메뉴 건너뛰기




Volumn 31, Issue 3-4, 2007, Pages 232-241

Theoretical assessment of a new experimental protocol for determining kinetic values describing mechanism (time)-based enzyme inhibition

Author keywords

Drug interactions; Enzyme inactivation; Genetic algorithm; Mechanism based inhibition; Simulation

Indexed keywords

1 [(2 ETHYL 4 METHYL 1H IMIDAZOL 5 YL)METHYL] 4 [4 (TRIFLUOROMETHYL) 2 PYRIDINYL]PIPERAZINE; 2 PHENYL 2 (1 PIPERIDINYL)PROPANE; BENZAMIDE DERIVATIVE; CYTOCHROME P450; DELAVIRDINE; DILTIAZEM; ETHINYLESTRADIOL; GESTODENE; L 754394; MENTHOFURAN; MIBEFRADIL; N (2 HYDROXY 1 INDANYL) 5 [2 (1,1 DIMETHYLETHYLAMINOCARBONYL)] 4 [(FURO[2,3 B]PYRIDIN 5 YL)METHYLPIPERAZIN 1 YL] 4 HYDROXY 2 PHENYLMETHYLPENTANAMIDE; N (3,5 DICHLORO 4 PYRIDYL) 4 METHOXY 3 (PROP 2 YNYLOXY)BENZAMIDE; PHENCYCLIDINE; PIPERAZINE DERIVATIVE; PIPERIDINE DERIVATIVE; SUPROFEN; THIOTEPA; TICLOPIDINE; UNCLASSIFIED DRUG; VERAPAMIL;

EID: 34249274907     PISSN: 09280987     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejps.2007.04.005     Document Type: Article
Times cited : (25)

References (49)
  • 1
    • 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., and Grime K. Automated assessment of time-dependent inhibition of human cytochrome P450 enzymes using liquid chromatography-tandem mass spectrometry analysis. Drug Metab. Dispos. 33 (2005) 1637-1647
    • (2005) Drug Metab. Dispos. , vol.33 , pp. 1637-1647
    • Atkinson, A.1    Kenny, J.R.2    Grime, K.3
  • 2
    • 0037369622 scopus 로고    scopus 로고
    • Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine: Comparison with fluoxetine and quinidine
    • Bertelsen K.M., Venkatakrishnan K., von Moltke L.L., Obach R.S., and Greenblatt D.J. Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine: Comparison with fluoxetine and quinidine. Drug Metab. Dispos. 31 (2003) 289-293
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 289-293
    • Bertelsen, K.M.1    Venkatakrishnan, K.2    von Moltke, L.L.3    Obach, R.S.4    Greenblatt, D.J.5
  • 5
    • 0035991642 scopus 로고    scopus 로고
    • Prediction of aqueous solubility of organic compounds using a quantitative structure-property relationship
    • Chen X.Q., Cho S.J., Li Y., and Venkatesh S. Prediction of aqueous solubility of organic compounds using a quantitative structure-property relationship. J. Pharm. Sci. 91 (2002) 1838-1852
    • (2002) J. Pharm. Sci. , vol.91 , pp. 1838-1852
    • Chen, X.Q.1    Cho, S.J.2    Li, Y.3    Venkatesh, S.4
  • 6
    • 0029553030 scopus 로고
    • Potent and selective inactivation of human liver microsomal cytochrome P-450 isoforms by L-754,394, an investigational human immune deficiency virus protease inhibitor
    • Chiba M., Nishime J.A., and Lin J.H. Potent and selective inactivation of human liver microsomal cytochrome P-450 isoforms by L-754,394, an investigational human immune deficiency virus protease inhibitor. J. Pharmacol. Exp. Ther. 275 (1995) 1527-1534
    • (1995) J. Pharmacol. Exp. Ther. , vol.275 , pp. 1527-1534
    • Chiba, M.1    Nishime, J.A.2    Lin, J.H.3
  • 7
    • 0033861911 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochromes P4502B1 and P4502B6 by 2-phenyl-2-(1-piperidinyl) propane
    • Chun J., Kent U.M., Moss R.M., Sayre L.M., and Hollenberg P.F. Mechanism-based inactivation of cytochromes P4502B1 and P4502B6 by 2-phenyl-2-(1-piperidinyl) propane. Drug Metab. Dispos. 28 (2000) 905-911
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 905-911
