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Volumn 2, Issue 4, 2006, Pages 629-645

Luminogenic cytochrome P450 assays

Author keywords

CYP; CYP induction; CYP inhibition; Cytochrome P450; Drug metabolism; Drug drug interaction; Fluorescent P450 assay; Hepatocyte; High throughput screening; Liver microsomes; Luminescent P450 assay; P450 Glo ; Recombinant CYP enzymes

Indexed keywords

ASTEMIZOLE; CERIVASTATIN; CYTOCHROME P450; CYTOCHROME P450 1A1; CYTOCHROME P450 1A2; CYTOCHROME P450 1B1; CYTOCHROME P450 2C19; CYTOCHROME P450 2C8; CYTOCHROME P450 2C9; CYTOCHROME P450 2D6; CYTOCHROME P450 3A4; CYTOCHROME P450 3A7; CYTOCHROME P450 4A11; FIREFLY LUCIFERASE; MIBEFRADIL; TERFENADINE; ENZYME INHIBITOR; FLUORESCENT DYE; LUCIFERASE; LUMINESCENT AGENT;

EID: 33747828962     PISSN: 17425255     EISSN: None     Source Type: Journal    
DOI: 10.1517/17425255.2.4.629     Document Type: Review
Times cited : (165)

References (84)
  • 1
    • 0026750647 scopus 로고
    • The human hepatic cytochromes P450 involved in drug metabolism
    • WRIGHTON SA, STEVENS JC: The human hepatic cytochromes P450 involved in drug metabolism. Crit. Rev. Tox. (1992) 22(1):1-21.
    • (1992) Crit. Rev. Tox , vol.22 , Issue.1 , pp. 1-21
    • WRIGHTON, S.A.1    STEVENS, J.C.2
  • 2
    • 10744232330 scopus 로고    scopus 로고
    • BJORNSSON TD, CALLAHAN JT, EINOLF HJ et al.: The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab. Dispos. (2003) 31(7):815-832. A widely referenced guidance manual for in vitro DDI studies.
    • BJORNSSON TD, CALLAHAN JT, EINOLF HJ et al.: The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab. Dispos. (2003) 31(7):815-832. A widely referenced guidance manual for in vitro DDI studies.
  • 3
    • 0036226275 scopus 로고    scopus 로고
    • in vivo and clinical aspects
    • PELKONEN O: Human CYPs: in vivo and clinical aspects. Drug Metab. Rev. (2002) 34(1&2):37-46.
    • (2002) Drug Metab. Rev , vol.34 , Issue.1-2 , pp. 37-46
    • PELKONEN, O.1    Human, C.Y.P.2
  • 4
    • 27644596457 scopus 로고    scopus 로고
    • WEINKERS LC, HEATH GH: Predicting in vivo drug interactions from in vitro drug discovery data. Nat. Rev. Drug Disc. (2005) 4:825-833. An excellent overview of the principles of in vitro metabolism and DDI work.
    • WEINKERS LC, HEATH GH: Predicting in vivo drug interactions from in vitro drug discovery data. Nat. Rev. Drug Disc. (2005) 4:825-833. An excellent overview of the principles of in vitro metabolism and DDI work.
  • 5
    • 26944495704 scopus 로고    scopus 로고
    • High throughput P450 screens in early drug discovery
    • ZLOKARNIK G, GROOTENHUIS PDJ, WATSON JB: High throughput P450 screens in early drug discovery. Drug Disc. Today (2005) 10(21):1443-1450.
    • (2005) Drug Disc. Today , vol.10 , Issue.21 , pp. 1443-1450
    • ZLOKARNIK, G.1    GROOTENHUIS, P.D.J.2    WATSON, J.B.3
  • 6
    • 0033549087 scopus 로고    scopus 로고
    • The safety of newly approved medicines: Do recent market removals mean there is a problem?
    • FRIEDMAN MA, WOODCOCK JL, LUMPKIN MM, SHUREN JE, HASS AE, THOMPSON I.J: The safety of newly approved medicines: do recent market removals mean there is a problem? JAMA (1999) 281(18):1728-1734.
    • (1999) JAMA , vol.281 , Issue.18 , pp. 1728-1734
    • FRIEDMAN, M.A.1    WOODCOCK, J.L.2    LUMPKIN, M.M.3    SHUREN, J.E.4    HASS, A.E.5    THOMPSON, I.J.6
  • 7
    • 0028818229 scopus 로고
    • Species similarities and differences in pharmacokinetics
    • LIN JH: Species similarities and differences in pharmacokinetics. Drug Metab. Dispos. (1995) 23(10):1008-1021.
    • (1995) Drug Metab. Dispos , vol.23 , Issue.10 , pp. 1008-1021
    • LIN, J.H.1
  • 8
    • 6944221357 scopus 로고    scopus 로고
    • Drug-drug interactions for UDP-glucuronosyltransferase substrates: A pharmacokinetic explanation for typically observed low exposure (AUC/AUC) ratios
    • WILLIAMS JA, HYLAND R, JONES BC et al.: Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUC/AUC) ratios. Drug Metab. Dispos. (2004) 32(11):1201-1208.
