메뉴 건너뛰기




Volumn 101, Issue , 2014, Pages 221-237

A cocktail approach for assessing the in vitro activity of human cytochrome P450s: An overview of current methodologies

Author keywords

Cocktail; CYP phenotyping; Drug drug interactions; Human liver microsomes; In vitro methodology

Indexed keywords

CYTOCHROME P450; CYTOCHROME P450 1A2; CYTOCHROME P450 2A6; CYTOCHROME P450 2B6; CYTOCHROME P450 2C19; CYTOCHROME P450 2C8; CYTOCHROME P450 2C9; CYTOCHROME P450 2D6; CYTOCHROME P450 2E1; CYTOCHROME P450 3A; ORGANIC SOLVENT;

EID: 84908350475     PISSN: 07317085     EISSN: 1873264X     Source Type: Journal    
DOI: 10.1016/j.jpba.2014.03.018     Document Type: Review
Times cited : (85)

References (177)
  • 1
    • 84861646776 scopus 로고    scopus 로고
    • Foundation review: reactions and enzymes in the metabolism of drugs and other xenobiotics
    • Testa B., Pedretti A., Vistoli G. Foundation review: reactions and enzymes in the metabolism of drugs and other xenobiotics. Drug Discovery Today 2012, 17:549-560.
    • (2012) Drug Discovery Today , vol.17 , pp. 549-560
    • Testa, B.1    Pedretti, A.2    Vistoli, G.3
  • 2
    • 0037068964 scopus 로고    scopus 로고
    • Clinical importance of the cytochromes P450
    • Nebert D.W., Russell D.W. Clinical importance of the cytochromes P450. Lancet 2002, 360:1155-1162.
    • (2002) Lancet , vol.360 , pp. 1155-1162
    • Nebert, D.W.1    Russell, D.W.2
  • 3
    • 84863920443 scopus 로고    scopus 로고
    • Contributions of human enzymes in carcinogen metabolism
    • Rendic S., Guengerich F.P. Contributions of human enzymes in carcinogen metabolism. Chem. Res. Toxicol. 2012, 25:1316-1383.
    • (2012) Chem. Res. Toxicol. , vol.25 , pp. 1316-1383
    • Rendic, S.1    Guengerich, F.P.2
  • 4
    • 70149110672 scopus 로고    scopus 로고
    • Polymorphism of human cytochrome P450 enzymes and its clinical impact
    • Zhou S.F., Liu J.P., Chowbay B. Polymorphism of human cytochrome P450 enzymes and its clinical impact. Drug Metab. Rev. 2009, 41:89-295.
    • (2009) Drug Metab. Rev. , vol.41 , pp. 89-295
    • Zhou, S.F.1    Liu, J.P.2    Chowbay, B.3
  • 6
    • 0031794361 scopus 로고    scopus 로고
    • Inhibition and induction of cytochrome P450 and the clinical implications
    • Lin J.H., Lu A.Y.H. Inhibition and induction of cytochrome P450 and the clinical implications. Clin. Pharmacokinet. 1998, 35:361-390.
    • (1998) Clin. Pharmacokinet. , vol.35 , pp. 361-390
    • Lin, J.H.1    Lu, A.Y.H.2
  • 7
    • 77955507698 scopus 로고    scopus 로고
    • A review of LC-MS techniques and high-throughput approaches used to investigate drug metabolism by cytochrome P450s
    • Youdim K.A., Saunders K.C. A review of LC-MS techniques and high-throughput approaches used to investigate drug metabolism by cytochrome P450s. J. Chromatogr. B 2010, 878:1326-1336.
    • (2010) J. Chromatogr. B , vol.878 , pp. 1326-1336
    • Youdim, K.A.1    Saunders, K.C.2
  • 8
    • 0025285552 scopus 로고
    • A cocktail strategy to assess in vivo oxidative drug-metabolism in humans
    • Breimer D.D., Schellens J.H.M. A cocktail strategy to assess in vivo oxidative drug-metabolism in humans. Trends Pharmacol. Sci. 1990, 11:223-225.
    • (1990) Trends Pharmacol. Sci. , vol.11 , pp. 223-225
    • Breimer, D.D.1    Schellens, J.H.M.2
  • 9
    • 4344576481 scopus 로고    scopus 로고
    • A simplified analytical method for a phenotyping cocktail of major CYP450 biotransformation routes
    • Jerdi M.C., Daali Y., Oestreicher M.K., Cherkaoui S., Dayer P. A simplified analytical method for a phenotyping cocktail of major CYP450 biotransformation routes. J. Pharmaceut. Biomed. 2004, 35:1203-1212.
    • (2004) J. Pharmaceut. Biomed. , vol.35 , pp. 1203-1212
    • Jerdi, M.C.1    Daali, Y.2    Oestreicher, M.K.3    Cherkaoui, S.4    Dayer, P.5
  • 10
    • 84892698531 scopus 로고    scopus 로고
    • Simultaneous LC-MS/MS quantification of P-glycoprotein and cytochrome P450 probe substrates and their metabolites in DBS and plasma
    • Bosilkovska M., Déglon J., Samer C., Walder B., Desmeules J., Staub C., Daali Y. Simultaneous LC-MS/MS quantification of P-glycoprotein and cytochrome P450 probe substrates and their metabolites in DBS and plasma. Bioanalysis 2014, 6:151-164.
    • (2014) Bioanalysis , vol.6 , pp. 151-164
    • Bosilkovska, M.1    Déglon, J.2    Samer, C.3    Walder, B.4    Desmeules, J.5    Staub, C.6    Daali, Y.7
  • 11
    • 0037803539 scopus 로고    scopus 로고
    • How useful is the 'cocktail approach' for evaluating human hepatic drug metabolizing capacity using cytochrome P450 phenotyping probes in vivo?
    • Tanaka E., Kurata N., Yasuhara H. How useful is the 'cocktail approach' for evaluating human hepatic drug metabolizing capacity using cytochrome P450 phenotyping probes in vivo?. J. Clin. Pharm. Ther. 2003, 28:157-165.
    • (2003) J. Clin. Pharm. Ther. , vol.28 , pp. 157-165
    • Tanaka, E.1    Kurata, N.2    Yasuhara, H.3
  • 12
    • 1642494659 scopus 로고    scopus 로고
    • Cocktail approaches and strategies in drug development: valuable tool or flawed science?
    • Zhou H.H., Tong Z., McLeod J.F. Cocktail approaches and strategies in drug development: valuable tool or flawed science?. J. Clin. Pharmacol. 2004, 44:120-134.
    • (2004) J. Clin. Pharmacol. , vol.44 , pp. 120-134
    • Zhou, H.H.1    Tong, Z.2    McLeod, J.F.3
  • 13
    • 33846607427 scopus 로고    scopus 로고
    • Appropriate phenotyping procedures for drug metabolizing enzymes and transporters in humans and their simultaneous use in the cocktail approach
    • Fuhr U., Jetter A., Kirchheiner J. Appropriate phenotyping procedures for drug metabolizing enzymes and transporters in humans and their simultaneous use in the cocktail approach. Clin. Pharmacol. Ther. 2007, 81:270-283.
    • (2007) Clin. Pharmacol. Ther. , vol.81 , pp. 270-283
    • Fuhr, U.1    Jetter, A.2    Kirchheiner, J.3
  • 14
    • 3242733232 scopus 로고    scopus 로고
    • Probing the world of cytochrone P450 enzymes
    • Frye R.E. Probing the world of cytochrone P450 enzymes. Mol. Interventions 2004, 4:157-162.
    • (2004) Mol. Interventions , vol.4 , pp. 157-162
    • Frye, R.E.1
  • 15
    • 0036893593 scopus 로고    scopus 로고
    • Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions
    • Yuan R., Madani S., Wei X.X., Reynolds K., Huang S.M. Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions. Drug Metab. Dispos. 2002, 30:1311-1319.
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 1311-1319
    • Yuan, R.1    Madani, S.2    Wei, X.X.3    Reynolds, K.4    Huang, S.M.5
  • 16
    • 0037272197 scopus 로고    scopus 로고
    • Strategies and molecular probes to investigate the role of cytochrome P450 in drug metabolism - focus on in vitro studies
    • Donato M.T., Castell J.V. Strategies and molecular probes to investigate the role of cytochrome P450 in drug metabolism - focus on in vitro studies. Clin. Pharmacokinet. 2003, 42:153-178.
    • (2003) Clin. Pharmacokinet. , vol.42 , pp. 153-178
    • Donato, M.T.1    Castell, J.V.2
  • 17
    • 38949094492 scopus 로고    scopus 로고
    • Cytochrome P450 and chemical toxicology
    • Guengerich F.P. Cytochrome P450 and chemical toxicology. Chem. Res. Toxicol. 2008, 21:70-83.
    • (2008) Chem. Res. Toxicol. , vol.21 , pp. 70-83
    • Guengerich, F.P.1
  • 18
    • 0034770465 scopus 로고    scopus 로고
    • Human drug metabolism and the cytochromes P450: application and relevance of in vitro models
    • Venkatakrishnan K., von Moltke L.L., Greenblatt D.J. Human drug metabolism and the cytochromes P450: application and relevance of in vitro models. J. Clin. Pharmacol. 2001, 41:1149-1179.
    • (2001) J. Clin. Pharmacol. , vol.41 , pp. 1149-1179
    • Venkatakrishnan, K.1    von Moltke, L.L.2    Greenblatt, D.J.3
  • 19
    • 36849043262 scopus 로고    scopus 로고
    • Evaluation of cytochrome P450 activity in vitro, using dermal and hepatic microsomes from four species and two keratinocyte cell lines in culture
    • Rolsted K., Kissmeyer A.M., Rist G.M., Hansen S.H. Evaluation of cytochrome P450 activity in vitro, using dermal and hepatic microsomes from four species and two keratinocyte cell lines in culture. Arch. Dermatol. Res. 2008, 300:10-18.
    • (2008) Arch. Dermatol. Res. , vol.300 , pp. 10-18
    • Rolsted, K.1    Kissmeyer, A.M.2    Rist, G.M.3    Hansen, S.H.4
  • 20
    • 22344440846 scopus 로고    scopus 로고
    • The use of a substrate cassette strategy to improve the capacity and throughput of cytochrome P450 induction studies in human hepatocytes
    • Mohutsky M.A., Petullo D.M., Wrighton S.A. The use of a substrate cassette strategy to improve the capacity and throughput of cytochrome P450 induction studies in human hepatocytes. Drug Metab. Dispos. 2005, 33:920-923.
    • (2005) Drug Metab. Dispos. , vol.33 , pp. 920-923
    • Mohutsky, M.A.1    Petullo, D.M.2    Wrighton, S.A.3
  • 21
    • 46449089949 scopus 로고    scopus 로고
    • Evaluation of HepaRG cells as an in vitro model for human drug metabolism studies
    • Kanebratt K.P., Andersson T.B. Evaluation of HepaRG cells as an in vitro model for human drug metabolism studies. Drug Metab. Dispos. 2008, 36:1444-1452.
    • (2008) Drug Metab. Dispos. , vol.36 , pp. 1444-1452
    • Kanebratt, K.P.1    Andersson, T.B.2
  • 22
    • 83055193621 scopus 로고    scopus 로고
    • Upgrading cytochrome P450 activity in HepG2 cells co-transfected with adenoviral vectors for drug hepatotoxicity assessment
    • Tolosa L., Donato M.T., Perez-Cataldo G., Castell J.V., Gomez-Lechon M.J. Upgrading cytochrome P450 activity in HepG2 cells co-transfected with adenoviral vectors for drug hepatotoxicity assessment. Toxicol. In Vitro 2012, 26:1272-1277.
