Oxidation. Drug Metab. Dispos. 2001, 29, 1051-1056.
-
(2001)
Drug Metab. Dispos
, vol.29
, pp. 1051-1056
-
-
Yasar, U.1
Tybring, G.2
Hidestrand, M.3
Oscarson, M.4
Ingelman-Sundberg, M.5
Dahl, M.-L.6
Eliasson, E.7
-
40
-
-
3142512630
-
Stereoselective Glucuronidation and Hydroxylation of Etodolac by UGT1A9 and CYP2C9 in Man
-
Tougou, K.; Gotou, H.; Ohno, Y.; Nakamura, A. Stereoselective Glucuronidation and Hydroxylation of Etodolac by UGT1A9 and CYP2C9 in Man. Xenobiotica 2004, 34, 449-461.
-
(2004)
Xenobiotica
, vol.34
, pp. 449-461
-
-
Tougou, K.1
Gotou, H.2
Ohno, Y.3
Nakamura, A.4
-
41
-
-
0030978662
-
Biotransformation of Mestranol to Ethinyl Estradiol In Vitro: The Role of Cytochrome P-450 2C9 and Metabolie Inhibitors
-
Schmider, J.; Greenblatt, D. J.; Von Moltke, L. L.; Karsov, D.; Vena, R.; Friedman, H. L.; Shader, R. I. Biotransformation of Mestranol to Ethinyl Estradiol In Vitro: The Role of Cytochrome P-450 2C9 and Metabolie Inhibitors. J. Clin. Pharmacol. 1997, 37, 193-200.
-
(1997)
J. Clin. Pharmacol
, vol.37
, pp. 193-200
-
-
Schmider, J.1
Greenblatt, D.J.2
Von Moltke, L.L.3
Karsov, D.4
Vena, R.5
Friedman, H.L.6
Shader, R.I.7
-
42
-
-
21444435755
-
Role of Human Liver Cytochrome P450 2C9 in the Metabolism of a Novel a4b1/a4b7 Dual Antagonist
-
Tsuda-Tsukimoto, M.; Ogasawara, Y.; Kume, T. Role of Human Liver Cytochrome P450 2C9 in the Metabolism of a Novel a4b1/a4b7 Dual Antagonist. Drug Metab. Pharmacokinet. 2005, 20, 127-134.
-
(2005)
Drug Metab. Pharmacokinet
, vol.20
, pp. 127-134
-
-
Tsuda-Tsukimoto, M.1
Ogasawara, Y.2
Kume, T.3
-
43
-
-
0032937343
-
The 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Inhibitor Fluvastatin: Effect on Human Cytochrome P-450 and Implications for Metabolic Drug Interactions
-
Fischer, V.; Johanson, L.; Heitz, F.; Tullman, R.; Graham, E.; Baldeck, J. P.; Robinson, W. T. The 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Inhibitor Fluvastatin: Effect on Human Cytochrome P-450 and Implications for Metabolic Drug Interactions. Drug Metab. Dispos. 1999, 27, 410-416.
-
(1999)
Drug Metab. Dispos
, vol.27
, pp. 410-416
-
-
Fischer, V.1
Johanson, L.2
Heitz, F.3
Tullman, R.4
Graham, E.5
Baldeck, J.P.6
Robinson, W.T.7
-
44
-
-
0029790413
-
Metabolism of Aceclofenac in Humans
-
Bort, R.; Ponsoda, X.; Carrasco, E.; Gomez-Lechon, M. J.; Castell, J. V. Metabolism of Aceclofenac in Humans. Drug Metab. Dispos. 1996, 24, 834-841.
-
(1996)
Drug Metab. Dispos
, vol.24
, pp. 834-841
-
-
Bort, R.1
Ponsoda, X.2
Carrasco, E.3
Gomez-Lechon, M.J.4
Castell, J.V.5
-
45
-
-
24344435153
-
CYP2C-Catalyzed δ-(9)-Tetrahydrocannabinol Metabolism: Kinetics, Pharmacogenetics and Interaction with Phenytoin
-
Bland, T. M.; Haining, R. L.; Tracy, T. S.; Callery, P. S. CYP2C-Catalyzed δ-(9)-Tetrahydrocannabinol Metabolism: Kinetics, Pharmacogenetics and Interaction with Phenytoin. Biochem. Pharmacol. 2005, 70, 1096-1103.