    • (2004) Drug Metab. Dispos , vol.32 , Issue.11 , pp. 1201-1208
    • WILLIAMS, J.A.1    HYLAND, R.2    JONES, B.C.3
  • 9
    • 33645471252 scopus 로고    scopus 로고
    • FURGE LL, GUENGERICH FP: Cytochrome P450 enzymes in drug metabolism and chemical toxicity. Biochem. Mol. Biol. Ed. (2006) 34(2):66-74.
    • FURGE LL, GUENGERICH FP: Cytochrome P450 enzymes in drug metabolism and chemical toxicity. Biochem. Mol. Biol. Ed. (2006) 34(2):66-74.
  • 11
    • 11144349691 scopus 로고    scopus 로고
    • High volume bioassays to assess CYP3A4-mediated drug interactions: Induction and inhibition in a single cell line
    • YUEY M-F, KAWAHARA M, RAUCY J: High volume bioassays to assess CYP3A4-mediated drug interactions: induction and inhibition in a single cell line. Drug Metab Dispos. (2005) 33(1):38-48.
    • (2005) Drug Metab Dispos , vol.33 , Issue.1 , pp. 38-48
    • YUEY, M.-F.1    KAWAHARA, M.2    RAUCY, J.3
  • 12
    • 1642273510 scopus 로고    scopus 로고
    • Induction of drug metabolism enzymes and MDR1 using a novel human hepatocyte cell line
    • MILLS BM, ROSE KA, SADAGOPAN N, SAHI J, MORAIS SMF: Induction of drug metabolism enzymes and MDR1 using a novel human hepatocyte cell line. J. Pharm. Exp. Ther. (2004) 309(1):303-309.
    • (2004) J. Pharm. Exp. Ther , vol.309 , Issue.1 , pp. 303-309
    • MILLS, B.M.1    ROSE, K.A.2    SADAGOPAN, N.3    SAHI, J.4    MORAIS, S.M.F.5
  • 13
    • 0033822059 scopus 로고    scopus 로고
    • A fluorescent cell-based assay for cytochrome P450 isozyme 1A2 induction and inhibition
    • KELLY JH, SUSSMAN NL: A fluorescent cell-based assay for cytochrome P450 isozyme 1A2 induction and inhibition. J. Biomol. Screen. (2000) 5(4):249-254.
    • (2000) J. Biomol. Screen , vol.5 , Issue.4 , pp. 249-254
    • KELLY, J.H.1    SUSSMAN, N.L.2
  • 14
    • 0037379409 scopus 로고    scopus 로고
    • Effects of prototypical enzyme inducers on cytochrome P450 expression in cultured hepatocytes
    • MADAN A, GRAHAM RA, CARROLL KM et al.: Effects of prototypical enzyme inducers on cytochrome P450 expression in cultured hepatocytes. Drug Metab. Dispos. (2003) 31(4):421-431.
    • (2003) Drug Metab. Dispos , vol.31 , Issue.4 , pp. 421-431
    • MADAN, A.1    GRAHAM, R.A.2    CARROLL, K.M.3
  • 16
    • 23944516070 scopus 로고    scopus 로고
    • Human CYP2C8 is transcriptionally regulated by the nuclear receptors constitutive androstane receptor, pregnane X receptor, glucocorticoid receptor, and hepatic nuclear factor 4-α
    • FERGUSON SS, CHEN Y, LECLUYSE EL, GOLDSTEIN JA: Human CYP2C8 is transcriptionally regulated by the nuclear receptors constitutive androstane receptor, pregnane X receptor, glucocorticoid receptor, and hepatic nuclear factor 4-α. Mol. Pharmacol. (2005) 68(3):747-757.
    • (2005) Mol. Pharmacol , vol.68 , Issue.3 , pp. 747-757
    • FERGUSON, S.S.1    CHEN, Y.2    LECLUYSE, E.L.3    GOLDSTEIN, J.A.4
  • 17
    • 0042844649 scopus 로고    scopus 로고
    • Identification of constitutive androstane receptor and glucocorticoid receptor binding sites in the CYP2C19 promoter
    • CHEN Y, FERGUSON SS, NEGISGI M, GOLDSTEIN JA: Identification of constitutive androstane receptor and glucocorticoid receptor binding sites in the CYP2C19 promoter. Mol. Pharmacol. (2003) 64(2):316-324.
    • (2003) Mol. Pharmacol , vol.64 , Issue.2 , pp. 316-324
    • CHEN, Y.1    FERGUSON, S.S.2    NEGISGI, M.3    GOLDSTEIN, J.A.4
  • 18
    • 0033990325 scopus 로고    scopus 로고
    • Role of the aromatic hydrocarbon receptor and [Ah] gene battery in the oxidative stress response, cell cycle control, and apoptosis
    • NEBERT DW, ROE AL, DIETER MZ, SOLIS WA, YANG Y, DALTON TP: Role of the aromatic hydrocarbon receptor and [Ah] gene battery in the oxidative stress response, cell cycle control, and apoptosis. Biochem. Pharm. (1999) 59:65-85.
    • (1999) Biochem. Pharm , vol.59 , pp. 65-85
    • NEBERT, D.W.1    ROE, A.L.2    DIETER, M.Z.3    SOLIS, W.A.4    YANG, Y.5    DALTON, T.P.6
  • 19
    • 0037228554 scopus 로고    scopus 로고
    • Differential regulation of human CYP4A genes by peroxisome proliferators and dexamethasone
    • SAVAS U, HSU MH, JOHNSON EF: Differential regulation of human CYP4A genes by peroxisome proliferators and dexamethasone. Arch. Biochem. Biophys. (2003) 409(1):212-220.
