메뉴 건너뛰기




Volumn 45, Issue 11, 2015, Pages 961-977

A comprehensive assay for nine major cytochrome P450 enzymes activities with 16 probe reactions on human liver microsomes by a single LC/MS/MS run to support reliable in vitro inhibitory drug-drug interaction evaluation

Author keywords

Cytochrome P450; drug drug interaction; GT0918; human liver microsomes; in vitro cocktail; LC MS MS; MDV3100

Indexed keywords

AMFEBUTAMONE; CHLORZOXAZONE; COUMARIN; 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 3A4; CYTOCHROME P450 INHIBITOR; DEXTROMETHORPHAN; DICLOFENAC; ENZALUTAMIDE; GT 0918; MEPHENYTOIN; MIDAZOLAM; NIFEDIPINE; OMEPRAZOLE; ORGANIC SOLVENT; PACLITAXEL; PHENACETIN; POLYUNSATURATED FATTY ACID; S MEPHENYTOIN; TESTOSTERONE; TOLBUTAMIDE; UNCLASSIFIED DRUG; XENOBIOTIC AGENT;

EID: 84942252011     PISSN: 00498254     EISSN: 13665928     Source Type: Journal    
DOI: 10.3109/00498254.2015.1036954     Document Type: Article
Times cited : (41)

References (80)
  • 1
    • 0035155095 scopus 로고    scopus 로고
    • Application of higher throughput screening (HTS) inhibition assays to evaluate the interaction of antiparasitic drugs with cytochrome P450s
    • Bapiro TE, Egnell AC, Hasler JA, Masimirembwa CM. (2001). Application of higher throughput screening (HTS) inhibition assays to evaluate the interaction of antiparasitic drugs with cytochrome P450s. Drug Metab Dispos 29: 30-5
    • (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
  • 2
    • 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 Jr WF, Ackermann JM, Crespi CL. (1999). Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450. Drug Metab Dispos 27: 246-9
    • (1999) Drug Metab Dispos , vol.27 , pp. 246-249
    • Busby, W.F.1    Ackermann, J.M.2    Crespi, C.L.3
  • 3
    • 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 DA. (1998). Effect of common organic solvents on in vitro cytochrome P450-mediated metabolic activities in human liver microsomes. Drug Metab Dispos 26: 1-4
    • (1998) Drug Metab Dispos , vol.26 , pp. 1-4
    • Chauret, N.1    Gauthier, A.2    Nicoll-Griffith, D.A.3
  • 4
    • 84856356243 scopus 로고    scopus 로고
    • Development and validation of a fast and sensitive uplc-ms/ms method for the quantification of six probe metabolites for the in vitro determination of cytochrome p450 activity
    • De Bock L, Boussery K, Colin P, et al. (2012). Development and validation of a fast and sensitive UPLC-MS/MS method for the quantification of six probe metabolites for the in vitro determination of cytochrome P450 activity. Talanta 89: 209-16
    • (2012) Talanta , vol.89 , pp. 209-216
    • De Bock, L.1    Boussery, K.2    Colin, P.3
  • 5
    • 0035157254 scopus 로고    scopus 로고
    • A method for the simultaneous evaluation of the activities of seven major human drugmetabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry
    • Dierks EA, Stams KR, Lim HK, et al. (2001). A method for the simultaneous evaluation of the activities of seven major human drugmetabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry. Drug Metab Dispos 29: 23-9
    • (2001) Drug Metab Dispos , vol.29 , pp. 23-29
    • Dierks, E.A.1    Stams, K.R.2    Lim, H.K.3
  • 6
    • 84903783030 scopus 로고    scopus 로고
    • Development and validation of a liquid-chromatography high-resolution tandem mass spectrometry approach for quantification of nine cytochrome p450 (CYP) model substrate metabolites in an in vitro CYP inhibition cocktail
    • Dinger J, Meyer MR, Maurer HH. (2014). Development and validation of a liquid-chromatography high-resolution tandem mass spectrometry approach for quantification of nine cytochrome P450 (CYP) model substrate metabolites in an in vitro CYP inhibition cocktail. Anal Bioanal Chem 406: 4453-64
    • (2014) Anal Bioanal Chem , vol.406 , pp. 4453-4464
    • Dinger, J.1    Meyer, M.R.2    Maurer, H.H.3
  • 7
    • 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 JD. (2007). In vitro LC-MS cocktail assays to simultaneously determine human cytochrome P450 activities. Biopharm Drug Dispos 28: 257-62
    • (2007) Biopharm Drug Dispos , vol.28 , pp. 257-262
    • Dixit, V.1    Hariparsad, N.2    Desai, P.3    Unadkat, J.D.4
  • 8
    • 3042544349 scopus 로고    scopus 로고
    • Fluorescence-based assays for screening nine cytochrome P450 (P450) activities in intact cells expressing individual human P450 enzymes