-
(2005)
Biochem. Pharmacol
, vol.70
, pp. 1096-1103
-
-
Bland, T.M.1
Haining, R.L.2
Tracy, T.S.3
Callery, P.S.4
-
46
-
-
0036843479
-
Effects of Fibrates on Metabolism of Statins in Human Hepatocytes
-
Prueksaritanont, T.; Tang, C.; Qiu, Y.; Mu, L.; Subramanian, R.; Lin, J. H. Effects of Fibrates on Metabolism of Statins in Human Hepatocytes. Drug Metab. Dispos. 2002, 30, 1280-1287.
-
(2002)
Drug Metab. Dispos
, vol.30
, pp. 1280-1287
-
-
Prueksaritanont, T.1
Tang, C.2
Qiu, Y.3
Mu, L.4
Subramanian, R.5
Lin, J.H.6
-
47
-
-
0034150775
-
359 Variants: Enzyme Kinetic Study with Seven Substrates
-
359 Variants: Enzyme Kinetic Study with Seven Substrates. Pharmacogenetics 2000, 10, 95-104.
-
(2000)
Pharmacogenetics
, vol.10
, pp. 95-104
-
-
Takanashi, K.1
Tainaka, H.2
Kobayashi, K.3
Yasumori, T.4
Hosakawa, M.5
Chiba, K.6
-
48
-
-
18844392062
-
Role of CYP2C9 and its Variants (CYP2C9*3 and CYP2C9*13) in the Metabolism of Lornoxicam in Humans
-
Guo, Y.; Zhang, Y.; Wang. Y.; Chen, X.; Si, D.; Zhong, D.; Fawcett, J. P.; Zhou, H. Role of CYP2C9 and its Variants (CYP2C9*3 and CYP2C9*13) in the Metabolism of Lornoxicam in Humans. Drug Metab. Dispos. 2005, 33, 749-753.
-
(2005)
Drug Metab. Dispos
, vol.33
, pp. 749-753
-
-
Guo, Y.1
Zhang, Y.2
Wang, Y.3
Chen, X.4
Si, D.5
Zhong, D.6
Fawcett, J.P.7
Zhou, H.8
-
49
-
-
0033777269
-
Human Hepatic Metabolism of a Novel 2-carboxyindole Glycine Antagonist for Stroke: In Vitro-In Vivo Correlations
-
Gilissen, R. A. H. J.; Ferrari, L.; Barnaby, R. J.; Kajbaf, M. Human Hepatic Metabolism of a Novel 2-carboxyindole Glycine Antagonist for Stroke: In Vitro-In Vivo Correlations. Xenobiotica 2000, 30, 843-856.
-
(2000)
Xenobiotica
, vol.30
, pp. 843-856
-
-
Gilissen, R.A.H.J.1
Ferrari, L.2
Barnaby, R.J.3
Kajbaf, M.4
-
50
-
-
0036146585
-
Oxidation of the Flavonoids Galangin and Kaempferide by Human Liver Microsomes and CYP1A1, CYP1A2, and CYP2C9
-
Otake, Y.; Walle, T. Oxidation of the Flavonoids Galangin and Kaempferide by Human Liver Microsomes and CYP1A1, CYP1A2, and CYP2C9. Drug Metab. Dispos. 2002, 30, 103-105.
-
(2002)
Drug Metab. Dispos
, vol.30
, pp. 103-105
-
-
Otake, Y.1
Walle, T.2
-
51
-
-
0029039791
-
Arachidonic Acid Metabolism by Human Cytochrome P450s 2C8, 2C9, 2E1, and 1A2: Regioselective Oxygenation and Evidence for a Role for CYP2C Enzymes in Arachidonic Acid Epoxygenation in Human Liver Microsomes
-
Rifkind, A. B.; Lee, C.; Chang, T. K. H.; Waxman, D. J. Arachidonic Acid Metabolism by Human Cytochrome P450s 2C8, 2C9, 2E1, and 1A2: Regioselective Oxygenation and Evidence for a Role for CYP2C Enzymes in Arachidonic Acid Epoxygenation in Human Liver Microsomes. Arch. Biochem. Biophys. 1995, 320, 380-389.