    • (2003) Arch. Biochem. Biophys , vol.409 , Issue.1 , pp. 212-220
    • SAVAS, U.1    HSU, M.H.2    JOHNSON, E.F.3
  • 20
    • 24944492194 scopus 로고    scopus 로고
    • Utility of recombinant cytochrome P450 enzymes: A drug metabolism perspective
    • TANG W, WANG RW, LU, AYH: Utility of recombinant cytochrome P450 enzymes: a drug metabolism perspective. Curr. Drug Metab. (2005) 6:503-517.
    • (2005) Curr. Drug Metab , vol.6 , pp. 503-517
    • TANG, W.1    WANG, R.W.2    LU, A.Y.H.3
  • 21
    • 0003518480 scopus 로고
    • John Wiley & Sons, Canada , A classic text on rapid equilibrium and steady-state enzyme systems
    • SEGEL IH: Enzyme kinetics. John Wiley & Sons, Canada (1975). A classic text on rapid equilibrium and steady-state enzyme systems.
    • (1975) Enzyme kinetics
    • SEGEL, I.H.1
  • 22
    • 0031777718 scopus 로고    scopus 로고
    • ITO K, IWATSUBO T, KANAMITSU S, NAKAJIMA Y, SUGIYAMA Y: Quantitative prediction of in vivo drug clearance and drug interactions from in vitro data on metabolism, together with binding and transport. Ann. Rev. Pharmacol. Toxicol. (1998) 38:461-499. A good description of how in vitro data is used to predict in vivo effects.
    • ITO K, IWATSUBO T, KANAMITSU S, NAKAJIMA Y, SUGIYAMA Y: Quantitative prediction of in vivo drug clearance and drug interactions from in vitro data on metabolism, together with binding and transport. Ann. Rev. Pharmacol. Toxicol. (1998) 38:461-499. A good description of how in vitro data is used to predict in vivo effects.
  • 23
    • 0032480765 scopus 로고    scopus 로고
    • Site-directed mutagenesis of histidine 245 in firefly luciferase: A proposed model of the active site
    • BRANCHINI BR, MAGYAR RA, MURTIASHAW MH, ANDERSON SM, ZIMMER M: Site-directed mutagenesis of histidine 245 in firefly luciferase: a proposed model of the active site. Biochemistry (1998) 37(44):15311-15319.
    • (1998) Biochemistry , vol.37 , Issue.44 , pp. 15311-15319
    • BRANCHINI, B.R.1    MAGYAR, R.A.2    MURTIASHAW, M.H.3    ANDERSON, S.M.4    ZIMMER, M.5
  • 25
    • 0034973773 scopus 로고    scopus 로고
    • GUENGERICH FP: Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity. Chem. Res. Toxicol. (2001) 14(6):611-650. An excellent review of the CYP reaction cycle and reaction mechanisms.
    • GUENGERICH FP: Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity. Chem. Res. Toxicol. (2001) 14(6):611-650. An excellent review of the CYP reaction cycle and reaction mechanisms.
  • 26
    • 33846269843 scopus 로고    scopus 로고
    • CALI JJ, HO S, MA D et al.: Bioluminescent P450 assays that use D-luciferin derivatives as substrates for CYP1A1, 1A2, 1B1, 2C8, 2C9, 2J2, 3A4, 3A7,4A11, 4F3B, 4F12 and 19. Proceedings of the 14th International Conference on Cytochrome P450s-Medimond S.r.l. International Proceedings. (2005):77-84.
    • CALI JJ, HO S, MA D et al.: Bioluminescent P450 assays that use D-luciferin derivatives as substrates for CYP1A1, 1A2, 1B1, 2C8, 2C9, 2J2, 3A4, 3A7,4A11, 4F3B, 4F12 and 19. Proceedings of the 14th International Conference on Cytochrome P450s-Medimond S.r.l. International Proceedings. (2005):77-84.
  • 27
    • 33846332233 scopus 로고    scopus 로고
    • P450-Glo™ CYP2C19 and CYP2D6 assays
    • Includes a discussion of CYP2D6 and -2C19 luminogenic substrate selectivity
    • CALI JJ, SOBOL M, MA D, GOOD T, LIU D: P450-Glo™ CYP2C19 and CYP2D6 assays. Cell Notes (2006) 14:20-24. Includes a discussion of CYP2D6 and -2C19 luminogenic substrate selectivity.
    • (2006) Cell Notes , vol.14 , pp. 20-24
    • CALI, J.J.1    SOBOL, M.2    MA, D.3    GOOD, T.4    LIU, D.5
  • 28
    • 28744439821 scopus 로고    scopus 로고
    • Catalytic activities of human cytochrome P450 2C9*1, 2C9*3 and 2C9*13
    • GUO Y, WANG Y, SI D, FAWCETT PJ, ZHONG D, ZHOU H: Catalytic activities of human cytochrome P450 2C9*1, 2C9*3 and 2C9*13. Xenobiotica (2005) 35(9):853-861.
