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Volumn 43, Issue 4, 2003, Pages 1308-1315

Use of robust classification techniques for the prediction of human cytochrome P450 2D6 inhibition

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EID: 0041698413     PISSN: 00952338     EISSN: None     Source Type: Journal    
DOI: 10.1021/ci030283p     Document Type: Article
Times cited : (182)

References (70)
  • 1
    • 0042430306 scopus 로고    scopus 로고
    • Pharmaceutical Research and Manufacturers of America: Washington, DC
    • Pharmaceutical Industry 2001 Profile; Pharmaceutical Research and Manufacturers of America: Washington, DC, 2001.
    • (2001) Pharmaceutical Industry 2001 Profile
  • 3
    • 0031975185 scopus 로고    scopus 로고
    • Update: Clinically significant cytochrome P-450 drug interactions
    • Michalets, E. L. Update: Clinically Significant Cytochrome P-450 Drug Interactions. Pharmacotherapy 1998, 18, 84-112.
    • (1998) Pharmacotherapy , vol.18 , pp. 84-112
    • Michalets, E.L.1
  • 5
    • 0028237729 scopus 로고
    • Interindividual variations in human liver cytochrome P450 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 P450 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
  • 7
    • 0029025655 scopus 로고
    • Recent advances: The cytochrome P450 enzymes
    • Slaughter, R. L.; Edwards, D. J. Recent Advances: The Cytochrome P450 Enzymes. Ann. Pharmacother. 1995, 29, 619-624.
    • (1995) Ann. Pharmacother. , vol.29 , pp. 619-624
    • Slaughter, R.L.1    Edwards, D.J.2
  • 8
    • 0031768733 scopus 로고    scopus 로고
    • In vitro characterization of cytochrome P450 2D6 inhibition by classic histamine H1 receptor antagonists
    • Hamelin, B. A.; Bouayad, A.; Drolet, B.; Gravel, A.; Turgeon, J. In vitro Characterization of Cytochrome P450 2D6 Inhibition by Classic Histamine H1 Receptor Antagonists. Drug Metab. Dispos. 1998, 26, 536-539.
    • (1998) Drug Metab. Dispos. , vol.26 , pp. 536-539
    • Hamelin, B.A.1    Bouayad, A.2    Drolet, B.3    Gravel, A.4    Turgeon, J.5
  • 9
    • 0036328632 scopus 로고    scopus 로고
    • Inhibition of risperidone metabolism by fluoxetine in patients with schizophrenia: A clinically relevant pharmacokinetic drug interaction
    • Spina, E.; Avenosa, A.; Scordo, M. G.; Ancione, M.; Madia, A.; Gatti, G.; Perucca, E. Inhibition of Risperidone Metabolism by Fluoxetine in Patients with Schizophrenia: a Clinically Relevant Pharmacokinetic Drug Interaction. J. Clin. Psychopharmacol. 2002, 22, 419-423.
    • (2002) J. Clin. Psychopharmacol. , vol.22 , pp. 419-423
    • Spina, E.1    Avenosa, A.2    Scordo, M.G.3    Ancione, M.4    Madia, A.5    Gatti, G.6    Perucca, E.7
  • 11
    • 0030430035 scopus 로고    scopus 로고
    • Cytochrome P450-mediated metabolism of the HIV-1 protease inhibitor ritonavir (ABT-538) in human liver microsomes
    • Kumar, G. N.; Rodrigues, A. D.; Buko, A. M.; Dinssen, J. F. Cytochrome P450-mediated Metabolism of the HIV-1 Protease Inhibitor Ritonavir (ABT-538) in Human Liver Microsomes. J. Pharmacol. Exp. Ther. 1996, 277, 423-431.
    • (1996) J. Pharmacol. Exp. Ther. , vol.277 , pp. 423-431
    • Kumar, G.N.1    Rodrigues, A.D.2    Buko, A.M.3    Dinssen, J.F.4
  • 12
    • 0032817291 scopus 로고    scopus 로고
    • Investigation of classification methods for the prediction of activity in diverse chemical libraries
    • Dixon, S. L.; Villar, H. O. Investigation of Classification methods for the Prediction of Activity in Diverse Chemical Libraries. J. Comput.-Aided Mol. Design 1999, 13, 533-545.