    • Chun, J.1    Kent, U.M.2    Moss, R.M.3    Sayre, L.M.4    Hollenberg, P.F.5
  • 8
    • 0037671388 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochrome P450 2B6 by a novel terminal acetylene inhibitor
    • Fan P.W., Gu C., Marsh S.A., and Stevens J.C. Mechanism-based inactivation of cytochrome P450 2B6 by a novel terminal acetylene inhibitor. Drug Metab. Dispos. 31 (2003) 28-36
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 28-36
    • Fan, P.W.1    Gu, C.2    Marsh, S.A.3    Stevens, J.C.4
  • 9
    • 0032893695 scopus 로고    scopus 로고
    • Improved reliability of the rapid microtiter plate assay using recombinant enzyme in predicting CYP2D6 inhibition in human liver microsomes
    • Favreau L.V., Palamanda J.R., Lin C.-c., and Nomeir A.A. Improved reliability of the rapid microtiter plate assay using recombinant enzyme in predicting CYP2D6 inhibition in human liver microsomes. Drug Metab. Dispos. 27 (1999) 436-439
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 436-439
    • Favreau, L.V.1    Palamanda, J.R.2    Lin, C.-c.3    Nomeir, A.A.4
  • 10
    • 34249334251 scopus 로고    scopus 로고
    • FDA, 2006. Guidance for industry: drug interaction studies - study design, data analysis, and implications for dosing and labeling.
  • 11
    • 33645980647 scopus 로고    scopus 로고
    • A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation
    • Ghanbari F., Rowland-Yeo K., Bloomer J.C., Clarke S.E., Lennard M.S., Tucker G.T., and Rostami-Hodjegan A. A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation. Curr. Drug Metab. 7 (2006) 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
  • 13
    • 0025184340 scopus 로고
    • Mechanism-based inactivation of human liver microsomal cytochrome P-450 IIIA4 by gestodene
    • Guengerich F.P. Mechanism-based inactivation of human liver microsomal cytochrome P-450 IIIA4 by gestodene. Chem. Res. Toxicol. 3 (1990) 363-371
    • (1990) Chem. Res. Toxicol. , vol.3 , pp. 363-371
    • Guengerich, F.P.1
  • 14
    • 0035699870 scopus 로고    scopus 로고
    • Inhibition by ticlopidine and its derivatives of human liver cytochrome P450. Mechanism-based inactivation of CYP2C19 by ticlopidine
    • Ha-Duong N.T., Dijols S., Macherey A.C., Dansette P.M., and Mansuy D. Inhibition by ticlopidine and its derivatives of human liver cytochrome P450. Mechanism-based inactivation of CYP2C19 by ticlopidine. Biol. React. Intermed. Vi (2001) 145-148
    • (2001) Biol. React. Intermed. , vol.Vi , pp. 145-148
    • Ha-Duong, N.T.1    Dijols, S.2    Macherey, A.C.3    Dansette, P.M.4    Mansuy, D.5
  • 15
    • 4243195884 scopus 로고    scopus 로고
    • Metabolism of N,N',N"-triethylenethiophosphoramide by CYP2B1 and CYP2B6 results in the inactivation of both isoforms by two distinct mechanisms
    • Harleton E., Webster M., Bumpus N.N., Kent U.M., Rae J.M., and Hollenberg P.F. Metabolism of N,N',N"-triethylenethiophosphoramide by CYP2B1 and CYP2B6 results in the inactivation of both isoforms by two distinct mechanisms. J. Pharmacol. Exp. Ther. 310 (2004) 1011-1019
    • (2004) J. Pharmacol. Exp. Ther. , vol.310 , pp. 1011-1019
    • Harleton, E.1    Webster, M.2    Bumpus, N.N.3    Kent, U.M.4    Rae, J.M.5    Hollenberg, P.F.6
  • 16
    • 0036226707 scopus 로고    scopus 로고
    • Characteristics and common properties of inhibitors, inducers, and activators of CYP enzymes
    • Hollenberg P.F. Characteristics and common properties of inhibitors, inducers, and activators of CYP enzymes. Drug Metab. Rev. 34 (2002) 17-35