    • (2012) Toxicol. In Vitro , vol.26 , pp. 1272-1277
    • Tolosa, L.1    Donato, M.T.2    Perez-Cataldo, G.3    Castell, J.V.4    Gomez-Lechon, M.J.5
  • 23
    • 84908348297 scopus 로고    scopus 로고
    • In situ evaluation of CYP1A2, CYP2B6 and CYP3A4/5 induction in human hepatocytes with a cocktail of probe substrates
    • Amunom I., Brawner S., Simpson J., Sawi J., Campbell R., Neat J., Parkinson A. In situ evaluation of CYP1A2, CYP2B6 and CYP3A4/5 induction in human hepatocytes with a cocktail of probe substrates. Drug Metab. Rev. 2009, 41:89.
    • (2009) Drug Metab. Rev. , vol.41 , pp. 89
    • Amunom, I.1    Brawner, S.2    Simpson, J.3    Sawi, J.4    Campbell, R.5    Neat, J.6    Parkinson, A.7
  • 24
    • 84865844666 scopus 로고    scopus 로고
    • In situ evaluation of CYP1A2, CYP2B6 and CYP3A4/5 induction in cultured human hepatocytes with a cocktail of probe substrates: a comparison of percent positive control values
    • Lyon K., Amunom I., Neat J.N., Holsapple J., Buckley D., Parkinson A. In situ evaluation of CYP1A2, CYP2B6 and CYP3A4/5 induction in cultured human hepatocytes with a cocktail of probe substrates: a comparison of percent positive control values. Drug Metab. Rev. 2010, 42:134-135.
    • (2010) Drug Metab. Rev. , vol.42 , pp. 134-135
    • Lyon, K.1    Amunom, I.2    Neat, J.N.3    Holsapple, J.4    Buckley, D.5    Parkinson, A.6
  • 25
    • 79954612110 scopus 로고    scopus 로고
    • Simultaneous assessment of cytochrome P450 activity in cultured human hepatocytes for compound-mediated induction of CYP3A4, CYP2B6, and CYP1A2, J
    • Rhodes S.P., Otten J.N., Hingorani G.P., Hartley D.P., Franklin R.B. Simultaneous assessment of cytochrome P450 activity in cultured human hepatocytes for compound-mediated induction of CYP3A4, CYP2B6, and CYP1A2, J. Pharmacol. Toxicol. 2011, 63:223-226.
    • (2011) Pharmacol. Toxicol. , vol.63 , pp. 223-226
    • Rhodes, S.P.1    Otten, J.N.2    Hingorani, G.P.3    Hartley, D.P.4    Franklin, R.B.5
  • 26
    • 84870669368 scopus 로고    scopus 로고
    • An 'all-inclusive' 96-well cytochrome P450 induction method: measuring enzyme activity, mRNA levels, protein levels, and cytotoxicity from one well using cryopreserved human hepatocytes
    • Halladay J.S., Wong S., Khojasteh S.C., Grepper S. An 'all-inclusive' 96-well cytochrome P450 induction method: measuring enzyme activity, mRNA levels, protein levels, and cytotoxicity from one well using cryopreserved human hepatocytes. J. Pharmacol. Toxicol. 2012, 66:270-275.
    • (2012) J. Pharmacol. Toxicol. , vol.66 , pp. 270-275
    • Halladay, J.S.1    Wong, S.2    Khojasteh, S.C.3    Grepper, S.4
  • 27
    • 25144525190 scopus 로고    scopus 로고
    • High-throughput screening of inhibitory potential of nine cytochrome P450 enzymes in vitro using liquid chromatography/tandem mass spectrometry
    • Kim M.J., Kim H., Cha I.J., Park J.S., Shon J.H., Liu K.H., Shin J.G. High-throughput screening of inhibitory potential of nine cytochrome P450 enzymes in vitro using liquid chromatography/tandem mass spectrometry. Rapid Commun. Mass Spectrom. 2005, 19:2651-2658.
    • (2005) Rapid Commun. Mass Spectrom. , vol.19 , pp. 2651-2658
    • Kim, M.J.1    Kim, H.2    Cha, I.J.3    Park, J.S.4    Shon, J.H.5    Liu, K.H.6    Shin, J.G.7
  • 29
    • 33747890072 scopus 로고    scopus 로고
    • Characterization of the cytochrome P450 enzymes involved in the metabolism of a new cardioprotective agent KR-33028
    • Kim H., Yoon Y.J., Kim H., Kang S., Cheon H.G., Yoo S.E., Shin J.G., Liu K.H. Characterization of the cytochrome P450 enzymes involved in the metabolism of a new cardioprotective agent KR-33028. Toxicol. Lett. 2006, 166:105-114.
    • (2006) Toxicol. Lett. , vol.166 , pp. 105-114
    • Kim, H.1    Yoon, Y.J.2    Kim, H.3    Kang, S.4    Cheon, H.G.5    Yoo, S.E.6    Shin, J.G.7    Liu, K.H.8
  • 30
    • 50249111587 scopus 로고    scopus 로고
    • In vitro metabolism of a novel PPAR gamma agonist, KR-62980, and its stereoisomer, KR-63198, in human liver microsomes and by recombinant cytochrome P450s
    • Kim K.B., Seo K.A., Yoon Y.J., Bae M.A., Cheon H.G., Shin J.G., Liu K.H. In vitro metabolism of a novel PPAR gamma agonist, KR-62980, and its stereoisomer, KR-63198, in human liver microsomes and by recombinant cytochrome P450s. Xenobiotica 2008, 38:1165-1176.
    • (2008) Xenobiotica , vol.38 , pp. 1165-1176
    • Kim, K.B.1    Seo, K.A.2    Yoon, Y.J.3    Bae, M.A.4    Cheon, H.G.5    Shin, J.G.6    Liu, K.H.7
  • 31
    • 79956371619 scopus 로고    scopus 로고
    • In vitro metabolism and transport of the new dipeptidyl peptidase 4 inhibitors, KR66222 and KR66223
    • Ahn H.J., Kim K.B., Liu K.H., Shin J.G., Ahn J.H., Kim M.S., Bae M.A., Song I.S. In vitro metabolism and transport of the new dipeptidyl peptidase 4 inhibitors, KR66222 and KR66223. Xenobiotica 2011, 41:445-455.
    • (2011) Xenobiotica , vol.41 , pp. 445-455
    • Ahn, H.J.1    Kim, K.B.2    Liu, K.H.3    Shin, J.G.4    Ahn, J.H.5    Kim, M.S.6    Bae, M.A.7    Song, I.S.8
  • 32
    • 84871253396 scopus 로고    scopus 로고
    • High-throughput screening of inhibitory effects of Bo-yang-hwan-o-tang on human cytochrome P450 isoforms in vitro using UPLC/MS/MS
    • Lee M., Park J., Lim M.S., Seong S.J., Lee J., Seo J.J., Park Y.K., Lee H.W., Yoon Y.R. High-throughput screening of inhibitory effects of Bo-yang-hwan-o-tang on human cytochrome P450 isoforms in vitro using UPLC/MS/MS. Anal. Sci. 2012, 28:1197-1201.
    • (2012) Anal. Sci. , vol.28 , pp. 1197-1201
    • Lee, M.1    Park, J.2    Lim, M.S.3    Seong, S.J.4    Lee, J.5    Seo, J.J.6    Park, Y.K.7    Lee, H.W.8    Yoon, Y.R.9
  • 33
    • 33847416297 scopus 로고    scopus 로고
    • The development of a cocktail CYP2B6, CYP2C8, and CYP3A5 inhibition assay and a preliminary assessment of utility in a drug discovery setting
    • O'Donnell C.J., Grime K., Courtney P., Slee D., Riley R.J. The development of a cocktail CYP2B6, CYP2C8, and CYP3A5 inhibition assay and a preliminary assessment of utility in a drug discovery setting. Drug Metab. Dispos. 2007, 35:381-385.
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 381-385
    • O'Donnell, C.J.1    Grime, K.2    Courtney, P.3    Slee, D.4    Riley, R.J.5
  • 34
    • 84865192528 scopus 로고    scopus 로고
    • Evaluation of P450 inhibition and induction by artemisinin antimalarials in human liver microsomes and primary human hepatocytes
    • Xing J., Kirby B.J., Whittington D., Wan Y.K., Goodlett D.R. Evaluation of P450 inhibition and induction by artemisinin antimalarials in human liver microsomes and primary human hepatocytes. Drug Metab. Dispos. 2012, 40:1757-1764.
    • (2012) Drug Metab. Dispos. , vol.40 , pp. 1757-1764
    • Xing, J.1    Kirby, B.J.2    Whittington, D.3    Wan, Y.K.4    Goodlett, D.R.5
  • 35
    • 84862227329 scopus 로고    scopus 로고
    • In vitro ADME profiling using high-throughput rapidfire mass spectrometry: cytochrome P450 inhibition and metabolic stability assays
    • Wu X., Wang J., Tan L., Bui J., Gjerstad E., McMillan K., Zhang W. In vitro ADME profiling using high-throughput rapidfire mass spectrometry: cytochrome P450 inhibition and metabolic stability assays. J. Biomol. Screen. 2012, 17:761-772.
    • (2012) J. Biomol. Screen. , vol.17 , pp. 761-772
    • Wu, X.1    Wang, J.2    Tan, L.3    Bui, J.4    Gjerstad, E.5    McMillan, K.6    Zhang, W.7
  • 36
    • 33947603205 scopus 로고    scopus 로고
    • Comparison of cytochrome P450 inhibition assays for drug discovery using human liver microsomes with LC-MS, rhCYP450 isozymes with fluorescence, and double cocktail with LC-MS
    • Di L., Kerns E.H., Li S.Q., Carter G.T. Comparison of cytochrome P450 inhibition assays for drug discovery using human liver microsomes with LC-MS, rhCYP450 isozymes with fluorescence, and double cocktail with LC-MS. Int. J. Pharm. 2007, 335:1-11.
    • (2007) Int. J. Pharm. , vol.335 , pp. 1-11
    • Di, L.1    Kerns, E.H.2    Li, S.Q.3    Carter, G.T.4
  • 37
    • 69249220270 scopus 로고    scopus 로고
    • Cocktail-substrate assay system for mechanism-based inhibition of CYP2C9, CYP2D6, and CYP3A using human liver microsomes at an early stage of drug development
    • Mori K., Hashimoto H., Takatsu H., Tsuda-Tsukimoto M., Kume T. Cocktail-substrate assay system for mechanism-based inhibition of CYP2C9, CYP2D6, and CYP3A using human liver microsomes at an early stage of drug development. Xenobiotica 2009, 39:415-422.
    • (2009) Xenobiotica , vol.39 , pp. 415-422
    • Mori, K.1    Hashimoto, H.2    Takatsu, H.3    Tsuda-Tsukimoto, M.4    Kume, T.5
  • 38
    • 34547494526 scopus 로고    scopus 로고
    • In vitro LC-MS cocktail assays to simultaneously determine human cytochrome P450 activities
    • Dixit V., Hariparsad N., Desai P., Unadkat J.D. In vitro LC-MS cocktail assays to simultaneously determine human cytochrome P450 activities. Biopharm. Drug Dispos. 2007, 28:257-262.