    • (1999) J. Comput.-Aided Mol. Design , vol.13 , pp. 533-545
    • Dixon, S.L.1    Villar, H.O.2
  • 14
    • 0027314831 scopus 로고
    • Development of a pharmacophore for inhibition of human liver cytochrome P-450 2D6: Molecular modeling and inhibition studies
    • Strobl, G. R.; von Kruedener, S.; Steockigt, J.; Guengerich, F. P.; Wolff, T. Development of a Pharmacophore for Inhibition of Human Liver Cytochrome P-450 2D6: Molecular Modeling and Inhibition Studies. J. Med. Chem. 1993, 36, 1136-1145.
    • (1993) J. Med. Chem. , vol.36 , pp. 1136-1145
    • Strobl, G.R.1    Von Kruedener, S.2    Steockigt, J.3    Guengerich, F.P.4    Wolff, T.5
  • 15
    • 0032870308 scopus 로고    scopus 로고
    • Multiple cytochrome P-450s involved in the metabolism of terbinfine suggest a limited potential for drug-drug interactions
    • Vickers, A. E. M.; Sinclair, J. R.; Zollinger, M.; Heitz, F.; Glanzel, U.; Johanson, L.; Fischer, V. Multiple Cytochrome P-450s Involved in the Metabolism of Terbinfine 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    Glanzel, U.5    Johanson, L.6    Fischer, V.7
  • 17
    • 0032849040 scopus 로고    scopus 로고
    • Three and four-dimensional-quantitative structure activity relationship (3D/4D-QSAR) analysis of CYP2D6 inhibitors
    • Ekins, S.; Bravi, G.; Binkley, S.; Gillespie, J. S.; Ring, B. J.; Wikel, J. H.; Wrighton, S. A. Three and Four-Dimensional-Quantitative Structure Activity Relationship (3D/4D-QSAR) Analysis of CYP2D6 Inhibitors. Pharmacogenetics 1999, 9.
    • (1999) Pharmacogenetics , pp. 9
    • Ekins, S.1    Bravi, G.2    Binkley, S.3    Gillespie, J.S.4    Ring, B.J.5    Wikel, J.H.6    Wrighton, S.A.7
  • 18
    • 0030996094 scopus 로고    scopus 로고
    • The in vivo interaction of dexmedetomidine with human liver microsomal cytochrome P4502D6 (CYP2D6)
    • Rodrigues, A. D.; Roberts, E. M. The in vivo Interaction of Dexmedetomidine with Human Liver Microsomal Cytochrome P4502D6 (CYP2D6). Drug Metab. Dispos. 1997, 25, 651-655.
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 651-655
    • Rodrigues, A.D.1    Roberts, E.M.2
  • 19
    • 0029008593 scopus 로고
    • Computer prediction and experimental validation of cytochrome P4502D6-dependent oxidation of GBR 12909
    • de Groot, M. J.; Bijloo, G. J.; Hansen, K. T.; Vermeulen, N. P. E. Computer Prediction and Experimental Validation of Cytochrome P4502D6-Dependent Oxidation of GBR 12909. Drug Metab. Dispos. 1995, 23, 667-669.
    • (1995) Drug Metab. Dispos. , vol.23 , pp. 667-669
    • De Groot, M.J.1    Bijloo, G.J.2    Hansen, K.T.3    Vermeulen, N.P.E.4
  • 20
  • 21
    • 0032870729 scopus 로고    scopus 로고
    • Effect of antipsychotic drugs on human liver cytochrome P-450 (CYP) isoforms in vitro: Preferred inhibition of CYP2D6
    • Shin, J.-G.; Soukhova, N.; Flockhart, D. A. Effect of Antipsychotic Drugs on Human Liver Cytochrome P-450 (CYP) Isoforms in vitro: Preferred Inhibition of CYP2D6. Drug Metab. Dispos. 1999, 27, 1078-1084.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 1078-1084
    • Shin, J.-G.1    Soukhova, N.2    Flockhart, D.A.3
  • 22
    • 0028816462 scopus 로고
    • Mepyramine, a histamine HI receptor antagonist, inhibits the metabolic activity of rat and human P450 2D forms
    • Hiroi, T.; Ohishi, N.; Imaoka, S.; Yabusaki, Y.; Fukui, H.; Funae, Y. Mepyramine, a Histamine HI Receptor Antagonist, Inhibits the Metabolic Activity of Rat and Human P450 2D Forms. J. Pharmacol. Exp. Ther. 1995, 272, 939-944.
