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Volumn 24, Issue 5, 2007, Pages 842-858

The evolving role of drug metabolism in drug discovery and development

Author keywords

Drug discovery and development; Drug interactions clearance; Drug metabolism; Exposure; Idiosyncratic drug toxicity; Inhibition; Integration of emerging sciences; Pharmacogenetics; Pharmacogenomics; Transporters

Indexed keywords

ATORVASTATIN; CARBAMAZEPINE; CELL NUCLEUS RECEPTOR; CLARITHROMYCIN; CLOZAPINE; CYTOCHROME P450; DAPSONE; DICLOFENAC; DIGOXIN; DRUG METABOLIZING ENZYME; FEXOFENADINE; GENE PRODUCT; HALOTHANE; INDOMETACIN; ISONIAZID; MULTIDRUG RESISTANCE PROTEIN 2; ORGANIC ANION TRANSPORTER; PARACETAMOL; PHENACETIN; PROCAINAMIDE; PROPAFENONE; QUINIDINE; TACRINE; TALINOLOL; TAMOXIFEN; TICLOPIDINE; TIENILIC ACID; TROGLITAZONE; UNINDEXED DRUG; VALPROIC ACID;

EID: 34247631742     PISSN: 07248741     EISSN: 1573904X     Source Type: Journal    
DOI: 10.1007/s11095-006-9217-9     Document Type: Review
Times cited : (62)

References (197)
  • 1
    • 0000739622 scopus 로고
    • The enzymatic deamination of amphetamine (benzedrine)
    • J. Axelrod. The enzymatic deamination of amphetamine (benzedrine) J. Biol. Chem. 214:753-763 (1955).
    • (1955) J. Biol. Chem , vol.214 , pp. 753-763
    • Axelrod, J.1
  • 2
    • 0013571647 scopus 로고
    • Conversion by the human of the testis hormone, testosterone, into the urinary androgen, androsterone
    • R. I. Dorfman, J. W. Cook, and J. B. Hamilton. Conversion by the human of the testis hormone, testosterone, into the urinary androgen, androsterone J. Biol. Chem. 130:285-295 (1939).
    • (1939) J. Biol. Chem , vol.130 , pp. 285-295
    • Dorfman, R.I.1    Cook, J.W.2    Hamilton, J.B.3
  • 3
    • 84961026584 scopus 로고
    • On the protective action of certain polycyclic aromatic hydrocarbons against carcinogenesis by aminoazo dyes and 2-acetylaminofluorene
    • E. C. Miller, J. A. Miller, R. R. Brown, and J. C. Macdonald. On the protective action of certain polycyclic aromatic hydrocarbons against carcinogenesis by aminoazo dyes and 2-acetylaminofluorene Cancer Res. 18:469-477 (1958).
    • (1958) Cancer Res , vol.18 , pp. 469-477
    • Miller, E.C.1    Miller, J.A.2    Brown, R.R.3    Macdonald, J.C.4
  • 4
    • 0001315679 scopus 로고
    • The metabolism of 4- dimethylaminoazobenzene by rat liver homogenates
    • G. C. Mueller and J. A. Miller. The metabolism of 4- dimethylaminoazobenzene by rat liver homogenates J. Biol. Chem. 176:535-544 (1948).
    • (1948) J. Biol. Chem , vol.176 , pp. 535-544
    • Mueller, G.C.1    Miller, J.A.2
  • 5
    • 0001477544 scopus 로고
    • The metabolism of methylated aminoazo dyes. II. Oxidative demethylation by rat liver homogenates
    • G. C. Mueller and J. A. Miller. The metabolism of methylated aminoazo dyes. II. Oxidative demethylation by rat liver homogenates J. Biol. Chem. 202:579-587 (1953).
    • (1953) J. Biol. Chem , vol.202 , pp. 579-587
    • Mueller, G.C.1    Miller, J.A.2
  • 6
    • 2642661712 scopus 로고
    • Conversion of androstenedione to estrone by placental microsomes
    • K. J. Ryan. Conversion of androstenedione to estrone by placental microsomes Biochim. Biophys. Acta 27:658-659 (1958).
    • (1958) Biochim. Biophys. Acta , vol.27 , pp. 658-659
    • Ryan, K.J.1
  • 9
    • 30344448851 scopus 로고    scopus 로고
    • Phase I and II drug metabolism: Terminology that we should phase out?
    • P. D. Josephy, F. P. Guengerich, and J. O. Miners. Phase I and II drug metabolism: terminology that we should phase out? Drug Metab. Rev.37:575-580 (2005).
    • (2005) Drug Metab. Rev , vol.37 , pp. 575-580
    • Josephy, P.D.1    Guengerich, F.P.2    Miners, J.O.3
  • 10
    • 0004779396 scopus 로고
    • Mechanisms of oxygen metabolism
    • H. S. Mason. Mechanisms of oxygen metabolism Science 125:1185-1188 (1957).
    • (1957) Science , vol.125 , pp. 1185-1188
    • Mason, H.S.1
  • 11
    • 0001426302 scopus 로고
    • Photochemical action spectrum of the terminal oxidase of mixed function oxidase systems
    • D. Y. Cooper, S. Levin, S. Narasimhulu, and O. Rosenthal. Photochemical action spectrum of the terminal oxidase of mixed function oxidase systems Science 147:400-402 (1965).
    • (1965) Science , vol.147 , pp. 400-402
    • Cooper, D.Y.1    Levin, S.2    Narasimhulu, S.3    Rosenthal, O.4
  • 12
    • 0001045385 scopus 로고
    • A new cytochrome in liver microsomes
    • T. Omura and R. Sato. A new cytochrome in liver microsomes J. Biol. Chem. 237:1375-1376 (1962).
    • (1962) J. Biol. Chem , vol.237 , pp. 1375-1376
    • Omura, T.1    Sato, R.2
  • 13
    • 0000747371 scopus 로고
    • The light reversible carbon monoxide inhibition of the steroid C21-hydroxylase system of the adrenal cortex
    • R. W. Estabrook, D. Y. Cooper, and O. Rosenthal. The light reversible carbon monoxide inhibition of the steroid C21-hydroxylase system of the adrenal cortex Biochem. Z. 338:741-755 (1963).
    • (1963) Biochem. Z , vol.338 , pp. 741-755
    • Estabrook, R.W.1    Cooper, D.Y.2    Rosenthal, O.3
  • 14
    • 0014429295 scopus 로고
    • Role of hemoprotein P-450 in fatty acid omega-hydroxylation in a soluble enzyme system from liver microsomes
    • A. Y. Lu and M. J. Coon. Role of hemoprotein P-450 in fatty acid omega-hydroxylation in a soluble enzyme system from liver microsomes J. Biol. Chem. 243:1331-1332 (1968).
    • (1968) J. Biol. Chem , vol.243 , pp. 1331-1332
    • Lu, A.Y.1    Coon, M.J.2
  • 15
    • 0345275779 scopus 로고    scopus 로고
    • A passion for P450s (rememberances of the early history of research on cytochrome P450)
    • R. W. Estabrook. A passion for P450s (rememberances of the early history of research on cytochrome P450) Drug Metab. Dispos. 31:1461-1473 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , pp. 1461-1473
    • Estabrook, R.W.1
  • 16
    • 3042519587 scopus 로고    scopus 로고
    • Cytochrome P450: What have we learned and what are the future issues?
    • F. P. Guengerich. Cytochrome P450: what have we learned and what are the future issues? Drug Metab. Rev. 36:159-197 (2004).
    • (2004) Drug Metab. Rev , vol.36 , pp. 159-197
    • Guengerich, F.P.1
  • 17
    • 0016683448 scopus 로고
    • Purified liver microsomal cytochrome P-450. Separation and characterization of multiple forms
    • D. A. Haugen, T. A. van der Hoeven, and M. J. Coon. Purified liver microsomal cytochrome P-450. Separation and characterization of multiple forms. J. Biol. Chem. 250:3567-3570 (1975).
    • (1975) J. Biol. Chem , vol.250 , pp. 3567-3570
    • Haugen, D.A.1    van der Hoeven, T.A.2    Coon, M.J.3
  • 19
    • 0018680603 scopus 로고
    • Multiple forms of inducible drug-metabolizing enzymes: A reasonable mechanism by which any organism can cope with adversity
    • D. W. Nebert. Multiple forms of inducible drug-metabolizing enzymes: a reasonable mechanism by which any organism can cope with adversity Mol. Cell. Biochem. 27:27-46 (1979).
    • (1979) Mol. Cell. Biochem , vol.27 , pp. 27-46
    • Nebert, D.W.1
  • 20
    • 0014486037 scopus 로고
    • Induction of drug metabolism. II. Qualitative differences in the microsomal N-demethylating systems stimulated by polycyclic hydrocarbons and by phenobarbital
    • N. E. Sladek and G. J. Mannering. Induction of drug metabolism. II. Qualitative differences in the microsomal N-demethylating systems stimulated by polycyclic hydrocarbons and by phenobarbital Mol. Pharmacol. 5:186-199 (1969).
    • (1969) Mol. Pharmacol , vol.5 , pp. 186-199
    • Sladek, N.E.1    Mannering, G.J.2
  • 21
    • 0036890399 scopus 로고    scopus 로고
    • The cytochrome P450 superfamily: Biochemistry, evolution and drug metabolism in humans
    • P. B. Danielson. The cytochrome P450 superfamily: biochemistry, evolution and drug metabolism in humans Curr. Drug Metab. 3:561-597 (2002).
    • (2002) Curr. Drug Metab , vol.3 , pp. 561-597
    • Danielson, P.B.1
  • 22
    • 0015499044 scopus 로고
    • Evidence for superoxide generation by NADPH-cytochrome c reductase of rat liver microsomes
    • S. D. Aust, D. L. Roerig, and T. C. Pederson. Evidence for superoxide generation by NADPH-cytochrome c reductase of rat liver microsomes Biochem. Biophys. Res. Commun. 47:1133-1137 (1972).
    • (1972) Biochem. Biophys. Res. Commun , vol.47 , pp. 1133-1137
    • Aust, S.D.1    Roerig, D.L.2    Pederson, T.C.3
  • 23
    • 0017800253 scopus 로고
    • Aliphatic hydroxylation by highly purified liver microsomal cytochrome P-450. Evidence for a carbon radical intermediate
    • J. T. Groves and G. A. McClusky. Aliphatic hydroxylation by highly purified liver microsomal cytochrome P-450. Evidence for a carbon radical intermediate Biochem. Biophys. Res. Commun. 81:154-160 (1978).