    • (2005) Xenobiotica , vol.35 , Issue.9 , pp. 853-861
    • GUO, Y.1    WANG, Y.2    SI, D.3    FAWCETT, P.J.4    ZHONG, D.5    ZHOU, H.6
  • 29
    • 33846335032 scopus 로고    scopus 로고
    • Comparison of 'high throughput' micromethods for determination of cytochrome P450 activities with classical methods using HPLC for product identification
    • ANZENBACHEROVA E, VEINLICHOVA A, MASEK V ANZENBACHER P: Comparison of 'high throughput' micromethods for determination of cytochrome P450 activities with classical methods using HPLC for product identification. Biomed. Pap. Med. Fac. Univ. Palacky Olomouc Czech Repub. (2005) 149(2):353-355.
    • (2005) Biomed. Pap. Med. Fac. Univ. Palacky Olomouc Czech Repub , vol.149 , Issue.2 , pp. 353-355
    • ANZENBACHEROVA, E.1    VEINLICHOVA, A.2    MASEK, V.3    ANZENBACHER, P.4
  • 34
    • 0033607201 scopus 로고    scopus 로고
    • Diclofenac and its derivatives as tools for studying human cytochromes P450 active sites: Particular efficiency and regioselectivity of P450 2Cs
    • MANCY A, ANTIGNAC M, MINOLETTI C et al.: Diclofenac and its derivatives as tools for studying human cytochromes P450 active sites: particular efficiency and regioselectivity of P450 2Cs. Biochemistry (1999) 38:14264-14270.
    • (1999) Biochemistry , vol.38 , pp. 14264-14270
    • MANCY, A.1    ANTIGNAC, M.2    MINOLETTI, C.3
  • 35
    • 0036264528 scopus 로고    scopus 로고
    • 4-Hydroxylation of debrisoquine by human CYP1A1 and its inhibition by quinidine and quinine
    • GRANVIL CP, KRAUSZ KW, GELBOIN HV, IDLE JR, GONZALEZ FJ: 4-Hydroxylation of debrisoquine by human CYP1A1 and its inhibition by quinidine and quinine. J. Pharmacol. Exp. Ther. (2002) 301(3):1025-1032.
    • (2002) J. Pharmacol. Exp. Ther , vol.301 , Issue.3 , pp. 1025-1032
    • GRANVIL, C.P.1    KRAUSZ, K.W.2    GELBOIN, H.V.3    IDLE, J.R.4    GONZALEZ, F.J.5
  • 36
    • 0033664783 scopus 로고    scopus 로고
    • Substrate-dependent modulation of CYP3A4 catalytic activity: Analysis of 27 test compounds with four fluorometric substrates
    • STRESSER DM, BLANCHARD AP, TURNER SD et al.: Substrate-dependent modulation of CYP3A4 catalytic activity: analysis of 27 test compounds with four fluorometric substrates. Drug Metab. Dispos. (2000) 28(12):1440-1448.
    • (2000) Drug Metab. Dispos , vol.28 , Issue.12 , pp. 1440-1448
    • STRESSER, D.M.1    BLANCHARD, A.P.2    TURNER, S.D.3
  • 37
    • 0031466149 scopus 로고    scopus 로고
    • Nonspecific binding to microsomes: Impact on scale-up of in vitro intrinsic clearance to hepatic clearance as assessed through examination of warfarin, imipramine, and propranolol
    • OBACH RS: Nonspecific binding to microsomes: impact on scale-up of in vitro intrinsic clearance to hepatic clearance as assessed through examination of warfarin, imipramine, and propranolol. Drug Metab. Dispos. (1997) 25(12):1359-1369.
    • (1997) Drug Metab. Dispos , vol.25 , Issue.12 , pp. 1359-1369
    • OBACH, R.S.1
  • 38
    • 14044251501 scopus 로고    scopus 로고
    • The binding of drugs to hepatocytes and its relationship to physicochemical properties
    • AUSTIN RP, BARTON P, MOHMED S, RILEY RJ: The binding of drugs to hepatocytes and its relationship to physicochemical properties. Drug Metab. Dispos. (2005) 33(3):419-425.
    • (2005) Drug Metab. Dispos , vol.33 , Issue.3 , pp. 419-425
    • AUSTIN, R.P.1    BARTON, P.2    MOHMED, S.3    RILEY, R.J.4
  • 39
    • 0033003760 scopus 로고    scopus 로고
    • A simple statistical parameter for use in evaluation and validation of high throughput screening assays
    • A quantitative approach for measuring assay quality
    • ZHANG J-H, CHUNG TDY, OLDENBURG KR: A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J. Biomol. Scr. (1999) 4:67-73. A quantitative approach for measuring assay quality.
    • (1999) J. Biomol. Scr , vol.4 , pp. 67-73
    • J-H, Z.1    CHUNG TDY, O.K.R.2
  • 41
    • 0034093628 scopus 로고    scopus 로고
    • Human cytochrome P450 3A4: In vitro drug-drug interactions patterns are substrate-dependent
    • WANG RW, NEWTON DJ, LIU N, ATKINS WM, LU AYH: Human cytochrome P450 3A4: in vitro drug-drug interactions patterns are substrate-dependent. Drug Metab. Dispos. (2000) 28(3):360-366.