    • (2002) Drug Metab. Rev. , vol.34 , pp. 17-35
    • Hollenberg, P.F.1
  • 17
    • 1342331932 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochrome P450 2D6 by 1-[(2-ethyl-4-methyl-1H-imidazol-5-yl)methyl]-4-[4-(trifluoromethyl)-2-p yridinyl]piperazine: kinetic characterization and evidence for apoprotein adduction
    • Hutzler J.M., Steenwyk R.C., Smith E.B., Walker G.S., and Wienkers L.C. Mechanism-based inactivation of cytochrome P450 2D6 by 1-[(2-ethyl-4-methyl-1H-imidazol-5-yl)methyl]-4-[4-(trifluoromethyl)-2-p yridinyl]piperazine: kinetic characterization and evidence for apoprotein adduction. Chem. Res. Toxicol. 17 (2004) 174-184
    • (2004) Chem. Res. Toxicol. , vol.17 , pp. 174-184
    • Hutzler, J.M.1    Steenwyk, R.C.2    Smith, E.B.3    Walker, G.S.4    Wienkers, L.C.5
  • 18
    • 0031723235 scopus 로고    scopus 로고
    • Prediction of pharmacokinetic alterations caused by drug-drug interactions: metabolic interaction in the liver
    • Ito K., Iwatsubo T., Kanamitsu S., Ueda K., Suzuki H., and Sugiyama Y. Prediction of pharmacokinetic alterations caused by drug-drug interactions: metabolic interaction in the liver. Pharmacol. Rev. 50 (1998) 387-412
    • (1998) Pharmacol. Rev. , vol.50 , pp. 387-412
    • Ito, K.1    Iwatsubo, T.2    Kanamitsu, S.3    Ueda, K.4    Suzuki, H.5    Sugiyama, Y.6
  • 19
    • 0032773854 scopus 로고    scopus 로고
    • Diltiazem inhibition of cytochrome P-450 3A activity is due to metabolite intermediate complex formation
    • Jones D.R., Gorski J.C., Hamman M.A., Mayhew B.S., Rider S., and Hall S.D. Diltiazem inhibition of cytochrome P-450 3A activity is due to metabolite intermediate complex formation. J. Pharmacol. Exp. Ther. 290 (1999) 1116-1125
    • (1999) J. Pharmacol. Exp. Ther. , vol.290 , pp. 1116-1125
    • Jones, D.R.1    Gorski, J.C.2    Hamman, M.A.3    Mayhew, B.S.4    Rider, S.5    Hall, S.D.6
  • 20
    • 4143108324 scopus 로고    scopus 로고
    • Substrate depletion approach for determining in vitro metabolic clearance: time dependencies in hepatocyte and microsomal incubations
    • Jones H.M., and Houston J.B. Substrate depletion approach for determining in vitro metabolic clearance: time dependencies in hepatocyte and microsomal incubations. Drug Metab. Dispos. 32 (2004) 973-982
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 973-982
    • Jones, H.M.1    Houston, J.B.2
  • 21
    • 0037671381 scopus 로고    scopus 로고
    • The mechanism-based inactivation of human cytochrome P4502B6 by phencyclidine
    • Jushchyshyn M.I., Kent U.M., and Hollenberg P.F. The mechanism-based inactivation of human cytochrome P4502B6 by phencyclidine. Drug Metab. Dispos. 31 (2003) 46-52
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 46-52
    • Jushchyshyn, M.I.1    Kent, U.M.2    Hollenberg, P.F.3
  • 22
    • 0036151664 scopus 로고    scopus 로고
    • Effect of 17-alpha-ethynylestradiol on activities of cytochrome P4502B (P450 2B) enzymes: characterization of inactivation of P450s 2B1 and 2B6 and identification of metabolites
    • Kent U.M., Mills D.E., Rajnarayanan R.V., Alworth W.L., and Hollenberg P.F. Effect of 17-alpha-ethynylestradiol on activities of cytochrome P4502B (P450 2B) enzymes: characterization of inactivation of P450s 2B1 and 2B6 and identification of metabolites. J. Pharmacol. Exp. Ther. 300 (2002) 549-558
    • (2002) J. Pharmacol. Exp. Ther. , vol.300 , pp. 549-558