-
(1995)
Arch. Biochem. Biophys
, vol.320
, pp. 380-389
-
-
Rifkind, A.B.1
Lee, C.2
Chang, T.K.H.3
Waxman, D.J.4
-
52
-
-
20944438105
-
Chlorpropamide 2-Hydroxylation is Catalysed by CYP2C9 and CYP2C19 In Vitro: Chlorpropamide Disposition is Influenced by CYP2C9, but not by CYP2C19 Genetic Polymorphism
-
Shon, J.-H.; Yoon, Y.-R.; Kim, M.-J.; Kim, K.-A.; Lim, Y.-C.; Liu, K.-H.; Shin, D.-H.; Lee, C.-H.; Cha, I.-J.; Shin, J.-G. Chlorpropamide 2-Hydroxylation is Catalysed by CYP2C9 and CYP2C19 In Vitro: Chlorpropamide Disposition is Influenced by CYP2C9, but not by CYP2C19 Genetic Polymorphism. Br. J. Clin. Pharmacol. 2005, 59, 552-563.
-
(2005)
Br. J. Clin. Pharmacol
, vol.59
, pp. 552-563
-
-
Shon, J.-H.1
Yoon, Y.-R.2
Kim, M.-J.3
Kim, K.-A.4
Lim, Y.-C.5
Liu, K.-H.6
Shin, D.-H.7
Lee, C.-H.8
Cha, I.-J.9
Shin, J.-G.10
-
53
-
-
0031985363
-
Metabolism of Meloxicam in Human Liver Involves Cytochromes P4502C9 and 3A4
-
Chesné, C.; Guyomard, C.; Guillouzo, A.; Schmids, J.; Ludwig, E.; Sauter, T. Metabolism of Meloxicam in Human Liver Involves Cytochromes P4502C9 and 3A4. Xenobiotica 1998, 28, 1-13.
-
(1998)
Xenobiotica
, vol.28
, pp. 1-13
-
-
Chesné, C.1
Guyomard, C.2
Guillouzo, A.3
Schmids, J.4
Ludwig, E.5
Sauter, T.6
-
54
-
-
2942562619
-
450 2C9 and 3A4 as the Major Catalysts of Phenprocoumon Hydroxylation In Vitro
-
450 2C9 and 3A4 as the Major Catalysts of Phenprocoumon Hydroxylation In Vitro. Eur. J. Clin. Pharmacol. 2004, 60, 173-182.
-
(2004)
Eur. J. Clin. Pharmacol
, vol.60
, pp. 173-182
-
-
Ufer, M.1
Svensson, J.O.2
Krausz, K.W.3
Gelboin, H.V.4
Rane, A.5
Tybring, G.6
-
55
-
-
0032797632
-
Hepatic metabolism of Diclofenac: Role of Human CYP in the Minor Oxidative Pathways
-
Bort, R.; Macé, K.; Boobis, A.; Gómez-Lechón, M. J.; Pfeifer, A.; Castell, J. Hepatic metabolism of Diclofenac: Role of Human CYP in the Minor Oxidative Pathways. Biochem. Pharmacol. 1999, 58, 787-796.
-
(1999)
Biochem. Pharmacol
, vol.58
, pp. 787-796
-
-
Bort, R.1
Macé, K.2
Boobis, A.3
Gómez-Lechón, M.J.4
Pfeifer, A.5
Castell, J.6
-
56
-
-
0033786365
-
Cytochrome P4502C9 is the Principal Catalyst of Racemic Acenocoumarol Hydroxylation Reactions in Human Liver Microsomes
-
Thijssen, H. H.; Flinois, J. P.; Beaune, P. H. Cytochrome P4502C9 is the Principal Catalyst of Racemic Acenocoumarol Hydroxylation Reactions in Human Liver Microsomes. Drug Metab. Dispos. 2000, 28, 1284-1290.
-
(2000)
Drug Metab. Dispos
, vol.28
, pp. 1284-1290
-
-
Thijssen, H.H.1
Flinois, J.P.2
Beaune, P.H.3
-
57
-
-
0028785979
-
Identification of the Human Liver Cytochrome P450 Enzymes Involved in the Metabolism of Zileuton (ABT-077) and its N-dehydroxylated Metabolite, Abbott-66193
-
Machinist, J. M.; Mayer, M. D.; Shet, M. S.; Ferrero, J. L.; Rodrigues, A. D. Identification of the Human Liver Cytochrome P450 Enzymes Involved in the Metabolism of Zileuton (ABT-077) and its N-dehydroxylated Metabolite, Abbott-66193. Drug Metab. Dispos. 1995, 23, 1163-1174.