    • (2000) Drug Metab. Dispos , vol.28 , Issue.3 , pp. 360-366
    • WANG, R.W.1    NEWTON, D.J.2    LIU, N.3    ATKINS, W.M.4    LU, A.Y.H.5
  • 42
    • 0034705191 scopus 로고    scopus 로고
    • Elucidation of distinct binding sites for cytochrome P450 3A4
    • HOSEA NA, MILLER GP, GUENGERICH FP: Elucidation of distinct binding sites for cytochrome P450 3A4. Biochemistry (2000) 39:5929-5939.
    • (2000) Biochemistry , vol.39 , pp. 5929-5939
    • HOSEA, N.A.1    MILLER, G.P.2    GUENGERICH, F.P.3
  • 43
    • 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: Dapsone activation of CYP2C9-mediated metabolism: evidence for activation of multiple substrates and a two-site model. Drug Metab. Dispos. (2001) 29(7):1029-1034.
    • (2001) Drug Metab. Dispos , vol.29 , Issue.7 , pp. 1029-1034
    • HUTZLER, J.M.1    HAUER, M.J.2    TRACY, T.S.3
  • 44
    • 2942711686 scopus 로고    scopus 로고
    • Differential contributions of active site residues in substrate recognition sites 1 and 5 to cytochrome P450 2C8 substrate selectivity and regioselectivity
    • KERDPIN O, ELLIOT DJ, BOYE SL, BIRKETT DJ, YOOVATHAWORN K, MINERS JO: Differential contributions of active site residues in substrate recognition sites 1 and 5 to cytochrome P450 2C8 substrate selectivity and regioselectivity. Biochemistry (2004) 43(24):7834-7842.
    • (2004) Biochemistry , vol.43 , Issue.24 , pp. 7834-7842
    • KERDPIN, O.1    ELLIOT, D.J.2    BOYE, S.L.3    BIRKETT, D.J.4    YOOVATHAWORN, K.5    MINERS, J.O.6
  • 45
    • 0035964178 scopus 로고    scopus 로고
    • Phenylalanine and tryptophan scanning mutagenesis of CYP3A4 substrate recognition site residues and effect on substrate oxidation and cooperativity
    • DOMANSKI TL, HE Y-A, KHAN KK, ROUSSEL F, WANG Q, HALPERT JR: Phenylalanine and tryptophan scanning mutagenesis of CYP3A4 substrate recognition site residues and effect on substrate oxidation and cooperativity. Biochemistry (2001) 40:10150-10160.
    • (2001) Biochemistry , vol.40 , pp. 10150-10160
    • DOMANSKI, T.L.1    HE, Y.-A.2    KHAN, K.K.3    ROUSSEL, F.4    WANG, Q.5    HALPERT, J.R.6
  • 46
    • 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
    • TESTINA SA Jr, PATONAY G: 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. (2003) 30(5):1459-1467.
    • (2003) J. Pharm. Biomed. Anal , vol.30 , Issue.5 , pp. 1459-1467
    • TESTINA Jr, S.A.1    PATONAY, G.2
  • 47
    • 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 KS, BEATTIE IG, RILEY RJ: Cytochrome P450 inhibition using recombinant proteins and mass spectrometry/multiple reaction monitoring technology in a cassette incubation. Drug Metab. Dispos. (2003) 31(7):955-966.
    • (2003) Drug Metab. Dispos , vol.31 , Issue.7 , pp. 955-966
    • WEAVER, R.1    GRAHAM, K.S.2    BEATTIE, I.G.3    RILEY, R.J.4
  • 48
    • 0032970480 scopus 로고    scopus 로고
    • Fully automated analysis of activities catalysed by the major human liver cytochrome P450 (CYP) enzymes: Assessment of human CYP inhibition potential
    • MOODY GC, GRIFFIN SJ, MATHER AN, MCGINNITY DF, RILEY RJ: Fully automated analysis of activities catalysed by the major human liver cytochrome P450 (CYP) enzymes: assessment of human CYP inhibition potential. Xenobiotica (1999) 29(1):53-75.
    • (1999) Xenobiotica , vol.29 , Issue.1 , pp. 53-75
    • MOODY, G.C.1    GRIFFIN, S.J.2    MATHER, A.N.3    MCGINNITY, D.F.4    RILEY, R.J.5
  • 49
    • 17844378465 scopus 로고    scopus 로고
    • The potential for CYP2D6 inhibition screening using a novel scintillation proximity assay-based approach
    • DELAPORTE E, SLAUGHTER DE, EGAN MA et al.: The potential for CYP2D6 inhibition screening using a novel scintillation proximity assay-based approach. J. Biomol. Screen. (2001) 6(4):225-231.
    • (2001) J. Biomol. Screen , vol.6 , Issue.4 , pp. 225-231
    • DELAPORTE, E.1    SLAUGHTER, D.E.2    EGAN, M.A.3
  • 51
    • 0025179066 scopus 로고
    • Fluorescnece assay for per-cell estimation of cytochrome P450-dependent monooxygenase activitities in keratinocyte suspensions and cultures
    • REINERS JJ, CANTU AR, PAVONE A, SMITH SC, GARDNER CR, LASKIN DL: Fluorescnece assay for per-cell estimation of cytochrome P450-dependent monooxygenase activitities in keratinocyte suspensions and cultures. Anal. Biochem. (1990) 188:317-324.