    • Kent, U.M.1    Mills, D.E.2    Rajnarayanan, R.V.3    Alworth, W.L.4    Hollenberg, P.F.5
  • 23
    • 0031848620 scopus 로고    scopus 로고
    • (R)-(+)-menthofuran is a potent, mechanism-based inactivator of human liver cytochrome P450 2A6
    • Khojasteh-Bakht S.C., Koenigs L.L., Peter R.M., Trager W.F., and Nelson S.D. (R)-(+)-menthofuran is a potent, mechanism-based inactivator of human liver cytochrome P450 2A6. Drug Metab. Dispos. 26 (1998) 701-704
    • (1998) Drug Metab. Dispos. , vol.26 , pp. 701-704
    • Khojasteh-Bakht, S.C.1    Koenigs, L.L.2    Peter, R.M.3    Trager, W.F.4    Nelson, S.D.5
  • 24
    • 73649151319 scopus 로고
    • Esters of methanesulfonic acid as irreversible inhibitiors of acetylcholinesterase
    • Kitz R., and Wilson I.B. Esters of methanesulfonic acid as irreversible inhibitiors of acetylcholinesterase. J. Biol. Chem. 237 (1962) 3245-3249
    • (1962) J. Biol. Chem. , vol.237 , pp. 3245-3249
    • Kitz, R.1    Wilson, I.B.2
  • 25
    • 0036196318 scopus 로고    scopus 로고
    • Mechanism-based inactivation of cytochrome P450 3A4 by 17 alpha-ethynylestradiol: evidence for heme destruction and covalent binding to protein
    • Lin H.L., Kent U.M., and Hollenberg P.F. Mechanism-based inactivation of cytochrome P450 3A4 by 17 alpha-ethynylestradiol: evidence for heme destruction and covalent binding to protein. J. Pharmacol. Exp. Ther. 301 (2002) 160-167
    • (2002) J. Pharmacol. Exp. Ther. , vol.301 , pp. 160-167
    • Lin, H.L.1    Kent, U.M.2    Hollenberg, P.F.3
  • 26
    • 0031794361 scopus 로고    scopus 로고
    • Inhibition and induction of cytochrome P450 and the clinical implications
    • Lin J.H., and Lu A.Y. Inhibition and induction of cytochrome P450 and the clinical implications. Clin. Pharmacokinet. 35 (1998) 361-390
    • (1998) Clin. Pharmacokinet. , vol.35 , pp. 361-390
    • Lin, J.H.1    Lu, A.Y.2
  • 27
    • 33947235192 scopus 로고    scopus 로고
    • Comparison of methods for analyzing kinetic data from mechanism-based enzyme inactivation: application to nitric oxide synthase
    • Maurer T., and Fung H.L. Comparison of methods for analyzing kinetic data from mechanism-based enzyme inactivation: application to nitric oxide synthase. AAPS PharmSci. 2 (2000) E8
    • (2000) AAPS PharmSci. , vol.2
    • Maurer, T.1    Fung, H.L.2
  • 28
    • 0033831197 scopus 로고    scopus 로고
    • An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation
    • Mayhew B.S., Jones D.R., and Hall S.D. An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation. Drug Metab. Dispos. 28 (2000) 1031-1037
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 1031-1037
    • Mayhew, B.S.1    Jones, D.R.2    Hall, S.D.3
  • 29
    • 0142150012 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human recombinant P4502C9 by the nonsteroidal anti-inflammatory drug suprofen
    • O'Donnell J.P., Dalvie D.K., Kalgutkar A.S., and Obach R.S. Mechanism-based inactivation of human recombinant P4502C9 by the nonsteroidal anti-inflammatory drug suprofen. Drug Metab. Dispos. 31 (2003) 1369-1377
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 1369-1377
    • O'Donnell, J.P.1    Dalvie, D.K.2    Kalgutkar, A.S.3    Obach, R.S.4
  • 30
    • 0035987898 scopus 로고    scopus 로고
    • Measurement of Michaelis constants for cytochrome P450-mediated biotransformation reactions using a substrate depletion approach
    • Obach R.S., and Reed-Hagen A.E. Measurement of Michaelis constants for cytochrome P450-mediated biotransformation reactions using a substrate depletion approach. Drug Metab. Dispos. 30 (2002) 831-837