    • Donato MT, Jimenez N, Castell JV, Gomez-Lechon MJ. (2004). Fluorescence-based assays for screening nine cytochrome P450 (P450) activities in intact cells expressing individual human P450 enzymes. Drug Metab Dispos 32: 699-706
    • (2004) Drug Metab Dispos , vol.32 , pp. 699-706
    • Donato, M.T.1    Jimenez, N.2    Castell, J.V.3    Gomez-Lechon, M.J.4
  • 9
    • 0031962621 scopus 로고    scopus 로고
    • Differential selectivity of cytochrome P450 inhibitors against probe substrates in human and rat liver microsomes
    • Eagling VA, Tjia JF, Back DJ. (1998). Differential selectivity of cytochrome P450 inhibitors against probe substrates in human and rat liver microsomes. Br J Clin Pharmacol 45: 107-14
    • (1998) Br J Clin Pharmacol , vol.45 , pp. 107-114
    • Eagling, V.A.1    Tjia, J.F.2    Back, D.J.3
  • 10
    • 0033861616 scopus 로고    scopus 로고
    • Identification of CYP3A4 as the enzyme involved in the mono-N-dealkylation of disopyramide enantiomers in humans
    • Echizen H, Tanizaki M, Tatsuno J, et al. (2000). Identification of CYP3A4 as the enzyme involved in the mono-N-dealkylation of disopyramide enantiomers in humans. Drug Metab Dispos 28: 937-44
    • (2000) Drug Metab Dispos , vol.28 , pp. 937-944
    • Echizen, H.1    Tanizaki, M.2    Tatsuno, J.3
  • 11
    • 40849102689 scopus 로고    scopus 로고
    • Cyp2c19 inhibition: The impact of substrate probe selection on in vitro inhibition profiles
    • Foti RS, Wahlstrom JL. (2008). CYP2C19 inhibition: the impact of substrate probe selection on in vitro inhibition profiles. Drug Metab Dispos 36: 523-8
    • (2008) Drug Metab Dispos , vol.36 , pp. 523-528
    • Foti, R.S.1    Wahlstrom, J.L.2
  • 12
    • 84867671775 scopus 로고    scopus 로고
    • Impact of organic solvents on cytochrome p450 probe reactions: Filling the gap with (s)-warfarin and midazolam hydroxylation
    • Gonzalez-Perez V, Connolly EA, Bridges AS, et al. (2012). Impact of organic solvents on cytochrome P450 probe reactions: filling the gap with (S)-Warfarin and midazolam hydroxylation. Drug Metab Dispos 40: 2136-42
    • (2012) Drug Metab Dispos , vol.40 , pp. 2136-2142
    • Gonzalez-Perez, V.1    Connolly, E.A.2    Bridges, A.S.3
  • 13
    • 36048939609 scopus 로고    scopus 로고
    • Mechanisms of cytochrome P450 substrate oxidation: MiniReview
    • Guengerich FP. (2007). Mechanisms of cytochrome P450 substrate oxidation: MiniReview. J Biochem Mol Toxicol 21: 163-8
    • (2007) J Biochem Mol Toxicol , vol.21 , pp. 163-168
    • Guengerich, F.P.1
  • 14
    • 84892909662 scopus 로고    scopus 로고
    • Cyp2e1 hydroxylation of aniline involves negative cooperativity
    • Hartman JH, Knott K, Miller GP. (2014). CYP2E1 hydroxylation of aniline involves negative cooperativity. Biochem Pharmacol 87: 523-33
    • (2014) Biochem Pharmacol , vol.87 , pp. 523-533
    • Hartman, J.H.1    Knott, K.2    Miller, G.P.3
  • 15
    • 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 HC, Xie ZY, et al. (2007). 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 21: 635-43
    • (2007) Rapid Commun Mass Spectrom , vol.21 , pp. 635-643
    • He, F.1    Bi, H.C.2    Xie, Z.Y.3
  • 16
    • 0033820249 scopus 로고    scopus 로고
    • Cyp2b6 mediates the in vitro hydroxylation of bupropion: Potential drug interactions with other antidepressants
    • Hesse LM, Venkatakrishnan K, Court MH, et al. (2000). CYP2B6 mediates the in vitro hydroxylation of bupropion: potential drug interactions with other antidepressants. Drug Metab Dispos 28: 1176-83
    • (2000) Drug Metab Dispos , vol.28 , pp. 1176-1183
    • Hesse, L.M.1    Venkatakrishnan, K.2    Court, M.H.3
  • 17
    • 34047163480 scopus 로고    scopus 로고
    • Inhibitory effects of neurotransmitters and steroids on human cyp2a6
    • Higashi E, Nakajima M, Katoh M, et al. (2007). Inhibitory effects of neurotransmitters and steroids on human CYP2A6. Drug Metab Dispos 35: 508-14
    • (2007) Drug Metab Dispos , vol.35 , pp. 508-514
    • Higashi, E.1    Nakajima, M.2    Katoh, M.3
  • 18
    • 44049087422 scopus 로고    scopus 로고
    • New era in drug interaction evaluation: Us food and drug administration update on CYP enzymes, transporters, and the guidance process
    • Huang SM, Strong JM, Zhang L, et al. (2008). New era in drug interaction evaluation: US Food and Drug Administration update on CYP enzymes, transporters, and the guidance process. J Clin Pharm 48: 662-70
    • (2008) J Clin Pharm , vol.48 , pp. 662-670
    • Huang, S.M.1    Strong, J.M.2    Zhang, L.3
  • 19