    • (1990) Anal. Biochem , vol.188 , pp. 317-324
    • REINERS, J.J.1    CANTU, A.R.2    PAVONE, A.3    SMITH, S.C.4    GARDNER, C.R.5    LASKIN, D.L.6
  • 53
    • 18844404436 scopus 로고    scopus 로고
    • Using IMAP technology to identify kinase inhibitors: Comparison with a substrate depletion approach and analysis of the nature of false positives
    • SINGH P, LILLYWHITE B, BANNAGHAN C, BROAD P: Using IMAP technology to identify kinase inhibitors: comparison with a substrate depletion approach and analysis of the nature of false positives. Comb. Chem. High Throughput Screen. (2005) 8(4):319-325.
    • (2005) Comb. Chem. High Throughput Screen , vol.8 , Issue.4 , pp. 319-325
    • SINGH, P.1    LILLYWHITE, B.2    BANNAGHAN, C.3    BROAD, P.4
  • 54
    • 0034013033 scopus 로고    scopus 로고
    • Assessment of specificity of eight chemical inhibitors using cDNA-expressed cytochromes P450
    • SAI Y, DAI R, YANG TJ et al.: Assessment of specificity of eight chemical inhibitors using cDNA-expressed cytochromes P450. Xenobiotica (2000) 30(4):327-343.
    • (2000) Xenobiotica , vol.30 , Issue.4 , pp. 327-343
    • SAI, Y.1    DAI, R.2    YANG, T.J.3
  • 55
    • 0028174881 scopus 로고
    • Evaluation of triaceryloleandomycin, α-naphthoflavone and diethyldithiocarbamate as selective chemical probes for inhibition of human cytochromes P450
    • CHANG TKH, GONZALEZ FJ, WAXMAN DJ: Evaluation of triaceryloleandomycin, α-naphthoflavone and diethyldithiocarbamate as selective chemical probes for inhibition of human cytochromes P450. Arch. Biochem. Biophys. (1994) 311(2):437-442.
    • (1994) Arch. Biochem. Biophys , vol.311 , Issue.2 , pp. 437-442
    • CHANG, T.K.H.1    GONZALEZ, F.J.2    WAXMAN, D.J.3
  • 56
    • 1642498315 scopus 로고    scopus 로고
    • Highly selective inhibition of human CYP3A in vitro by azamulin and evidence that inhibition is irreversible
    • STRESSER DM, BROUDY MI, HO T et al.: Highly selective inhibition of human CYP3A in vitro by azamulin and evidence that inhibition is irreversible. Drug Metab. Dispos. (2004) 32(1):105-112.
    • (2004) Drug Metab. Dispos , vol.32 , Issue.1 , pp. 105-112
    • STRESSER, D.M.1    BROUDY, M.I.2    HO, T.3
  • 57
    • 0033966832 scopus 로고    scopus 로고
    • Fluvoxamine-clozapine drug interaction: Inhibition in vitro of five cytochrome P450 isoforms involved in clozapine metabolism
    • OLESEN OV, LINNET K: Fluvoxamine-clozapine drug interaction: inhibition in vitro of five cytochrome P450 isoforms involved in clozapine metabolism. J. Clin. Psychopharmacol. (2000) 20(1):35-42.
    • (2000) J. Clin. Psychopharmacol , vol.20 , Issue.1 , pp. 35-42
    • OLESEN, O.V.1    LINNET, K.2
  • 58
    • 0031570357 scopus 로고    scopus 로고
    • Microtiter plate assays for inhibition of human, drug-metabolizing cytochrome P450
    • CRESPI CL, MILLER VP, PENMAN BW: Microtiter plate assays for inhibition of human, drug-metabolizing cytochrome P450. Anal. Biochem. (1997) 248:188-190.
    • (1997) Anal. Biochem , vol.248 , pp. 188-190
    • CRESPI, C.L.1    MILLER, V.P.2    PENMAN, B.W.3
  • 60
    • 0033997634 scopus 로고    scopus 로고
    • Automated high throughput human CYP isoform activity assay using SPE-LC/MS method: Application in CYP inhibition evaluation
    • YIN H, RACHA J, LI S-Y, OLEJNIK N, SATOH H, MOORE D: Automated high throughput human CYP isoform activity assay using SPE-LC/MS method: application in CYP inhibition evaluation. Xenobiotica (2000) 30(2):141-154.
    • (2000) Xenobiotica , vol.30 , Issue.2 , pp. 141-154
    • YIN, H.1    RACHA, J.2    LI, S.-Y.3    OLEJNIK, N.4    SATOH, H.5    MOORE, D.6
  • 61
    • 0037378805 scopus 로고    scopus 로고
    • Cytochrome P450 2C8 and flavin-containing monooxygenases are involved in the metabolism of tazarotenic acid in humans
    • ATTAR M, DONG D, LING K-HJ, TANG-LIU DD-S: Cytochrome P450 2C8 and flavin-containing monooxygenases are involved in the metabolism of tazarotenic acid in humans. Drug Metab. Dispos. (2003) 31(4):476-481.
    • (2003) Drug Metab. Dispos , vol.31 , Issue.4 , pp. 476-481
    • ATTAR, M.1    DONG, D.2    LING, K.-H.J.3    TANG-LIU, D.D.-S.4
  • 62
    • 0036266778 scopus 로고    scopus 로고
    • Trimethoprim and sulfamethoxazole are selective inhibitors of CYP2C8 and CYP2C9, respectively
    • WEN X, WANG J-S, BACKMAN JT, LAITILA J, NEUVONEN PJ: Trimethoprim and sulfamethoxazole are selective inhibitors of CYP2C8 and CYP2C9, respectively. Drug Metab. Dispos. (2002) 30(6):631-635.