-
(1995)
Drug Metab. Dispos
, vol.23
, pp. 1163-1174
-
-
Machinist, J.M.1
Mayer, M.D.2
Shet, M.S.3
Ferrero, J.L.4
Rodrigues, A.D.5
-
58
-
-
0027491277
-
Cytochrome P450 2C9 is Responsible for Hydroxylation of the Naphthoquinone Antimalarial Drug 58C80 in Human Liver
-
Weaver, R. J.; Dickins, M.; Burke, D. M. Cytochrome P450 2C9 is Responsible for Hydroxylation of the Naphthoquinone Antimalarial Drug 58C80 in Human Liver. Biochem. Pharmacol. 1993, 46, 1183-1197.
-
(1993)
Biochem. Pharmacol
, vol.46
, pp. 1183-1197
-
-
Weaver, R.J.1
Dickins, M.2
Burke, D.M.3
-
59
-
-
10744225323
-
Stereoselective Metabolism of Lansoprazole by Human Liver Cytochrome P450 Enzymes
-
Kim, K.-A.; Kim, M.-J.; Park, J.-Y.; Shon, J.-H.; Yoon, Y.-R.; Lee, S.-S.; Liu, K.-H.; Chun, J.-H.; Hyun, M.-H.; Shin, J.-G. Stereoselective Metabolism of Lansoprazole by Human Liver Cytochrome P450 Enzymes. Drug Metab. Dispos. 2003, 31, 1227-1234.
-
(2003)
Drug Metab. Dispos
, vol.31
, pp. 1227-1234
-
-
Kim, K.-A.1
Kim, M.-J.2
Park, J.-Y.3
Shon, J.-H.4
Yoon, Y.-R.5
Lee, S.-S.6
Liu, K.-H.7
Chun, J.-H.8
Hyun, M.-H.9
Shin, J.-G.10
-
60
-
-
0032986686
-
Zolpidem Metabolism In Vitro: Responsible Cytochromes, Chemical Inhibitors, and In Vivo Correlations
-
Von Moltke, L. L.; Greenblatt, D. J.; Granda, B. W.; Duan, S. X.; Grassi, J. M.; Venkatakrishnan, K.; Harmatz, J. S.; Shader, R. I. Zolpidem Metabolism In Vitro: Responsible Cytochromes, Chemical Inhibitors, and In Vivo Correlations. Br. J. Clin. Pharmacol. 1999, 48, 89-97.
-
(1999)
Br. J. Clin. Pharmacol
, vol.48
, pp. 89-97
-
-
Von Moltke, L.L.1
Greenblatt, D.J.2
Granda, B.W.3
Duan, S.X.4
Grassi, J.M.5
Venkatakrishnan, K.6
Harmatz, J.S.7
Shader, R.I.8
-
61
-
-
0034176412
-
Identification of CYP2C9 as a Human Liver Microsomal Linoleic Acid Epoxygenase
-
Draper, A. J.; Hammock, B. D. Identification of CYP2C9 as a Human Liver Microsomal Linoleic Acid Epoxygenase. Arch. Biochem. Biophys. 2000, 376, 199-205.
-
(2000)
Arch. Biochem. Biophys
, vol.376
, pp. 199-205
-
-
Draper, A.J.1
Hammock, B.D.2
-
62
-
-
0029970205
-
Metabolic Activation of the Potent Carcinogen Dibenzo[a,h]anthracene by cDNA-Expressed Human Cytochromes P450
-
Shou, M.; Krausz, K. W.; Gonzalez, F. J.; Gelboin, H. V. Metabolic Activation of the Potent Carcinogen Dibenzo[a,h]anthracene by cDNA-Expressed Human Cytochromes P450. Arch. Biochem. Biophys. 1996, 328, 201-207.
-
(1996)
Arch. Biochem. Biophys
, vol.328
, pp. 201-207
-
-
Shou, M.1
Krausz, K.W.2
Gonzalez, F.J.3
Gelboin, H.V.4
-
63
-
-
0034014319
-
-
Tang, C.; Shou, M.; Mei, Q.; Rushmore, T. H.; Rodrigues, A. D. Major Role of Human Liver Microsomal Cytochrome P450 2C9 (CYP2C9) in the Oxidative Metabolism of Celecoxib, a Novel Cyclooxygenase-II Inhibitor. J. Pharmacol. Exp. Ther. 2000, 293, 453-459.