    • 33846577441 scopus 로고    scopus 로고
    • Drug interaction studies: Study design, data analysis, and implications for dosing and labeling
    • Huang SM, Temple R, Throckmorton DC, Lesko LJ. (2007). Drug interaction studies: study design, data analysis, and implications for dosing and labeling. Clin Pharm Ther 81: 298-304
    • (2007) Clin Pharm Ther , vol.81 , pp. 298-304
    • Huang, S.M.1    Temple, R.2    Throckmorton, D.C.3    Lesko, L.J.4
  • 20
    • 2642555502 scopus 로고    scopus 로고
    • Effectormediated alteration of substrate orientation in cytochrome P450 2C9
    • Hummel MA, Gannett PM, Aguilar JS, Tracy TS. (2004). Effectormediated alteration of substrate orientation in cytochrome P450 2C9. Biochemistry 43: 7207-14
    • (2004) Biochemistry , vol.43 , pp. 7207-7214
    • Hummel, M.A.1    Gannett, P.M.2    Aguilar, J.S.3    Tracy, T.S.4
  • 21
    • 44949121516 scopus 로고    scopus 로고
    • Substrate proton to heme distances in cyp2c9 allelic variants and alterations by the heterotropic activator, dapsone
    • Hummel MA, Gannett PM, Aguilar J, Tracy TS. (2008). Substrate proton to heme distances in CYP2C9 allelic variants and alterations by the heterotropic activator, dapsone. Arch Biochem Biophys 475: 175-83
    • (2008) Arch Biochem Biophys , vol.475 , pp. 175-183
    • Hummel, M.A.1    Gannett, P.M.2    Aguilar, J.3    Tracy, T.S.4
  • 22
    • 58149463629 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochrome P450 2C9 by tienilic acid and (+/)-suprofen: A comparison of kinetics and probe substrate selection
    • Hutzler JM, Balogh LM, Zientek M, et al. (2009). Mechanism-based inactivation of cytochrome P450 2C9 by tienilic acid and (+/)-suprofen: a comparison of kinetics and probe substrate selection. Drug Metab Dispos 37: 59-65
    • (2009) Drug Metab Dispos , vol.37 , pp. 59-65
    • Hutzler, J.M.1    Balogh, L.M.2    Zientek, M.3
  • 23
    • 0034934070 scopus 로고    scopus 로고
    • Minimal in vivo activation of CYP2C9-mediated flurbiprofen metabolism by dapsone
    • Hutzler JM, Frye RF, Korzekwa KR, et al. (2001a). Minimal in vivo activation of CYP2C9-mediated flurbiprofen metabolism by dapsone. Eur J Pharm Sci 14: 47-52
    • (2001) Eur J Pharm Sci , vol.14 , pp. 47-52
    • Hutzler, J.M.1    Frye, R.F.2    Korzekwa, K.R.3
  • 24
    • 0034956877 scopus 로고    scopus 로고
    • Dapsone activation of CYP2C9-mediated metabolism: Evidence for activation of multiple substrates and a two-site model
    • Hutzler JM, Hauer MJ, Tracy TS. (2001b). Dapsone activation of CYP2C9-mediated metabolism: evidence for activation of multiple substrates and a two-site model. Drug Metab Dispos 29: 1029-34
    • (2001) Drug Metab Dispos , vol.29 , pp. 1029-1034
    • Hutzler, J.M.1    Hauer, M.J.2    Tracy, T.S.3
  • 25
    • 0036842029 scopus 로고    scopus 로고
    • Activation of cyp2c9-mediated metabolism by a series of dapsone analogs: Kinetics and structural requirements
    • Hutzler JM, Kolwankar D, Hummel MA, Tracy TS. (2002). Activation of CYP2C9-mediated metabolism by a series of dapsone analogs: kinetics and structural requirements. Drug Metab Dispos 30: 1194-200
    • (2002) Drug Metab Dispos , vol.30 , pp. 1194-1200
    • Hutzler, J.M.1    Kolwankar, D.2    Hummel, M.A.3    Tracy, T.S.4
  • 26
    • 0036201594 scopus 로고    scopus 로고
    • Atypical kinetic profiles in drug metabolism reactions
    • Hutzler JM, Tracy TS. (2002). Atypical kinetic profiles in drug metabolism reactions. Drug Metab Dispos 30: 355-62
    • (2002) Drug Metab Dispos , vol.30 , pp. 355-362
    • Hutzler, J.M.1    Tracy, T.S.2
  • 27
    • 15844394255 scopus 로고    scopus 로고
    • Identification of residues 99, 220, and 221 of human cytochrome P450 2C19 as key determinants of omeprazole activity
    • Ibeanu GC, Ghanayem BI, Linko P, et al. (1996). Identification of residues 99, 220, and 221 of human cytochrome P450 2C19 as key determinants of omeprazole activity. J Biol Chem 271: 12496-501
    • (1996) J Biol Chem , vol.271 , pp. 12496-12501
    • Ibeanu, G.C.1    Ghanayem, B.I.2    Linko, P.3
  • 28
    • 38949100528 scopus 로고    scopus 로고
    • Cytochrome P450 inactivation by pharmaceuticals and phytochemicals: Therapeutic relevance
    • Johnson WW. (2008). Cytochrome P450 inactivation by pharmaceuticals and phytochemicals: therapeutic relevance. Drug Metab Rev 40: 101-47
    • (2008) Drug Metab Rev , vol.40 , pp. 101-147
    • Johnson, W.W.1
  • 29
    • 0019180050 scopus 로고