    • (2007) Biopharm. Drug Dispos. , vol.28 , pp. 257-262
    • Dixit, V.1    Hariparsad, N.2    Desai, P.3    Unadkat, J.D.4
  • 39
    • 0033775984 scopus 로고    scopus 로고
    • High-throughput cytochrome P450 inhibition screening via cassette probe-dosing strategy. IV. Validation of a direct injection on-line guard cartridge extraction/tandem mass spectrometry method for simultaneous CYP3A4, 2D6 and 2E1 inhibition assessment
    • Bu H.Z., Knuth K., Magis L., Teitelbaum P. High-throughput cytochrome P450 inhibition screening via cassette probe-dosing strategy. IV. Validation of a direct injection on-line guard cartridge extraction/tandem mass spectrometry method for simultaneous CYP3A4, 2D6 and 2E1 inhibition assessment. Rapid Commun. Mass Spectrom. 2000, 14:1943-1948.
    • (2000) Rapid Commun. Mass Spectrom. , vol.14 , pp. 1943-1948
    • Bu, H.Z.1    Knuth, K.2    Magis, L.3    Teitelbaum, P.4
  • 40
    • 56749185575 scopus 로고    scopus 로고
    • Efficient assessment of the utility of immortalized Fa2N-4 cells for cytochrome P450 (CYP) induction studies using multiplex quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) and substrate cassette methodologies
    • Kenny J.R., Chen L., McGinnity D.F., Grime K., Shakesheff K.M., Thomson B., Riley R. Efficient assessment of the utility of immortalized Fa2N-4 cells for cytochrome P450 (CYP) induction studies using multiplex quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) and substrate cassette methodologies. Xenobiotica 2008, 38:1500-1517.
    • (2008) Xenobiotica , vol.38 , pp. 1500-1517
    • Kenny, J.R.1    Chen, L.2    McGinnity, D.F.3    Grime, K.4    Shakesheff, K.M.5    Thomson, B.6    Riley, R.7
  • 43
    • 84908346431 scopus 로고    scopus 로고
    • Assessment of cytochrome P450 (1A2, 2B6, 2C9 and 3A4) induction in cryopreserved human hepatocytes cultured in 48-well plates using the cocktail strategy
    • Gerin B., Dell'Aiera S., Boekens H., Smith S., Chanteux H. Assessment of cytochrome P450 (1A2, 2B6, 2C9 and 3A4) induction in cryopreserved human hepatocytes cultured in 48-well plates using the cocktail strategy. Drug Metab. Rev. 2010, 42:132.
    • (2010) Drug Metab. Rev. , vol.42 , pp. 132
    • Gerin, B.1    Dell'Aiera, S.2    Boekens, H.3    Smith, S.4    Chanteux, H.5
  • 44
    • 84865858512 scopus 로고    scopus 로고
    • Plateable cryopreserved human hepatocytes for the assessment of cytochrome P450 inducibility: experimental condition-related variables affecting their response to inducers
    • Alexandre E., Baze A., Parmentier C., Desbans C., Pekthong D., Gerin B., Wack C., Bachellier P., Heyd B., Weber J.C., Richert L. Plateable cryopreserved human hepatocytes for the assessment of cytochrome P450 inducibility: experimental condition-related variables affecting their response to inducers. Xenobiotica 2012, 42:968-979.
    • (2012) Xenobiotica , vol.42 , pp. 968-979
    • Alexandre, E.1    Baze, A.2    Parmentier, C.3    Desbans, C.4    Pekthong, D.5    Gerin, B.6    Wack, C.7    Bachellier, P.8    Heyd, B.9    Weber, J.C.10    Richert, L.11
  • 45
    • 84872573356 scopus 로고    scopus 로고
    • Application of a substrate cocktail approach in the assessment of cytochrome P450 induction using cultured human hepatocytes
    • Pelletier R.D., Lai W.G., Wong Y.N. Application of a substrate cocktail approach in the assessment of cytochrome P450 induction using cultured human hepatocytes. J. Biomol. Screen. 2013, 18:199-210.
    • (2013) J. Biomol. Screen. , vol.18 , pp. 199-210
    • Pelletier, R.D.1    Lai, W.G.2    Wong, Y.N.3
  • 46
    • 84861231597 scopus 로고    scopus 로고
    • Quantification of human hepatocyte cytochrome P450 enzymes and transporters induced by HIV protease inhibitors using newly validated LC-MS/MS cocktail assays and RT-PCR
    • Liu L., Mugundu G.M., Kirby B.J., Samineni D., Desai P.B., Unadkat J.D. Quantification of human hepatocyte cytochrome P450 enzymes and transporters induced by HIV protease inhibitors using newly validated LC-MS/MS cocktail assays and RT-PCR. Biopharm. Drug Dispos. 2012, 33:207-217.
    • (2012) Biopharm. Drug Dispos. , vol.33 , pp. 207-217
    • Liu, L.1    Mugundu, G.M.2    Kirby, B.J.3    Samineni, D.4    Desai, P.B.5    Unadkat, J.D.6
  • 47
    • 84871623034 scopus 로고    scopus 로고
    • Direct and metabolism-dependent cytochrome P450 inhibition assays for evaluating drug-drug interactions
    • Lee K.S., Kim S.K. Direct and metabolism-dependent cytochrome P450 inhibition assays for evaluating drug-drug interactions. J. Appl. Toxicol. 2013, 33:100-108.
    • (2013) J. Appl. Toxicol. , vol.33 , pp. 100-108
    • Lee, K.S.1    Kim, S.K.2
  • 48
    • 84866789818 scopus 로고    scopus 로고
    • In vitro and in vivo assessment of cytochrome P450-mediated herb-drug interaction of Ssang-hwa-tang
    • Lee S.Y., Lee J.Y., Kang W., Kwon K.I., Oh S.J., Ma J.Y., Kim S.K. In vitro and in vivo assessment of cytochrome P450-mediated herb-drug interaction of Ssang-hwa-tang. Food Chem. 2013, 136:450-457.
    • (2013) Food Chem. , vol.136 , pp. 450-457
    • Lee, S.Y.1    Lee, J.Y.2    Kang, W.3    Kwon, K.I.4    Oh, S.J.5    Ma, J.Y.6    Kim, S.K.7
  • 49
    • 38549128284 scopus 로고    scopus 로고
    • A new in vitro approach for the simultaneous determination of phase I and phase II enzymatic activities of human hepatocyte preparations
    • Lahoz A., Donata M.T., Montero S., Castell J.V., Gomez-Lechon M.J. A new in vitro approach for the simultaneous determination of phase I and phase II enzymatic activities of human hepatocyte preparations. Rapid Commun. Mass Spectrom. 2008, 22:240-244.
    • (2008) Rapid Commun. Mass Spectrom. , vol.22 , pp. 240-244
    • Lahoz, A.1    Donata, M.T.2    Montero, S.3    Castell, J.V.4    Gomez-Lechon, M.J.5
  • 50
    • 73249138950 scopus 로고    scopus 로고
    • A rapid ultra-performance liquid chromatography/tandem mass spectrometric methodology for the in vitro analysis of pooled and cocktail cytochrome P450 assays
    • Alden P.G., Plumb R.S., Jones M.D., Rainville P.D., Shave D. A rapid ultra-performance liquid chromatography/tandem mass spectrometric methodology for the in vitro analysis of pooled and cocktail cytochrome P450 assays. Rapid Commun. Mass Spectrom. 2010, 24:147-154.
    • (2010) Rapid Commun. Mass Spectrom. , vol.24 , pp. 147-154
    • Alden, P.G.1    Plumb, R.S.2    Jones, M.D.3    Rainville, P.D.4    Shave, D.5
  • 51
    • 0037974571 scopus 로고    scopus 로고
    • Cytochrome P450 inhibition using recombinant proteins and mass spectrometry/multiple reaction monitoring technology in a cassette incubation
    • Weaver R., Graham K.S., Beattie I.G., Riley R.J. Cytochrome P450 inhibition using recombinant proteins and mass spectrometry/multiple reaction monitoring technology in a cassette incubation. Drug Metab. Dispos. 2003, 31:955-966.
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 955-966
    • Weaver, R.1    Graham, K.S.2    Beattie, I.G.3    Riley, R.J.4
  • 52
    • 27544446643 scopus 로고    scopus 로고
    • Automated assessment of time-dependent inhibition of human cytochrome P450 enzymes using liquid chromatography-tandem mass spectrometry analysis
    • Atkinson A., Kenny J.R., Grime K. Automated assessment of time-dependent inhibition of human cytochrome P450 enzymes using liquid chromatography-tandem mass spectrometry analysis. Drug Metab. Dispos. 2005, 33:1637-1647.
    • (2005) Drug Metab. Dispos. , vol.33 , pp. 1637-1647
    • Atkinson, A.1    Kenny, J.R.2    Grime, K.3
  • 53
    • 33746047547 scopus 로고    scopus 로고
    • Evaluation of time-dependent cytochrome P450 inhibition using cultured human hepatocytes
    • McGinnity D.F., Berry A.J., Kenny J.R., Grime K., Riley R.J. Evaluation of time-dependent cytochrome P450 inhibition using cultured human hepatocytes. Drug Metab. Dispos. 2006, 34:1291-1300.
    • (2006) Drug Metab. Dispos. , vol.34 , pp. 1291-1300
    • McGinnity, D.F.1    Berry, A.J.2    Kenny, J.R.3    Grime, K.4    Riley, R.J.5
  • 54
    • 84871856516 scopus 로고    scopus 로고
    • A sensitive and specific CYP cocktail assay for the simultaneous assessment of human cytochrome P450 activities in primary cultures of human hepatocytes using LC-MS/MS
    • Pillai V.C., Strom S.C., Caritis S.N., Venkataramanan R. A sensitive and specific CYP cocktail assay for the simultaneous assessment of human cytochrome P450 activities in primary cultures of human hepatocytes using LC-MS/MS. J. Pharm. Biomed. Anal. 2013, 74:126-132.
    • (2013) J. Pharm. Biomed. Anal. , vol.74 , pp. 126-132
    • Pillai, V.C.1    Strom, S.C.2    Caritis, S.N.3    Venkataramanan, R.4
  • 55
    • 11244269638 scopus 로고    scopus 로고
    • Use of a cocktail of probe substrates for drug-metabolizing enzymes for the assessment of the metabolic capacity of hepatocyte preparations
    • Floby E., Briem S., Terelius Y., Sohlenius-Sternbeck A.K. Use of a cocktail of probe substrates for drug-metabolizing enzymes for the assessment of the metabolic capacity of hepatocyte preparations. Xenobiotica 2004, 34:949-959.
    • (2004) Xenobiotica , vol.34 , pp. 949-959
    • Floby, E.1    Briem, S.2    Terelius, Y.3    Sohlenius-Sternbeck, A.K.4
  • 57
    • 0037212558 scopus 로고    scopus 로고
    • High-throughput inhibition screening of major human cytochrome P450 enzymes using an in vitro cocktail and liquid chromatography-tandem mass spectrometry
    • Testino S.A., Patonay G. High-throughput inhibition screening of major human cytochrome P450 enzymes using an in vitro cocktail and liquid chromatography-tandem mass spectrometry. J. Pharmaceut. Biomed. 2003, 30:1459-1467.
    • (2003) J. Pharmaceut. Biomed. , vol.30 , pp. 1459-1467
    • Testino, S.A.1    Patonay, G.2
  • 58
    • 84871539611 scopus 로고    scopus 로고
    • Discovery and characterization of novel, potent, and selective cytochrome P450 2J2 inhibitors
    • Ren S., Zeng J., Mei Y., Zhang J.Z.H., Yan S.F., Fei J., Chen L. Discovery and characterization of novel, potent, and selective cytochrome P450 2J2 inhibitors. Drug Metab. Dispos. 2013, 41:60-71.