    • (1995) J. Pharmacol. Exp. Ther. , vol.272 , pp. 939-944
    • Hiroi, T.1    Ohishi, N.2    Imaoka, S.3    Yabusaki, Y.4    Fukui, H.5    Funae, Y.6
  • 23
    • 0033917295 scopus 로고    scopus 로고
    • Inhibition of human cytochrome P450 enzymes by constituents of St. John's Wort, an herbal preparation used in the treatment of depression
    • Oback, R. S. Inhibition of Human Cytochrome P450 Enzymes by Constituents of St. John's Wort, an Herbal Preparation Used in the Treatment of Depression. J. Pharmacol. Exp. Ther. 2000, 294, 88-95.
    • (2000) J. Pharmacol. Exp. Ther. , vol.294 , pp. 88-95
    • Oback, R.S.1
  • 24
    • 0030834105 scopus 로고    scopus 로고
    • Venlafaxine: In vitro inhibition of CYP2D6-dependent imipramine and desipramine metabolism; comparative studies with selected SSRIs, and effects on human hepatic CYP3A4, CYP2C9 and CYP1A2
    • Ball, S. E.; Ahern, D.; Scatina, J.; Kao, J. Venlafaxine: in vitro Inhibition of CYP2D6-Dependent Imipramine and Desipramine Metabolism; Comparative Studies with Selected SSRIs, and Effects on Human Hepatic CYP3A4, CYP2C9 and CYP1A2. Br. J. Clin. Pharmacol. 1997, 43, 619-626.
    • (1997) Br. J. Clin. Pharmacol , vol.43 , pp. 619-626
    • Ball, S.E.1    Ahern, D.2    Scatina, J.3    Kao, J.4
  • 25
    • 0035155095 scopus 로고    scopus 로고
    • Application of higher throughput screening (HTS) inhibition assays to evaluate the interaction of antiparasitic drugs with cytochrome P450s
    • Bapiro, T. E.; Egnell, A.-C.; Hasler, J. A.; Masimirembwa, C. M. Application of Higher Throughput Screening (HTS) Inhibition Assays to Evaluate the Interaction of Antiparasitic Drugs with Cytochrome P450s. Drug Metab. Dispos. 2001, 29, 30-35.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 30-35
    • Bapiro, T.E.1    Egnell, A.-C.2    Hasler, J.A.3    Masimirembwa, C.M.4
  • 26
    • 0027410086 scopus 로고
    • The metabolism of aprindine in relation to the sparteine/debrisoquine polymorphism
    • Ebner, T.; Eichelbaum, M. The Metabolism of Aprindine in Relation to the Sparteine/Debrisoquine Polymorphism. Br. J. Clin. Pharmacol. 1993, 35, 426-430.
    • (1993) Br. J. Clin. Pharmacol. , vol.35 , pp. 426-430
    • Ebner, T.1    Eichelbaum, M.2
  • 27
    • 0032750751 scopus 로고    scopus 로고
    • Cytoohrome P-450-mediated metabolism of the individual enantiomers of the antidepressant agent reboxetine in human liver microsomes
    • Wienkers, L. C.; Allievi, C.; Hauer, M. J.; Wynalda, M. A. Cytoohrome P-450-Mediated Metabolism of the Individual Enantiomers of the Antidepressant Agent Reboxetine in Human Liver Microsomes. Drug Metab. Dispos. 1999, 27, 1334-1340.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 1334-1340
    • Wienkers, L.C.1    Allievi, C.2    Hauer, M.J.3    Wynalda, M.A.4
  • 28
    • 0034128040 scopus 로고    scopus 로고
    • In vitro inhibition of the cytochrome P450 (CYP450) system by the antiplatelet drug ticlopidine: Potent effect on CYP2C19 and CYP2D6
    • Ko, J. W.; Desta, Z.; Soukhova, N. V.; Tracy, T.; Flockhart, D. A. In vitro Inhibition of the Cytochrome P450 (CYP450) System by the Antiplatelet Drug Ticlopidine: Potent Effect on CYP2C19 and CYP2D6. Br. J. Clin. Pharmacol. 2000, 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
  • 30
    • 0026666976 scopus 로고
    • The antipsychotic clozapine is metabolized by the polymorphic human microsomal and recombinant cytochrome P450 2D6
    • Fischer, V.; Vogels, B.; Maurer, O.; Tynes, R. E. The Antipsychotic Clozapine is Metabolized by the Polymorphic Human Microsomal and Recombinant Cytochrome P450 2D6. J. Pharmacol. Exp. Ther. 1992, 200, 1355-1360.
