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Volumn 8, Issue 1, 2014, Pages 43-50

Comparison of catalytic properties of cytochromes p450 3a4 and 3a5 by molecular docking simulation

Author keywords

Accessibility; Affinity; CYP3A4; CYP3A5; Docking simulation; Metabolic activity

Indexed keywords

CAREBASTINE; CYTOCHROME P450 3A4; CYTOCHROME P450 3A5; ENDOSULFAN; ESTRADIOL; FLUINDOSTATIN; HALOPERIDOL; HEME; ITRACONAZOLE; MIDAZOLAM; TRIAZOLAM; VINCRISTINE; CYP3A4 PROTEIN, HUMAN; CYP3A5 PROTEIN, HUMAN; CYTOCHROME P450 3A;

EID: 84925387124     PISSN: 18723128     EISSN: None     Source Type: Journal    
DOI: 10.2174/1872312807666131229121228     Document Type: Article
Times cited : (18)

References (26)
  • 1
    • 0030428256 scopus 로고    scopus 로고
    • Cytochrome P4503A (CYP3A) metabolism: Prediction of in vivo activity in humans
    • [1] Wilkinson G.R. Cytochrome P4503A (CYP3A) metabolism: prediction of in vivo activity in humans. J. Pharmacokinet. Biopharm., 1996, 24, 475-490.
    • (1996) J. Pharmacokinet. Biopharm , vol.24 , pp. 475-490
    • Wilkinson, G.R.1
  • 2
    • 31344443943 scopus 로고    scopus 로고
    • Significance of the minor cytochrome P450 3A isoforms
    • [2] Daly, A.K. Significance of the minor cytochrome P450 3A isoforms. Clin. Pharmacokinet., 2006, 45, 13-31.
    • (2006) Clin. Pharmacokinet , vol.45 , pp. 13-31
    • Daly, A.K.1
  • 3
    • 33645990311 scopus 로고    scopus 로고
    • A literature review of enzyme kinetic parameters for CYP3A4-mediated metabolic reactions of 113 drugs in human liver microsomes: Structure-kinetics relationship assessment
    • [3] Bu, H.Z. A literature review of enzyme kinetic parameters for CYP3A4-mediated metabolic reactions of 113 drugs in human liver microsomes: structure-kinetics relationship assessment. Current Drug Metab., 2006, 7, 231-249.
    • (2006) Current Drug Metab , vol.7 , pp. 231-249
    • Bu, H.Z.1
  • 6
    • 38849106780 scopus 로고    scopus 로고
    • Comparison of kinetic parameters for drug oxidation rates and substrate inhibition potential mediated by cytochrome P450 3A4 and 3A5
    • [6] Niwa, T.; Murayama, N.; Emoto, C.; Yamazaki, H. Comparison of kinetic parameters for drug oxidation rates and substrate inhibition potential mediated by cytochrome P450 3A4 and 3A5. Curr. Drug Metab., 2008, 9, 20-33.
    • (2008) Curr. Drug Metab , vol.9 , pp. 20-33
    • Niwa, T.1    Murayama, N.2    Emoto, C.3    Yamazaki, H.4
  • 7
    • 77953296304 scopus 로고    scopus 로고
    • Comparison of the contributions of cytochrome P450 3A4 and 3A5 in drug oxidation rates and substrate inhibition
    • [7] Niwa, T.; Murayama, N.; Yamazaki, H. Comparison of the contributions of cytochrome P450 3A4 and 3A5 in drug oxidation rates and substrate inhibition. J. Health Sci., 2010, 56, 239-256.
    • (2010) J. Health Sci , vol.56 , pp. 239-256
    • Niwa, T.1    Murayama, N.2    Yamazaki, H.3
  • 8
    • 58149468203 scopus 로고    scopus 로고
    • Drug interactions of thalidomide with midazolam and cyclosporine A: Heterotropic cooperativity of human cytochrome P450 3A5
    • [8] Okada, Y.; Murayama, N.; Yanagida, C.; Shimizu, M.; Guengerich, F.P.; Yamazaki, H. Drug interactions of thalidomide with midazolam and cyclosporine A: heterotropic cooperativity of human cytochrome P450 3A5. Drug Metab. Dispos., 2009, 37, 18-23.
    • (2009) Drug Metab. Dispos , vol.37 , pp. 18-23
    • Okada, Y.1    Murayama, N.2    Yanagida, C.3    Shimizu, M.4    Guengerich, F.P.5    Yamazaki, H.6
  • 12
    • 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
    • [12] Patki, K.C.; Von Moltke, L.L.; Greenblatt, D.J. In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes P450: role of CYP3A4 and CYP3A5. Drug Metab. Dispos., 2003, 31, 938-944.
    • (2003) Drug Metab. Dispos , vol.31 , pp. 938-944
    • Patki, K.C.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 13
    • 9444270510 scopus 로고    scopus 로고
    • Utility of recombinant enzyme kinetics in prediction of human clearance: impact of variability, CYP3A5, and CYP2C19 on CYP3A4 probe substrates
    • [13] Galetin, A.; Brown, C.; Hallifax, D.; Ito, K.; Houston, J.B. Utility of recombinant enzyme kinetics in prediction of human clearance: impact of variability, CYP3A5, and CYP2C19 on CYP3A4 probe substrates. Drug Metab. Dispos., 2004, 32, 1411-1420.
    • (2004) Drug Metab. Dispos , vol.32 , pp. 1411-1420
    • Galetin, A.1    Brown, C.2    Hallifax, D.3    Ito, K.4    Houston, J.B.5
  • 15
    • 39749180482 scopus 로고    scopus 로고