    • (2013) Drug Metab. Dispos. , vol.41 , pp. 60-71
    • Ren, S.1    Zeng, J.2    Mei, Y.3    Zhang, J.Z.H.4    Yan, S.F.5    Fei, J.6    Chen, L.7
  • 59
    • 33846458253 scopus 로고    scopus 로고
    • Induction of cytochrome P450: assessment in an immortalized human hepatocyte cell line (Fa2N4) using a novel higher throughput cocktail assay
    • Youdim K.A., Tyman C.A., Jones B.C., Hyland R. Induction of cytochrome P450: assessment in an immortalized human hepatocyte cell line (Fa2N4) using a novel higher throughput cocktail assay. Drug Metab. Dispos. 2007, 35:275-282.
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 275-282
    • Youdim, K.A.1    Tyman, C.A.2    Jones, B.C.3    Hyland, R.4
  • 60
    • 34247261031 scopus 로고    scopus 로고
    • Analytical approaches to determine cytochrome P450 inhibitory potential of new chemical entities in drug discovery
    • Smith D., Sadagopan N., Zientek M., Reddy A., Cohen L. Analytical approaches to determine cytochrome P450 inhibitory potential of new chemical entities in drug discovery. J. Chromatogr. B 2007, 850:455-463.
    • (2007) J. Chromatogr. B , vol.850 , pp. 455-463
    • Smith, D.1    Sadagopan, N.2    Zientek, M.3    Reddy, A.4    Cohen, L.5
  • 61
    • 55549132252 scopus 로고    scopus 로고
    • Development of an in vitro drug-drug interaction assay to simultaneously monitor five cytochrome P450 isoforms and performance assessment using drug library compounds
    • Zientek M., Miller H., Smith D., Dunklee M.B., Heinle L., Thurston A., Lee C., Hyland R., Fahmi O., Burdette D. Development of an in vitro drug-drug interaction assay to simultaneously monitor five cytochrome P450 isoforms and performance assessment using drug library compounds. J. Pharmacol. Toxicol. Methods 2008, 58:206-214.
    • (2008) J. Pharmacol. Toxicol. Methods , vol.58 , pp. 206-214
    • Zientek, M.1    Miller, H.2    Smith, D.3    Dunklee, M.B.4    Heinle, L.5    Thurston, A.6    Lee, C.7    Hyland, R.8    Fahmi, O.9    Burdette, D.10
  • 62
    • 49949086869 scopus 로고    scopus 로고
    • An automated, high-throughput, 384 well cytochrome P450 cocktail IC50 assay using a rapid resolution LC-MS/MS end-point
    • Youdim K.A., Lyons R., Payne L., Jones B.C., Saunders K. An automated, high-throughput, 384 well cytochrome P450 cocktail IC50 assay using a rapid resolution LC-MS/MS end-point. J. Pharmaceut. Biomed. 2008, 48:92-99.
    • (2008) J. Pharmaceut. Biomed. , vol.48 , pp. 92-99
    • Youdim, K.A.1    Lyons, R.2    Payne, L.3    Jones, B.C.4    Saunders, K.5
  • 63
    • 78649542235 scopus 로고    scopus 로고
    • Quantifying and predicting the promiscuity and isoform specificity of small-molecule cytochrome P450 inhibitors
    • Nath A., Zientek M.A., Burke B.J., Jiang Y., Atkins W.M. Quantifying and predicting the promiscuity and isoform specificity of small-molecule cytochrome P450 inhibitors. Drug Metab. Dispos. 2010, 38:2195-2203.
    • (2010) Drug Metab. Dispos. , vol.38 , pp. 2195-2203
    • Nath, A.1    Zientek, M.A.2    Burke, B.J.3    Jiang, Y.4    Atkins, W.M.5
  • 64
    • 0035015324 scopus 로고    scopus 로고
    • High-throughput cytochrome P450 (CYP) inhibition screening via a cassette probe-dosing strategy. VI. Simultaneous evaluation of inhibition potential of drugs on human hepatic isozymes CYP2A6, 3A4, 2C9, 2D6 and 2E1
    • Bu H.Z., Magis L., Knuth K., Teitelbaum P. High-throughput cytochrome P450 (CYP) inhibition screening via a cassette probe-dosing strategy. VI. Simultaneous evaluation of inhibition potential of drugs on human hepatic isozymes CYP2A6, 3A4, 2C9, 2D6 and 2E1. Rapid Commun. Mass Spectrom. 2001, 15:741-748.
    • (2001) Rapid Commun. Mass Spectrom. , vol.15 , pp. 741-748
    • Bu, H.Z.1    Magis, L.2    Knuth, K.3    Teitelbaum, P.4
  • 65
    • 79953243156 scopus 로고    scopus 로고
    • A cocktail of metabolic probes demonstrates the relevance of primary human hepatocyte cultures in a microfluidic biochip for pharmaceutical drug screening
    • Prot J.M., Videau O., Brochot C., Legallais C., Benech H., Leclerc E. A cocktail of metabolic probes demonstrates the relevance of primary human hepatocyte cultures in a microfluidic biochip for pharmaceutical drug screening. Int. J. Pharm. 2011, 408:67-75.
    • (2011) Int. J. Pharm. , vol.408 , pp. 67-75
    • Prot, J.M.1    Videau, O.2    Brochot, C.3    Legallais, C.4    Benech, H.5    Leclerc, E.6
  • 66
    • 84872168458 scopus 로고    scopus 로고
    • Evaluation of seven drug metabolisms and clearances by cryopreserved human primary hepatocytes cultivated in microfluidic biochips
    • Baudoin R., Prot J.M., Nicolas G., Brocheton J., Brochot C., Legallais C., Benech H., Leclerc E. Evaluation of seven drug metabolisms and clearances by cryopreserved human primary hepatocytes cultivated in microfluidic biochips. Xenobiotica 2013, 43:140-152.
    • (2013) Xenobiotica , vol.43 , pp. 140-152
    • Baudoin, R.1    Prot, J.M.2    Nicolas, G.3    Brocheton, J.4    Brochot, C.5    Legallais, C.6    Benech, H.7    Leclerc, E.8
  • 67
    • 53749100013 scopus 로고    scopus 로고
    • Assessment of cytochrome P450 induction in human hepatocytes using the cocktail strategy plus liquid chromatography tandem mass spectrometry
    • Lahoz A., Donato M.T., Picazo L., Castell J.V., Gomez-Lechon M.J. Assessment of cytochrome P450 induction in human hepatocytes using the cocktail strategy plus liquid chromatography tandem mass spectrometry. Drug Metab. Lett. 2008, 2:205-209.
    • (2008) Drug Metab. Lett. , vol.2 , pp. 205-209
    • Lahoz, A.1    Donato, M.T.2    Picazo, L.3    Castell, J.V.4    Gomez-Lechon, M.J.5
  • 69
    • 43249092372 scopus 로고    scopus 로고
    • Sub one minute inhibition assays for the major cytochrome P450 enzymes utilizing ultra-performance liquid chromatography/tandem mass spectrometry
    • Rainville P.D., Wheaton J.P., Alden P.G., Plumb R.S. Sub one minute inhibition assays for the major cytochrome P450 enzymes utilizing ultra-performance liquid chromatography/tandem mass spectrometry. Rapid Commun. Mass Spectrom. 2008, 22:1345-1350.
    • (2008) Rapid Commun. Mass Spectrom. , vol.22 , pp. 1345-1350
    • Rainville, P.D.1    Wheaton, J.P.2    Alden, P.G.3    Plumb, R.S.4
  • 71
    • 0037175449 scopus 로고    scopus 로고
    • Rapid and quantitative determination of metabolites from multiple cytochrome P450 probe substrates by gradient liquid chromatography-electrospray ionization-ion trap mass spectrometry
    • Zhang T.Y., Zhu Y.X., Gunaratna C. Rapid and quantitative determination of metabolites from multiple cytochrome P450 probe substrates by gradient liquid chromatography-electrospray ionization-ion trap mass spectrometry. J. Chromatogr. B 2002, 780:371-379.
    • (2002) J. Chromatogr. B , vol.780 , pp. 371-379
    • Zhang, T.Y.1    Zhu, Y.X.2    Gunaratna, C.3
  • 72
    • 33847360957 scopus 로고    scopus 로고
    • Rapid determination of six metabolites from multiple cytochrome P450 probe substrates in human liver microsome by liquid chromatography/mass spectrometry: application to high-throughput inhibition screening of terpenoids
    • He F., Bi H.C., Xie Z.Y., Zuo Z., Li J.K., Li X., Zhao L.Z., Chen X., Huang M. Rapid determination of six metabolites from multiple cytochrome P450 probe substrates in human liver microsome by liquid chromatography/mass spectrometry: application to high-throughput inhibition screening of terpenoids. Rapid Commun. Mass Spectrom. 2007, 21:635-643.
    • (2007) Rapid Commun. Mass Spectrom. , vol.21 , pp. 635-643
    • He, F.1    Bi, H.C.2    Xie, Z.Y.3    Zuo, Z.4    Li, J.K.5    Li, X.6    Zhao, L.Z.7    Chen, X.8    Huang, M.9
  • 73
    • 4644223218 scopus 로고    scopus 로고
    • Simultaneous determination of the inhibitory potency of herbal extracts on the activity of six major cytochrome P450 enzymes using liquid chromatography mass spectrometry and automated online extraction
    • Unger M., Frank A. Simultaneous determination of the inhibitory potency of herbal extracts on the activity of six major cytochrome P450 enzymes using liquid chromatography mass spectrometry and automated online extraction. Rapid Commun. Mass Spectrom. 2004, 18:2273-2281.
    • (2004) Rapid Commun. Mass Spectrom. , vol.18 , pp. 2273-2281
    • Unger, M.1    Frank, A.2
  • 74
    • 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
    • Dierks E.A., Stams K.R., Lim H.K., Cornelius G., Zhang H.L., Ball S.E. 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. 2001, 29:23-29.
    • (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.L.5    Ball, S.E.6
  • 75
    • 0033811314 scopus 로고    scopus 로고
    • High-throughput cytochrome P450 (CYP) inhibition screening via cassette probe-dosing strategy. I. Development of direct injection/on-line guard cartridge extraction/tandem mass spectrometry for the simultaneous detection of CYP probe substrates and their metabolites
    • Bu H.Z., Magis L., Knuth K., Teitelbaum P. High-throughput cytochrome P450 (CYP) inhibition screening via cassette probe-dosing strategy. I. Development of direct injection/on-line guard cartridge extraction/tandem mass spectrometry for the simultaneous detection of CYP probe substrates and their metabolites. Rapid Commun. Mass Spectrom. 2000, 14:1619-1624.
    • (2000) Rapid Commun. Mass Spectrom. , vol.14 , pp. 1619-1624
    • Bu, H.Z.1    Magis, L.2    Knuth, K.3    Teitelbaum, P.4
  • 76
    • 35649025731 scopus 로고    scopus 로고
    • Analysis of potential drug-drug interactions for anticancer agents in human liver microsomes by high throughput liquid chromatography/mass spectrometry assay
    • Moreno-Farre J., Workman P., Raynaud F. Analysis of potential drug-drug interactions for anticancer agents in human liver microsomes by high throughput liquid chromatography/mass spectrometry assay. Aust. J. Cancer 2007, 6:55-69.