    • (1992) J. Pharmacol. Exp. Ther. , vol.200 , pp. 1355-1360
    • Fischer, V.1    Vogels, B.2    Maurer, O.3    Tynes, R.E.4
  • 31
    • 0028194864 scopus 로고
    • Inhibition of desipramine hydroxylation in vitro by serotonin-reuptake-inhibitor antidepressants, and by quinidine and ketoconazole: A model system to predict drug interactions in vivo
    • Von Moltke, L. L. D. J. G.; Cotreau-Bibbo, M. M.; Duan, S. X.; Harmatz, J. S.; Jerold, S.; Shader, R. I. Inhibition of Desipramine Hydroxylation in vitro by Serotonin-reuptake-inhibitor Antidepressants, and by Quinidine and ketoconazole: a Model System to Predict Drug Interactions in vivo. J Pharmacol. Exp. Ther. 1994, 268, 1278-1283.
    • (1994) J Pharmacol. Exp. Ther. , vol.268 , pp. 1278-1283
    • Von Moltke, L.L.D.J.G.1    Cotreau-Bibbo, M.M.2    Duan, S.X.3    Harmatz, J.S.4    Jerold, S.5    Shader, R.I.6
  • 32
    • 0034014925 scopus 로고    scopus 로고
    • Identification of the major human liver cytochrome P450 isoform(s) responsible for the formation of the primary metabolites of ziprasidone and prediction of possible drug interactions
    • Prakash, C.; Kamel, A.; Cui, D.; Whalen, R. D.; Miceli, J. J.; Tweedie, D. Identification of the Major Human Liver Cytochrome P450 Isoform(s) Responsible for the Formation of the Primary Metabolites of Ziprasidone and Prediction of Possible Drug Interactions. Br. J. Clin. Pharmacol. 2000, 49, 35S-42S.
    • (2000) Br. J. Clin. Pharmacol. , vol.49
    • Prakash, C.1    Kamel, A.2    Cui, D.3    Whalen, R.D.4    Miceli, J.J.5    Tweedie, D.6
  • 33
    • 0035155252 scopus 로고    scopus 로고
    • Interaction of delavirdine with human liver microsomal cytochrome P450: Inhibition of CYP2C9, CYP2C19, and CYP2D6
    • Voorman, R. L.; Payne, N. A.; Wienkers, L. C.; Hauer, M. J.; Sanders, P. E. Interaction of Delavirdine with Human Liver Microsomal Cytochrome P450: Inhibition of CYP2C9, CYP2C19, and CYP2D6. Drug Metab. Dispos. 2001, 29, 41-47.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 41-47
    • Voorman, R.L.1    Payne, N.A.2    Wienkers, L.C.3    Hauer, M.J.4    Sanders, P.E.5
  • 34
    • 0028316987 scopus 로고
    • Atypical metabolism of deprenyl and its enantiomer, (S)-(+), a-dimethyl-N-propynylphen-ethylamine, by cytochrome P450 2D6
    • Grace, J. M.; Kinter, M. T.; MacDonald, T. L. Atypical Metabolism of Deprenyl and its Enantiomer, (S)-(+), a-Dimethyl-N-Propynylphen-ethylamine, by Cytochrome P450 2D6. Chem. Res. Toxlcol. 1994, 7, 286-290.