    • The effect of solvents on drug metabolism in vitro
    • Kawalek JC, Andrews AW. (1980). The effect of solvents on drug metabolism in vitro. Drug Metab Disposition 8: 380-4
    • (1980) Drug Metab Disposition , vol.8 , pp. 380-384
    • Kawalek, J.C.1    Andrews, A.W.2
  • 31
    • 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 MJ, Kim H, Cha IJ, et al. (2005). High-throughput screening of inhibitory potential of nine cytochrome P450 enzymes in vitro using liquid chromatography/tandem mass spectrometry. Rapid commun Mass Spectrom 19: 2651-8
    • (2005) Rapid Commun Mass Spectrom , vol.19 , pp. 2651-2658
    • Kim, M.J.1    Kim, H.2    Cha, I.J.3
  • 32
    • 0030811096 scopus 로고    scopus 로고
    • Evaluation of omeprazole and lansoprazole as inhibitors of cytochrome P450 isoforms
    • Ko JW, Sukhova N, Thacker D, et al. (1997). Evaluation of omeprazole and lansoprazole as inhibitors of cytochrome P450 isoforms. Drug Metab Dispos 25: 853-62
    • (1997) Drug Metab Dispos , vol.25 , pp. 853-862
    • Ko, J.W.1    Sukhova, N.2    Thacker, D.3
  • 33
    • 0000574406 scopus 로고    scopus 로고
    • Evaluation of atypical cytochrome P450 kinetics with two-substrate models: Evidence that multiple substrates can simultaneously bind to cytochrome P450 active sites
    • Korzekwa KR, Krishnamachary N, Shou M, et al. (1998). Evaluation of atypical cytochrome P450 kinetics with two-substrate models: evidence that multiple substrates can simultaneously bind to cytochrome P450 active sites. Biochemistry 37: 4137-47
    • (1998) Biochemistry , vol.37 , pp. 4137-4147
    • Korzekwa, K.R.1    Krishnamachary, N.2    Shou, M.3
  • 34
    • 84869119884 scopus 로고    scopus 로고
    • Reliable highthroughput 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, et al. (2012). Reliable highthroughput method for inhibition assay of 8 cytochrome P450 isoforms using cocktail of probe substrates and stable isotope-labeled internal standards. Drug Metab Pharmacokinet 27: 520-9
    • (2012) Drug Metab Pharmacokinet , vol.27 , pp. 520-529
    • Kozakai, K.1    Yamada, Y.2    Oshikata, M.3
  • 35
    • 33750547308 scopus 로고    scopus 로고
    • CYP2C9 inhibition: Impact of probe selection and pharmacogenetics on in vitro inhibition profiles
    • Kumar V, Wahlstrom JL, Rock DA, et al. (2006). CYP2C9 inhibition: impact of probe selection and pharmacogenetics on in vitro inhibition profiles. Drug Metab Dispos 34: 1966-75
    • (2006) Drug Metab Dispos , vol.34 , pp. 1966-1975
    • Kumar, V.1    Wahlstrom, J.L.2    Rock, D.A.3
  • 36
    • 84871623034 scopus 로고    scopus 로고
    • Direct and metabolism-dependent cytochrome P450 inhibition assays for evaluating drug-drug interactions
    • Lee KS, Kim SK. (2013). Direct and metabolism-dependent cytochrome P450 inhibition assays for evaluating drug-drug interactions. J Appl Toxicol 33: 00-8
    • (2013) J Appl Toxicol , vol.33 , pp. 00-8
    • Lee, K.S.1    Kim, S.K.2
  • 37
    • 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 XQ, Bjorkman A, Andersson TB, et al. (2002). Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: a new high affinity and turnover enzyme-specific probe substrate. J Pharm Exp Ther 300: 399-407
    • (2002) J Pharm Exp Ther , vol.300 , pp. 399-407
    • Li, X.Q.1    Bjorkman, A.2    Andersson, T.B.3
  • 38
    • 84856294149 scopus 로고    scopus 로고
    • Inhibitory effects of wogonin on catalytic activity of cytochrome P450 enzyme in human liver microsomes
    • Li T, Li N, Guo Q, et al. (2011). Inhibitory effects of wogonin on catalytic activity of cytochrome P450 enzyme in human liver microsomes. Eur J Drug Metab Pharmacokinet 36: 249-56
    • (2011) Eur J Drug Metab Pharmacokinet , vol.36 , pp. 249-256
    • Li, T.1    Li, N.2    Guo, Q.3
  • 39
    • 16244384507 scopus 로고    scopus 로고
    • Stereoselective inhibition of cytochrome P450 forms by lansoprazole and omeprazole in vitro
    • Liu KH, Kim MJ, Shon JH, et al. (2005). Stereoselective inhibition of cytochrome P450 forms by lansoprazole and omeprazole in vitro. Xenobiotica 35: 27-38
    • (2005) Xenobiotica , vol.35 , pp. 27-38
    • Liu, K.H.1    Kim, M.J.2    Shon, J.H.3
  • 40
    • 0030825141 scopus 로고    scopus 로고
    • Effect of albumin on the estimation, in vitro, of phenytoin vmax and km values: Implications for clinical correlation
    • Ludden LK, Ludden TM, Collins JM, et al. (1997). Effect of albumin on the estimation, in vitro, of phenytoin Vmax and Km values: implications for clinical correlation. J Pharm Exp Ther 282: 391-6