-
Tang, C.; Shou, M.; Mei, Q.; Rushmore, T. H.; Rodrigues, A. D. Major Role of Human Liver Microsomal Cytochrome P450 2C9 (CYP2C9) in the Oxidative Metabolism of Celecoxib, a Novel Cyclooxygenase-II Inhibitor. J. Pharmacol. Exp. Ther. 2000, 293, 453-459.
-
-
-
-
64
-
-
0037403687
-
Identification of the Cytochrome P450 Enzymes Involved in the N-Oxidation of Voriconazole
-
Hyland, R.; Jones, B. C.; Smith, D. A. Identification of the Cytochrome P450 Enzymes Involved in the N-Oxidation of Voriconazole. Drug Metab. Dispos. 2003, 31, 540-547.
-
(2003)
Drug Metab. Dispos
, vol.31
, pp. 540-547
-
-
Hyland, R.1
Jones, B.C.2
Smith, D.A.3
-
65
-
-
0035010954
-
Involvement of CYP2B6 in N-Demethylation of Ketamine in Human Liver Microsomes
-
Yanagihara, Y.; Kariya, S.; Ohtani, M.; Uchino, K.; Aoyama, T.; Yamamura, Y.; Iga, T. Involvement of CYP2B6 in N-Demethylation of Ketamine in Human Liver Microsomes. Drug Metab. Dispos. 2001, 29, 887-890.
-
(2001)
Drug Metab. Dispos
, vol.29
, pp. 887-890
-
-
Yanagihara, Y.1
Kariya, S.2
Ohtani, M.3
Uchino, K.4
Aoyama, T.5
Yamamura, Y.6
Iga, T.7
-
66
-
-
0035039489
-
Identification of the Cytochrome P450 Enzymes Involved in the N-Demethylation of Sildenafil
-
Hyland, R.; Roe, E. G. H.; Jones, B. C.; Smith, D. A. Identification of the Cytochrome P450 Enzymes Involved in the N-Demethylation of Sildenafil. Br. J. Clin. Pharmacol. 2001, 17, 239-248.
-
(2001)
Br. J. Clin. Pharmacol
, vol.17
, pp. 239-248
-
-
Hyland, R.1
Roe, E.G.H.2
Jones, B.C.3
Smith, D.A.4
-
67
-
-
0032870308
-
Multiple Cytochrome P-450s Involved in the Metabolism of Terbinafine Suggest a Limited Potential for Drug-Drug Interactions
-
Vickers, A. E. M.; Sinclair, J. R.; Zollinger, M.; Heitz, F.; Glänzel, U.; Johanson, L.; Fischer, V. Multiple Cytochrome P-450s Involved in the Metabolism of Terbinafine Suggest a Limited Potential for Drug-Drug Interactions. Drug Metab. Dispos. 1999, 27, 1029-1038.
-
(1999)
Drug Metab. Dispos
, vol.27
, pp. 1029-1038
-
-
Vickers, A.E.M.1
Sinclair, J.R.2
Zollinger, M.3
Heitz, F.4
Glänzel, U.5
Johanson, L.6
Fischer, V.7
-
68
-
-
0030783057
-
Hepatic Microsomal Metabolism of Montelukast, a Potent Leukotriene D4 Receptor Antagonist in Humans
-
Chiba, M.; Xu, X.; Nishime, J. A.; Balani, S. K.; Lin, J. H. Hepatic Microsomal Metabolism of Montelukast, a Potent Leukotriene D4 Receptor Antagonist in Humans. Drug Metab. Dispos. 1997, 25, 1022-1031.
-
(1997)
Drug Metab. Dispos
, vol.25
, pp. 1022-1031
-
-
Chiba, M.1
Xu, X.2
Nishime, J.A.3
Balani, S.K.4
Lin, J.H.5
-
69
-
-
0030831766
-
Human CYP2C9 and CYP2A6 Mediate Formation of the Hepatotoxin 4-Ene-Valproic Acid
-
Sadeque, A. J. M.; Fisher, M. B.; Korzekwa, K. R.; Gonzalez, F. J.; Rettie, A. E. Human CYP2C9 and CYP2A6 Mediate Formation of the Hepatotoxin 4-Ene-Valproic Acid. J. Pharmacol. Exp. Ther. 1997, 283, 698-703.
