메뉴 건너뛰기




Volumn 35, Issue 12, 2007, Pages 2159-2165

Progress curve analysis of CYP1A2 inhibition: A more informative approach to the assessment of mechanism-based inactivation?

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 1A2; DIHYDRALAZINE; FURAFYLLINE; OLTIPRAZ; PAROXETINE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; RESVERATROL;

EID: 36349009310     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.107.017236     Document Type: Article
Times cited : (31)

References (24)
  • 1
    • 27444445468 scopus 로고    scopus 로고
    • Prediction of in vivo drug-drug interactions from in-vitro data: Impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant
    • Brown HS, Ito K, Galetin A, and Houston JB (2005) Prediction of in vivo drug-drug interactions from in-vitro data: impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant. Br J Clin Pharmacol 60:508-518.
    • (2005) Br J Clin Pharmacol , vol.60 , pp. 508-518
    • Brown, H.S.1    Ito, K.2    Galetin, A.3    Houston, J.B.4
  • 2
    • 0035192944 scopus 로고    scopus 로고
    • Differential inhibition & inactivation of Human CYP1 enzymes by trans resveratrol: Evidence for mechanism-based inhibition of CYP1A2
    • Chang TKH, Chen J, and Lee WBK (2001) Differential inhibition & inactivation of Human CYP1 enzymes by trans resveratrol: evidence for mechanism-based inhibition of CYP1A2. J Pharmacol Exp Ther 299:874-882.
    • (2001) J Pharmacol Exp Ther , vol.299 , pp. 874-882
    • Chang, T.K.H.1    Chen, J.2    Lee, W.B.K.3
  • 3
    • 0035949433 scopus 로고    scopus 로고
    • Structural and mechanistic insight into the inhibition of aspartic proteases by a slow-tight binding inhibitor from an extremophilic Bacillus sp.: Correlation of the kinetic parameters with the inhibitor induced conformational changes
    • Dash C, Phadtare S, Deshpande V, and Rao M (2001) Structural and mechanistic insight into the inhibition of aspartic proteases by a slow-tight binding inhibitor from an extremophilic Bacillus sp.: correlation of the kinetic parameters with the inhibitor induced conformational changes. Biochemistry 40:11525-11532.
    • (2001) Biochemistry , vol.40 , pp. 11525-11532
    • Dash, C.1    Phadtare, S.2    Deshpande, V.3    Rao, M.4
  • 4
    • 33645980647 scopus 로고    scopus 로고
    • A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro to in vivo extrapolation
    • Ghanbari F, Rowland-Yeo K, Bloomer JC, Clarke SE, Lennard MS, Tucker GT, and Rostami-Hodjegan A (2006) A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro to in vivo extrapolation. Curr Drug Metab 7:315-334.
    • (2006) Curr Drug Metab , vol.7 , pp. 315-334
    • Ghanbari, F.1    Rowland-Yeo, K.2    Bloomer, J.C.3    Clarke, S.E.4    Lennard, M.S.5    Tucker, G.T.6    Rostami-Hodjegan, A.7
  • 5
    • 18844369894 scopus 로고    scopus 로고
    • Impact of parallel pathways of drug elimination and multiple cytochrome P450 involvement on drug-drug interactions: CYP2D6 paradigm
    • Ito K, Halifax D, Obach RS, and Houston JB (2005) Impact of parallel pathways of drug elimination and multiple cytochrome P450 involvement on drug-drug interactions: CYP2D6 paradigm. Drug Metab Dispos 33:837-844.
    • (2005) Drug Metab Dispos , vol.33 , pp. 837-844
    • Ito, K.1    Halifax, D.2    Obach, R.S.3    Houston, J.B.4
  • 6
    • 73649151319 scopus 로고
    • Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase
    • Kitz R and Wilson IB (1962) Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase. J Biol Chem 237:3245-3249.
    • (1962) J Biol Chem , vol.237 , pp. 3245-3249
    • Kitz, R.1    Wilson, I.B.2
  • 7
    • 0027380074 scopus 로고
    • Isoform-selective mechanism-based inhibition of human cytochrome P450 1A2 by furafylline
    • Kunze KL and Trager WF (1993) Isoform-selective mechanism-based inhibition of human cytochrome P450 1A2 by furafylline. Chem Res Toxicol 6:646-656.
    • (1993) Chem Res Toxicol , vol.6 , pp. 646-656
    • Kunze, K.L.1    Trager, W.F.2
  • 8
    • 0034014663 scopus 로고    scopus 로고
    • Inhibition of human cytochrome P450 enzymes by 1,2-dithiole-3-thione, oltipraz and its derivatives, and sulphaphane
    • Langouet S, Furge L, Kerriguy N, Nakamura K, Guillouzo A, and Guengerich FP (2000) Inhibition of human cytochrome P450 enzymes by 1,2-dithiole-3-thione, oltipraz and its derivatives, and sulphaphane. Chem Res Toxicol 13:245-252.
    • (2000) Chem Res Toxicol , vol.13 , pp. 245-252
    • Langouet, S.1    Furge, L.2    Kerriguy, N.3    Nakamura, K.4    Guillouzo, A.5    Guengerich, F.P.6
  • 9
    • 0031794361 scopus 로고    scopus 로고
    • Inhibition and induction of cytochrome P450 and the clinical implications
    • Lin JH and Lu AYH (1998) Inhibition and induction of cytochrome P450 and the clinical implications. Clin Pharmacokinet 35:361-390.