    • (1997) J Pharm Exp Ther , vol.282 , pp. 391-396
    • Ludden, L.K.1    Ludden, T.M.2    Collins, J.M.3
  • 41
    • 80054737088 scopus 로고    scopus 로고
    • Bovine serum albumin decreases Km values of human UDP-glucuronosyltransferases 1A9 and 2B7 and increases Vmax values of UGT1A9
    • Manevski N, Moreolo PS, Yli-Kauhaluoma J, Finel M. (2011). Bovine serum albumin decreases Km values of human UDP-glucuronosyltransferases 1A9 and 2B7 and increases Vmax values of UGT1A9. Drug Metab Dispos 39: 2117-29
    • (2011) Drug Metab Dispos , vol.39 , pp. 2117-2129
    • Manevski, N.1    Moreolo, P.S.2    Yli-Kauhaluoma, J.3    Finel, M.4
  • 42
    • 0032874278 scopus 로고    scopus 로고
    • Heterologous expression and kinetic characterization of human cytochromes P-450: Validation of a pharmaceutical tool for drug metabolism research
    • Masimirembwa CM, Otter C, Berg M, et al. (1999). Heterologous expression and kinetic characterization of human cytochromes P-450: validation of a pharmaceutical tool for drug metabolism research. Drug Metab Dispos 27: 1117-22
    • (1999) Drug Metab Dispos , vol.27 , pp. 1117-1122
    • Masimirembwa, C.M.1    Otter, C.2    Berg, M.3
  • 43
    • 77649141812 scopus 로고    scopus 로고
    • New insights into the structural features and functional relevance of human cytochrome P450 2C9
    • Mo SL, Zhou ZW, Yang LP, et al. (2009). New insights into the structural features and functional relevance of human cytochrome P450 2C9. Part I. Curr Drug Metab 10: 1075-126
    • (2009) Part I. Curr Drug Metab , vol.10 , pp. 1075-1126
    • Mo, S.L.1    Zhou, Z.W.2    Yang, L.P.3
  • 44
    • 0037068964 scopus 로고    scopus 로고
    • Clinical importance of the cytochromes P450
    • Nebert DW, Russell DW. (2002). Clinical importance of the cytochromes P450. Lancet 360: 1155-62
    • (2002) Lancet , vol.360 , pp. 1155-1162
    • Nebert, D.W.1    Russell, D.W.2
  • 45
    • 72949085043 scopus 로고    scopus 로고
    • Effects of organic solvents on the time-dependent inhibition of CYP3A4 by diazepam
    • Nishiya Y, Nakamura K, Okudaira N, et al. (2010). Effects of organic solvents on the time-dependent inhibition of CYP3A4 by diazepam. Xenobiotica 40: 1-8
    • (2010) Xenobiotica , vol.40 , pp. 1-8
    • Nishiya, Y.1    Nakamura, K.2    Okudaira, N.3
  • 46
    • 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 CJ, Grime K, Courtney P, et al. (2007). 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 35: 381-5
    • (2007) Drug Metab Dispos , vol.35 , pp. 381-385
    • O'Donnell, C.J.1    Grime, K.2    Courtney, P.3
  • 47
    • 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 JN, Hingorani GP, Hartley DP, et al. (2011). An in vitro, high throughput, seven CYP cocktail inhibition assay for the evaluation of new chemical entities using LC-MS/MS. Drug Metab Lett 5: 17-24
    • (2011) Drug Metab Lett , vol.5 , pp. 17-24
    • Otten, J.N.1    Hingorani, G.P.2    Hartley, D.P.3
  • 48
    • 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 KC, Von Moltke LL, Greenblatt DJ. (2003). 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 31: 938-44
    • (2003) Drug Metab Dispos , vol.31 , pp. 938-944
    • Patki, K.C.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 49
    • 15244345304 scopus 로고    scopus 로고
    • Prediction of drug metabolism and interactions on the basis of in vitro investigations
    • Pelkonen O, Turpeinen M, Uusitalo J, et al. (2005). Prediction of drug metabolism and interactions on the basis of in vitro investigations. Basic Clin Pharmacol Toxicol 96: 167-75
    • (2005) Basic Clin Pharmacol Toxicol , vol.96 , pp. 167-175
    • Pelkonen, O.1    Turpeinen, M.2    Uusitalo, J.3
  • 50
    • 84892371509 scopus 로고    scopus 로고
    • A high-throughput inhibition screening of major human cytochrome P450 enzymes using an in vitro cocktail and liquid chromatography-tandem mass spectrometry
    • Qin CZ, Ren X, Tan ZR, et al. (2014). A high-throughput inhibition screening of major human cytochrome P450 enzymes using an in vitro cocktail and liquid chromatography-tandem mass spectrometry. Biomed chromatogr 28: 197-203
    • (2014) Biomed Chromatogr , vol.28 , pp. 197-203
    • Qin, C.Z.1    Ren, X.2    Tan, Z.R.3
  • 51
    • 84871539611 scopus 로고    scopus 로고
    • Discovery and characterization of novel, potent, and selective cytochrome P450 2J2 inhibitors