-
(1997)
J. Pharmacol. Exp. Ther
, vol.283
, pp. 698-703
-
-
Sadeque, A.J.M.1
Fisher, M.B.2
Korzekwa, K.R.3
Gonzalez, F.J.4
Rettie, A.E.5
-
70
-
-
0038687263
-
Sulfaphenazole Derivatives as Tools for Comparing Cytochrome P450 2C5 and Human Cytochromes P450 2Cs: Identification of a New High Affinity Substrate Common to Those Enzymes
-
Marques-Soares, C.; Dijols, S.; Macherey, A.-C.; Wester, M. R.; Johnson, E. F.; Dansette, P. M.; Mansuy, D. Sulfaphenazole Derivatives as Tools for Comparing Cytochrome P450 2C5 and Human Cytochromes P450 2Cs: Identification of a New High Affinity Substrate Common to Those Enzymes. Biochemistry 2003, 42, 6363-6369.
-
(2003)
Biochemistry
, vol.42
, pp. 6363-6369
-
-
Marques-Soares, C.1
Dijols, S.2
Macherey, A.-C.3
Wester, M.R.4
Johnson, E.F.5
Dansette, P.M.6
Mansuy, D.7
-
71
-
-
0033815944
-
-
Margolis, J. M.; O'Donnell, J. P.; Mankowski, D. C.; Ekins, S.; Obach, R. S. (R)-, (S)-, and Racemic Fluoxetine N-Demethylation by Human Cytochrome P450 Enzymes. Drug Metab. Dispos. 2000, 28, 1187-1191.
-
Margolis, J. M.; O'Donnell, J. P.; Mankowski, D. C.; Ekins, S.; Obach, R. S. (R)-, (S)-, and Racemic Fluoxetine N-Demethylation by Human Cytochrome P450 Enzymes. Drug Metab. Dispos. 2000, 28, 1187-1191.
-
-
-
-
72
-
-
0024354143
-
Expression of a Human Liver Cytochrome P-450 Protein with Tolbutamide Hydroxylase Activity in Saccharomyces cerevisiae
-
Brian, W. R.; Srivastava, P. K.; Umbenhauer, D. R.; Lloyd, R. S.; Guengerich, F. P. Expression of a Human Liver Cytochrome P-450 Protein with Tolbutamide Hydroxylase Activity in Saccharomyces cerevisiae. Biochemistry 1989, 28, 4993-4999.
-
(1989)
Biochemistry
, vol.28
, pp. 4993-4999
-
-
Brian, W.R.1
Srivastava, P.K.2
Umbenhauer, D.R.3
Lloyd, R.S.4
Guengerich, F.P.5
-
73
-
-
0033855822
-
CYP2C8/9 Mediate Dapsone N-Hydroxylation at Clinical Concentrations of Dapsone
-
Winter, H. R.; Wang, Y.; Unadkat, J. D. CYP2C8/9 Mediate Dapsone N-Hydroxylation at Clinical Concentrations of Dapsone. Drug Metab. Dispos. 2000, 28, 865-868.
-
(2000)
Drug Metab. Dispos
, vol.28
, pp. 865-868
-
-
Winter, H.R.1
Wang, Y.2
Unadkat, J.D.3
-
74
-
-
0031434742
-
Metabolism of Clozapine by cDNA-Expressed Human Cytochrome P450 Enzymes
-
Linnet, K.; Olesen, O. V. Metabolism of Clozapine by cDNA-Expressed Human Cytochrome P450 Enzymes. Drug Metab. Dispos. 1997, 25, 1379-1382.
-
(1997)
Drug Metab. Dispos
, vol.25
, pp. 1379-1382
-
-
Linnet, K.1
Olesen, O.V.2
-
75
-
-
0030848298
-
In Vitro Identification of the Human Cytochrome P450 Enzymes Involved in the Metabolism of R-(+)- and S-(-)-Carvedilol
-
Oldham, H. G.; Clarke, S. E. In Vitro Identification of the Human Cytochrome P450 Enzymes Involved in the Metabolism of R-(+)- and S-(-)-Carvedilol. Drug Metab. Dispos. 1997, 25, 970-977.
-
(1997)
Drug Metab. Dispos
, vol.25
, pp. 970-977
-
-
Oldham, H.G.1
Clarke, S.E.2
-
76
-
-
0031918465
-
Tolterodine, a New Muscarinic Receptor Antagonist, is Metabolized by Cytochromes P450 2D6 and 3A in Human Liver Microsomes
-
Postlind, H.; Danielson, A.; Lindgren, A.; Andersson, S. H. G. Tolterodine, a New Muscarinic Receptor Antagonist, is Metabolized by Cytochromes P450 2D6 and 3A in Human Liver Microsomes. Drug Metab. Dispos. 1998, 26, 289-293.