    • (2002) Drug Metab. Dispos , vol.30 , Issue.6 , pp. 631-635
    • WEN, X.1    WANG, J.-S.2    BACKMAN, J.T.3    LAITILA, J.4    NEUVONEN, P.J.5
  • 63
    • 0023924549 scopus 로고
    • In vitro inhibition studies of tolbutamide hydroxylase activity of human liver microsomes by azotes, sulphonamides and quinolines
    • BACK DJ, TJIA JF, KARBWANG J COLBERT J: In vitro inhibition studies of tolbutamide hydroxylase activity of human liver microsomes by azotes, sulphonamides and quinolines. Br. J. Clin. Pharm. (1988) 26:23-29.
    • (1988) Br. J. Clin. Pharm , vol.26 , pp. 23-29
    • BACK, D.J.1    TJIA, J.F.2    KARBWANG, J.3    COLBERT, J.4
  • 64
    • 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 KS, BEATTIE IG, RILEY RJ: Cytochrome P450 inhibition using recombinant proteins and mass spectrometry/multiple reaction monitoring technology in a cassette incubation. Drug Metab. Dispos. (2003) 31(7):955-966.
    • (2003) Drug Metab. Dispos , vol.31 , Issue.7 , pp. 955-966
    • WEAVER, R.1    GRAHAM, K.S.2    BEATTIE, I.G.3    RILEY, R.J.4
  • 65
    • 0033954725 scopus 로고    scopus 로고
    • In vitro inhibitory effects of troglitazone and its metabolites on drug oxidation activities of human cytochrome P450 enzymes: Comparison with pioglitazone and rosiglitazone
    • YAMAZAKI H, SUZUKI M, TANE K, SHIMADA N, NAKAJIMA M, YOKOI T: In vitro inhibitory effects of troglitazone and its metabolites on drug oxidation activities of human cytochrome P450 enzymes: comparison with pioglitazone and rosiglitazone. Xenobiotica (2000) 30(1):61-70.
    • (2000) Xenobiotica , vol.30 , Issue.1 , pp. 61-70
    • YAMAZAKI, H.1    SUZUKI, M.2    TANE, K.3    SHIMADA, N.4    NAKAJIMA, M.5    YOKOI, T.6
  • 66
    • 0035144768 scopus 로고    scopus 로고
    • DESTA Z, SOUKHOVA NV, FLOCKHART DA: Inhibition of cytochrome P450 (CYP450 isoforms by isoniazid: potent inhibition of CYP2C19 and CYP3A. Antimicrob. Agents Chemother. (2001) 45(2):382-392.
    • DESTA Z, SOUKHOVA NV, FLOCKHART DA: Inhibition of cytochrome P450 (CYP450 isoforms by isoniazid: potent inhibition of CYP2C19 and CYP3A. Antimicrob. Agents Chemother. (2001) 45(2):382-392.
  • 67
    • 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.: Stereoselective inhibition of cytochrome P450 forms by lansoprazole and omeprazole in vitro. Xenobiotica (2005) 35(1):27-38.
    • (2005) Xenobiotica , vol.35 , Issue.1 , pp. 27-38
    • LIU, K.H.1    KIM, M.J.2    SHON, J.H.3
  • 68
    • 0141520307 scopus 로고    scopus 로고
    • High-throughput screening to estimate single or multiple enzymes involved in drug metabolism: Microtitre plate assay using a combination of recombinant CYP2D6 and human liver microsomes
    • YAMAMOTO T, SUZUKI A, KOHNO Y: High-throughput screening to estimate single or multiple enzymes involved in drug metabolism: microtitre plate assay using a combination of recombinant CYP2D6 and human liver microsomes. Xenobiotica (2003) 33(8):823-839.
    • (2003) Xenobiotica , vol.33 , Issue.8 , pp. 823-839
    • YAMAMOTO, T.1    SUZUKI, A.2    KOHNO, Y.3
  • 70
    • 0035032365 scopus 로고    scopus 로고
    • Development of a miniaturized 384-well high throughput screen for detection of substrates of cytochrome P450 2D6 and 3A4 metabolism
    • KARIV I, FERESHTEH MP, OLDENBURG KR: Development of a miniaturized 384-well high throughput screen for detection of substrates of cytochrome P450 2D6 and 3A4 metabolism. J. Biomol. Screen. (2001) 6(2):91-99.
    • (2001) J. Biomol. Screen , vol.6 , Issue.2 , pp. 91-99
    • KARIV, I.1    FERESHTEH, M.P.2    OLDENBURG, K.R.3
  • 71
    • 17844378465 scopus 로고    scopus 로고
    • The potential for CYP2D6 inhibition screening using a novel scintillation proximity assay-based approach
    • DELAPORTE E, SLAUGHTER DE, EGAN MA et al.: The potential for CYP2D6 inhibition screening using a novel scintillation proximity assay-based approach. J. Biomol. Screen. (2001) 6(4):225-231.