    • (1978) Biochem. Biophys. Res. Commun , vol.81 , pp. 154-160
    • Groves, J.T.1    McClusky, G.A.2
  • 24
    • 0034973773 scopus 로고    scopus 로고
    • Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity
    • F. P. Guengerich. Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity Chem. Res. Toxicol. 14:611-650 (2001).
    • (2001) Chem. Res. Toxicol , vol.14 , pp. 611-650
    • Guengerich, F.P.1
  • 28
    • 0015240625 scopus 로고
    • Effect of superoxide generation and dismutation on hydroxylation reactions catalyzed by liver microsomal cytochrome P-450
    • H. W. Strobel and M. J. Coon. Effect of superoxide generation and dismutation on hydroxylation reactions catalyzed by liver microsomal cytochrome P-450 J. Biol. Chem. 246:7826-7829 (1971).
    • (1971) J. Biol. Chem , vol.246 , pp. 7826-7829
    • Strobel, H.W.1    Coon, M.J.2
  • 31
    • 0022590907 scopus 로고
    • Congenital adrenal hyperplasia
    • W. L. Miller. Congenital adrenal hyperplasia N. Engl. J. Med. 314:1321-1322 (1986).
    • (1986) N. Engl. J. Med , vol.314 , pp. 1321-1322
    • Miller, W.L.1
  • 32
    • 0037068964 scopus 로고    scopus 로고
    • Clinical importance of the cytochromes P450
    • D. W. Nebert and D. W. Russell. Clinical importance of the cytochromes P450 Lancet 360:1155-1162 (2002).
    • (2002) Lancet , vol.360 , pp. 1155-1162
    • Nebert, D.W.1    Russell, D.W.2
  • 33
    • 0019519171 scopus 로고
    • Searches for ultimate chemical carcinogens and their reactions with cellular macromolecules
    • E. C. Miller and J. A. Miller. Searches for ultimate chemical carcinogens and their reactions with cellular macromolecules Cancer 47:2327-2345 (1981).
    • (1981) Cancer , vol.47 , pp. 2327-2345
    • Miller, E.C.1    Miller, J.A.2
  • 34
    • 0015336883 scopus 로고
    • The relevance of chemicobiological interactions for the toxic and carcinogenic effects of aromatic amines. V. The pharmacokinetics of related aromatic amines in blood
    • U. Groth and H. G. Neumann. The relevance of chemicobiological interactions for the toxic and carcinogenic effects of aromatic amines. V. The pharmacokinetics of related aromatic amines in blood Chem. Biol. Interact. 4:409-419 (1972).
    • (1972) Chem. Biol. Interact , vol.4 , pp. 409-419
    • Groth, U.1    Neumann, H.G.2
  • 37
    • 25444527734 scopus 로고    scopus 로고
    • A comparison of the covalent binding of clozapine, procainamide, and vesnarinone to human neutrophils in vitro and rat tissues in vitro and in vivo
    • I. Gardner, M. Popovic, N. Zahid, and J. P. Uetrecht. A comparison of the covalent binding of clozapine, procainamide, and vesnarinone to human neutrophils in vitro and rat tissues in vitro and in vivo Chem. Res. Toxicol. 18:1384-1394 (2005).
    • (2005) Chem. Res. Toxicol , vol.18 , pp. 1384-1394
    • Gardner, I.1    Popovic, M.2    Zahid, N.3    Uetrecht, J.P.4
  • 39
    • 0030927213 scopus 로고    scopus 로고
    • Protein targets of xenobiotic reactive intermediates
    • N. R. Pumford and N. C. Halmes. Protein targets of xenobiotic reactive intermediates Annu. Rev. Pharmacol. Toxicol. 37:91-117 (1997).
    • (1997) Annu. Rev. Pharmacol. Toxicol , vol.37 , pp. 91-117
    • Pumford, N.R.1    Halmes, N.C.2
  • 40
    • 0035147506 scopus 로고    scopus 로고
    • Prediction of a new drug's potential to cause idiosyncratic reactions
    • J. Uetrecht. Prediction of a new drug's potential to cause idiosyncratic reactions Curr. Opin. Drug. Discov. Dev. 4:55-59 (2001).
    • (2001) Curr. Opin. Drug. Discov. Dev , vol.4 , pp. 55-59
    • Uetrecht, J.1
  • 41
    • 13844319935 scopus 로고    scopus 로고
    • Drug bioactivation, covalent binding to target proteins and toxicity relevance
    • S. Zhou, E. Chan, W. Duan, M. Huang, and Y. Z. Chen. Drug bioactivation, covalent binding to target proteins and toxicity relevance Drug Metab. Rev. 37:41-213 (2005).
    • (2005) Drug Metab. Rev , vol.37 , pp. 41-213
    • Zhou, S.1    Chan, E.2    Duan, W.3    Huang, M.4    Chen, Y.Z.5
  • 42
    • 24944510505 scopus 로고    scopus 로고
    • Cytochrome p450 enzymes mechanism based inhibitors: Common sub-structures and reactivity
    • E. Fontana, P. M. Dansette, and S. M. Poli. Cytochrome p450 enzymes mechanism based inhibitors: common sub-structures and reactivity Curr. Drug Metab. 6:413-454 (2005).
    • (2005) Curr. Drug Metab , vol.6 , pp. 413-454
    • Fontana, E.1    Dansette, P.M.2    Poli, S.M.3
  • 46
    • 27844564267 scopus 로고    scopus 로고
    • Implications of pharmacogenomics for drug development and clinical practice
    • G. S. Ginsburg, R. P. Konstance, J. S. Allsbrook, and K. A. Schulman. Implications of pharmacogenomics for drug development and clinical practice Arch. Intern. Med. 165:2331-2336 (2005).
    • (2005) Arch. Intern. Med , vol.165 , pp. 2331-2336
    • Ginsburg, G.S.1    Konstance, R.P.2    Allsbrook, J.S.3    Schulman, K.A.4
  • 48
    • 0032748555 scopus 로고    scopus 로고
    • Pharmacogenetics and pharmacogenomics: Why is this relevant to the clinical geneticist?
    • D. W. Nebert. Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist? Clin. Genet. 56:247-258 (1999).
    • (1999) Clin. Genet , vol.56 , pp. 247-258
    • Nebert, D.W.1
  • 49
    • 0242330670 scopus 로고    scopus 로고
    • The drugs don't work: Expectations and the shaping of pharmacogenetics
    • A. Hedgecoe and P. Martin. The drugs don't work: expectations and the shaping of pharmacogenetics Soc. Stud. Sci. 33:327-364 (2003).
    • (2003) Soc. Stud. Sci , vol.33 , pp. 327-364
    • Hedgecoe, A.1    Martin, P.2
  • 50
    • 0034621009 scopus 로고    scopus 로고
    • Science, medicine, and the future: Pharmacogenetics
    • C. R. Wolf, G. Smith, and R. L. Smith. Science, medicine, and the future: Pharmacogenetics BMJ 320:987-990 (2000).
    • (2000) BMJ , vol.320 , pp. 987-990
    • Wolf, C.R.1    Smith, G.2    Smith, R.L.3
  • 51
    • 0037271322 scopus 로고    scopus 로고
    • Cross-species sequence comparisons: A review of methods and available resources
    • K. A. Frazer, L. Elnitski, D. M. Church, I. Dubchak, and R. C. Hardison. Cross-species sequence comparisons: a review of methods and available resources. Genome Res. 13:1-12 (2003).
    • (2003) Genome Res , vol.13 , pp. 1-12
    • Frazer, K.A.1    Elnitski, L.2    Church, D.M.3    Dubchak, I.4    Hardison, R.C.5
  • 52
    • 0034762015 scopus 로고    scopus 로고
    • K. A. Frazer, J. B. Sheehan, R. P. Stokowski, X. Chen, R. Hosseini, J. F. Cheng, S. P. Fodor, D. R. Cox, and N. Patil. Evolutionarily conserved sequences on human chromosome 21 Genome Res. 11:1651-1659 (2001).
    • K. A. Frazer, J. B. Sheehan, R. P. Stokowski, X. Chen, R. Hosseini, J. F. Cheng, S. P. Fodor, D. R. Cox, and N. Patil. Evolutionarily conserved sequences on human chromosome 21 Genome Res. 11:1651-1659 (2001).
  • 54
    • 2942703753 scopus 로고    scopus 로고
    • Gene expression profile in the livers of rats orally administered ethinylestradiol for 28 days using a microarray technique
    • N. Kato, M. Shibutani, H. Takagi, C. Uneyama, K. Y. Lee, S. Takigami, K. Mashima, and M. Hirose. Gene expression profile in the livers of rats orally administered ethinylestradiol for 28 days using a microarray technique Toxicology 200:179-192 (2004).
    • (2004) Toxicology , vol.200 , pp. 179-192
    • Kato, N.1    Shibutani, M.2    Takagi, H.3    Uneyama, C.4    Lee, K.Y.5    Takigami, S.6    Mashima, K.7    Hirose, M.8
  • 56
    • 0014693146 scopus 로고
    • Steady-state plasma levels of nortriptyline in twins: Influence of genetic factors and drug therapy
    • B. Alexanderson, D. A. Evans, and F. Sjoqvist. Steady-state plasma levels of nortriptyline in twins: influence of genetic factors and drug therapy Br. Med. J. 4:764-768 (1969).
    • (1969) Br. Med. J , vol.4 , pp. 764-768
    • Alexanderson, B.1    Evans, D.A.2    Sjoqvist, F.3
  • 57
    • 0014128388 scopus 로고    scopus 로고
    • W. Hammer and F. Sjoqvist. Plasma levels of monomethylated tricyclic antidepressants during treatment with imipramine-like compounds Life Sci. 6:1895-1903 (1967).
    • W. Hammer and F. Sjoqvist. Plasma levels of monomethylated tricyclic antidepressants during treatment with imipramine-like compounds Life Sci. 6:1895-1903 (1967).
  • 58
    • 0022464795 scopus 로고
    • Polymorphic oxidation of debrisoquine and sparteine
    • M. Eichelbaum. Polymorphic oxidation of debrisoquine and sparteine Prog. Clin. Biol. Res. 214:157-167 (1986).
    • (1986) Prog. Clin. Biol. Res , vol.214 , pp. 157-167
    • Eichelbaum, M.1
  • 59
    • 0035514968 scopus 로고    scopus 로고
    • The Paton Prize Award. The discovery of the debrisoquine hydroxylation polymorphism: Scientific and clinical impact and consequences
    • R. L. Smith. The Paton Prize Award. The discovery of the debrisoquine hydroxylation polymorphism: scientific and clinical impact and consequences Toxicology 168:11-19 (2001).