-
(1998)
Drug Metab. Dispos
, vol.26
, pp. 289-293
-
-
Postlind, H.1
Danielson, A.2
Lindgren, A.3
Andersson, S.H.G.4
-
77
-
-
31844440321
-
Human Cytochrome P450 Enzymes of Importance for the Bioactivation of Methyleugenol to the Proximate Carcinogen 1′-Hydroxymethyleugenol
-
Jeurissen, S. M. F.; Bogaards, J. J. P.; Boersma, M. G.; Ter Horst, J. P. F.; Awad, H. M.; Fiamegos, Y. C.; Van Beek, T. A.; Alink, G. M.; Sudhölter, E. J. R.; Cnubben, N. H. P.; Rietjens, I. M. C. M. Human Cytochrome P450 Enzymes of Importance for the Bioactivation of Methyleugenol to the Proximate Carcinogen 1′-Hydroxymethyleugenol. Chem. Res. Toxicol. 2006, 19, 111-116.
-
(2006)
Chem. Res. Toxicol
, vol.19
, pp. 111-116
-
-
Jeurissen, S.M.F.1
Bogaards, J.J.P.2
Boersma, M.G.3
Ter Horst, J.P.F.4
Awad, H.M.5
Fiamegos, Y.C.6
Van Beek, T.A.7
Alink, G.M.8
Sudhölter, E.J.R.9
Cnubben, N.H.P.10
Rietjens, I.M.C.M.11
-
78
-
-
0036707621
-
Metabolism of the Endocrine Disruptor Pesticide-Methoxychlor by Human P450s: Pathways Involving a Novel Catechol Metabolite
-
Hu, Y.; Kupfer, D. Metabolism of the Endocrine Disruptor Pesticide-Methoxychlor by Human P450s: Pathways Involving a Novel Catechol Metabolite. Drug Metab. Dispos. 2002, 30, 1035-1042.
-
(2002)
Drug Metab. Dispos
, vol.30
, pp. 1035-1042
-
-
Hu, Y.1
Kupfer, D.2
-
79
-
-
4243125326
-
Identification of the Main Human Cytochrome P450 Enzymes Involved in Safrole 1′-Hydroxylation
-
Ueng, Y.-F.; Hsieh, C.-H.; Don, M.-J.; Chi, C.-W.; Ho, L.-K. Identification of the Main Human Cytochrome P450 Enzymes Involved in Safrole 1′-Hydroxylation. Chem. Res. Toxicol. 2004, 17, 1151-1156.
-
(2004)
Chem. Res. Toxicol
, vol.17
, pp. 1151-1156
-
-
Ueng, Y.-F.1
Hsieh, C.-H.2
Don, M.-J.3
Chi, C.-W.4
Ho, L.-K.5
-
80
-
-
2442599224
-
Role of Individual Human Cytochrome P450 Enzymes in the In Vitro Metabolism of Hydromorphone
-
Benetton, S. A.; Borges, V. M.; Chang, T. K. H.; McErlane, K. M. Role of Individual Human Cytochrome P450 Enzymes in the In Vitro Metabolism of Hydromorphone. Xenobiotica 2004, 34, 335-344.
-
(2004)
Xenobiotica
, vol.34
, pp. 335-344
-
-
Benetton, S.A.1
Borges, V.M.2
Chang, T.K.H.3
McErlane, K.M.4
-
81
-
-
0001357271
-
Identification of Enzymes Responsible for the Metabolism of Phenobarbital
-
San Diego, CA, International Society for the Study of Xenobiotics; p
-
Hargreaves, J. A.; Howald, W. N.; Racha, J. K.; Levy, R. H. Identification of Enzymes Responsible for the Metabolism of Phenobarbital. In Proceedings of the Seventh North American ISSX Meeting, San Diego, CA, 1996; International Society for the Study of Xenobiotics; p 259.
-
(1996)
Proceedings of the Seventh North American ISSX Meeting
, pp. 259
-
-
Hargreaves, J.A.1
Howald, W.N.2
Racha, J.K.3
Levy, R.H.4
-
82
-
-
0032820022
-
Cytochrome P-450 3A4 and 2C8 are Involved in Zopiclone Metabolism
-
Becquemont, L.; Mouajjah, S.; Escaffre, O.; Beaune, P.; Funck-Brentano, C.; Jaillon, P. Cytochrome P-450 3A4 and 2C8 are Involved in Zopiclone Metabolism. Drug Metab. Dispos. 1999, 27, 1068-1073.