    • (1994) Chem. Res. Toxlcol. , vol.7 , pp. 286-290
    • Grace, J.M.1    Kinter, M.T.2    MacDonald, T.L.3
  • 35
    • 0029979348 scopus 로고    scopus 로고
    • Inhibition of cytochrome P450 by nefazodone in vitro: Studies of dextromethorphan O- and N-demethylation
    • Schmider, J.; Greenblatt, D. J.; von Moltke, L. J.; Harmatz, J. S.; Shader, R. I. Inhibition of Cytochrome P450 by Nefazodone in vitro: Studies of Dextromethorphan O- and N-demethylation. Br. J. Clin. Pharmacol 1996, 41, 339-343.
    • (1996) Br. J. Clin. Pharmacol , vol.41 , pp. 339-343
    • Schmider, J.1    Greenblatt, D.J.2    Von Moltke, L.J.3    Harmatz, J.S.4    Shader, R.I.5
  • 36
    • 0028080520 scopus 로고
    • The inhibitory effect of amiodarone and desethylamiodarone on dextromethorphan O-demethylation in human and rat liver microsomes
    • Jaruratanasirikul, S.; Hortiwakul, R. The Inhibitory Effect of Amiodarone and Desethylamiodarone on Dextromethorphan O-demethylation in Human and Rat Liver Microsomes. J. Pharm. Pharmacol. 1994, 46, 933-935.
    • (1994) J. Pharm. Pharmacol. , vol.46 , pp. 933-935
    • Jaruratanasirikul, S.1    Hortiwakul, R.2
  • 38
    • 0344765487 scopus 로고    scopus 로고
    • Characterization of the selectivity and mechanism of human cytochrome P450 inhibition by the human immunodeficiency virus-protease inhbitor nelfinavir mesylate
    • Lillibridge, J. H.; Liang, B. H.; Kerr, B. M.; Webber, S.; Quart, B.; Shetty, B. V.; Lee, C. A. Characterization of the Selectivity and Mechanism of Human Cytochrome P450 Inhibition by the Human Immunodeficiency Virus-Protease Inhbitor Nelfinavir Mesylate. Drug Metab. Dispos. 1998, 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
  • 39
    • 0035144768 scopus 로고    scopus 로고
    • Inhibition of cytochrome P450 (CYP450) isoforms by isoniazid: Potent inhibition of CYP2C19 and CYP3A
    • Desta, Z.; Soukhova, N. V.; Flockhart, D. A. Inhibition of Cytochrome P450 (CYP450) Isoforms by Isoniazid: Potent Inhibition of CYP2C19 and CYP3A. Antimicrob. Agents Chemother. 2001, 45, 382-392.
    • (2001) Antimicrob. Agents Chemother. , vol.45 , pp. 382-392
    • Desta, Z.1    Soukhova, N.V.2    Flockhart, D.A.3
  • 40
    • 0032910986 scopus 로고    scopus 로고
    • Preclinical and in vitro assessment of the potential of D0870, an antifungal agent, for producing clinical drug interactions
    • McKillop, D.; Back, D. J.; McCormick, A. D.; Evans, J. A.; Tjia, J. Preclinical and in vitro Assessment of the Potential of D0870, an Antifungal Agent, for Producing Clinical Drug Interactions. Xenobiotica 1999, 29, 395-408.
    • (1999) Xenobiotica , vol.29 , pp. 395-408
    • McKillop, D.1    Back, D.J.2    McCormick, A.D.3    Evans, J.A.4    Tjia, J.5
  • 41
    • 0036177763 scopus 로고    scopus 로고
    • The gastroprokinetic and antiemetic drug metoclopramide is a substrate and inhibitor of cytochrome P450 2D6
    • Destra, Z.; Wu, G. M.; Morocho, A. M.; Flockhart, D. A. The Gastroprokinetic and Antiemetic Drug Metoclopramide Is a Substrate and Inhibitor of Cytochrome P450 2D6. Drug Metab. Dispos. 2002, 30, 336-343.