    • (2001) Toxicology , vol.168 , pp. 11-19
    • Smith, R.L.1
  • 60
    • 0029028932 scopus 로고
    • Geographical/interracial differences in polymorphic drug oxidation. Current state of knowledge of cytochromes P450 (CYP) 2D6 and 2C19
    • L. Bertilsson. Geographical/interracial differences in polymorphic drug oxidation. Current state of knowledge of cytochromes P450 (CYP) 2D6 and 2C19 Clin. Pharmacokinet. 29:192-209 (1995).
    • (1995) Clin. Pharmacokinet , vol.29 , pp. 192-209
    • Bertilsson, L.1
  • 61
    • 0345240943 scopus 로고    scopus 로고
    • Correlation between genotype and phenotype of the human arylamine N-acetyltransferase type 1 (NAT1)
    • C. Bruhn, J. Brockmoller, I. Cascorbi, I. Roots, and H. H. Borchert. Correlation between genotype and phenotype of the human arylamine N-acetyltransferase type 1 (NAT1) Biochem. Pharmacol. 58:1759-1764 (1999).
    • (1999) Biochem. Pharmacol , vol.58 , pp. 1759-1764
    • Bruhn, C.1    Brockmoller, J.2    Cascorbi, I.3    Roots, I.4    Borchert, H.H.5
  • 62
    • 0030758131 scopus 로고    scopus 로고
    • Identification of the polymorphically expressed CYP2C19 and the wild-type CYP2C9-ILE359 allele as low-Km catalysts of cyclophosphamide and ifosfamide activation
    • T. K. Chang, L. Yu, J. A. Goldstein, and D. J. Waxman. Identification of the polymorphically expressed CYP2C19 and the wild-type CYP2C9-ILE359 allele as low-Km catalysts of cyclophosphamide and ifosfamide activation Pharmacogenetics 7:211-221 (1997).
    • (1997) Pharmacogenetics , vol.7 , pp. 211-221
    • Chang, T.K.1    Yu, L.2    Goldstein, J.A.3    Waxman, D.J.4
  • 64
    • 0035660166 scopus 로고    scopus 로고
    • S. Garte, L. Gaspari, A. K. Alexandrie, C. Ambrosone, H. Autrup, J. L. Autrup, H. Baranova, L. Bathum, S. Benhamou, P. Boffetta, C. Bouchardy, K. Breskvar, J. Brockmoller, I. Cascorbi, M. L. Clapper, C. Coutelle, A. Daly, M. Dell'Omo, V. Dolzan, C. M. Dresler, A. Fryer, A. Haugen, D. W. Hein, A. Hildesheim, A. Hirvonen, L. L. Hsieh, M. Ingelman-Sundberg, I. Kalina, D. Kang, M. Kihara, C. Kiyohara, P. Kremers, P. Lazarus, L. Le Marchand, M. C. Lechner, E. M. van Lieshout, S. London, J. J. Manni, C. M. Maugard, S. Morita, V. Nazar-Stewart, K. Noda, Y. Oda, F. F. Parl, R. Pastorelli, I. Persson, W. H. Peters, A. Rannug, T. Rebbeck, A. Risch, L. Roelandt, M. Romkes, D. Ryberg, J. Salagovic, B. Schoket, J. Seidegard, P. G. Shields, E. Sim, D. Sinnet, R. C. Strange, I. Stucker, H. Sugimura, J. To-Figueras, P. Vineis, M. C. Yu, and E. Taioli. Metabolic gene polymorphism frequencies in control populations. Cancer Epidemiol. Biomark. Prev. 10:1239-1248 2001
    • S. Garte, L. Gaspari, A. K. Alexandrie, C. Ambrosone, H. Autrup, J. L. Autrup, H. Baranova, L. Bathum, S. Benhamou, P. Boffetta, C. Bouchardy, K. Breskvar, J. Brockmoller, I. Cascorbi, M. L. Clapper, C. Coutelle, A. Daly, M. Dell'Omo, V. Dolzan, C. M. Dresler, A. Fryer, A. Haugen, D. W. Hein, A. Hildesheim, A. Hirvonen, L. L. Hsieh, M. Ingelman-Sundberg, I. Kalina, D. Kang, M. Kihara, C. Kiyohara, P. Kremers, P. Lazarus, L. Le Marchand, M. C. Lechner, E. M. van Lieshout, S. London, J. J. Manni, C. M. Maugard, S. Morita, V. Nazar-Stewart, K. Noda, Y. Oda, F. F. Parl, R. Pastorelli, I. Persson, W. H. Peters, A. Rannug, T. Rebbeck, A. Risch, L. Roelandt, M. Romkes, D. Ryberg, J. Salagovic, B. Schoket, J. Seidegard, P. G. Shields, E. Sim, D. Sinnet, R. C. Strange, I. Stucker, H. Sugimura, J. To-Figueras, P. Vineis, M. C. Yu, and E. Taioli. Metabolic gene polymorphism frequencies in control populations. Cancer Epidemiol. Biomark. Prev. 10:1239-1248 (2001).
  • 65
    • 0028590127 scopus 로고
    • Biochemistry and molecular biology of the human CYP2C subfamily
    • J. A. Goldsteinand and S. M. Moraisde. Biochemistry and molecular biology of the human CYP2C subfamily Pharmacogenetics 4:285-299 (1994).
    • (1994) Pharmacogenetics , vol.4 , pp. 285-299
    • Goldsteinand, J.A.1    Moraisde, S.M.2
  • 67
    • 18244379610 scopus 로고    scopus 로고
    • M. Iwasaki, Y. Yoshimura, S. Asahi, K. Saito, S. Sakai, S. Morita, O. Takenaka, T. Inoda, E. Kashiyama, A. Aoyama, T. Nakabayashi, S. Omori, T. Kuwabara, T. Izumi, K. Nakamura, K. Takanaka, Y. Nakayama, M. Takeuchi, H. Nakamura, S. Kametani, Y. Terauchi, T. Hashizume, S. Nagayama, T. Kume, M. Achira, H. Kawai, T. Kawashiro, A. Nakamura, Y. Nakai, A. Kagayama, T. Shiraga, T. Niwa, T. Yoshimura, J. Morita, F. Ohsawa, M. Tani, N. Osawa, K. Ida, and K. Noguchi. Functional characterization of single nucleotide polymorphisms with amino acid substitution in CYP1A2, CYP2A6, and CYP2B6 found in the Japanese population Drug Metab. Pharmacokinet. 19:444-452 (2004).
    • M. Iwasaki, Y. Yoshimura, S. Asahi, K. Saito, S. Sakai, S. Morita, O. Takenaka, T. Inoda, E. Kashiyama, A. Aoyama, T. Nakabayashi, S. Omori, T. Kuwabara, T. Izumi, K. Nakamura, K. Takanaka, Y. Nakayama, M. Takeuchi, H. Nakamura, S. Kametani, Y. Terauchi, T. Hashizume, S. Nagayama, T. Kume, M. Achira, H. Kawai, T. Kawashiro, A. Nakamura, Y. Nakai, A. Kagayama, T. Shiraga, T. Niwa, T. Yoshimura, J. Morita, F. Ohsawa, M. Tani, N. Osawa, K. Ida, and K. Noguchi. Functional characterization of single nucleotide polymorphisms with amino acid substitution in CYP1A2, CYP2A6, and CYP2B6 found in the Japanese population Drug Metab. Pharmacokinet. 19:444-452 (2004).
  • 69
    • 0030995879 scopus 로고    scopus 로고
    • Molecular mechanisms of genetic polymorphisms of drug metabolism
    • U. A. Meyer and U. M. Zanger. Molecular mechanisms of genetic polymorphisms of drug metabolism Annu. Rev. Pharmacol. Toxicol. 37:269-296 (1997).
    • (1997) Annu. Rev. Pharmacol. Toxicol , vol.37 , pp. 269-296
    • Meyer, U.A.1    Zanger, U.M.2
  • 70
    • 0026760963 scopus 로고
    • Six-base deletion occurring in messages of human cytochrome P-450 in the CYP2C subfamily results in reduction of tolbutamide hydroxylase activity
    • S. Ohgiya, M. Komori, H. Ohi, K. Shiramatsu, N. Shinriki, and T. Kamataki. Six-base deletion occurring in messages of human cytochrome P-450 in the CYP2C subfamily results in reduction of tolbutamide hydroxylase activity Biochem. Int. 27:1073-1081 (1992).
    • (1992) Biochem. Int , vol.27 , pp. 1073-1081
    • Ohgiya, S.1    Komori, M.2    Ohi, H.3    Shiramatsu, K.4    Shinriki, N.5    Kamataki, T.6
  • 71
    • 28744442089 scopus 로고    scopus 로고
    • Isosorbide dinitrate and hydralazine hydrochloride: A review of efficacy and safety
    • K. C. Ferdinand. Isosorbide dinitrate and hydralazine hydrochloride: a review of efficacy and safety Expert Rev. Cardiovasc. Ther. 3:993-1001 (2005).
    • (2005) Expert Rev. Cardiovasc. Ther , vol.3 , pp. 993-1001
    • Ferdinand, K.C.1
  • 72
    • 33745250457 scopus 로고    scopus 로고
    • Prescribing BiDil: Is it black and white?
    • S. B. Hagaand and G. S. Ginsburg. Prescribing BiDil: is it black and white? J. Am. Coll. Cardiol. 48:12-14 (2006).
    • (2006) J. Am. Coll. Cardiol , vol.48 , pp. 12-14
    • Hagaand, S.B.1    Ginsburg, G.S.2
  • 75
    • 0001718982 scopus 로고
    • Studies on pig liver microsomes. I. Enzymic and pigment composition of different microsomal fractions
    • D. Garfinkel. Studies on pig liver microsomes. I. Enzymic and pigment composition of different microsomal fractions Arch. Biochem. Biophys. 77:493-509 (1958).
    • (1958) Arch. Biochem. Biophys , vol.77 , pp. 493-509
    • Garfinkel, D.1
  • 76
    • 0001202995 scopus 로고
    • Pigments of rat liver microsomes
    • M. Klingenberg. Pigments of rat liver microsomes Arch. Biochem. Biophys. 75:376-386 (1958).