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 831-837
    • Obach, R.S.1    Reed-Hagen, A.E.2
  • 31
    • 4644267926 scopus 로고    scopus 로고
    • Two major grapefruit juice components differ in intestinal CYP3A4 inhibition kinetic and binding properties
    • Paine M.F., Criss A.B., and Watkins P.B. Two major grapefruit juice components differ in intestinal CYP3A4 inhibition kinetic and binding properties. Drug Metab. Dispos. 32 (2004) 1146-1153
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 1146-1153
    • Paine, M.F.1    Criss, A.B.2    Watkins, P.B.3
  • 32
    • 0033026601 scopus 로고    scopus 로고
    • Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: an in vitro investigation with human liver preparations
    • Prueksaritanont T., Ma B., Tang C.Y., Meng Y., Assang C., Lu P., Reider P.J., Lin J.H., and Baillie T.A. Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: an in vitro investigation with human liver preparations. Br. J. Clin. Pharmacol. 47 (1999) 291-298
    • (1999) Br. J. Clin. Pharmacol. , vol.47 , pp. 291-298
    • Prueksaritanont, T.1    Ma, B.2    Tang, C.Y.3    Meng, Y.4    Assang, C.5    Lu, P.6    Reider, P.J.7    Lin, J.H.8    Baillie, T.A.9
  • 33
    • 0030927213 scopus 로고    scopus 로고
    • Protein targets of xenobiotic reactive intermediates
    • Pumford N.R., and Halmes N.C. Protein targets of xenobiotic reactive intermediates. Annu. Rev. Pharmacol. Toxicol. 37 (1997) 91-117
    • (1997) Annu. Rev. Pharmacol. Toxicol. , vol.37 , pp. 91-117
    • Pumford, N.R.1    Halmes, N.C.2
  • 34
    • 1242314687 scopus 로고    scopus 로고
    • A quantitative structure-property relationship for predicting drug solubility in PEG 400/water cosolvent systems
    • Rytting E., Lentz K.A., Chen X.Q., Qian F., and Venkatesh S. A quantitative structure-property relationship for predicting drug solubility in PEG 400/water cosolvent systems. Pharm. Res. 21 (2004) 237-244
    • (2004) Pharm. Res. , vol.21 , pp. 237-244
    • Rytting, E.1    Lentz, K.A.2    Chen, X.Q.3    Qian, F.4    Venkatesh, S.5
  • 36
    • 0028930481 scopus 로고
    • Mechanism-based enzyme inactivators
    • Silverman R.B. Mechanism-based enzyme inactivators. Meth. Enzymol. 249 (1995) 240-283
    • (1995) Meth. Enzymol. , vol.249 , pp. 240-283
    • Silverman, R.B.1
  • 37
    • 0019882269 scopus 로고
    • Kinetics of suicide substrates. Steady-state treatments and computer-aided exact solutions
    • Tatsunami S., Yago N., and Hosoe M. Kinetics of suicide substrates. Steady-state treatments and computer-aided exact solutions. Biochim. Biophys. Acta 662 (1981) 226-235
    • (1981) Biochim. Biophys. Acta , vol.662 , pp. 226-235
    • Tatsunami, S.1    Yago, N.2    Hosoe, M.3
  • 38
    • 0142010701 scopus 로고    scopus 로고
    • Drug metabolism and drug interactions: application and clinical value of in vitro models
    • Venkatakrishnan K., von Moltke L.L., Obach R.S., and Greenblatt D.J. Drug metabolism and drug interactions: application and clinical value of in vitro models. Curr. Drug Metab. 4 (2003) 423-459
    • (2003) Curr. Drug Metab. , vol.4 , pp. 423-459
    • Venkatakrishnan, K.1    von Moltke, L.L.2    Obach, R.S.3    Greenblatt, D.J.4
  • 39
    • 0033948964 scopus 로고    scopus 로고
    • Potent mechanism-based inhibition of human CYP3A in vitro by amprenavir and ritonavir: comparison with ketoconazole