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 336-343
    • Destra, Z.1    Wu, G.M.2    Morocho, A.M.3    Flockhart, D.A.4
  • 42
    • 0033029616 scopus 로고    scopus 로고
    • Inhibitory effects of azelastine and its metabolites on drug oxidation catalyzed by human cytochrome P4050 enzymes
    • Nakajima, M.; Ohyama, K.; Nakamura, S.; Shimada, N.; Yamazaki, H.; Yokoi, T. Inhibitory Effects of Azelastine and its Metabolites on Drug Oxidation Catalyzed by Human Cytochrome P4050 Enzymes. Drug Metab. Dispos. 1999, 27, 792-797.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 792-797
    • Nakajima, M.1    Ohyama, K.2    Nakamura, S.3    Shimada, N.4    Yamazaki, H.5    Yokoi, T.6
  • 43
    • 0028812667 scopus 로고
    • An investigation of the interaction between halofantrine, CYP2D6 and CYP3A4: Studies with human liver microsomes and heterologous enzyme expression systems
    • Halliday, R. C.; Jones, B. C.; Smith, D. A.; Kitteringham, N. R.; Park, B. K. An Investigation of the Interaction between Halofantrine, CYP2D6 and CYP3A4: Studies with Human Liver Microsomes and Heterologous Enzyme Expression Systems. Br. J. Clin. Pharmacol. 1995, 40, 369-378.
    • (1995) Br. J. Clin. Pharmacol. , vol.40 , pp. 369-378
    • Halliday, R.C.1    Jones, B.C.2    Smith, D.A.3    Kitteringham, N.R.4    Park, B.K.5
  • 45
    • 0034932451 scopus 로고    scopus 로고
    • Inhibition and inactivation of human cytochrome P450 isoforms by phenethylisothiocyanate
    • Nakajima, M.; Yoshida, R.; Shimada, N.; Yamazaki, H.; Yokoi, T. Inhibition and Inactivation of Human Cytochrome P450 Isoforms by Phenethylisothiocyanate. Drug Metab. Dispos. 2001, 29, 1110-1113.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 1110-1113
    • Nakajima, M.1    Yoshida, R.2    Shimada, N.3    Yamazaki, H.4    Yokoi, T.5
  • 46
    • 0034821488 scopus 로고    scopus 로고
    • In vitro metabolism of tegaserod in human liver and intestine: Assessment of drug interactions
    • Vickers, A. E. M.; Zollinger, M.; Dannecker, R.; Tynes, R.; Heitz, F.; Fischer, V, In vitro Metabolism of Tegaserod in Human Liver and Intestine: Assessment of Drug Interactions. Drug Metab. Dispos. 2001, 29, 1269-1276.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 1269-1276
    • Vickers, A.E.M.1    Zollinger, M.2    Dannecker, R.3    Tynes, R.4    Heitz, F.5    Fischer, V.6
  • 47
    • 0034960661 scopus 로고    scopus 로고
    • Metabolism of ipecac alkaloids cephaeline and emetine by human hepatic microsomal cytochrome P450s and their inhibitory effects on P450 enzyme activities
    • Asano, T.; Kushida, H.; Sadakane, C.; Ishihar, K.; Wakui, Y.; Yangisawa, T.; Kimura, M.; Kamei, H.; Yoshida, T. Metabolism of Ipecac Alkaloids Cephaeline and Emetine by Human Hepatic Microsomal Cytochrome P450s and their Inhibitory Effects on P450 Enzyme Activities. Biol. Pharm. Bull. 2001, 24, 678-682.
    • (2001) Biol. Pharm. Bull. , vol.24 , pp. 678-682
    • Asano, T.1    Kushida, H.2    Sadakane, C.3    Ishihar, K.4    Wakui, Y.5    Yangisawa, T.6    Kimura, M.7    Kamei, H.8    Yoshida, T.9
  • 49
    • 0029983702 scopus 로고    scopus 로고
    • In vitro interaction of the antipsychotic agent olanzapine with human cytochrome P450 CYP2C9, CYP2C19, CYP2D6, and CYP3A
    • Ring, B. J.; Binkley, S. N.; Vandenbranden, M.; Wrighton, S. A. In vitro Interaction of the Antipsychotic Agent Olanzapine with Human Cytochrome P450 CYP2C9, CYP2C19, CYP2D6, and CYP3A. Br. J. Clin. Pharm. 1996.
    • (1996) Br. J. Clin. Pharm.