    • (2007) Aust. J. Cancer , vol.6 , pp. 55-69
    • Moreno-Farre, J.1    Workman, P.2    Raynaud, F.3
  • 77
    • 77957320051 scopus 로고    scopus 로고
    • Effects of eupatilin and jaceosidin on cytochrome P450 enzyme activities in human liver microsomes
    • Ji H.Y., Kim S.Y., Kim D.K., Jeong J.H., Lee H.S. Effects of eupatilin and jaceosidin on cytochrome P450 enzyme activities in human liver microsomes. Molecules 2010, 15:6466-6475.
    • (2010) Molecules , vol.15 , pp. 6466-6475
    • Ji, H.Y.1    Kim, S.Y.2    Kim, D.K.3    Jeong, J.H.4    Lee, H.S.5
  • 78
    • 80052230944 scopus 로고    scopus 로고
    • Corydaline inhibits multiple cytochrome P450 and UDP-glucuronosyltransferase enzyme activities in human liver microsomes
    • Ji H.Y., Liu K.H., Lee H., Im S.R., Shim H.J., Son M., Lee H.S. Corydaline inhibits multiple cytochrome P450 and UDP-glucuronosyltransferase enzyme activities in human liver microsomes. Molecules 2011, 16:6591-6602.
    • (2011) Molecules , vol.16 , pp. 6591-6602
    • Ji, H.Y.1    Liu, K.H.2    Lee, H.3    Im, S.R.4    Shim, H.J.5    Son, M.6    Lee, H.S.7
  • 79
    • 84861028053 scopus 로고    scopus 로고
    • Effect of a new prokinetic agent DA-9701 formulated with corydalis tuber and pharbitidis semen on cytochrome P450 and UDP-glucuronosyltransferase enzyme activities in human liver microsomes
    • Ji H.Y., Liu K.H., Jeong J.H., Lee D.Y., Shim H.J., Son M., Lee H.S. Effect of a new prokinetic agent DA-9701 formulated with corydalis tuber and pharbitidis semen on cytochrome P450 and UDP-glucuronosyltransferase enzyme activities in human liver microsomes. Evid. Based Complement Altern. 2012, 1-7.
    • (2012) Evid. Based Complement Altern. , pp. 1-7
    • Ji, H.Y.1    Liu, K.H.2    Jeong, J.H.3    Lee, D.Y.4    Shim, H.J.5    Son, M.6    Lee, H.S.7
  • 80
    • 79551633386 scopus 로고    scopus 로고
    • An in vitro, high throughput, seven CYP cocktail inhibition assay for the evaluation of new chemical entities using LC-MS/MS
    • Otten J.N., Hingorani G.P., Hartley D.P., Kragerud S.D., Franklin R.B. An in vitro, high throughput, seven CYP cocktail inhibition assay for the evaluation of new chemical entities using LC-MS/MS. Drug Metab. Lett. 2011, 5:17-24.
    • (2011) Drug Metab. Lett. , vol.5 , pp. 17-24
    • Otten, J.N.1    Hingorani, G.P.2    Hartley, D.P.3    Kragerud, S.D.4    Franklin, R.B.5
  • 81
    • 77955989559 scopus 로고    scopus 로고
    • Profiling induction of cytochrome P450 enzyme activity by statins using a new liquid chromatography-tandem mass spectrometry cocktail assay in human hepatocytes
    • Feidt D.M., Klein K., Hofmann U., Riedmaier S., Knobeloch D., Thasler W.E., Weiss T.S., Schwab M., Zanger U.M. Profiling induction of cytochrome P450 enzyme activity by statins using a new liquid chromatography-tandem mass spectrometry cocktail assay in human hepatocytes. Drug Metab. Dispos. 2010, 38:1589-1597.
    • (2010) Drug Metab. Dispos. , vol.38 , pp. 1589-1597
    • Feidt, D.M.1    Klein, K.2    Hofmann, U.3    Riedmaier, S.4    Knobeloch, D.5    Thasler, W.E.6    Weiss, T.S.7    Schwab, M.8    Zanger, U.M.9
  • 85
    • 84869119884 scopus 로고    scopus 로고
    • Reliable high-throughput method for inhibition assay of 8 cytochrome P450 isoforms using cocktail of probe substrates and stable isotope-labeled internal standards
    • Kozakai K., Yamada Y., Oshikata M., Kawase T., Suzuki E., Haramaki Y., Taniguchi H. Reliable high-throughput method for inhibition assay of 8 cytochrome P450 isoforms using cocktail of probe substrates and stable isotope-labeled internal standards. Drug Metab. Pharmacokinet. 2012, 27:520-529.
    • (2012) Drug Metab. Pharmacokinet. , vol.27 , pp. 520-529
    • Kozakai, K.1    Yamada, Y.2    Oshikata, M.3    Kawase, T.4    Suzuki, E.5    Haramaki, Y.6    Taniguchi, H.7
  • 86
    • 84875692768 scopus 로고    scopus 로고
    • In vitro inhibitory effect of luotonin A on human CYP1A
    • Jahng Y., Kwon O.K., Lee S. In vitro inhibitory effect of luotonin A on human CYP1A. Arch. Pharm. Res. 2012, 35:2199-2203.
    • (2012) Arch. Pharm. Res. , vol.35 , pp. 2199-2203
    • Jahng, Y.1    Kwon, O.K.2    Lee, S.3
  • 88
    • 11144242471 scopus 로고    scopus 로고
    • Multiple P450 substrates in a single run: rapid and comprehensive in vitro interaction assay
    • Turpeinen M., Jouko U., Jorma J., Olavi P. Multiple P450 substrates in a single run: rapid and comprehensive in vitro interaction assay. Eur. J. Pharm. Sci. 2005, 24:123-132.
    • (2005) Eur. J. Pharm. Sci. , vol.24 , pp. 123-132
    • Turpeinen, M.1    Jouko, U.2    Jorma, J.3    Olavi, P.4
  • 90
  • 91
    • 34447343085 scopus 로고    scopus 로고
    • In vitro interaction cocktail assay for nine major cytochrome P450 enzymes with 13 probe reactions and a single LC/MSMS run: analytical validation and testing with monoclonal anti-CYP antibodies
    • Tolonen A., Petsalo A., Turpeinen M., Uusitalo J., Pelkonen O. In vitro interaction cocktail assay for nine major cytochrome P450 enzymes with 13 probe reactions and a single LC/MSMS run: analytical validation and testing with monoclonal anti-CYP antibodies. J. Mass Spectrom. 2007, 42:960-966.
    • (2007) J. Mass Spectrom. , vol.42 , pp. 960-966
    • Tolonen, A.1    Petsalo, A.2    Turpeinen, M.3    Uusitalo, J.4    Pelkonen, O.5
  • 92
    • 44649188476 scopus 로고    scopus 로고
    • Identification of the human cytochrome P450 enzymes involved in the in vitro biotransformation of lynestrenol and norethindrone
    • Korhonen T., Turpeinen M., Tolonen A., Laine K., Pelkonen O. Identification of the human cytochrome P450 enzymes involved in the in vitro biotransformation of lynestrenol and norethindrone. J. Steroid Biochem. 2008, 110:56-66.
    • (2008) J. Steroid Biochem. , vol.110 , pp. 56-66
    • Korhonen, T.1    Turpeinen, M.2    Tolonen, A.3    Laine, K.4    Pelkonen, O.5
  • 93
    • 77952297444 scopus 로고    scopus 로고
    • Metabolism of carbosulfan II. Human interindividual variability in its in vitro hepatic biotransformation and the identification of the cytochrome P450 isoforms involved
    • Abass K., Reponen P., Mattila S., Pelkonen O. Metabolism of carbosulfan II. Human interindividual variability in its in vitro hepatic biotransformation and the identification of the cytochrome P450 isoforms involved. Chem. Biol. Interact. 2010, 185:163-173.
    • (2010) Chem. Biol. Interact. , vol.185 , pp. 163-173
    • Abass, K.1    Reponen, P.2    Mattila, S.3    Pelkonen, O.4
  • 94
    • 77949457681 scopus 로고    scopus 로고
    • Rapid screening of commercially available herbal products for the inhibition of major human hepatic cytochrome P450 enzymes using the N-in-one cocktail
    • Sevior D.K., Hokkanen J., Tolonen A., Abass K., Tursas L., Pelkonen O., Ahokas J.T. Rapid screening of commercially available herbal products for the inhibition of major human hepatic cytochrome P450 enzymes using the N-in-one cocktail. Xenobiotica 2010, 40:245-254.
    • (2010) Xenobiotica , vol.40 , pp. 245-254
    • Sevior, D.K.1    Hokkanen, J.2    Tolonen, A.3    Abass, K.4    Tursas, L.5    Pelkonen, O.6    Ahokas, J.T.7
  • 95
    • 79251598311 scopus 로고    scopus 로고
    • Metabolism of hyperforin, the active constituent of St. John's wort, in human liver microsomes
    • Hokkanen J., Tolonen A., Mattila S., Turpeinen M. Metabolism of hyperforin, the active constituent of St. John's wort, in human liver microsomes. Eur. J. Pharm. Sci. 2011, 42:273-284.
    • (2011) Eur. J. Pharm. Sci. , vol.42 , pp. 273-284
    • Hokkanen, J.1    Tolonen, A.2    Mattila, S.3    Turpeinen, M.4
  • 96
    • 78651377521 scopus 로고    scopus 로고
    • Metabolism of alpha-thujone in human hepatic preparations in vitro
    • Abass K., Reponen P., Mattila S., Pelkonen O. Metabolism of alpha-thujone in human hepatic preparations in vitro. Xenobiotica 2011, 41:101-111.
    • (2011) Xenobiotica , vol.41 , pp. 101-111
    • Abass, K.1    Reponen, P.2    Mattila, S.3    Pelkonen, O.4
  • 97
    • 84877792756 scopus 로고    scopus 로고
    • The inhibition of major human hepatic cytochrome P450 enzymes by 18 pesticides: comparison of the N-in-one and single substrate approaches
    • Abass K., Pelkonen O. The inhibition of major human hepatic cytochrome P450 enzymes by 18 pesticides: comparison of the N-in-one and single substrate approaches. Toxicol. In Vitro 2012, 27:1584-1588.
    • (2012) Toxicol. In Vitro , vol.27 , pp. 1584-1588
    • Abass, K.1    Pelkonen, O.2
  • 100
    • 2442690439 scopus 로고    scopus 로고
    • Validated assays for human cytochrome P450 activities
    • Walsky R.L., Obach R.S. Validated assays for human cytochrome P450 activities. Drug Metab. Dispos. 2004, 32:647-660.
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 647-660
    • Walsky, R.L.1    Obach, R.S.2
  • 101
    • 0037974573 scopus 로고    scopus 로고
    • In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes P450: role of CYP3A4 and CYP3A5
    • Patki K.C., von Moltke L.L., Greenblatt D.J. In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes P450: role of CYP3A4 and CYP3A5. Drug Metab. Dispos. 2003, 31:938-944.
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 938-944
    • Patki, K.C.1    von Moltke, L.L.2    Greenblatt, D.J.3
  • 102
    • 0042531825 scopus 로고    scopus 로고
    • In vitro activation of 7-benzyloxyresorufin O-debenzylation and nifedipine oxidation in human liver microsomes
    • Niwa T., Shiraga T., Yamasaki S., Ishibashi K., Ohno Y., Kagayama A. In vitro activation of 7-benzyloxyresorufin O-debenzylation and nifedipine oxidation in human liver microsomes. Xenobiotica 2003, 33:717-729.