    • Ren S, Zeng J, Mei Y, et al. (2013). Discovery and characterization of novel, potent, and selective cytochrome P450 2J2 inhibitors. Drug Metab Dispos 41: 60-71
    • (2013) Drug Metab Dispos , vol.41 , pp. 60-71
    • Ren, S.1    Zeng, J.2    Mei, Y.3
  • 52
    • 42449124602 scopus 로고    scopus 로고
    • The albumin effect and in vitro-in vivo extrapolation: Sequestration of long-chain unsaturated fatty acids enhances phenytoin hydroxylation by human liver microsomal and recombinant cytochrome P450 2C9
    • Rowland A, Elliot DJ, Knights KM, et al. (2008). The albumin effect and in vitro-in vivo extrapolation: sequestration of long-chain unsaturated fatty acids enhances phenytoin hydroxylation by human liver microsomal and recombinant cytochrome P450 2C9. Drug Metab Dispos 36: 870-7
    • (2008) Drug Metab Dispos , vol.36 , pp. 870-877
    • Rowland, A.1    Elliot, D.J.2    Knights, K.M.3
  • 53
    • 33947398317 scopus 로고    scopus 로고
    • Binding of inhibitory fatty acids is responsible for the enhancement of UDP-glucuronosyltransferase 2B7 activity by albumin: Implications for in vitro-in vivo extrapolation
    • Rowland A, Gaganis P, Elliot DJ, et al. (2007). Binding of inhibitory fatty acids is responsible for the enhancement of UDP-glucuronosyltransferase 2B7 activity by albumin: implications for in vitro-in vivo extrapolation. J Pharmacol Exp Ther 321: 137-47
    • (2007) J Pharmacol Exp Ther , vol.321 , pp. 137-147
    • Rowland, A.1    Gaganis, P.2    Elliot, D.J.3
  • 54
    • 27244462157 scopus 로고    scopus 로고
    • Covalent alteration of the CYP3A4 active site: Evidence for multiple substrate binding domains
    • Schrag ML, Wienkers LC. (2001). Covalent alteration of the CYP3A4 active site: evidence for multiple substrate binding domains. Arch Biochem Biophys 391: 49-55
    • (2001) Arch Biochem Biophys , vol.391 , pp. 49-55
    • Schrag, M.L.1    Wienkers, L.C.2
  • 55
    • 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 DK, Hokkanen J, Tolonen A, et al. (2010). Rapid screening of commercially available herbal products for the inhibition of major human hepatic cytochrome P450 enzymes using the N-in-one cocktail. Xenobiotica 40: 245-54
    • (2010) Xenobiotica , vol.40 , pp. 245-254
    • Sevior, D.K.1    Hokkanen, J.2    Tolonen, A.3
  • 56
    • 0033564235 scopus 로고    scopus 로고
    • Sigmoidal kinetic model for two co-operative substrate-binding sites in a cytochrome P450 3A4 active site: An example of the metabolism of diazepam and its derivatives
    • Shou M, Mei Q, Ettore Jr MW, et al. (1999). Sigmoidal kinetic model for two co-operative substrate-binding sites in a cytochrome P450 3A4 active site: an example of the metabolism of diazepam and its derivatives. Biochem J 340: 845-53
    • (1999) Biochem J , vol.340 , pp. 845-853
    • Shou, M.1    Mei, Q.2    Ettore, M.W.3
  • 57
    • 84864545260 scopus 로고    scopus 로고
    • Evaluation of inhibition selectivity for human cytochrome P450 2A enzymes
    • Stephens ES, Walsh AA, Scott EE. (2012). Evaluation of inhibition selectivity for human cytochrome P450 2A enzymes. Drug Metab Dispos 40: 1797-802
    • (2012) Drug Metab Dispos , vol.40 , pp. 1797-1802
    • Stephens, E.S.1    Walsh, A.A.2    Scott, E.E.3
  • 58
    • 0036259919 scopus 로고    scopus 로고
    • Effect of albumin on phenytoin and tolbutamide metabolism in human liver microsomes: An impact more than protein binding
    • Tang C, Lin Y, Rodrigues AD, Lin JH. (2002). Effect of albumin on phenytoin and tolbutamide metabolism in human liver microsomes: an impact more than protein binding. Drug Metab Dispos 30: 648-54
    • (2002) Drug Metab Dispos , vol.30 , pp. 648-654
    • Tang, C.1    Lin, Y.2    Rodrigues, A.D.3    Lin, J.H.4
  • 59
    • 0034007499 scopus 로고    scopus 로고
    • Substrate-dependent effect of acetonitrile on human liver microsomal cytochrome p450 2c9 (cyp2c9) activity
    • Tang C, Shou M, Rodrigues AD. (2000). Substrate-dependent effect of acetonitrile on human liver microsomal cytochrome P450 2C9 (CYP2C9) activity. Drug Metab Dispos 28: 567-72
    • (2000) Drug Metab Dispos , vol.28 , pp. 567-572
    • Tang, C.1    Shou, M.2    Rodrigues, A.D.3
  • 60
    • 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 Jr SA, Patonay G. (2003). High-throughput inhibition screening of major human cytochrome P450 enzymes using an in vitro cocktail and liquid chromatography-tandem mass spectrometry. J Pharm Biomed Anal 30: 1459-67