    • Ring, B.J.1    Binkley, S.N.2    Vandenbranden, M.3    Wrighton, S.A.4
  • 50
    • 0033791657 scopus 로고    scopus 로고
    • In vitro evaluation of the disposition of a novel cysteine protease inhibitor
    • Jacobsen, W.; Christians, U.; Benet, L. Z. In vitro Evaluation of the Disposition of a Novel Cysteine Protease Inhibitor. Drug Metab. Dispos. 2000, 28, 1343-1351.
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 1343-1351
    • Jacobsen, W.1    Christians, U.2    Benet, L.Z.3
  • 51
    • 0032937343 scopus 로고    scopus 로고
    • 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.; Bladeck, 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    Bladeck, J.-P.6    Robinson, W.T.7
  • 52
    • 0030812885 scopus 로고    scopus 로고
    • In vitro metabolism of simvastatin in humans [SET] identification of metabolizing enzymes and effect of the drug on hepatic P450s
    • Prueksaritanont, T.; Gorhan, L. M.; Ma, B.; Liu, L.; Yu, X.; Zhao, J. J.; Slaughter, D. E.; Arison, B. H.; Vyas, K. P. In vitro Metabolism of Simvastatin in Humans [SET] Identification of Metabolizing Enzymes and Effect of the Drug on Hepatic P450s. Drug Metab. Dispos. 1997, 25, 1191-1199.
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 1191-1199
    • Prueksaritanont, T.1    Gorhan, L.M.2    Ma, B.3    Liu, L.4    Yu, X.5    Zhao, J.J.6    Slaughter, D.E.7    Arison, B.H.8    Vyas, K.P.9
  • 53
    • 0029920517 scopus 로고    scopus 로고
    • Significance of metabolism in the disposition and action of the antidysrythmic drug, dofetilide. In vitro studies and correlation with in vivo data
    • Walker, D. K.; Alabaster, C. T.; Congrave, G. S.; Hargreaves, M. B.; Hyland, R. J.; Jones, B. C.; Reed, L. J.; Smith, D. A. Significance of Metabolism in the Disposition and Action of the Antidysrythmic Drug, Dofetilide. In vitro Studies and Correlation with in vivo Data. Drug Metab. Dispos. 1996, 24, 447-455.
    • (1996) Drug Metab. Dispos. , vol.24 , pp. 447-455
    • Walker, D.K.1    Alabaster, C.T.2    Congrave, G.S.3    Hargreaves, M.B.4    Hyland, R.J.5    Jones, B.C.6    Reed, L.J.7    Smith, D.A.8
  • 54
    • 0032963256 scopus 로고    scopus 로고
    • In vitro evaluation of potential drug interactions with levetiracetam, a new antiepileptic agent
    • Nicolas, J.-M.; Collart, P.; Gerin, B.; Mather, G.; Trager, W.; Levy, R.; Roba, J. In vitro Evaluation of Potential Drug Interactions with Levetiracetam, a New Antiepileptic Agent. Drug Metab. Dispos. 1999, 27, 250-254.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 250-254
    • Nicolas, J.-M.1    Collart, P.2    Gerin, B.3    Mather, G.4    Trager, W.5    Levy, R.6    Roba, J.7
  • 55
    • 0032977948 scopus 로고    scopus 로고
    • Lack of single-dose disulfiram effects on cytochrome P-450 2c9, 2C19, 2D6, and 3A4 activities: Evidence for specificity toward P-450 2E1
    • Kharasch, E. D.; Hankins, D. C.; Jubert, C. T.; Thummel, K. E.; Taraday, J. K. Lack of Single-Dose Disulfiram Effects on Cytochrome P-450 2c9, 2C19, 2D6, and 3A4 Activities: Evidence for Specificity toward P-450 2E1. Drug Metab. Dispos. 1999, 27, 717-723.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 717-723
    • Kharasch, E.D.1    Hankins, D.C.2    Jubert, C.T.3    Thummel, K.E.4    Taraday, J.K.5
  • 56
    • 0034048206 scopus 로고    scopus 로고
    • In vitro inhibition and induction of human hepatic cytochrome P450 enzymes by modafinil
    • Robertson, P.; Decory, H. H.; Madan, A.; Parkinson, A. In vitro Inhibition and Induction of Human Hepatic Cytochrome P450 Enzymes by Modafinil. Drug Metab. Dispos. 2000, 28, 664-671.