-
(1999)
Drug Metab. Dispos
, vol.27
, pp. 1068-1073
-
-
Becquemont, L.1
Mouajjah, S.2
Escaffre, O.3
Beaune, P.4
Funck-Brentano, C.5
Jaillon, P.6
-
83
-
-
0031058342
-
Cytochromes P450 Mediating the N-Demethylation of Amitriptyline
-
Ghahramani, P.; Ellis, S. W.; Lennard, M. S.; Ramsay, L. E.; Tucker, G. T. Cytochromes P450 Mediating the N-Demethylation of Amitriptyline. Br. J. Clin. Pharmacol. 1997, 43, 137-144.
-
(1997)
Br. J. Clin. Pharmacol
, vol.43
, pp. 137-144
-
-
Ghahramani, P.1
Ellis, S.W.2
Lennard, M.S.3
Ramsay, L.E.4
Tucker, G.T.5
-
84
-
-
18544389188
-
The Influence of CYP2B6, CYP2C9 and CYP2D6 Genotypes on the Formation of the Potent Antioestrogen Z-4-Hydroxytamoxifen in Human Liver
-
Coller, J. K.; Krebsfaenger, N.; Klein, K.; Endrizzi, K.; Wolbold, R.; Lang, T.; Nussler, A.; Neuhaus, P.; Zanger, U. M.; Eichelbaum, M.; Murdter, T. E. The Influence of CYP2B6, CYP2C9 and CYP2D6 Genotypes on the Formation of the Potent Antioestrogen Z-4-Hydroxytamoxifen in Human Liver. Br. J. Clin. Pharmacol. 2002, 54, 157-167.
-
(2002)
Br. J. Clin. Pharmacol
, vol.54
, pp. 157-167
-
-
Coller, J.K.1
Krebsfaenger, N.2
Klein, K.3
Endrizzi, K.4
Wolbold, R.5
Lang, T.6
Nussler, A.7
Neuhaus, P.8
Zanger, U.M.9
Eichelbaum, M.10
Murdter, T.E.11
-
85
-
-
0001167520
-
Zafirlukast is a Substrate for CYP2C9 and an Inhibitor of CYP2C9 and CYP3A In Vitro
-
Grimm, S. W.; Stams, K. R.; Aaron, E. J. Zafirlukast is a Substrate for CYP2C9 and an Inhibitor of CYP2C9 and CYP3A In Vitro. Int. Soc. Study Xenobiot. Proc. 1996, 10, 392.
-
(1996)
Int. Soc. Study Xenobiot. Proc
, vol.10
, pp. 392
-
-
Grimm, S.W.1
Stams, K.R.2
Aaron, E.J.3
-
86
-
-
0036239908
-
Metabolism of (+)- and (-)-Limonenes to Respective Carveols and Perillyl Alcohols by CYP2C9 and CYP2C19 in Human Liver Microsomes
-
Miyazawa, M.; Shindo, M.; Shimada, T. Metabolism of (+)- and (-)-Limonenes to Respective Carveols and Perillyl Alcohols by CYP2C9 and CYP2C19 in Human Liver Microsomes. Drug Metab. Dispos. 2002, 30, 602-607.
-
(2002)
Drug Metab. Dispos
, vol.30
, pp. 602-607
-
-
Miyazawa, M.1
Shindo, M.2
Shimada, T.3
-
87
-
-
34547673017
-
Comparison of Topological, Shape, and Docking Methods in Virtual Screening
-
McGaughey, G. B.; Sheridan, R. P.; Bayly, C. I.; Culberson, J. C.; Kreatsoulas, C.; Lindsley, S.; Maiorov, V.; Truchon, J.-F.; Cornell, W. D. Comparison of Topological, Shape, and Docking Methods in Virtual Screening. J. Chem. Inf. Model. 2007, 47, 1504-1519.
-
(2007)
J. Chem. Inf. Model
, vol.47
, pp. 1504-1519
-
-
McGaughey, G.B.1
Sheridan, R.P.2
Bayly, C.I.3
Culberson, J.C.4
Kreatsoulas, C.5
Lindsley, S.6
Maiorov, V.7
Truchon, J.-F.8
Cornell, W.D.9
|