    • (1958) Arch. Biochem. Biophys , vol.75 , pp. 376-386
    • Klingenberg, M.1
  • 77
    • 0014670327 scopus 로고
    • Resolution of the cytochrome P-450-containing omega-hydroxylation system of liver microsomes into three components
    • A. Y. Lu, K. W. Junk, and M. J. Coon. Resolution of the cytochrome P-450-containing omega-hydroxylation system of liver microsomes into three components J. Biol. Chem. 244:3714-3721 (1969).
    • (1969) J. Biol. Chem , vol.244 , pp. 3714-3721
    • Lu, A.Y.1    Junk, K.W.2    Coon, M.J.3
  • 78
    • 0014940845 scopus 로고
    • Genetic differences in the extent of aryl hydrocarbon hydroxylase induction in mouse fetal cell cultures
    • D. W. Nebert and L. L. Bausserman. Genetic differences in the extent of aryl hydrocarbon hydroxylase induction in mouse fetal cell cultures J. Biol. Chem. 245:6373-6382 (1970).
    • (1970) J. Biol. Chem , vol.245 , pp. 6373-6382
    • Nebert, D.W.1    Bausserman, L.L.2
  • 79
    • 0019291033 scopus 로고    scopus 로고
    • A. B. Okey, G. P. Bondy, M. E. Mason, D. W. Nebert, C. J. Forster-Gibson, J. Muncan, and M. J. Dufresne. Temperature-dependent cytosol-to-nucleus translocation of the Ah receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin in continuous cell culture lines J. Biol. Chem. 255:11415-11422 (1980).
    • A. B. Okey, G. P. Bondy, M. E. Mason, D. W. Nebert, C. J. Forster-Gibson, J. Muncan, and M. J. Dufresne. Temperature-dependent cytosol-to-nucleus translocation of the Ah receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin in continuous cell culture lines J. Biol. Chem. 255:11415-11422 (1980).
  • 80
    • 0015218622 scopus 로고
    • Aryl hydrocarbon hydroxylase induction in mammalian liver cell culture. I. Stimulation of enzyme activity in nonhepatic cells and in hepatic cells by phenobarbital, polycyclic hydrocarbons, and 2,2-bis(p-chlorophenyl)-1,1,1-trichloroethane
    • J. E. Gielen and D. W. Nebert. Aryl hydrocarbon hydroxylase induction in mammalian liver cell culture. I. Stimulation of enzyme activity in nonhepatic cells and in hepatic cells by phenobarbital, polycyclic hydrocarbons, and 2,2-bis(p-chlorophenyl)-1,1,1-trichloroethane J. Biol. Chem. 246:5189-5198 (1971).
    • (1971) J. Biol. Chem , vol.246 , pp. 5189-5198
    • Gielen, J.E.1    Nebert, D.W.2
  • 81
    • 0016875797 scopus 로고
    • Current models of steroid hormone action: A critique
    • J. Gorski and F. Gannon. Current models of steroid hormone action: a critique Annu. Rev. Physiol. 38:425-450 (1976).
    • (1976) Annu. Rev. Physiol , vol.38 , pp. 425-450
    • Gorski, J.1    Gannon, F.2
  • 82
    • 0017588083 scopus 로고
    • Cytosolic receptor for aryl hydrocarbon hydroxylase induction by polycyclic aromatic compounds. Evidence for structural and regulatory variants among established cell cultured lines
    • T. M. Guenthner and D. W. Nebert. Cytosolic receptor for aryl hydrocarbon hydroxylase induction by polycyclic aromatic compounds. Evidence for structural and regulatory variants among established cell cultured lines J. Biol. Chem. 252:8981-8989 (1977).
    • (1977) J. Biol. Chem , vol.252 , pp. 8981-8989
    • Guenthner, T.M.1    Nebert, D.W.2
  • 83
    • 0017145975 scopus 로고    scopus 로고
    • A. Poland, E. Glover, and A. S. Kende. Stereospecific, high affinity binding of 2,3,7,8-tetrachlorodibenzo-p-dioxin by hepatic cytosol. Evidence that the binding species is receptor for induction of aryl hydrocarbon hydroxylase J. Biol. Chem. 251:4936-4946 (1976).
    • A. Poland, E. Glover, and A. S. Kende. Stereospecific, high affinity binding of 2,3,7,8-tetrachlorodibenzo-p-dioxin by hepatic cytosol. Evidence that the binding species is receptor for induction of aryl hydrocarbon hydroxylase J. Biol. Chem. 251:4936-4946 (1976).
  • 84
    • 13144260727 scopus 로고    scopus 로고
    • G. Bertilsson, J. Heidrich, K. Svensson, M. Asman, L. Jendeberg, M. Sydow-Backman, R. Ohlsson, H. Postlind, P. Blomquist, and A. Berkenstam. Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction Proc. Natl. Acad. Sci. USA 95:12208-12213 (1998).
    • G. Bertilsson, J. Heidrich, K. Svensson, M. Asman, L. Jendeberg, M. Sydow-Backman, R. Ohlsson, H. Postlind, P. Blomquist, and A. Berkenstam. Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction Proc. Natl. Acad. Sci. USA 95:12208-12213 (1998).
  • 87
    • 0033617520 scopus 로고    scopus 로고
    • Orphan nuclear receptors: Shifting endocrinology into reverse
    • S. A. Kliewer, J. M. Lehmann, and T. M. Willson. Orphan nuclear receptors: shifting endocrinology into reverse Science 284:757-760 (1999).
    • (1999) Science , vol.284 , pp. 757-760
    • Kliewer, S.A.1    Lehmann, J.M.2    Willson, T.M.3
  • 88
    • 0034518420 scopus 로고    scopus 로고
    • The role of orphan nuclear receptors in the regulation of cholesterol homeostasis
    • J. J. Repa and D. J. Mangelsdorf. The role of orphan nuclear receptors in the regulation of cholesterol homeostasis Annu. Rev. Cell Dev. Biol. 16:459-481 (2000).
    • (2000) Annu. Rev. Cell Dev. Biol , vol.16 , pp. 459-481
    • Repa, J.J.1    Mangelsdorf, D.J.2
  • 89
    • 0036783335 scopus 로고    scopus 로고
    • Pharmacogenomics, regulation and signaling pathways of phase I and II drug metabolizing enzymes
    • T. H. Rushmore and A. N. Kong. Pharmacogenomics, regulation and signaling pathways of phase I and II drug metabolizing enzymes Curr. Drug Metab. 3:481-490 (2002).
    • (2002) Curr. Drug Metab , vol.3 , pp. 481-490
    • Rushmore, T.H.1    Kong, A.N.2
  • 90
    • 33644869283 scopus 로고    scopus 로고
    • Tissue distribution and pharmacodynamics: A complicated relationship
    • J. H. Lin. Tissue distribution and pharmacodynamics: a complicated relationship Curr. Drug Metab. 7:39-65 (2006).
    • (2006) Curr. Drug Metab , vol.7 , pp. 39-65
    • Lin, J.H.1
  • 91
    • 0034188949 scopus 로고    scopus 로고
    • Pharmacogenetic diagnostics of cytochrome P450 polymorphisms in clinical drug development and in drug treatment
    • J. Brockmoller, J. Kirchheiner, C. Meisel, and I. Roots. Pharmacogenetic diagnostics of cytochrome P450 polymorphisms in clinical drug development and in drug treatment Pharmacogenomics 1:125-151 (2000).
    • (2000) Pharmacogenomics , vol.1 , pp. 125-151
    • Brockmoller, J.1    Kirchheiner, J.2    Meisel, C.3    Roots, I.4
  • 92
    • 0022651601 scopus 로고
    • Pharmacokinetic drug interactions
    • M. Eichelbaum. Pharmacokinetic drug interactions J. Clin. Pharmacol. 26:469-473 (1986).
    • (1986) J. Clin. Pharmacol , vol.26 , pp. 469-473
    • Eichelbaum, M.1
  • 93
    • 0031742831 scopus 로고    scopus 로고
    • Relevance of pheno- and genotyping in clinical drug development
    • M. T. Zuhlsdorf. Relevance of pheno- and genotyping in clinical drug development Int. J. Clin. Pharmacol. Ther. 36:607-612 (1998).
    • (1998) Int. J. Clin. Pharmacol. Ther , vol.36 , pp. 607-612
    • Zuhlsdorf, M.T.1
  • 94
    • 0037421584 scopus 로고    scopus 로고
    • Inheritance and drug response
    • R. Weinshilboum. Inheritance and drug response N. Engl. J. Med. 348:529-537 (2003).
    • (2003) N. Engl. J. Med , vol.348 , pp. 529-537
    • Weinshilboum, R.1
  • 95
    • 0742321734 scopus 로고    scopus 로고
    • Human drug metabolising cytochrome P450 enzymes: Properties and polymorphisms
    • M. Ingelman-Sundberg. Human drug metabolising cytochrome P450 enzymes: properties and polymorphisms Naunyn-Schmiedebergs Arch. Pharmacol 369:89-104 (2004).
    • (2004) Naunyn-Schmiedebergs Arch. Pharmacol , vol.369 , pp. 89-104
    • Ingelman-Sundberg, M.1
  • 96
    • 0033569516 scopus 로고    scopus 로고
    • Pharmacogenomics: Translating functional genomics into rational therapeutics
    • W. E. Evans and M. V. Relling. Pharmacogenomics: translating functional genomics into rational therapeutics Science 286:487-491 (1999).
    • (1999) Science , vol.286 , pp. 487-491
    • Evans, W.E.1    Relling, M.V.2
  • 97
    • 0035056821 scopus 로고    scopus 로고
    • Pharmacogenetic application in drug development and clinical trials
    • M. M. Shi, M. R. Bleavins, and F. A. Iglesiade la. Pharmacogenetic application in drug development and clinical trials Drug Metab. Dispos. 29:591-595 (2001).
    • (2001) Drug Metab. Dispos , vol.29 , pp. 591-595
    • Shi, M.M.1    Bleavins, M.R.2    Iglesiade la, F.A.3
  • 98
    • 0031023815 scopus 로고    scopus 로고
    • M. W. Linder, R. A. Prough, and R. Valdes, Jr. Pharmacogenetics: a laboratory tool for optimizing therapeutic efficiency. Clin. Chem.43:254-266 (1997).
    • M. W. Linder, R. A. Prough, and R. Valdes, Jr. Pharmacogenetics: a laboratory tool for optimizing therapeutic efficiency. Clin. Chem.43:254-266 (1997).