    • Flavonoids diosmetin and luteolin inhibit midazolam metabolism by human liver microsomes and recombinant CYP 3A4 and CYP3A5 enzymes
    • [15] Quintieri, L.; Palatini, P.; Nassi, A.; Ruzza, P.; Floreani, M. Flavonoids diosmetin and luteolin inhibit midazolam metabolism by human liver microsomes and recombinant CYP 3A4 and CYP3A5 enzymes. Biochem. Pharmacol., 2008, 75, 1426-1437.
    • (2008) Biochem. Pharmacol , vol.75 , pp. 1426-1437
    • Quintieri, L.1    Palatini, P.2    Nassi, A.3    Ruzza, P.4    Floreani, M.5
  • 16
    • 0345016882 scopus 로고    scopus 로고
    • Effects of cytochrome b(5) on drug oxidation activities of human cytochrome P450 (CYP) 3As: Similarity of CYP3A5 with CYP3A4 but not CYP3A7
    • [16] Yamaori, S.; Yamazaki, H.; Suzuki, A.; Yamada, A.; Tani, H.; Kamidate, T.; Fujita, K.; Kamataki, T. Effects of cytochrome b(5) on drug oxidation activities of human cytochrome P450 (CYP) 3As: similarity of CYP3A5 with CYP3A4 but not CYP3A7. Biochem. Pharmacol., 2003, 66, 2333-2340.
    • (2003) Biochem. Pharmacol , vol.66 , pp. 2333-2340
    • Yamaori, S.1    Yamazaki, H.2    Suzuki, A.3    Yamada, A.4    Tani, H.5    Kamidate, T.6    Fujita, K.7    Kamataki, T.8
  • 18
    • 33751112296 scopus 로고    scopus 로고
    • Characterization of ebastine, hydroxyebastine, and carebastine metabolism by human liver microsomes and expressed cytochrome P450 enzymes: Major roles for CYP2J2 and CYP3A
    • [18] Liu, K.H.; Kim, M.G.; Lee, D.J.; Yoon, Y.J.; Kim, M.J.; Shon, J.H.; Choi, C.S.; Choi, Y.K.; Desta, Z.; Shin, J.G. Characterization of ebastine, hydroxyebastine, and carebastine metabolism by human liver microsomes and expressed cytochrome P450 enzymes: major roles for CYP2J2 and CYP3A. Drug Metab. Dispos., 2006, 34, 1793-1797.
    • (2006) Drug Metab. Dispos , vol.34 , pp. 1793-1797
    • Liu, K.H.1    Kim, M.G.2    Lee, D.J.3    Yoon, Y.J.4    Kim, M.J.5    Shon, J.H.6    Choi, C.S.7    Choi, Y.K.8    Desta, Z.9    Shin, J.G.10
  • 19
    • 0032937343 scopus 로고    scopus 로고
    • The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor fluvastatin: Effect on human cytochrome P-450 and implications for metabolic drug interactions
    • [19] Fischer, V.; Johanson, L.; Heitz, F.; Tullman, R.; Graham, E.; Baldeck, J.P.; Robinson, W.T. The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor fluvastatin: effect on human cytochrome P-450 and implications for metabolic drug interactions. Drug Metab. Dispos., 1999, 27, 410-416.
    • (1999) Drug Metab. Dispos , vol.27 , pp. 410-416
    • Fischer, V.1    Johanson, L.2    Heitz, F.3    Tullman, R.4    Graham, E.5    Baldeck, J.P.6    Robinson, W.T.7
  • 20
    • 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
    • [20] Kalgutkar, A.S.; Taylor, T.J.; Venkatakrishnan, K.; Isin, E.M. 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, 243-249.
    • (2003) Drug Metab. Dispos , vol.31 , pp. 243-249
    • Kalgutkar, A.S.1    Taylor, T.J.2    Venkatakrishnan, K.3    Isin, E.M.4
  • 22
    • 0842347425 scopus 로고    scopus 로고
    • Differential enantioselectivity and product-dependent activation and inhibition in metabolism of verapamil by human CYP3As
    • [22] Shen, L.; Fitzloff, J.F.; Cook, C.S. Differential enantioselectivity and product-dependent activation and inhibition in metabolism of verapamil by human CYP3As. Drug Metab. Dispos., 2004, 32, 186-196.
    • (2004) Drug Metab. Dispos , vol.32 , pp. 186-196
    • Shen, L.1    Fitzloff, J.F.2    Cook, C.S.3
  • 24
    • 0032956839 scopus 로고    scopus 로고
    • Inhibition of cytochrome P-450 3A (CYP3A) in human intestinal and liver microsomes: Comparison of Ki values and impact of CYP3A5 expression
    • [24] Gibbs, M.A.; Thummel, K.E.; Shen, D.D.; Kunze, K.L. Inhibition of cytochrome P-450 3A (CYP3A) in human intestinal and liver microsomes: comparison of Ki values and impact of CYP3A5 expression. Drug Metab. Dispos., 1999, 27, 180-187.
    • (1999) Drug Metab. Dispos , vol.27 , pp. 180-187
    • Gibbs, M.A.1    Thummel, K.E.2    Shen, D.D.3    Kunze, K.L.4
  • 25
    • 77952016964 scopus 로고    scopus 로고
    • Potential impact of cytochrome P450 3A5 in human liver on drug interactions with triazoles
    • [25] Yamazaki, H.; Nakamoto, M.; Shimizu, M.; Murayama, N.; Niwa, T. Potential impact of cytochrome P450 3A5 in human liver on drug interactions with triazoles. Br. J. Clin. Pharmacol., 2010, 69, 593-597.
    • (2010) Br. J. Clin. Pharmacol , vol.69 , pp. 593-597
    • Yamazaki, H.1    Nakamoto, M.2    Shimizu, M.3    Murayama, N.4    Niwa, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.