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 664-671
    • Robertson, P.1    Decory, H.H.2    Madan, A.3    Parkinson, A.4
  • 57
    • 0032727054 scopus 로고    scopus 로고
    • Characterization of the in vitro biotransformation of the HIV-1 reverse transcriptase inhibitor nevirapine by human hepatic cytochromes P-450
    • Erickson, D. A.; Mather, G.; Trager, W. F.; Levy, R. H.; Keirns, J. J. Characterization of the in vitro Biotransformation of the HIV-1 Reverse Transcriptase Inhibitor Nevirapine by Human Hepatic Cytochromes P-450. Drug Metab. Dispos. 1999, 27, 1488-1495.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 1488-1495
    • Erickson, D.A.1    Mather, G.2    Trager, W.F.3    Levy, R.H.4    Keirns, J.J.5
  • 58
    • 0030908183 scopus 로고    scopus 로고
    • Inhibition of human drug metabolizing cytochromes P450 by anastrozole, a potent and selective inhibitor of aromatase
    • Grimm, S. W.; Dyroff, M. C. Inhibition of Human Drug Metabolizing Cytochromes P450 by Anastrozole, a Potent and Selective Inhibitor of Aromatase. Drug Metab. Dispos. 1997, 25, 598-602.
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 598-602
    • Grimm, S.W.1    Dyroff, M.C.2
  • 61
    • 0032702307 scopus 로고    scopus 로고
    • In vitro inhibition of human liver drug metabolizing enzymes by second generation antihistamines
    • Nicolas, J.-M.; Whomsley, R.; Collart, P.; Roba, J. In vitro Inhibition of Human Liver Drug Metabolizing Enzymes by Second Generation Antihistamines. Chem.-Biol. Interact. 1999, 123, 63-79.
    • (1999) Chem.-Biol. Interact. , vol.123 , pp. 63-79
    • Nicolas, J.-M.1    Whomsley, R.2    Collart, P.3    Roba, J.4
  • 64
    • 0034013033 scopus 로고    scopus 로고
    • Assessment of specificity of eight chemical inhibitors using cDNA-expressed cytochromes P450
    • Sai, Y.; Dai, R.; Yang, T. J.; Krausz, K. W.; Gonzalez, F. J.; Gelboin, H. V.; Shou, M. Assessment of Specificity of Eight Chemical Inhibitors Using cDNA-Expressed Cytochromes P450. Xenobiotica 2000, 50, 327-343.
    • (2000) Xenobiotica , vol.50 , pp. 327-343
    • Sai, Y.1    Dai, R.2    Yang, T.J.3    Krausz, K.W.4    Gonzalez, F.J.5    Gelboin, H.V.6    Shou, M.7
  • 67
    • 0030211964 scopus 로고    scopus 로고
    • Bagging predictors
    • Breiman, L. Bagging Predictors. Machine Learning 1996, 24, 123-140.
    • (1996) Machine Learning , vol.24 , pp. 123-140
    • Breiman, L.1
  • 68
    • 0042931027 scopus 로고    scopus 로고
    • Accelrys: San Diego, CA
    • 2, ccM ed.; Accelrys: San Diego, CA, 2001.
    • (2001) 2, ccM Ed.
  • 69
    • 0035829402 scopus 로고    scopus 로고
    • One-dimensional molecular representations and similarity calculations: Methodology and validation
    • Dixon, S. L.; Kenneth, M.; Merz, J. One-Dimensional Molecular Representations and Similarity Calculations: Methodology and Validation. J. Med. Chem. 2001, 44, 3795-3809.
    • (2001) J. Med. Chem. , vol.44 , pp. 3795-3809
    • Dixon, S.L.1    Kenneth, M.2    Merz, J.3
  • 70
    • 0042931028 scopus 로고    scopus 로고
    • Insightful Corporation: Seattle, WA
    • S-PLUS 6.1 for Windows; Insightful Corporation: Seattle, WA, 2001.
    • (2001) S-PLUS 6.1 for Windows


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.