  • 99
    • 0032899811 scopus 로고    scopus 로고
    • Merits and limitations of recombinant models for the study of human P450-mediated drug metabolism and toxicity: An intralaboratory comparison
    • T. Friedberg, M. P. Pritchard, M. Bandera, S. P. Hanlon, D. Yao, L. A. McLaughlin, S. Ding, B. Burchell, and C. R. Wolf. Merits and limitations of recombinant models for the study of human P450-mediated drug metabolism and toxicity: an intralaboratory comparison Drug Metab. Rev. 31:523-544 (1999).
    • (1999) Drug Metab. Rev , vol.31 , pp. 523-544
    • Friedberg, T.1    Pritchard, M.P.2    Bandera, M.3    Hanlon, S.P.4    Yao, D.5    McLaughlin, L.A.6    Ding, S.7    Burchell, B.8    Wolf, C.R.9
  • 100
    • 2642549957 scopus 로고    scopus 로고
    • Transgenic analysis of human drug-metabolizing enzymes: Preclinical drug development and toxicology
    • C. J. Henderson and C. R. Wolf. Transgenic analysis of human drug-metabolizing enzymes: preclinical drug development and toxicology Mol. Interv. 3:331-343 (2003).
    • (2003) Mol. Interv , vol.3 , pp. 331-343
    • Henderson, C.J.1    Wolf, C.R.2
  • 101
    • 26944498056 scopus 로고    scopus 로고
    • Challenges in current drug delivery from the potential application of pharmacogenomics and personalized medicine in clinical practice
    • I. S. Vizirianakis. Challenges in current drug delivery from the potential application of pharmacogenomics and personalized medicine in clinical practice Curr. Drug Deliv. 1:73-80 (2004).
    • (2004) Curr. Drug Deliv , vol.1 , pp. 73-80
    • Vizirianakis, I.S.1
  • 102
    • 0037186881 scopus 로고    scopus 로고
    • The Gerhard Zbinden memorial lecture: Application of biochemical and genetic approaches to understanding pathways of chemical toxicity
    • C. R. Wolf. The Gerhard Zbinden memorial lecture: application of biochemical and genetic approaches to understanding pathways of chemical toxicity Toxicol. Lett. 127:3-17 (2002).
    • (2002) Toxicol. Lett , vol.127 , pp. 3-17
    • Wolf, C.R.1
  • 103
    • 0025861818 scopus 로고    scopus 로고
    • P. M. Holland, R. D. Abramson, R. Watson, and D. H. Gelfand. Detection of specific polymerase chain reaction product by utilizing the 5′-3′ exonuclease activity of Thermus aquaticus DNA polymerase Proc. Natl. Acad. Sci. USA 88:7276-7280 (1991).
    • P. M. Holland, R. D. Abramson, R. Watson, and D. H. Gelfand. Detection of specific polymerase chain reaction product by utilizing the 5′-3′ exonuclease activity of Thermus aquaticus DNA polymerase Proc. Natl. Acad. Sci. USA 88:7276-7280 (1991).
  • 104
    • 0032544336 scopus 로고    scopus 로고
    • Genetic variation as a guide to drug development
    • P. W. Kleyn and E. S. Vesell. Genetic variation as a guide to drug development Science 281:1820-1821 (1998).
    • (1998) Science , vol.281 , pp. 1820-1821
    • Kleyn, P.W.1    Vesell, E.S.2
  • 108
    • 18144399225 scopus 로고    scopus 로고
    • Systems biology in drug safety and metabolism: Integration of microarray, real-time PCR and enzyme approaches
    • L. G. Yengi. Systems biology in drug safety and metabolism: integration of microarray, real-time PCR and enzyme approaches Pharmacogenomics 6:185-192 (2005).
    • (2005) Pharmacogenomics , vol.6 , pp. 185-192
    • Yengi, L.G.1
  • 109
    • 84984934048 scopus 로고    scopus 로고
    • DNA microarrays in drug discovery and development
    • C. Debouck and P. N. Goodfellow. DNA microarrays in drug discovery and development Nat. Genet. 21:48-50 (1999).
    • (1999) Nat. Genet , vol.21 , pp. 48-50
    • Debouck, C.1    Goodfellow, P.N.2
  • 112
    • 0037790603 scopus 로고    scopus 로고
    • Inactivation of the hepatic cytochrome P450 system by conditional deletion of hepatic cytochrome P450 reductase
    • C. J. Henderson, D. M. Otto, D. Carrie, M. A. Magnuson, A. W. McLaren, I. Rosewell, and C. R. Wolf. Inactivation of the hepatic cytochrome P450 system by conditional deletion of hepatic cytochrome P450 reductase. J. Biol. Chem. 278:13480-13486 (2003).
    • (2003) J. Biol. Chem , vol.278 , pp. 13480-13486
    • Henderson, C.J.1    Otto, D.M.2    Carrie, D.3    Magnuson, M.A.4    McLaren, A.W.5    Rosewell, I.6    Wolf, C.R.7
  • 114
    • 0027083454 scopus 로고
    • A simplified method for the culturing of primary adult rat and human hepatocytes as multicellular spheroids
    • A. P. Li, S. M. Colburn, and D. J. Beck. A simplified method for the culturing of primary adult rat and human hepatocytes as multicellular spheroids In Vitro Cell Dev. Biol. 28A:673-677 (1992).
    • (1992) In Vitro Cell Dev. Biol , vol.28 A , pp. 673-677
    • Li, A.P.1    Colburn, S.M.2    Beck, D.J.3
  • 116
    • 0029584276 scopus 로고
    • Substrates of human hepatic cytochrome P450 3A4
    • A. P. Li, D. L. Kaminski, and A. Rasmussen. Substrates of human hepatic cytochrome P450 3A4 Toxicology 104:1-8 (1995).
    • (1995) Toxicology , vol.104 , pp. 1-8
    • Li, A.P.1    Kaminski, D.L.2    Rasmussen, A.3
  • 118
    • 0346942394 scopus 로고    scopus 로고
    • Monitoring expression of genes involved in drug metabolism and toxicology using DNA microarrays
    • D. Gerhold, M. Lu, J. Xu, C. Austin, C. T. Caskey, and T. Rushmore. Monitoring expression of genes involved in drug metabolism and toxicology using DNA microarrays Physiol. Genomics. 5:161-170 (2001).
    • (2001) Physiol. Genomics , vol.5 , pp. 161-170
    • Gerhold, D.1    Lu, M.2    Xu, J.3    Austin, C.4    Caskey, C.T.5    Rushmore, T.6
  • 119
    • 1942421316 scopus 로고    scopus 로고
    • Integrating in vitro kinetic data from compounds exhibiting induction, reversible inhibition and mechanism-based inactivation: In vitro study design
    • D. J. McConn and Z. Zhao. Integrating in vitro kinetic data from compounds exhibiting induction, reversible inhibition and mechanism-based inactivation: in vitro study design Curr. Drug Metab. 5:141-146 (2004).
    • (2004) Curr. Drug Metab , vol.5 , pp. 141-146
    • McConn, D.J.1    Zhao, Z.2
  • 121
    • 1642301013 scopus 로고    scopus 로고
    • Sex difference in induction of hepatic CYP2B and CYP3A subfamily enzymes by nicardipine and nifedipine in rats
    • Y. Konno, M. Sekimoto, K. Nemoto, and M. Degawa. Sex difference in induction of hepatic CYP2B and CYP3A subfamily enzymes by nicardipine and nifedipine in rats Toxicol. Appl. Pharmacol. 196:20-28 (2004).
    • (2004) Toxicol. Appl. Pharmacol , vol.196 , pp. 20-28
    • Konno, Y.1    Sekimoto, M.2    Nemoto, K.3    Degawa, M.4
  • 122
    • 17644387518 scopus 로고    scopus 로고
    • Selective downregulation of hepatic cytochrome P450 expression and activity in a rat model of inflammatory pain
    • D. Projean, S. Dautrey, H. K. Vu, T. Groblewski, J. L. Brazier, and J. Ducharme. Selective downregulation of hepatic cytochrome P450 expression and activity in a rat model of inflammatory pain Pharm. Res. 22:62-70 (2005).
    • (2005) Pharm. Res , vol.22 , pp. 62-70
    • Projean, D.1    Dautrey, S.2    Vu, H.K.3    Groblewski, T.4    Brazier, J.L.5    Ducharme, J.6
  • 123
    • 0034189084 scopus 로고    scopus 로고
    • Current pharmacogenomic approaches to clinical drug development
    • M. P. Murphy. Current pharmacogenomic approaches to clinical drug development Pharmacogenomics 1:115-123 (2000).
    • (2000) Pharmacogenomics , vol.1 , pp. 115-123
    • Murphy, M.P.1
  • 124
    • 0032702726 scopus 로고    scopus 로고
    • The orphan human pregnane X receptor mediates the transcriptional activation of CYP3A4 by rifampicin through a distal enhancer module
    • B. Goodwin, E. Hodgson, and C. Liddle. The orphan human pregnane X receptor mediates the transcriptional activation of CYP3A4 by rifampicin through a distal enhancer module Mol. Pharmacol. 56:1329-1339 (1999).
    • (1999) Mol. Pharmacol , vol.56 , pp. 1329-1339
    • Goodwin, B.1    Hodgson, E.2    Liddle, C.3
  • 125
    • 0042468096 scopus 로고    scopus 로고
    • Impact of drug transporter studies on drug discovery and development
    • N. Mizuno, T. Niwa, Y. Yotsumoto, and Y. Sugiyama. Impact of drug transporter studies on drug discovery and development Pharmacol. Rev. 55:425-461 (2003).
    • (2003) Pharmacol. Rev , vol.55 , pp. 425-461
    • Mizuno, N.1    Niwa, T.2    Yotsumoto, Y.3    Sugiyama, Y.4
  • 126
    • 18844425783 scopus 로고    scopus 로고
    • Transporters and their impact on drug disposition
    • P. M. Beringer and R. L. Slaughter. Transporters and their impact on drug disposition Ann. Pharmacother. 39:1097-1108 (2005).
    • (2005) Ann. Pharmacother , vol.39 , pp. 1097-1108
    • Beringer, P.M.1    Slaughter, R.L.2
  • 127
    • 25144450046 scopus 로고    scopus 로고
    • Apical/basolateral surface expression of drug transporters and its role in vectorial drug transport
    • K. Ito, H. Suzuki, T. Horie, and Y. Sugiyama. Apical/basolateral surface expression of drug transporters and its role in vectorial drug transport Pharm. Res. 22:1559-1577 (2005).