    • (2003) Xenobiotica , vol.33 , pp. 717-729
    • Niwa, T.1    Shiraga, T.2    Yamasaki, S.3    Ishibashi, K.4    Ohno, Y.5    Kagayama, A.6
  • 104
    • 0032793678 scopus 로고    scopus 로고
    • Involvement of CYP2E1 as a low-affinity enzyme in phenacetin O-deethylation in human liver microsomes
    • Kobayashi K., Nakajima M., Oshima K., Shimada N., Yokoi T., Chiba K. Involvement of CYP2E1 as a low-affinity enzyme in phenacetin O-deethylation in human liver microsomes. Drug Metab. Dispos. 1999, 27:860-865.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 860-865
    • Kobayashi, K.1    Nakajima, M.2    Oshima, K.3    Shimada, N.4    Yokoi, T.5    Chiba, K.6
  • 105
    • 0031149716 scopus 로고    scopus 로고
    • Inhibition of coumarin 7-hydroxylase activity in human liver microsomes
    • Draper A.J., Madan A., Parkinson A. Inhibition of coumarin 7-hydroxylase activity in human liver microsomes. Arch. Biochem. Biophys. 1997, 341:47-61.
    • (1997) Arch. Biochem. Biophys. , vol.341 , pp. 47-61
    • Draper, A.J.1    Madan, A.2    Parkinson, A.3
  • 106
    • 0030056594 scopus 로고    scopus 로고
    • Specificity of substrate and inhibitor probes for cytochrome P450s: evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes
    • Ono S., Hatanaka T., Hotta H., Satoh T., Gonzalez F.J., Tsutsui M. Specificity of substrate and inhibitor probes for cytochrome P450s: evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes. Xenobiotica 1996, 26:681-693.
    • (1996) Xenobiotica , vol.26 , pp. 681-693
    • Ono, S.1    Hatanaka, T.2    Hotta, H.3    Satoh, T.4    Gonzalez, F.J.5    Tsutsui, M.6
  • 107
    • 0027444834 scopus 로고
    • Bioactivation and irreversible binding of the cognition activator tacrine using human and rat-liver microsomal preparations - species difference
    • Woolf T.F., Pool W.F., Bjorge S.M., Chang T., Goel O.P., Purchase C.F., Schroeder M.C., Kunze K.L., Trager W.F. Bioactivation and irreversible binding of the cognition activator tacrine using human and rat-liver microsomal preparations - species difference. Drug Metab. Dispos. 1993, 21:874-882.
    • (1993) Drug Metab. Dispos. , vol.21 , pp. 874-882
    • Woolf, T.F.1    Pool, W.F.2    Bjorge, S.M.3    Chang, T.4    Goel, O.P.5    Purchase, C.F.6    Schroeder, M.C.7    Kunze, K.L.8    Trager, W.F.9
  • 108
    • 0028240611 scopus 로고
    • The effect of enzyme-inhibition on the metabolism and activation of tacrine by human liver microsomes
    • Spaldin V., Madden S., Pool W.F., Woolf T.F., Park B.K. The effect of enzyme-inhibition on the metabolism and activation of tacrine by human liver microsomes. Br. J. Clin. Pharmacol. 1994, 38:15-22.
    • (1994) Br. J. Clin. Pharmacol. , vol.38 , pp. 15-22
    • Spaldin, V.1    Madden, S.2    Pool, W.F.3    Woolf, T.F.4    Park, B.K.5
  • 109
    • 0028106482 scopus 로고
    • Cytochrome-P450 specifities of alkoxyresorufin O-dealkylation in human and rat-liver
    • Burke M.D., Thompson S., Weaver R.J., Wolf C.R., Mayer R.T. Cytochrome-P450 specifities of alkoxyresorufin O-dealkylation in human and rat-liver. Biochem. Pharmacol. 1994, 48:923-936.
    • (1994) Biochem. Pharmacol. , vol.48 , pp. 923-936
    • Burke, M.D.1    Thompson, S.2    Weaver, R.J.3    Wolf, C.R.4    Mayer, R.T.5
  • 111
    • 0032942444 scopus 로고    scopus 로고
    • Involvement of cytochrome P-450 isozymes in melatonin metabolism and clinical implications
    • Yeleswaram K., Vachharajani N., Santone K. Involvement of cytochrome P-450 isozymes in melatonin metabolism and clinical implications. J. Pineal Res. 1999, 26:190-191.
    • (1999) J. Pineal Res. , vol.26 , pp. 190-191
    • Yeleswaram, K.1    Vachharajani, N.2    Santone, K.3
  • 113
    • 0035293495 scopus 로고    scopus 로고
    • Cytochrome P-450 isoforms involved in melatonin metabolism in human liver microsomes
    • Facciola G., Hidestrand M., von Bahr C., Tybring G. Cytochrome P-450 isoforms involved in melatonin metabolism in human liver microsomes. Eur. J. Clin. Pharmacol. 2001, 56:881-888.
    • (2001) Eur. J. Clin. Pharmacol. , vol.56 , pp. 881-888
    • Facciola, G.1    Hidestrand, M.2    von Bahr, C.3    Tybring, G.4
  • 116
    • 0034936401 scopus 로고    scopus 로고
    • Evaluation of the contribution of cytochrome P450 3A4 to human liver microsomal bupropion hydroxylation
    • Faucette S.R., Hawke R.L., Shord S.S., Lecluyse E.L., Lindley C.M. Evaluation of the contribution of cytochrome P450 3A4 to human liver microsomal bupropion hydroxylation. Drug Metab. Dispos. 2001, 29:1123-1129.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 1123-1129
    • Faucette, S.R.1    Hawke, R.L.2    Shord, S.S.3    Lecluyse, E.L.4    Lindley, C.M.5
  • 118
    • 0028036727 scopus 로고
    • Selective biotransformation of taxol to 6-alpha.hydroxytaxol by human cytochrome-P450 2C8
    • Rahman A., Korzekwa K.R., Grogan J., Gonzalez F.J., Harris J.W. Selective biotransformation of taxol to 6-alpha.hydroxytaxol by human cytochrome-P450 2C8. Cancer Res. 1994, 54:5543-5546.
    • (1994) Cancer Res. , vol.54 , pp. 5543-5546
    • Rahman, A.1    Korzekwa, K.R.2    Grogan, J.3    Gonzalez, F.J.4    Harris, J.W.5
  • 121
    • 0033507633 scopus 로고    scopus 로고
    • Enzymes in addition to CYP3A4 and 3A5 mediate N-demethylation of dextromethorphan in human liver microsomes
    • Wang Y., Unadkat J.D. Enzymes in addition to CYP3A4 and 3A5 mediate N-demethylation of dextromethorphan in human liver microsomes. Biopharm. Drug Dispos. 1999, 20:341-346.
    • (1999) Biopharm. Drug Dispos. , vol.20 , pp. 341-346
    • Wang, Y.1    Unadkat, J.D.2
  • 122
    • 33750711672 scopus 로고    scopus 로고
    • Evaluation of 227 drugs for in vitro inhibition of cytochrome P4502B6
    • Walsky R.L., Astuccio A.V., Obach R.S. Evaluation of 227 drugs for in vitro inhibition of cytochrome P4502B6. J. Clin. Pharmacol. 2006, 46:1426-1438.
    • (2006) J. Clin. Pharmacol. , vol.46 , pp. 1426-1438
    • Walsky, R.L.1    Astuccio, A.V.2    Obach, R.S.3
  • 123
    • 0036154008 scopus 로고    scopus 로고
    • Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: a new high affinity and turnover enzyme-specific probe substrate
    • Li X.Q., Bjorkman A., Andersson T.B., Ridderstrom M., Masimirembwa C.M. Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: a new high affinity and turnover enzyme-specific probe substrate. J. Pharmacol. Exp. Ther. 2002, 300:399-407.
    • (2002) J. Pharmacol. Exp. Ther. , vol.300 , pp. 399-407
    • Li, X.Q.1    Bjorkman, A.2    Andersson, T.B.3    Ridderstrom, M.4    Masimirembwa, C.M.5
  • 124
    • 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
  • 125
    • 84862658556 scopus 로고    scopus 로고
    • Comprehensive assessment of repaglinide metabolic pathways: impact of choice of in vitro system and relative enzyme contribution to in vitro clearance
    • Sall C., Houston J.B., Galetin A.A. Comprehensive assessment of repaglinide metabolic pathways: impact of choice of in vitro system and relative enzyme contribution to in vitro clearance. Drug Metab. Dispos. 2012, 40:1279-1289.
    • (2012) Drug Metab. Dispos. , vol.40 , pp. 1279-1289
    • Sall, C.1    Houston, J.B.2    Galetin, A.A.3
  • 126
    • 0042318871 scopus 로고    scopus 로고
    • CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide
    • Bidstrup T.B., Bjornsdottir I., Sidelmann U.G., Thomsen M.S., Hansen K.T. CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide. Br. J. Clin. Pharmacol. 2003, 56:305-314.
    • (2003) Br. J. Clin. Pharmacol. , vol.56 , pp. 305-314
    • Bidstrup, T.B.1    Bjornsdottir, I.2    Sidelmann, U.G.3    Thomsen, M.S.4    Hansen, K.T.5
  • 127
    • 25844448609 scopus 로고    scopus 로고
    • Metabolism of repaglinide by CYP2C8 and CYP3A4 in vitro: effect of fibrates and rifampicin
    • Kajosaari L.I., Laitila J., Neuvonen P.J., Backman J.T. Metabolism of repaglinide by CYP2C8 and CYP3A4 in vitro: effect of fibrates and rifampicin. Basic Clin. Pharmacol. 2005, 97:249-256.
    • (2005) Basic Clin. Pharmacol. , vol.97 , pp. 249-256
    • Kajosaari, L.I.1    Laitila, J.2    Neuvonen, P.J.3    Backman, J.T.4
  • 128
    • 0031757521 scopus 로고    scopus 로고
    • Comparative studies on the catalytic roles of cytochrome P450 2C9 and its Cys- and Leu-variants in the oxidation of Warfarin, flurbiprofen, and diclofenac by human liver microsomes
    • Yamazaki H., Inoue K., Chiba K., Ozawa N., Kawai T., Suzuki Y., Goldstein J.A., Guengerich F.P., Shimada T. Comparative studies on the catalytic roles of cytochrome P450 2C9 and its Cys- and Leu-variants in the oxidation of Warfarin, flurbiprofen, and diclofenac by human liver microsomes. Biochem. Pharmacol. 1998, 56:243-251.
    • (1998) Biochem. Pharmacol. , vol.56 , pp. 243-251
    • Yamazaki, H.1    Inoue, K.2    Chiba, K.3    Ozawa, N.4    Kawai, T.5    Suzuki, Y.6    Goldstein, J.A.7    Guengerich, F.P.8    Shimada, T.9
  • 129
    • 0033048695 scopus 로고    scopus 로고
    • Roles of human hepatic cytochrome P450s 2C9 and 3A4 in the metabolic activation of diclofenac
    • Tang W., Stearns R.A., Wang R.W., Chiu S.H.L., Baillie T.A. Roles of human hepatic cytochrome P450s 2C9 and 3A4 in the metabolic activation of diclofenac. Chem. Res. Toxicol. 1999, 12:192-199.
    • (1999) Chem. Res. Toxicol. , vol.12 , pp. 192-199
    • Tang, W.1    Stearns, R.A.2    Wang, R.W.3    Chiu, S.H.L.4    Baillie, T.A.5
  • 130
    • 0033048697 scopus 로고    scopus 로고
    • Metabolic activation of diclofenac by human cytochrome P450 3A4: role of 5-hydroxydiclofenac
    • Shen S.J., Marchick M.R., Davis M.R., Doss G.A., Pohl L.R. Metabolic activation of diclofenac by human cytochrome P450 3A4: role of 5-hydroxydiclofenac. Chem. Res. Toxicol. 1999, 12:214-222.