    • (2001) J. Biomol. Screen , vol.6 , Issue.4 , pp. 225-231
    • DELAPORTE, E.1    SLAUGHTER, D.E.2    EGAN, M.A.3
  • 72
    • 0033959578 scopus 로고    scopus 로고
    • Drug interactions with calcium channel blockers: Possible involvement of metabolite-intermediate complexation with CYP3A
    • MA B, PRUEKSARITANONT T, LIN JH: Drug interactions with calcium channel blockers: possible involvement of metabolite-intermediate complexation with CYP3A. Drug Metab. Dispos. (2000) 28(2):125-130.
    • (2000) Drug Metab. Dispos , vol.28 , Issue.2 , pp. 125-130
    • MA, B.1    PRUEKSARITANONT, T.2    LIN, J.H.3
  • 73
    • 85019511919 scopus 로고    scopus 로고
    • Substrate dependent inhibition profiles of fourteen drugs on CYP3A4 activity measured by a high throughput LCMS/MS method with four probe drugs, midazolam, testosterone, nifedipine and terfenadine
    • RACHA JK, ZHAO ZS, OLEJNIK N et al.: Substrate dependent inhibition profiles of fourteen drugs on CYP3A4 activity measured by a high throughput LCMS/MS method with four probe drugs, midazolam, testosterone, nifedipine and terfenadine. Drug Metab. Pharmacokinet. (2003) 18(2):128-138.
    • (2003) Drug Metab. Pharmacokinet , vol.18 , Issue.2 , pp. 128-138
    • RACHA, J.K.1    ZHAO, Z.S.2    OLEJNIK, N.3
  • 75
    • 0034950245 scopus 로고    scopus 로고
    • Development of a generalized, quantitative physicochemical model of CYP3A4 inhibition for use in early drug discovery
    • RILEY RJ, PARKER AJ, TRIGG S, MANNERS CN: Development of a generalized, quantitative physicochemical model of CYP3A4 inhibition for use in early drug discovery. Pharm. Res. (2001) 18(5):652-655.
    • (2001) Pharm. Res , vol.18 , Issue.5 , pp. 652-655
    • RILEY, R.J.1    PARKER, A.J.2    TRIGG, S.3    MANNERS, C.N.4
  • 76
    • 0037369521 scopus 로고    scopus 로고
    • Assessment of the contributions of CYP3A4 and CYP3A5 in the metabolism of the antipsychotic agent haloperidol to its potentially neurotoxic pyridinium metabolite and effect of antidepressants on the bioactivation pathway
    • KALGUTKAR AS, TAYLOR TJ, VENKATAKRISHNAN K, ISIN EM: Assessment of the contributions of CYP3A4 and CYP3A5 in the metabolism of the antipsychotic agent haloperidol to its potentially neurotoxic pyridinium metabolite and effect of antidepressants on the bioactivation pathway. Drug Metab. Dispos. (2003) 31(3):243-249.
    • (2003) Drug Metab. Dispos , vol.31 , Issue.3 , pp. 243-249
    • KALGUTKAR, A.S.1    TAYLOR, T.J.2    VENKATAKRISHNAN, K.3    ISIN, E.M.4
  • 77
    • 0842347425 scopus 로고    scopus 로고
    • Differential enantioselectivity and product-dependent activation and inhibition in metabolism of verapamil by human CYP3As
    • SHEN L, FITZLOFF JF, COOK CS: Differential enantioselectivity and product-dependent activation and inhibition in metabolism of verapamil by human CYP3As. Drug Metab. Dispos. (2004) 32(2):186-196.
    • (2004) Drug Metab. Dispos , vol.32 , Issue.2 , pp. 186-196
    • SHEN, L.1    FITZLOFF, J.F.2    COOK, C.S.3
  • 78
    • 0037389628 scopus 로고    scopus 로고
    • In vitro and pharmacophore insights into CYP3A enzymes
    • EKINS S, STRESSER DM, WILLIAMS JA: In vitro and pharmacophore insights into CYP3A enzymes. Trends Pharmacol. Sci. (2003) 24(4):161-166.
    • (2003) Trends Pharmacol. Sci , vol.24 , Issue.4 , pp. 161-166
    • EKINS, S.1    STRESSER, D.M.2    WILLIAMS, J.A.3
  • 79
    • 33846292064 scopus 로고    scopus 로고
    • Jackson Gastroenterology Patient ed
    • http://www.gicare.com/pated/cimetidine.htm Jackson Gastroenterology Patient ed. (1998).
    • (1998)
  • 80
    • 33846292413 scopus 로고    scopus 로고
    • http://www.promega.com/ Technical Resources, Promega Corp. website, see Technical Bulletin #325. Detailed luminogenic CYP assay protocols.
    • http://www.promega.com/ Technical Resources, Promega Corp. website, see Technical Bulletin #325. Detailed luminogenic CYP assay protocols.
  • 81
    • 33846316215 scopus 로고    scopus 로고
    • http://www.promega.com/ Technical Resources, Promega Corp. website, see Technical Bulletin #340. Detailed luminogenic CYP assay protocols.
    • http://www.promega.com/ Technical Resources, Promega Corp. website, see Technical Bulletin #340. Detailed luminogenic CYP assay protocols.
  • 82
    • 33846279615 scopus 로고    scopus 로고
    • screening kit protocols
    • http://www.invitrogen.com/content/sfs/man uals/O-13873-rl%20US%200405.pdf Vivid CYP450 screening kit protocols.


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