    • (2005) Pharm. Res , vol.22 , pp. 1559-1577
    • Ito, K.1    Suzuki, H.2    Horie, T.3    Sugiyama, Y.4
  • 128
    • 0028818229 scopus 로고
    • Species similarities and differences in pharmacokinetics
    • J. H. Lin. Species similarities and differences in pharmacokinetics Drug Metab. Dispos. 23:1008-1021 (1995).
    • (1995) Drug Metab. Dispos , vol.23 , pp. 1008-1021
    • Lin, J.H.1
  • 129
    • 21444450864 scopus 로고    scopus 로고
    • Biochemical and molecular pharmacological aspects of transporters as determinants of drug disposition
    • Y. Sai. Biochemical and molecular pharmacological aspects of transporters as determinants of drug disposition Drug Metab. Pharmacokinet. 20:91-99 (2005).
    • (2005) Drug Metab. Pharmacokinet , vol.20 , pp. 91-99
    • Sai, Y.1
  • 131
    • 0345505691 scopus 로고    scopus 로고
    • The role of multidrug transporters in drug availability, metabolism and toxicity
    • A. Bodo, E. Bakos, F. Szeri, A. Varadi, and B. Sarkadi. The role of multidrug transporters in drug availability, metabolism and toxicity Toxicol. Lett. 140-141:133-143 (2003).
    • (2003) Toxicol. Lett , vol.140-141 , pp. 133-143
    • Bodo, A.1    Bakos, E.2    Szeri, F.3    Varadi, A.4    Sarkadi, B.5
  • 133
    • 0036159433 scopus 로고    scopus 로고
    • Fruit juices inhibit organic anion transporting polypeptide-mediated drug uptake to decrease the oral availability of fexofenadine
    • G. K. Dresser, D. G. Bailey, B. F. Leake, U. I. Schwarz, P. A. Dawson, D. J. Freeman, and R. B. Kim. Fruit juices inhibit organic anion transporting polypeptide-mediated drug uptake to decrease the oral availability of fexofenadine Clin. Pharmacol. Ther. 71:11-20 (2002).
    • (2002) Clin. Pharmacol. Ther , vol.71 , pp. 11-20
    • Dresser, G.K.1    Bailey, D.G.2    Leake, B.F.3    Schwarz, U.I.4    Dawson, P.A.5    Freeman, D.J.6    Kim, R.B.7
  • 134
    • 0032793959 scopus 로고    scopus 로고
    • OATP and P-glycoprotein transporters mediate the cellular uptake and excretion of fexofenadine
    • M. Cvetkovic, B. Leake, M. F. Fromm, G. R. Wilkinson, and R. B. Kim. OATP and P-glycoprotein transporters mediate the cellular uptake and excretion of fexofenadine Drug Metab. Dispos. 27:866-871 (1999).
    • (1999) Drug Metab. Dispos , vol.27 , pp. 866-871
    • Cvetkovic, M.1    Leake, B.2    Fromm, M.F.3    Wilkinson, G.R.4    Kim, R.B.5
  • 135
  • 136
    • 0031760270 scopus 로고    scopus 로고
    • Diclofenac acyl glucuronide, a major biliary metabolite, is directly involved in small intestinal injury in rats
    • S. Seitz and U. A. Boelsterli. Diclofenac acyl glucuronide, a major biliary metabolite, is directly involved in small intestinal injury in rats Gastroenterology 115:1476-1482 (1998).
    • (1998) Gastroenterology , vol.115 , pp. 1476-1482
    • Seitz, S.1    Boelsterli, U.A.2
  • 137
    • 0033984873 scopus 로고    scopus 로고
    • Drug- and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver
    • B. Stieger, K. Fattinger, J. Madon, G. A. Kullak-Ublick, and P. J. Meier. Drug- and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver Gastroenterology 118:422-430 (2000).
    • (2000) Gastroenterology , vol.118 , pp. 422-430
    • Stieger, B.1    Fattinger, K.2    Madon, J.3    Kullak-Ublick, G.A.4    Meier, P.J.5
  • 138
    • 0035813014 scopus 로고    scopus 로고
    • Troglitazone-induced intrahepatic cholestasis by an interference with the hepatobiliary export of bile acids in male and female rats. Correlation with the gender difference in troglitazone sulfate formation and the inhibition of the canalicular bile salt export pump (Bsep) by troglitazone and troglitazone sulfate
    • C. Funk, M. Pantze, L. Jehle, C. Ponelle, G. Scheuermann, M. Lazendic, and R. Gasser. Troglitazone-induced intrahepatic cholestasis by an interference with the hepatobiliary export of bile acids in male and female rats. Correlation with the gender difference in troglitazone sulfate formation and the inhibition of the canalicular bile salt export pump (Bsep) by troglitazone and troglitazone sulfate Toxicology 167:83-98 (2001).
    • (2001) Toxicology , vol.167 , pp. 83-98
    • Funk, C.1    Pantze, M.2    Jehle, L.3    Ponelle, C.4    Scheuermann, G.5    Lazendic, M.6    Gasser, R.7
  • 141
    • 14044265064 scopus 로고    scopus 로고
    • Assessment of drug interactions in hepatobiliary transport using rhodamine 123 in sandwich-cultured rat hepatocytes
    • P. P. Annaert and K. L. Brouwer. Assessment of drug interactions in hepatobiliary transport using rhodamine 123 in sandwich-cultured rat hepatocytes Drug Metab. Dispos. 33:388-394 (2005).
    • (2005) Drug Metab. Dispos , vol.33 , pp. 388-394
    • Annaert, P.P.1    Brouwer, K.L.2
  • 142
    • 0034822280 scopus 로고    scopus 로고
    • P-glycoprotein-mediated in vitro biliary excretion in sandwich-cultured rat hepatocytes
    • P. P. Annaert, R. Z. Turncliff, C. L. Booth, D. R. Thakker, and K. L. Brouwer. P-glycoprotein-mediated in vitro biliary excretion in sandwich-cultured rat hepatocytes Drug Metab. Dispos. 29:1277-1283 (2001).
    • (2001) Drug Metab. Dispos , vol.29 , pp. 1277-1283
    • Annaert, P.P.1    Turncliff, R.Z.2    Booth, C.L.3    Thakker, D.R.4    Brouwer, K.L.5
  • 143
    • 15744367808 scopus 로고    scopus 로고
    • Polymorphisms in human organic anion-transporting polypeptide 1A2 (OATP1A2): Implications for altered drug disposition and central nervous system drug entry
    • W. Lee, H. Glaeser, L. H. Smith, R. L. Roberts, G. W. Moeckel, G. Gervasini, B. F. Leake, and R. B. Kim. Polymorphisms in human organic anion-transporting polypeptide 1A2 (OATP1A2): implications for altered drug disposition and central nervous system drug entry. J. Biol. Chem. 280:9610-9617 (2005).
    • (2005) J. Biol. Chem , vol.280 , pp. 9610-9617
    • Lee, W.1    Glaeser, H.2    Smith, L.H.3    Roberts, R.L.4    Moeckel, G.W.5    Gervasini, G.6    Leake, B.F.7    Kim, R.B.8
  • 144
    • 4944225107 scopus 로고    scopus 로고
    • Prediction of in vivo biliary clearance from the in vitro transcellular transport of organic anions across a double-transfected Madin-Darby canine kidney II monolayer expressing both rat organic anion transporting polypeptide 4 and multidrug resistance associated protein 2
    • M. Sasaki, H. Suzuki, J. Aoki, K. Ito, P. J. Meier, and Y. Sugiyama. Prediction of in vivo biliary clearance from the in vitro transcellular transport of organic anions across a double-transfected Madin-Darby canine kidney II monolayer expressing both rat organic anion transporting polypeptide 4 and multidrug resistance associated protein 2 Mol. Pharmacol. 66:450-459 (2004).
    • (2004) Mol. Pharmacol , vol.66 , pp. 450-459
    • Sasaki, M.1    Suzuki, H.2    Aoki, J.3    Ito, K.4    Meier, P.J.5    Sugiyama, Y.6
  • 146
    • 33646230798 scopus 로고    scopus 로고
    • Use of canalicular membrane vesicles (CMVs) from rats, dogs, monkeys and humans to assess drug transport across the canalicular membrane
    • A. D. Shilling, F. Azam, J. Kao, and L. Leung. Use of canalicular membrane vesicles (CMVs) from rats, dogs, monkeys and humans to assess drug transport across the canalicular membrane J. Pharmacol. Toxicol. Methods 53:186-197 (2006).
    • (2006) J. Pharmacol. Toxicol. Methods , vol.53 , pp. 186-197
    • Shilling, A.D.1    Azam, F.2    Kao, J.3    Leung, L.4
  • 147
    • 6944221357 scopus 로고    scopus 로고
    • Drug-drug interactions for UDP-glucuronosyltransferase substrates: A pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios
    • J. A. Williams, R. Hyland, B. C. Jones, D. A. Smith, S. Hurst, T. C. Goosen, V. Peterkin, J. R. Koup, and S. E. Ball. Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios Drug Metab. Dispos. 32:1201-1208 (2004).
    • (2004) Drug Metab. Dispos , vol.32 , pp. 1201-1208
    • Williams, J.A.1    Hyland, R.2    Jones, B.C.3    Smith, D.A.4    Hurst, S.5    Goosen, T.C.6    Peterkin, V.7    Koup, J.R.8    Ball, S.E.9
  • 148
    • 0344333422 scopus 로고    scopus 로고
    • Prediction of hepatic clearance from microsomes, hepatocytes, and liver slices
    • J. B. Houston and D. J. Carlile. Prediction of hepatic clearance from microsomes, hepatocytes, and liver slices Drug Metab. Rev. 29:891-922 (1997).
    • (1997) Drug Metab. Rev , vol.29 , pp. 891-922
    • Houston, J.B.1    Carlile, D.J.2
  • 149
    • 4143108324 scopus 로고    scopus 로고
    • Substrate depletion approach for determining in vitro metabolic clearance: Time dependencies in hepatocyte and microsomal incubations
    • H. M. Jones and J. B. Houston. Substrate depletion approach for determining in vitro metabolic clearance: time dependencies in hepatocyte and microsomal incubations Drug Metab. Dispos. 32:973-982 (2004).
    • (2004) Drug Metab. Dispos , vol.32 , pp. 973-982
    • Jones, H.M.1    Houston, J.B.2
  • 150
    • 0032733974 scopus 로고    scopus 로고
    • Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
    • R. S. Obach. Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: an examination of in vitro half-life approach and nonspecific binding to microsomes Drug Metab. Dispos. 27:1350-1359 (1999).