    • (1999) Chem. Res. Toxicol. , vol.12 , pp. 214-222
    • Shen, S.J.1    Marchick, M.R.2    Davis, M.R.3    Doss, G.A.4    Pohl, L.R.5
  • 131
    • 0027264432 scopus 로고
    • Cytochrome P450TB (CYP2C) - a major monooxygenase catalyzing diclofenac 4'-hydroxylation in human liver
    • Leemann T., Transon C., Dayer P. Cytochrome P450TB (CYP2C) - a major monooxygenase catalyzing diclofenac 4'-hydroxylation in human liver. Life Sci. 1993, 52:29-34.
    • (1993) Life Sci. , vol.52 , pp. 29-34
    • Leemann, T.1    Transon, C.2    Dayer, P.3
  • 134
    • 0027366623 scopus 로고
    • Oxidative-metabolism of omeprazole in human liver microsomes - cosegregation with S-mephenytoin 4'-hydroxylation
    • Chiba K., Kobayashi K., Manabe K., Tani M., Kamataki T., Ishizaki T. Oxidative-metabolism of omeprazole in human liver microsomes - cosegregation with S-mephenytoin 4'-hydroxylation. J. Pharmacol. Exp. Ther. 1993, 266:52-59.
    • (1993) J. Pharmacol. Exp. Ther. , vol.266 , pp. 52-59
    • Chiba, K.1    Kobayashi, K.2    Manabe, K.3    Tani, M.4    Kamataki, T.5    Ishizaki, T.6
  • 136
    • 0029858783 scopus 로고    scopus 로고
    • Human CYP2C19 is a major omeprazole 5-hydroxylase, as demonstrated with recombinant cytochrome P450 enzymes
    • Karam W.G., Goldstein J.A., Lasker J.M., Ghanayem B.I. Human CYP2C19 is a major omeprazole 5-hydroxylase, as demonstrated with recombinant cytochrome P450 enzymes. Drug Metab. Dispos. 1996, 24:1081-1087.
    • (1996) Drug Metab. Dispos. , vol.24 , pp. 1081-1087
    • Karam, W.G.1    Goldstein, J.A.2    Lasker, J.M.3    Ghanayem, B.I.4
  • 137
    • 0032836580 scopus 로고    scopus 로고
    • Effect of various salts on the stability of lansoprazole, omeprazole, and pantoprazole as determined by high-performance liquid chromatography
    • Ekpe A., Jacobsen T. Effect of various salts on the stability of lansoprazole, omeprazole, and pantoprazole as determined by high-performance liquid chromatography. Drug Dev. Ind. Pharm. 1999, 25:1057-1065.
    • (1999) Drug Dev. Ind. Pharm. , vol.25 , pp. 1057-1065
    • Ekpe, A.1    Jacobsen, T.2
  • 138
    • 27144526218 scopus 로고    scopus 로고
    • Enantiomer/enantiomer interactions between the S- and R-isomers of omeprazole in human cytochrome P450 enzymes: major role of CYP2C19 and CYP3A4
    • Li X.Q., Weidolf L., Simonsson R., Andersson T.B. Enantiomer/enantiomer interactions between the S- and R-isomers of omeprazole in human cytochrome P450 enzymes: major role of CYP2C19 and CYP3A4. J. Pharmacol. Exp. Ther. 2005, 315:777-787.
    • (2005) J. Pharmacol. Exp. Ther. , vol.315 , pp. 777-787
    • Li, X.Q.1    Weidolf, L.2    Simonsson, R.3    Andersson, T.B.4
  • 140
    • 0035065393 scopus 로고    scopus 로고
    • Competitive CYP2C9 inhibitors: enzyme inhibition studies, protein homology modeling, and three-dimensional quantitative structure-activity relationship analysis
    • Afzelius L., Zamora I., Ridderstrom M., Andersson T.B., Karlen A., Masimirembwa C.M. Competitive CYP2C9 inhibitors: enzyme inhibition studies, protein homology modeling, and three-dimensional quantitative structure-activity relationship analysis. Mol. Pharmacol. 2001, 59:909-919.
    • (2001) Mol. Pharmacol. , vol.59 , pp. 909-919
    • Afzelius, L.1    Zamora, I.2    Ridderstrom, M.3    Andersson, T.B.4    Karlen, A.5    Masimirembwa, C.M.6
  • 141
    • 0029974085 scopus 로고    scopus 로고
    • Human liver microsomal diazepam metabolism using cDNA-expressed cytochrome P450s: role of CYP2B6, 2C19 and the 3A subfamily
    • Ono S., Hatanaka T., Miyazawa S., Tsutsui M., Aoyama T., Gonzalez F.J., Satoh T. Human liver microsomal diazepam metabolism using cDNA-expressed cytochrome P450s: role of CYP2B6, 2C19 and the 3A subfamily. Xenobiotica 1996, 26:1155-1166.
    • (1996) Xenobiotica , vol.26 , pp. 1155-1166
    • Ono, S.1    Hatanaka, T.2    Miyazawa, S.3    Tsutsui, M.4    Aoyama, T.5    Gonzalez, F.J.6    Satoh, T.7
  • 142
    • 0030976985 scopus 로고    scopus 로고
    • Reappraisal of human CYP isoforms involved in imipramine N-demethylation and 2-hydroxylation: a study using microsomes obtained from putative extensive and poor metabolizers of S-mephenytoin and eleven recombinant human CYPs
    • Koyama E., Chiba K., Tani M., Ishizaki T. Reappraisal of human CYP isoforms involved in imipramine N-demethylation and 2-hydroxylation: a study using microsomes obtained from putative extensive and poor metabolizers of S-mephenytoin and eleven recombinant human CYPs. J. Pharmacol. Exp. Ther. 1997, 281:1199-1210.
    • (1997) J. Pharmacol. Exp. Ther. , vol.281 , pp. 1199-1210
    • Koyama, E.1    Chiba, K.2    Tani, M.3    Ishizaki, T.4
  • 145
    • 24944464940 scopus 로고    scopus 로고
    • Contribution of human hepatic cytochrome P450 isoforms to the metabolism of psychotropic drugs
    • Niwa T., Shiraga T., Ishii I., Kagayama A., Takagi A. Contribution of human hepatic cytochrome P450 isoforms to the metabolism of psychotropic drugs. Biol. Pharm. Bull. 2005, 28:1711-1716.
    • (2005) Biol. Pharm. Bull. , vol.28 , pp. 1711-1716
    • Niwa, T.1    Shiraga, T.2    Ishii, I.3    Kagayama, A.4    Takagi, A.5
  • 146
    • 0024548251 scopus 로고
    • In vitro characterization of the human cytochrome P450 involved in polymorphic oxidation of propafenone
    • Kroemer H.K., Mikus G., Kronbach T., Meyer U.A., Eichelbaum M. In vitro characterization of the human cytochrome P450 involved in polymorphic oxidation of propafenone. Clin. Pharmacol. Ther. 1989, 45:28-33.
    • (1989) Clin. Pharmacol. Ther. , vol.45 , pp. 28-33
    • Kroemer, H.K.1    Mikus, G.2    Kronbach, T.3    Meyer, U.A.4    Eichelbaum, M.5
  • 147
    • 0027460033 scopus 로고
    • Identification and characterization of the cytochrome-P450 enzymes involved in N-dealkylation of propafenone - molecular-base for interaction potential and variable disposition of active metabolites
    • Botsch S., Gautier J.C., Beaune P., Eichelbaum M., Kroemer H.K. Identification and characterization of the cytochrome-P450 enzymes involved in N-dealkylation of propafenone - molecular-base for interaction potential and variable disposition of active metabolites. Mol. Pharmacol. 1993, 43:120-126.
    • (1993) Mol. Pharmacol. , vol.43 , pp. 120-126
    • Botsch, S.1    Gautier, J.C.2    Beaune, P.3    Eichelbaum, M.4    Kroemer, H.K.5
  • 149
    • 0029898576 scopus 로고    scopus 로고
    • Structural requirements for activity of propafenone-type modulators in P-glycoprotein-mediated multidrug resistance
    • Chiba P., Ecker G., Schmid D., Drach J., Tell B., Goldenberg S., Gekeler V. Structural requirements for activity of propafenone-type modulators in P-glycoprotein-mediated multidrug resistance. Mol. Pharmacol. 1996, 49:1122-1130.
    • (1996) Mol. Pharmacol. , vol.49 , pp. 1122-1130
    • Chiba, P.1    Ecker, G.2    Schmid, D.3    Drach, J.4    Tell, B.5    Goldenberg, S.6    Gekeler, V.7
  • 150
    • 84873620874 scopus 로고    scopus 로고
    • Understanding the mechanism of cytochrome P450 3A4: recent advances and remaining problems
    • Sevrioukova I.F., Poulos T.L. Understanding the mechanism of cytochrome P450 3A4: recent advances and remaining problems. Dalton Trans. 2013, 42:3116-3126.
    • (2013) Dalton Trans. , vol.42 , pp. 3116-3126
    • Sevrioukova, I.F.1    Poulos, T.L.2
  • 152
    • 0031748173 scopus 로고    scopus 로고
    • In vitro and in vivo drug interactions involving human CYP3A
    • Thummel K.E., Wilkinson G.R. In vitro and in vivo drug interactions involving human CYP3A. Annu. Rev. Pharmacol. 1998, 38:389-430.
    • (1998) Annu. Rev. Pharmacol. , vol.38 , pp. 389-430
    • Thummel, K.E.1    Wilkinson, G.R.2
  • 154
    • 33748802003 scopus 로고    scopus 로고
    • Structural basis for ligand promiscuity in cytochrome P450 3A4
    • Ekroos M., Sjogren T. Structural basis for ligand promiscuity in cytochrome P450 3A4. Proc. Natl. Acad. Sci. U.S.A. 2006, 103:13682-13687.
    • (2006) Proc. Natl. Acad. Sci. U.S.A. , vol.103 , pp. 13682-13687
    • Ekroos, M.1    Sjogren, T.2
  • 157
    • 23044500208 scopus 로고    scopus 로고
    • CYP3A4 substrate selection and substitution in the prediction of potential drug-drug interactions
    • Galetin A., Ito K., Hallifax D., Houston J.B. CYP3A4 substrate selection and substitution in the prediction of potential drug-drug interactions. J. Pharmacol. Exp. Ther. 2005, 314:180-190.
    • (2005) J. Pharmacol. Exp. Ther. , vol.314 , pp. 180-190
    • Galetin, A.1    Ito, K.2    Hallifax, D.3    Houston, J.B.4
  • 158
    • 34250716928 scopus 로고    scopus 로고
    • Risk assessment for drug-drug interaction caused by metabolism-based inhibition of CYP3A using automated in vitro assay systems and its application in the early drug discovery process
    • Watanabe A., Nakamura K., Okudaira N., Okazaki O., Sudo K.I. Risk assessment for drug-drug interaction caused by metabolism-based inhibition of CYP3A using automated in vitro assay systems and its application in the early drug discovery process. Drug Metab. Dispos. 2007, 35:1232-1238.
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 1232-1238
    • Watanabe, A.1    Nakamura, K.2    Okudaira, N.3    Okazaki, O.4    Sudo, K.I.5
  • 159
    • 0035060326 scopus 로고    scopus 로고
    • Cytochrome P4502B6 and 2C9 do not metabolize midazolam: kinetic analysis and inhibition study with monoclonal antibodies
    • Hamaoka N., Oda Y., Hase I., Asada A., Cytochrome P4502B6 and 2C9 do not metabolize midazolam: kinetic analysis and inhibition study with monoclonal antibodies. Br. J. Anaesth. 2001, 86:540-544.