    • (1998) Clin Pharmacokinet , vol.35 , pp. 361-390
    • Lin, J.H.1    Lu, A.Y.H.2
  • 10
    • 0032706108 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochrome P450s 1A2 & 3A4 by dihydralazine in human liver microsomes
    • Masubuchi Y and Horie T (1999) Mechanism-based inactivation of cytochrome P450s 1A2 & 3A4 by dihydralazine in human liver microsomes. Chem Res Toxicol 12:1028-1032.
    • (1999) Chem Res Toxicol , vol.12 , pp. 1028-1032
    • Masubuchi, Y.1    Horie, T.2
  • 11
    • 0033743402 scopus 로고    scopus 로고
    • Impact of mechanism-based inactivation on inhibitor potency: Implications for rational drug discovery
    • Maurer ST, Tabrizi-Fard, and Fung HL (2000) Impact of mechanism-based inactivation on inhibitor potency: implications for rational drug discovery. J Pharm Sci 89:1404-1412.
    • (2000) J Pharm Sci , vol.89 , pp. 1404-1412
    • Maurer, S.T.1    Tabrizi-Fard2    Fung, H.L.3
  • 12
    • 0023728105 scopus 로고
    • The behavior and significance of slow-binding enzyme inhibitors
    • Morrison JF and Walsh CT (1988) The behavior and significance of slow-binding enzyme inhibitors. Adv Enzymol Relat Areas Mol Biol 61:201-301.
    • (1988) Adv Enzymol Relat Areas Mol Biol , vol.61 , pp. 201-301
    • Morrison, J.F.1    Walsh, C.T.2
  • 14
    • 33846449874 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions
    • Obach RS, Walsky RL, and Venkatakrishnan K (2007) Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions. Drug Metab Dispos 35:246-255.
    • (2007) Drug Metab Dispos , vol.35 , pp. 246-255
    • Obach, R.S.1    Walsky, R.L.2    Venkatakrishnan, K.3
  • 15
    • 0018722047 scopus 로고
    • Kinetic analysis of progress curves
    • Orson BA and Tipton KF (1979) Kinetic analysis of progress curves. Methods Enzymol 63:159-183.
    • (1979) Methods Enzymol , vol.63 , pp. 159-183
    • Orson, B.A.1    Tipton, K.F.2
  • 17
    • 0028930481 scopus 로고
    • Mechanism-based enzyme inactivators
    • Silverman RB (1995) Mechanism-based enzyme inactivators. Methods Enzymol 249:240-283.
    • (1995) Methods Enzymol , vol.249 , pp. 240-283
    • Silverman, R.B.1
  • 18
    • 0029089652 scopus 로고
    • Determination of human hepatic cytochrome P4501A2 activity in vitro use of tacrine as an isoenzyme-specific probe
    • Spaldin V, Madden S, Adams DA, Edwards RJ, Davies DS, and Park BK (1995) Determination of human hepatic cytochrome P4501A2 activity in vitro use of tacrine as an isoenzyme-specific probe. Drug Metab Dispos 23:929-934.
    • (1995) Drug Metab Dispos , vol.23 , pp. 929-934
    • Spaldin, V.1    Madden, S.2    Adams, D.A.3    Edwards, R.J.4    Davies, D.S.5    Park, B.K.6
  • 20
    • 0035192944 scopus 로고    scopus 로고
    • Differential inhibition and inactivation of human CYP1 enzymes by trans-resveratrol: Evidence for mechanism-based inactivation of CYP1A2
    • Thomas KH, Chang JC, and Lee WBK (2001) Differential inhibition and inactivation of human CYP1 enzymes by trans-resveratrol: evidence for mechanism-based inactivation of CYP1A2. J Pharmacol Exp Ther 299:874-882.
    • (2001) J Pharmacol Exp Ther , vol.299 , pp. 874-882
    • Thomas, K.H.1    Chang, J.C.2    Lee, W.B.K.3
  • 21
    • 0029853923 scopus 로고    scopus 로고
    • Phenacetin O-deethylation by human liver microsomes in vitro: Inhibition by chemical probes, SSRI antidepressants, nefazodone and venlafaxine
    • Von Moltke LL, Greenblatt DJ, Duan SX, Schmider J (1996) Phenacetin O-deethylation by human liver microsomes in vitro: inhibition by chemical probes, SSRI antidepressants, nefazodone and venlafaxine. Psychopharmacology 128:398-407.
    • (1996) Psychopharmacology , vol.128 , pp. 398-407
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Duan, S.X.3    Schmider, J.4
  • 23
    • 24644441043 scopus 로고    scopus 로고
    • Kinetic values for mechanism-based enzyme inhibition: Assessing the bias introduced by the conventional experimental protocol
    • Yang J, Jamei M, Rowland-Yeo K, Tucker GT, and Rostami-Hodjegan A (2005) Kinetic values for mechanism-based enzyme inhibition: assessing the bias introduced by the conventional experimental protocol. Eur J Pharm Sci 26:334-340.
    • (2005) Eur J Pharm Sci , vol.26 , pp. 334-340
    • Yang, J.1    Jamei, M.2    Rowland-Yeo, K.3    Tucker, G.T.4    Rostami-Hodjegan, A.5
  • 24
    • 18844445670 scopus 로고    scopus 로고
    • Evaluation of time-dependent inactivation of CYP3A in cryopreserved human hepatocytes
    • Zhao P, Kunze KL, and Lee CA (2004) Evaluation of time-dependent inactivation of CYP3A in cryopreserved human hepatocytes. Drug Metab Dispos 33:853-861.
    • (2004) Drug Metab Dispos , vol.33 , pp. 853-861
    • Zhao, P.1    Kunze, K.L.2    Lee, C.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.