    • (1999) Drug Metab. Dispos , vol.27 , pp. 1350-1359
    • Obach, R.S.1
  • 151
    • 19944427171 scopus 로고    scopus 로고
    • Simple strategies for reducing sample loads in in in vitro metabolic stability high-throughput screening experiments: A comparison between traditional, two-time-point and pooled sample analyses
    • S. X. Zhao, D. Forman, N. Wallace, B. J. Smith, D. Meyer, D. Kazolias, F. Gao, J. Soglia, M. Cole, and D. Nettleton. Simple strategies for reducing sample loads in in in vitro metabolic stability high-throughput screening experiments: a comparison between traditional, two-time-point and pooled sample analyses J. Pharm. Sci. 94:38-45 (2005).
    • (2005) J. Pharm. Sci , vol.94 , pp. 38-45
    • Zhao, S.X.1    Forman, D.2    Wallace, N.3    Smith, B.J.4    Meyer, D.5    Kazolias, D.6    Gao, F.7    Soglia, J.8    Cole, M.9    Nettleton, D.10
  • 152
    • 0037403950 scopus 로고    scopus 로고
    • Utility of hepatocytes in predicting drug metabolism: Comparison of hepatic intrinsic clearance in rats and humans in vivo and in vitro
    • Y. Naritomi, S. Terashita, A. Kagayama, and Y. Sugiyama. Utility of hepatocytes in predicting drug metabolism: comparison of hepatic intrinsic clearance in rats and humans in vivo and in vitro Drug Metab. Dispos. 31:580-588 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , pp. 580-588
    • Naritomi, Y.1    Terashita, S.2    Kagayama, A.3    Sugiyama, Y.4
  • 153
    • 23944451585 scopus 로고    scopus 로고
    • A unified model for predicting human hepatic, metabolic clearance from in vitro intrinsic clearance data in hepatocytes and microsomes
    • R. J. Riley, D. F. McGinnity, and R. P. Austin. A unified model for predicting human hepatic, metabolic clearance from in vitro intrinsic clearance data in hepatocytes and microsomes Drug Metab. Dispos. 33:1304-1311 (2005).
    • (2005) Drug Metab. Dispos , vol.33 , pp. 1304-1311
    • Riley, R.J.1    McGinnity, D.F.2    Austin, R.P.3
  • 154
    • 0036320379 scopus 로고    scopus 로고
    • Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: An application of serum incubation method
    • Y. Shibata, H. Takahashi, M. Chiba, and Y. Ishii. Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: an application of serum incubation method Drug Metab. Dispos. 30:892-896 (2002).
    • (2002) Drug Metab. Dispos , vol.30 , pp. 892-896
    • Shibata, Y.1    Takahashi, H.2    Chiba, M.3    Ishii, Y.4
  • 157
    • 33645809139 scopus 로고    scopus 로고
    • M. F. Paine, H. L. Hart, S. S. Ludington, R. L. Haining, A. E. Rettie, and D. C. Zeldin. The human intestinal cytochrome P450 pie Drug Metab. Dispos. 34:880-886 (2006).
    • M. F. Paine, H. L. Hart, S. S. Ludington, R. L. Haining, A. E. Rettie, and D. C. Zeldin. The human intestinal cytochrome P450 "pie" Drug Metab. Dispos. 34:880-886 (2006).
  • 158
    • 17644380257 scopus 로고    scopus 로고
    • Predicting drug disposition via application of BCS: Transport/absorption/ elimination interplay and development of a biopharmaceutics drug disposition classification system
    • C. Y. Wu and L. Z. Benet. Predicting drug disposition via application of BCS: transport/absorption/ elimination interplay and development of a biopharmaceutics drug disposition classification system Pharm. Res. 22:11-23 (2005).
    • (2005) Pharm. Res , vol.22 , pp. 11-23
    • Wu, C.Y.1    Benet, L.Z.2
  • 159
    • 0345866819 scopus 로고    scopus 로고
    • CYP3A4-transfected Caco-2 cells as a tool for understanding biochemical absorption barriers: Studies with sirolimus and midazolam
    • C. L. Cummins, W. Jacobsen, U. Christians, and L. Z. Benet. CYP3A4-transfected Caco-2 cells as a tool for understanding biochemical absorption barriers: studies with sirolimus and midazolam J. Pharmacol. Exp. Ther. 308:143-155 (2004).
    • (2004) J. Pharmacol. Exp. Ther , vol.308 , pp. 143-155
    • Cummins, C.L.1    Jacobsen, W.2    Christians, U.3    Benet, L.Z.4
  • 161
    • 33745498418 scopus 로고    scopus 로고
    • Pharmacokinetics and metabolic disposition of sirolimus in healthy male volunteers after a single oral dose
    • L. Y. Leung, H. K. Lim, M. W. Abell, and J. J. Zimmerman. Pharmacokinetics and metabolic disposition of sirolimus in healthy male volunteers after a single oral dose Ther. Drug Monit. 28:51-61 (2006).
    • (2006) Ther. Drug Monit , vol.28 , pp. 51-61
    • Leung, L.Y.1    Lim, H.K.2    Abell, M.W.3    Zimmerman, J.J.4
  • 162
    • 0027474601 scopus 로고
    • Mechanism of the cardiotoxic actions of terfenadine
    • R. L. Woosley, Y. Chen, J. P. Freiman, and R. A. Gillis. Mechanism of the cardiotoxic actions of terfenadine JAMA 269:1532-1536 (1993).
    • (1993) JAMA , vol.269 , pp. 1532-1536
    • Woosley, R.L.1    Chen, Y.2    Freiman, J.P.3    Gillis, R.A.4
  • 163
    • 0031952975 scopus 로고    scopus 로고
    • Fexofenadine
    • A. Markham and A. J. Wagstaff. Fexofenadine Drugs 55:269-274 (1998).
    • (1998) Drugs , vol.55 , pp. 269-274
    • Markham, A.1    Wagstaff, A.J.2
  • 164
    • 0142243111 scopus 로고    scopus 로고
    • Mechanism-based inhibition of human liver microsomal cytochrome P450 1A2 by zileuton, a 5-lipoxygenase inhibitor
    • P. Lu, M. L. Schrag, D. E. Slaughter, C. E. Raab, M. Shou, and A. D. Rodrigues. Mechanism-based inhibition of human liver microsomal cytochrome P450 1A2 by zileuton, a 5-lipoxygenase inhibitor Drug Metab. Dispos. 31:1352-1360 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , pp. 1352-1360
    • Lu, P.1    Schrag, M.L.2    Slaughter, D.E.3    Raab, C.E.4    Shou, M.5    Rodrigues, A.D.6
  • 165
    • 10044257558 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human cytochrome P4502C8 by drugs in vitro
    • T. M. Polasek, D. J. Elliot, B. C. Lewis, and J. O. Miners. Mechanism-based inactivation of human cytochrome P4502C8 by drugs in vitro. J. Pharmacol. Exp. Ther.311:996-1007 (2004).
    • (2004) J. Pharmacol. Exp. Ther , vol.311 , pp. 996-1007
    • Polasek, T.M.1    Elliot, D.J.2    Lewis, B.C.3    Miners, J.O.4
  • 166
    • 19944393579 scopus 로고    scopus 로고
    • Enzyme kinetics for clinically relevant CYP inhibition
    • Z. Y. Zhang and Y. N. Wong. Enzyme kinetics for clinically relevant CYP inhibition Curr. Drug Metab. 6:241-257 (2005).
    • (2005) Curr. Drug Metab , vol.6 , pp. 241-257
    • Zhang, Z.Y.1    Wong, Y.N.2
  • 168
    • 24944492194 scopus 로고    scopus 로고
    • Utility of recombinant cytochrome p450 enzymes: A drug metabolism perspective
    • W. Tang, R. W. Wang, and A. Y. Lu. Utility of recombinant cytochrome p450 enzymes: a drug metabolism perspective Curr. Drug Metab. 6:503-517 (2005).
    • (2005) Curr. Drug Metab , vol.6 , pp. 503-517
    • Tang, W.1    Wang, R.W.2    Lu, A.Y.3
  • 169
    • 29944439409 scopus 로고    scopus 로고
    • Mechanism-based inactivation and reversibility: Is there a new trend in the inactivation of cytochrome p450 enzymes?
    • A. L. Blobaum. Mechanism-based inactivation and reversibility: is there a new trend in the inactivation of cytochrome p450 enzymes? Drug Metab. Dispos. 34:1-7 (2006).
    • (2006) Drug Metab. Dispos , vol.34 , pp. 1-7
    • Blobaum, A.L.1
  • 170
    • 0035157254 scopus 로고    scopus 로고
    • A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry
    • E. A. Dierks, K. R. Stams, H. K. Lim, G. Cornelius, H. Zhang, and S. E. Ball. A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry Drug Metab. Dispos. 29:23-29 (2001).
    • (2001) Drug Metab. Dispos , vol.29 , pp. 23-29
    • Dierks, E.A.1    Stams, K.R.2    Lim, H.K.3    Cornelius, G.4    Zhang, H.5    Ball, S.E.6
  • 171
    • 18844369894 scopus 로고    scopus 로고
    • Impact of parallel pathways of drug elimination and multiple cytochrome P450 involvement on drug-drug interactions: CYP2D6 paradigm
    • K. Ito, D. Hallifax, R. S. Obach, and J. B. Houston. Impact of parallel pathways of drug elimination and multiple cytochrome P450 involvement on drug-drug interactions: CYP2D6 paradigm Drug Metab. Dispos. 33:837-844 (2005).
    • (2005) Drug Metab. Dispos , vol.33 , pp. 837-844
    • Ito, K.1    Hallifax, D.2    Obach, R.S.3    Houston, J.B.4
  • 172
    • 0033831197 scopus 로고    scopus 로고
    • An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation
    • B. S. Mayhew, D. R. Jones, and S. D. Hall. An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation Drug Metab. Dispos. 28:1031-1037 (2000).
    • (2000) Drug Metab. Dispos , vol.28 , pp. 1031-1037
    • Mayhew, B.S.1    Jones, D.R.2    Hall, S.D.3
  • 173
    • 0142150012 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human recombinant P450 2C9 by the nonsteroidal anti-inflammatory drug suprofen
    • J. P. O'Donnell, D. K. Dalvie, A. S. Kalgutkar, and R. S. Obach. Mechanism-based inactivation of human recombinant P450 2C9 by the nonsteroidal anti-inflammatory drug suprofen Drug Metab. Dispos. 31:1369-1377 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , pp. 1369-1377
    • O'Donnell, J.P.1    Dalvie, D.K.2    Kalgutkar, A.S.3    Obach, R.S.4
  • 174
    • 0842282550 scopus 로고    scopus 로고
    • Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites
    • Y. H. Wang, D. R. Jones, and S. D. Hall. Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites Drug Metab. Dispos. 32:259-266 (2004).