    • (2001) Br. J. Anaesth. , vol.86 , pp. 540-544
    • Hamaoka, N.1    Oda, Y.2    Hase, I.3    Asada, A.4
  • 160
    • 0022998708 scopus 로고
    • Characterization of rat and human-liver microsomal cytochrome-P450 forms involved in nifedipine oxidation, a prototype for genetic-polymorphism in oxidative drug-metabolism
    • Guengerich F.P., Martin M.V., Beaune P.H., Kremers P., Wolff T., Waxman D.J. Characterization of rat and human-liver microsomal cytochrome-P450 forms involved in nifedipine oxidation, a prototype for genetic-polymorphism in oxidative drug-metabolism. J. Biol. Chem. 1986, 261:5051-5060.
    • (1986) J. Biol. Chem. , vol.261 , pp. 5051-5060
    • Guengerich, F.P.1    Martin, M.V.2    Beaune, P.H.3    Kremers, P.4    Wolff, T.5    Waxman, D.J.6
  • 161
    • 0025860978 scopus 로고
    • Oxidation of dihydropyridine calcium-channel blockers and analogs by human liver cytochrome-P450 IIIA4
    • Guengerich F.P., Brian W.R., Iwasaki M., Sari M.A., Baarnhielm C., Berntsson P. Oxidation of dihydropyridine calcium-channel blockers and analogs by human liver cytochrome-P450 IIIA4. J. Med. Chem. 1991, 34:1838-1844.
    • (1991) J. Med. Chem. , vol.34 , pp. 1838-1844
    • Guengerich, F.P.1    Brian, W.R.2    Iwasaki, M.3    Sari, M.A.4    Baarnhielm, C.5    Berntsson, P.6
  • 162
    • 0029671251 scopus 로고    scopus 로고
    • Roles of cytochrome b5 in the oxidation of testosterone and nifedipine by recombinant cytochrome P450 3A4 and by human liver microsomes
    • Yamazaki H., Nakano M., Imai Y., Ueng Y.F., Guengerich F.P., Shimada T. Roles of cytochrome b5 in the oxidation of testosterone and nifedipine by recombinant cytochrome P450 3A4 and by human liver microsomes. Arch. Biochem. Biophys. 1996, 325:174-182.
    • (1996) Arch. Biochem. Biophys. , vol.325 , pp. 174-182
    • Yamazaki, H.1    Nakano, M.2    Imai, Y.3    Ueng, Y.F.4    Guengerich, F.P.5    Shimada, T.6
  • 163
    • 0027265750 scopus 로고
    • CYP2D6-dependent and CYP3A-dependent metabolism of dextromethorphan in humans
    • Jacqzaigrain E., Funckbrentano C., Cresteil T. CYP2D6-dependent and CYP3A-dependent metabolism of dextromethorphan in humans. Pharmacogenetics 1993, 3:197-204.
    • (1993) Pharmacogenetics , vol.3 , pp. 197-204
    • Jacqzaigrain, E.1    Funckbrentano, C.2    Cresteil, T.3
  • 164
    • 0027956791 scopus 로고
    • Characterization of dextromethorphan N-demethylation by human liver-microsomes - contribution of the cytochrome-P450 3A (CYP3A) subfamily
    • Gorski J.C., Jones D.R., Wrighton S.A., Hall S.D. Characterization of dextromethorphan N-demethylation by human liver-microsomes - contribution of the cytochrome-P450 3A (CYP3A) subfamily. Biochem. Pharmacol. 1994, 48:173-182.
    • (1994) Biochem. Pharmacol. , vol.48 , pp. 173-182
    • Gorski, J.C.1    Jones, D.R.2    Wrighton, S.A.3    Hall, S.D.4
  • 165
    • 0030889604 scopus 로고    scopus 로고
    • Metabolism of dextromethorphan in vitro: involvement of cytochromes P450 2D6 and 3A3/4, with a possible role of 2E1
    • Schmider J., Greenblatt D.J., Fogelman S.M., VonMoltke L.L., Shader R.I. Metabolism of dextromethorphan in vitro: involvement of cytochromes P450 2D6 and 3A3/4, with a possible role of 2E1. Biopharm. Drug Dispos. 1997, 18:227-240.
    • (1997) Biopharm. Drug Dispos. , vol.18 , pp. 227-240
    • Schmider, J.1    Greenblatt, D.J.2    Fogelman, S.M.3    VonMoltke, L.L.4    Shader, R.I.5
  • 166
    • 0034771887 scopus 로고    scopus 로고
    • Characterization of dextromethorphan O- and N-demethylation catalyzed by highly purified recombinant human CYP2D6
    • Yu A.M., Dong H.J., Lang D., Haining R.L. Characterization of dextromethorphan O- and N-demethylation catalyzed by highly purified recombinant human CYP2D6. Drug Metab. Dispos. 2001, 29:1362-1365.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 1362-1365
    • Yu, A.M.1    Dong, H.J.2    Lang, D.3    Haining, R.L.4
  • 167
    • 0034782996 scopus 로고    scopus 로고
    • Comparative contribution to dextromethorphan metabolism by cytochrome P450 isoforms in vitro: can dextromethorphan be used as a dual probe for both CYP2D6 and CYP3A activities?
    • Yu A.M., Haining R.L. Comparative contribution to dextromethorphan metabolism by cytochrome P450 isoforms in vitro: can dextromethorphan be used as a dual probe for both CYP2D6 and CYP3A activities?. Drug Metab. Dispos. 2001, 29:1514-1520.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 1514-1520
    • Yu, A.M.1    Haining, R.L.2
  • 168
    • 0031940804 scopus 로고    scopus 로고
    • Effect of common organic solvents on in vitro cytochrome P450-mediated metabolic activities in human liver microsomes
    • Chauret N., Gauthier A., Nicoll-Griffith D.A. Effect of common organic solvents on in vitro cytochrome P450-mediated metabolic activities in human liver microsomes. Drug Metab. Dispos. 1998, 26:1-4.
    • (1998) Drug Metab. Dispos. , vol.26 , pp. 1-4
    • Chauret, N.1    Gauthier, A.2    Nicoll-Griffith, D.A.3
  • 169
    • 0031921010 scopus 로고    scopus 로고
    • Evaluation of the selectivity of in vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities
    • Hickman D., Wang J.P., Wang Y., Unadkat J.D. Evaluation of the selectivity of in vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities. Drug Metab. Dispos. 1998, 26:207-215.
    • (1998) Drug Metab. Dispos. , vol.26 , pp. 207-215
    • Hickman, D.1    Wang, J.P.2    Wang, Y.3    Unadkat, J.D.4
  • 170
    • 0345490845 scopus 로고    scopus 로고
    • Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450
    • Busby W.F., Ackermann J.M., Crespi C.L. Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450. Drug Metab. Dispos. 1999, 27:246-249.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 246-249
    • Busby, W.F.1    Ackermann, J.M.2    Crespi, C.L.3
  • 171
    • 0035146956 scopus 로고    scopus 로고
    • Effects of organic solvents on the activities of cytochrome P450 isoforms, UDP-dependent glucuronyl transferase, and phenol sulfotransferase in human hepatocytes
    • Easterbrook J., Lu C., Sakai Y., Li A.P. Effects of organic solvents on the activities of cytochrome P450 isoforms, UDP-dependent glucuronyl transferase, and phenol sulfotransferase in human hepatocytes. Drug Metab. Dispos. 2001, 29:141-144.
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 141-144
    • Easterbrook, J.1    Lu, C.2    Sakai, Y.3    Li, A.P.4
  • 172
    • 70349088259 scopus 로고    scopus 로고
    • Contrasting Influence of NADPH and a NADPH-Regenerating System on the Metabolism of Carbonyl-Containing Compounds in Hepatic Microsomes
    • Mazur C.S., Kenneke J.F., Goldsmith M.R., Brown C. Contrasting Influence of NADPH and a NADPH-Regenerating System on the Metabolism of Carbonyl-Containing Compounds in Hepatic Microsomes. Drug Metab. Dispos. 2009, 37:1801-1805.
    • (2009) Drug Metab. Dispos. , vol.37 , pp. 1801-1805
    • Mazur, C.S.1    Kenneke, J.F.2    Goldsmith, M.R.3    Brown, C.4
  • 173
    • 0033674502 scopus 로고    scopus 로고
    • Comparison between cytochrome P450 (CYP) content and relative activity approaches to scaling from cDNA-expressed CYPs to human liver microsomes: ratios of accessory proteins as sources of discrepancies between the approaches
    • Venkatakrishnan K., Von Moltke L.L., Court M.H., Harmatz J.S., Crespi C.L., Greenblatt D.J. Comparison between cytochrome P450 (CYP) content and relative activity approaches to scaling from cDNA-expressed CYPs to human liver microsomes: ratios of accessory proteins as sources of discrepancies between the approaches. Drug Metab. Dispos. 2000, 28:1493-1504.
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 1493-1504
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Court, M.H.3    Harmatz, J.S.4    Crespi, C.L.5    Greenblatt, D.J.6
  • 174
    • 0034824312 scopus 로고    scopus 로고
    • Optimizing drug development: strategies to assess drug metabolism/transporter interaction potential - towards a consensus
    • Tucker G.T., Houston J.B., Huang S.M. Optimizing drug development: strategies to assess drug metabolism/transporter interaction potential - towards a consensus. Br. J. Clin. Pharmacol. 2001, 52:107-117.
    • (2001) Br. J. Clin. Pharmacol. , vol.52 , pp. 107-117
    • Tucker, G.T.1    Houston, J.B.2    Huang, S.M.3
  • 175
    • 2942571518 scopus 로고    scopus 로고
    • Protein precipitation for the analysis of a drug cocktail in plasma by LC-ESI-MS
    • Souverain S., Rudaz S., Veuthey J.L. Protein precipitation for the analysis of a drug cocktail in plasma by LC-ESI-MS. J. Pharmaceut. Biomed. 2004, 35:913-920.
    • (2004) J. Pharmaceut. Biomed. , vol.35 , pp. 913-920
    • Souverain, S.1    Rudaz, S.2    Veuthey, J.L.3
  • 176
    • 8444250979 scopus 로고    scopus 로고
    • Matrix effect in LC-ESI-MS and LC-APCI-MS with off-line and on-line extraction procedures
    • Souverain S., Rudaz S., Veuthey J.L. Matrix effect in LC-ESI-MS and LC-APCI-MS with off-line and on-line extraction procedures. J. Chromatogr. A 2004, 1058:61-66.
    • (2004) J. Chromatogr. A , vol.1058 , pp. 61-66
    • Souverain, S.1    Rudaz, S.2    Veuthey, J.L.3
  • 177
    • 2042546727 scopus 로고    scopus 로고
    • Cytochrome P450 2C8 (CYP2C8)-mediated hydroxylation of an endothelin ETA receptor antagonist in human liver microsomes
    • Ma B., Subramanian R., Schrag M.L., Rodrigues A.D., Tang C.Y. Cytochrome P450 2C8 (CYP2C8)-mediated hydroxylation of an endothelin ETA receptor antagonist in human liver microsomes. Drug Metab. Dispos. 2004, 32:473-478.
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 473-478
    • Ma, B.1    Subramanian, R.2    Schrag, M.L.3    Rodrigues, A.D.4    Tang, C.Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.