    • von Moltke L.L., Durol A.L.B., Duan S.X., and Greenblatt D.J. Potent mechanism-based inhibition of human CYP3A in vitro by amprenavir and ritonavir: comparison with ketoconazole. Eur. J. Clin. Pharmacol. 56 (2000) 259-261
    • (2000) Eur. J. Clin. Pharmacol. , vol.56 , pp. 259-261
    • von Moltke, L.L.1    Durol, A.L.B.2    Duan, S.X.3    Greenblatt, D.J.4
  • 40
    • 0032454713 scopus 로고    scopus 로고
    • Microsomal metabolism of delavirdine: evidence for mechanism-based inactivation of human cytochrome p450 3A
    • Voorman R.L., Maio S.M., Payne N.A., Zha Z.Y., Koeplinger K.A., and Wang X.H. Microsomal metabolism of delavirdine: evidence for mechanism-based inactivation of human cytochrome p450 3A. J. Pharmacol. Exp. Ther. 287 (1998) 381-388
    • (1998) J. Pharmacol. Exp. Ther. , vol.287 , pp. 381-388
    • Voorman, R.L.1    Maio, S.M.2    Payne, N.A.3    Zha, Z.Y.4    Koeplinger, K.A.5    Wang, X.H.6
  • 41
    • 0035155252 scopus 로고    scopus 로고
    • Interaction of delavirdine with human liver microsomal cytochrome P450: inhibition of CYP2C9, CYP2C19, and CYP2D6
    • Voorman R.L., Payne N.A., Wienkers L.C., Hauer M.J., and Sanders P.E. Interaction of delavirdine with human liver microsomal cytochrome P450: inhibition of CYP2C9, CYP2C19, and CYP2D6. Drug Metab. Dispos. 29 (2001) 41-47
    • (2001) Drug Metab. Dispos. , vol.29 , pp. 41-47
    • Voorman, R.L.1    Payne, N.A.2    Wienkers, L.C.3    Hauer, M.J.4    Sanders, P.E.5
  • 42
    • 0018993834 scopus 로고
    • Kinetics of suicide substrates
    • Waley S.G. Kinetics of suicide substrates. Biochem. J. 185 (1980) 771-773
    • (1980) Biochem. J. , vol.185 , pp. 771-773
    • Waley, S.G.1
  • 44
    • 2442690439 scopus 로고    scopus 로고
    • Validated assays for human cytochrome P450 activities
    • Walsky R.L., and Obach R.S. Validated assays for human cytochrome P450 activities. Drug Metab. Dispos. 32 (2004) 647-660
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 647-660
    • Walsky, R.L.1    Obach, R.S.2
  • 45
    • 0036786448 scopus 로고    scopus 로고
    • Quantitative structure/property relationship analysis of Caco-2 permeability using a genetic algorithm-based partial least squares method
    • Yamashita F., Wanchana S., and Hashida M. Quantitative structure/property relationship analysis of Caco-2 permeability using a genetic algorithm-based partial least squares method. J. Pharm. Sci. 91 (2002) 2230-2239
    • (2002) J. Pharm. Sci. , vol.91 , pp. 2230-2239
    • Yamashita, F.1    Wanchana, S.2    Hashida, M.3
  • 47
    • 24644441043 scopus 로고    scopus 로고
    • Kinetic values for mechanism-based inhibition: assessment of bias introduced by the conventional experimental protocol
    • Yang J., Jamei M., Yeo K.R., Rostami-Hodjegan A., and Tucker G.T. Kinetic values for mechanism-based inhibition: assessment of bias introduced by the conventional experimental protocol. Eur. J. Pharm. Sci. 26 (2005) 334-340
    • (2005) Eur. J. Pharm. Sci. , vol.26 , pp. 334-340
    • Yang, J.1    Jamei, M.2    Yeo, K.R.3    Rostami-Hodjegan, A.4    Tucker, G.T.5
  • 48
    • 0034854303 scopus 로고    scopus 로고
    • Inhibitory effects of verapamil and diltiazem on simvastatin metabolism in human liver microsomes
    • Yeo K.R., and Yeo W.W. Inhibitory effects of verapamil and diltiazem on simvastatin metabolism in human liver microsomes. Br. J. Clin. Pharmacol. 51 (2001) 461-470
    • (2001) Br. J. Clin. Pharmacol. , vol.51 , pp. 461-470
    • Yeo, K.R.1    Yeo, W.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.