    • (2003) J Pharm Biomed Anal , vol.30 , pp. 1459-1467
    • Testino, S.A.1    Patonay, G.2
  • 61
    • 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, et al. (2007). 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 42: 960-6
    • (2007) J Mass Spectrom , vol.42 , pp. 960-966
    • Tolonen, A.1    Petsalo, A.2    Turpeinen, M.3
  • 62
    • 0035916224 scopus 로고    scopus 로고
    • Identification of human cyp2c19 residues that confer s-mephenytoin 40-hydroxylation activity to cyp2c9
    • Tsao CC, Wester MR, Ghanayem B, et al. (2001). Identification of human CYP2C19 residues that confer S-mephenytoin 40-hydroxylation activity to CYP2C9. Biochemistry 40: 1937-44
    • (2001) Biochemistry , vol.40 , pp. 1937-1944
    • Tsao, C.C.1    Wester, M.R.2    Ghanayem, B.3
  • 63
    • 11144242471 scopus 로고    scopus 로고
    • Multiple P450 substrates in a single run: Rapid and comprehensive in vitro interaction assay
    • Turpeinen M, Uusitalo J, Jalonen J, Pelkonen O. (2005). Multiple P450 substrates in a single run: rapid and comprehensive in vitro interaction assay. Eur J Pharm Sci 24: 123-32
    • (2005) Eur J Pharm Sci , vol.24 , pp. 123-132
    • Turpeinen, M.1    Uusitalo, J.2    Jalonen, J.3    Pelkonen, O.4
  • 64
    • 84455163212 scopus 로고    scopus 로고
    • Prediction of cyp2d6 drug interactions from in vitro data: Evidence for substratedependent inhibition
    • VandenBrink BM, Foti RS, Rock DA, et al. (2012). Prediction of CYP2D6 drug interactions from in vitro data: evidence for substratedependent inhibition. Drug Metab Dispos 40: 47-53
    • (2012) Drug Metab Dispos , vol.40 , pp. 47-53
    • VandenBrink, B.M.1    Foti, R.S.2    Rock, D.A.3
  • 65
    • 35548954678 scopus 로고    scopus 로고
    • Effect of commonly used organic solvents on the kinetics of cytochrome p450 2b6-and 2c8-dependent activity in human liver microsomes
    • Vuppugalla R, Chang SY, Zhang H, et al. (2007). Effect of commonly used organic solvents on the kinetics of cytochrome P450 2B6-and 2C8-dependent activity in human liver microsomes. Drug Metab Dispos 35: 1990-5
    • (2007) Drug Metab Dispos , vol.35 , pp. 1990-1995
    • Vuppugalla, R.1    Chang, S.Y.2    Zhang, H.3
  • 66
    • 2442690439 scopus 로고    scopus 로고
    • Validated assays for human cytochrome P450 activities
    • Walsky RL, Obach RS. (2004). Validated assays for human cytochrome P450 activities. Drug Metab Dispos 32: 647-60
    • (2004) Drug Metab Dispos , vol.32 , pp. 647-660
    • Walsky, R.L.1    Obach, R.S.2
  • 67
    • 0033507633 scopus 로고    scopus 로고
    • Enzymes in addition to CYP3A4 and 3A5 mediate N-demethylation of dextromethorphan in human liver microsomes
    • Wang Y, Unadkat JD. (1999). Enzymes in addition to CYP3A4 and 3A5 mediate N-demethylation of dextromethorphan in human liver microsomes. Biopharm Drug Dispos 20: 341-6
    • (1999) Biopharm Drug Dispos , vol.20 , pp. 341-346
    • Wang, Y.1    Unadkat, J.D.2
  • 68
    • 76749166335 scopus 로고    scopus 로고
    • In vitro assessment of metabolic drug-drug interaction potential of apixaban through cytochrome P450 phenotyping, inhibition, and induction studies
    • Wang L, Zhang D, Raghavan N, et al. (2010). In vitro assessment of metabolic drug-drug interaction potential of apixaban through cytochrome P450 phenotyping, inhibition, and induction studies. Drug Metab Dispos 38: 448-58
    • (2010) Drug Metab Dispos , vol.38 , pp. 448-458
    • Wang, L.1    Zhang, D.2    Raghavan, N.3
  • 69
    • 79960952379 scopus 로고    scopus 로고
    • In vitro-in vivo extrapolation of CYP2C8-catalyzed paclitaxel 6alpha-hydroxylation: Effects of albumin on in vitro kinetic parameters and assessment of interindividual variability in predicted clearance
    • Wattanachai N, Polasek TM, Heath TM, et al. (2011). In vitro-in vivo extrapolation of CYP2C8-catalyzed paclitaxel 6alpha-hydroxylation: effects of albumin on in vitro kinetic parameters and assessment of interindividual variability in predicted clearance. Eur J Clin Pharmacol 67: 815-24
    • (2011) Eur J Clin Pharmacol , vol.67 , pp. 815-824
    • Wattanachai, N.1    Polasek, T.M.2    Heath, T.M.3
  • 70
    • 84859886181 scopus 로고    scopus 로고
    • Effect of albumin on human liver microsomal and recombinant CYP1A2 activities: Impact on in vitro-in vivo extrapolation of drug clearance
    • Wattanachai N, Tassaneeyakul W, Rowland A, et al. (2012). Effect of albumin on human liver microsomal and recombinant CYP1A2 activities: impact on in vitro-in vivo extrapolation of drug clearance. Drug Metab Dispos 40: 982-9