    • (2004) Drug Metab. Dispos , vol.32 , pp. 259-266
    • Wang, Y.H.1    Jones, D.R.2    Hall, S.D.3
  • 175
    • 24644441043 scopus 로고    scopus 로고
    • Kinetic values for mechanism-based enzyme inhibition: Assessing the bias introduced by the conventional experimental protocol
    • J. Yang, M. Jamei, K. R. Yeo, G. T. Tucker, and A. Rostami-Hodjegan. Kinetic values for mechanism-based enzyme inhibition: assessing the bias introduced by the conventional experimental protocol Eur. J. Pharm. Sci. 26:334-340 (2005).
    • (2005) Eur. J. Pharm. Sci , vol.26 , pp. 334-340
    • Yang, J.1    Jamei, M.2    Yeo, K.R.3    Tucker, G.T.4    Rostami-Hodjegan, A.5
  • 176
    • 0032619762 scopus 로고    scopus 로고
    • Knowledge-based expert systems for toxicity and metabolism prediction: DEREK, StAR and METEOR
    • N. Greene, P. N. Judson, J. J. Langowski, and C. A. Marchant. Knowledge-based expert systems for toxicity and metabolism prediction: DEREK, StAR and METEOR SAR QSAR Environ. Res. 10:299-314 (1999).
    • (1999) SAR QSAR Environ. Res , vol.10 , pp. 299-314
    • Greene, N.1    Judson, P.N.2    Langowski, J.J.3    Marchant, C.A.4
  • 177
    • 22944469767 scopus 로고    scopus 로고
    • Automated screening with confirmation of mechanism-based inactivation of CYP3A4, CYP2C9, CYP2C19, CYP2D6, and CYP1A2 in pooled human liver microsomes
    • H. K. Lim, N. Duczak Jr., L. Brougham, M. Elliot, K. Patel, and K. Chan. Automated screening with confirmation of mechanism-based inactivation of CYP3A4, CYP2C9, CYP2C19, CYP2D6, and CYP1A2 in pooled human liver microsomes Drug Metab. Dispos. 33:1211-1219 (2005).
    • (2005) Drug Metab. Dispos , vol.33 , pp. 1211-1219
    • Lim, H.K.1    Duczak Jr., N.2    Brougham, L.3    Elliot, M.4    Patel, K.5    Chan, K.6
  • 178
    • 0037369622 scopus 로고    scopus 로고
    • Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine: Comparison with fluoxetine and quinidine
    • K. M. Bertelsen, K. Venkatakrishnan, L. L. Von Moltke, R. S. Obach, and D. J. Greenblatt. Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine: comparison with fluoxetine and quinidine. Drug Metab. Dispos. 31:289-293 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , pp. 289-293
    • Bertelsen, K.M.1    Venkatakrishnan, K.2    Von Moltke, L.L.3    Obach, R.S.4    Greenblatt, D.J.5
  • 179
    • 0036219021 scopus 로고    scopus 로고
    • Selective serotonin reuptake inhibitors and cytochrome P-450 mediated drug-drug interactions: An update
    • A. Hemeryck and F. M. Belpaire. Selective serotonin reuptake inhibitors and cytochrome P-450 mediated drug-drug interactions: an update Curr. Drug Metab. 3:13-37 (2002).
    • (2002) Curr. Drug Metab , vol.3 , pp. 13-37
    • Hemeryck, A.1    Belpaire, F.M.2
  • 180
    • 18844426008 scopus 로고    scopus 로고
    • In vitro-in vivo extrapolation of CYP2D6 inactivation by paroxetine: Prediction of nonstationary pharmacokinetics and drug interaction magnitude
    • K. Venkatakrishnan and R. S. Obach. In vitro-in vivo extrapolation of CYP2D6 inactivation by paroxetine: prediction of nonstationary pharmacokinetics and drug interaction magnitude Drug Metab. Dispos. 33:845-852 (2005).
    • (2005) Drug Metab. Dispos , vol.33 , pp. 845-852
    • Venkatakrishnan, K.1    Obach, R.S.2
  • 181
    • 0033026601 scopus 로고    scopus 로고
    • Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: An in vitro investigation with human liver preparations
    • T. Prueksaritanont, B. Ma, C. Tang, Y. Meng, C. Assang, P. Lu, P. J. Reider, J. H. Lin, and T. A. Baillie. Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: an in vitro investigation with human liver preparations Br. J. Clin. Pharmacol. 47:291-298 (1999).
    • (1999) Br. J. Clin. Pharmacol , vol.47 , pp. 291-298
    • Prueksaritanont, T.1    Ma, B.2    Tang, C.3    Meng, Y.4    Assang, C.5    Lu, P.6    Reider, P.J.7    Lin, J.H.8    Baillie, T.A.9
  • 182
    • 0033863264 scopus 로고    scopus 로고
    • Mibefradil is a P-glycoprotein substrate and a potent inhibitor of both P-glycoprotein and CYP3A in vitro
    • C. Wandel, R. B. Kim, F. P. Guengerich, and A. J. Wood. Mibefradil is a P-glycoprotein substrate and a potent inhibitor of both P-glycoprotein and CYP3A in vitro Drug Metab. Dispos. 28:895-898 (2000).
    • (2000) Drug Metab. Dispos , vol.28 , pp. 895-898
    • Wandel, C.1    Kim, R.B.2    Guengerich, F.P.3    Wood, A.J.4
  • 184
    • 0035092715 scopus 로고    scopus 로고
    • Challenges and limitations of gene expression profiling in mechanistic and predictive toxicology
    • M. R. Fielden and T. R. Zacharewski. Challenges and limitations of gene expression profiling in mechanistic and predictive toxicology Toxicol. Sci. 60:6-10 (2001).
    • (2001) Toxicol. Sci , vol.60 , pp. 6-10
    • Fielden, M.R.1    Zacharewski, T.R.2
  • 186
    • 0038172423 scopus 로고    scopus 로고
    • Gene expression in two hepatic cell lines, cultured primary hepatocytes, and liver slices compared to the in vivo liver gene expression in rats: Possible implications for toxicogenomics use of in vitro systems
    • F. Boess, M. Kamber, S. Romer, R. Gasser, D. Muller, S. Albertini, and L. Suter. Gene expression in two hepatic cell lines, cultured primary hepatocytes, and liver slices compared to the in vivo liver gene expression in rats: possible implications for toxicogenomics use of in vitro systems. Toxicol. Sci.73:386-402 (2003).
    • (2003) Toxicol. Sci , vol.73 , pp. 386-402
    • Boess, F.1    Kamber, M.2    Romer, S.3    Gasser, R.4    Muller, D.5    Albertini, S.6    Suter, L.7
  • 190
    • 18944401259 scopus 로고    scopus 로고
    • Elucidating mechanisms of drug-induced toxicity
    • D. C. Liebler and F. P. Guengerich. Elucidating mechanisms of drug-induced toxicity. Nat. Rev. Drug Discov. 4:410-420 (2005).
    • (2005) Nat. Rev. Drug Discov , vol.4 , pp. 410-420
    • Liebler, D.C.1    Guengerich, F.P.2
  • 191
    • 0042831348 scopus 로고    scopus 로고
    • Screening for the potential of a drug candidate to cause idiosyncratic drug reactions
    • J. Uetrecht. Screening for the potential of a drug candidate to cause idiosyncratic drug reactions Drug Discov. Today 8:832-837 (2003).
    • (2003) Drug Discov. Today , vol.8 , pp. 832-837
    • Uetrecht, J.1
  • 192
    • 0038650987 scopus 로고    scopus 로고
    • Nuclear receptor, pregname X receptor, is required for induction of UDP-glucuronosyltranferases in mouse liver by pregnenolone-16 alpha-carbonitrile
    • C. Chen, J. L. Staudinger, and C. D. Klaassen. Nuclear receptor, pregname X receptor, is required for induction of UDP-glucuronosyltranferases in mouse liver by pregnenolone-16 alpha-carbonitrile Drug Metab. Dispos. 31:908-915 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , pp. 908-915
    • Chen, C.1    Staudinger, J.L.2    Klaassen, C.D.3
  • 193
    • 0021809352 scopus 로고
    • The effect of medroxyprogesterone acetate on the hepatic drug-metabolizing enzymes in normal and protein-deficient female rats
    • J. P. Nagpal, K. L. Khanduja, R. R. Sharma, S. Majumdar, R. Singh, M. P. Gupta, and S. C. Dogra. The effect of medroxyprogesterone acetate on the hepatic drug-metabolizing enzymes in normal and protein-deficient female rats Biochem. Med. 34:11-16 (1985).
    • (1985) Biochem. Med , vol.34 , pp. 11-16
    • Nagpal, J.P.1    Khanduja, K.L.2    Sharma, R.R.3    Majumdar, S.4    Singh, R.5    Gupta, M.P.6    Dogra, S.C.7
  • 194
    • 0022636569 scopus 로고
    • Time course of hepatic changes produced by medroxyprogesterone acetate in the rat
    • H. U. Saarni. Time course of hepatic changes produced by medroxyprogesterone acetate in the rat Gen. Pharmacol. 17:25-29 (1986).
    • (1986) Gen. Pharmacol , vol.17 , pp. 25-29
    • Saarni, H.U.1
  • 195
    • 34247641720 scopus 로고    scopus 로고
    • Application of pharmacogenomics in drug discovery and development: Correlations between transcriptional modulation and preclinical safety observation
    • L. G. Yengi, Q. Xiang, L. Shen, C. Appavu, J. Kao, and J. Scatina. Application of pharmacogenomics in drug discovery and development: correlations between transcriptional modulation and preclinical safety observation. Drug metab. Lett 1:(2007).
    • (2007) Drug metab. Lett , vol.1
    • Yengi, L.G.1    Xiang, Q.2    Shen, L.3    Appavu, C.4    Kao, J.5    Scatina, J.6
  • 196
    • 4344645978 scopus 로고    scopus 로고
    • Can the pharmaceutical industry reduce attrition rates?
    • I. Kola and J. Landis. Can the pharmaceutical industry reduce attrition rates? Nat. Rev. Drug Discov. 3:711-715 (2004).
    • (2004) Nat. Rev. Drug Discov , vol.3 , pp. 711-715
    • Kola, I.1    Landis, J.2


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