    • (2012) Drug Metab Dispos , vol.40 , pp. 982-989
    • Wattanachai, N.1    Tassaneeyakul, W.2    Rowland, A.3
  • 71
    • 0042265520 scopus 로고    scopus 로고
    • Crystal structure of human cytochrome P450 2C9 with bound warfarin
    • Williams PA, Cosme J, Ward A, et al. (2003). Crystal structure of human cytochrome P450 2C9 with bound warfarin. Nature 424: 464-8
    • (2003) Nature , vol.424 , pp. 464-468
    • Williams, P.A.1    Cosme, J.2    Ward, A.3
  • 72
    • 34047252007 scopus 로고    scopus 로고
    • Development and full validation of six inhibition assays for five major cytochrome p450 enzymes in human liver microsomes using an automated 96-well microplate incubation format and lc-ms/ms analysis
    • Yao M, Zhu M, Sinz MW, et al. (2007). Development and full validation of six inhibition assays for five major cytochrome P450 enzymes in human liver microsomes using an automated 96-well microplate incubation format and LC-MS/MS analysis. J Pharm Biomed Anal 44: 211-23
    • (2007) J Pharm Biomed Anal , vol.44 , pp. 211-223
    • Yao, M.1    Zhu, M.2    Sinz, M.W.3
  • 73
    • 84873176765 scopus 로고    scopus 로고
    • Characterization of intestinal and hepatic P450 enzymes in cynomolgus monkeys with typical substrates and inhibitors for human P450 enzymes
    • Yoda N, Emoto C, Date S, et al. (2012). Characterization of intestinal and hepatic P450 enzymes in cynomolgus monkeys with typical substrates and inhibitors for human P450 enzymes. Xenobiotica 42: 719-30
    • (2012) Xenobiotica , vol.42 , pp. 719-730
    • Yoda, N.1    Emoto, C.2    Date, S.3
  • 74
    • 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 XX, et al. (2002). Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions. Drug Metab Dispos 30: 1311-19
    • (2002) Drug Metab Dispos , vol.30 , pp. 1311-1319
    • Yuan, R.1    Madani, S.2    Wei, X.X.3
  • 75
    • 78049445726 scopus 로고    scopus 로고
    • Evaluation of cytochrome P450 inhibition assays using human liver microsomes by a cassette analysis/LC-MS/MS
    • Zambon S, Fontana S, Kajbaf M. (2010). Evaluation of cytochrome P450 inhibition assays using human liver microsomes by a cassette analysis/LC-MS/MS. Drug Metab Lett 4: 120-8
    • (2010) Drug Metab Lett , vol.4 , pp. 120-128
    • Zambon, S.1    Fontana, S.2    Kajbaf, M.3
  • 76
    • 0037175449 scopus 로고    scopus 로고
    • Rapid and quantitative determination of metabolites from multiple cytochrome P450 probe substrates by gradient liquid chromatography-electrospray ionizationion trap mass spectrometry
    • Zhang T, Zhu Y, Gunaratna C. (2002). Rapid and quantitative determination of metabolites from multiple cytochrome P450 probe substrates by gradient liquid chromatography-electrospray ionizationion trap mass spectrometry. J Chromatogr B 780: 371-9
    • (2002) J Chromatogr B , vol.780 , pp. 371-379
    • Zhang, T.1    Zhu, Y.2    Gunaratna, C.3
  • 77
    • 18844445670 scopus 로고    scopus 로고
    • Evaluation of time-dependent inactivation of CYP3A in cryopreserved human hepatocytes
    • Zhao P, Kunze KL, Lee CA. (2005). Evaluation of time-dependent inactivation of CYP3A in cryopreserved human hepatocytes. Drug Metab Dispos 33: 853-61
    • (2005) Drug Metab Dispos , vol.33 , pp. 853-861
    • Zhao, P.1    Kunze, K.L.2    Lee, C.A.3
  • 78
    • 16444377083 scopus 로고    scopus 로고
    • Mechanism-based inhibition of cytochrome P450 3A4 by therapeutic drugs
    • Zhou S, Yung CS, Cher GB, et al. (2005). Mechanism-based inhibition of cytochrome P450 3A4 by therapeutic drugs. Clin Pharmacokinet 44: 279-304
    • (2005) Clin Pharmacokinet , vol.44 , pp. 279-304
    • Zhou, S.1    Yung, C.S.2    Cher, G.B.3
  • 79
    • 70450245353 scopus 로고    scopus 로고
    • Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development
    • Zhou SF, Zhou ZW, Yang LP, Cai JP. (2009). Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development. Curr Med Chem 16: 3480-675
    • (2009) Curr Med Chem , vol.16 , pp. 3480-3675
    • Zhou, S.F.1    Zhou, Z.W.2    Yang, L.P.3    Cai, J.P.4
  • 80
    • 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, et al. (2008). 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 58: 206-14
    • (2008) J Pharmacol Toxicol Methods , vol.58 , pp. 206-214
    • Zientek, M.1    Miller, H.2    Smith, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.