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Volumn 25, Issue 12, 1997, Pages 1383-1388

In vitro biotransformation and identification of-human cytochrome P450 isozyme-dependent metabolism of tazofelone

Author keywords

[No Author keywords available]

Indexed keywords

ANTIINFLAMMATORY AGENT; COMPLEMENTARY DNA; CYTOCHROME P450; DRUG METABOLITE; MIDAZOLAM; SULFOXIDE; TAZOFELONE; TROLEANDOMYCIN; UNCLASSIFIED DRUG;

EID: 0031465252     PISSN: 00909556     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (24)

References (23)
  • 2
    • 0029025655 scopus 로고
    • Recent advances: The cytochrome P450 enzymes
    • R. L. Slaghter and D. J. Edwards. Recent advances: the cytochrome P450 enzymes. Ann. Pharmacother. 29, 619-624 (1995).
    • (1995) Ann. Pharmacother. , vol.29 , pp. 619-624
    • Slaghter, R.L.1    Edwards, D.J.2
  • 3
    • 0026750647 scopus 로고
    • The human hepatic cytochrome P450 involved in metabolism
    • S. A. Wrighton and J. C. Stevens: The human hepatic cytochrome P450 involved in metabolism. Crit. Rev. Toxicol. 22, 1-21 (1992).
    • (1992) Crit. Rev. Toxicol. , vol.22 , pp. 1-21
    • Wrighton, S.A.1    Stevens, J.C.2
  • 4
    • 0026677681 scopus 로고
    • The rational selection of drug interaction studies: Implication of recent advances in drug metabolism
    • G. T. Tucker: The rational selection of drug interaction studies: implication of recent advances in drug metabolism. Int. J. Clin. Pharmacol. Ther. Toxicol. 30, 550-553 (1992).
    • (1992) Int. J. Clin. Pharmacol. Ther. Toxicol. , vol.30 , pp. 550-553
    • Tucker, G.T.1
  • 6
    • 0345400689 scopus 로고    scopus 로고
    • Predicting rates of cytochrome P450 mediated bioactivation and its application to the design of safer chemicals
    • (S.C. DeVito, ed.), ACS Press, Washington, D.C.
    • J. P. Jones: Predicting rates of cytochrome P450 mediated bioactivation and its application to the design of safer chemicals. In "Designing Safer Chemicals" (S.C. DeVito, ed.), pp 117-137. ACS Press, Washington, D.C., 1996.
    • (1996) Designing Safer Chemicals , pp. 117-137
    • Jones, J.P.1
  • 7
    • 0016174577 scopus 로고
    • Preparation and properties of partially purified cytochrome P450 and reduced nicotinamide adenine dinucleotide phosphate cytochrome P450 reductase from rabbit liver microsomes
    • T. A. Van Der Hoeven and M. J. Coon: Preparation and properties of partially purified cytochrome P450 and reduced nicotinamide adenine dinucleotide phosphate cytochrome P450 reductase from rabbit liver microsomes. J. Biol. Chem. 249, 6302-6310 (1974).
    • (1974) J. Biol. Chem. , vol.249 , pp. 6302-6310
    • Van Der Hoeven, T.A.1    Coon, M.J.2
  • 8
    • 0027445449 scopus 로고
    • Isolation and characterization of human liver cytochrome P450 2C19: Correlation between 2C19 and S-mephenytoin 4′-hydroxylation
    • S. A. Wrighton, J. C. Stevens, G. W. Becker, and M. Vandenbranden: Isolation and characterization of human liver cytochrome P450 2C19: correlation between 2C19 and S-mephenytoin 4′-hydroxylation. Arch. Biochem. Biophys. 306, 240-245 (1993).
    • (1993) Arch. Biochem. Biophys. , vol.306 , pp. 240-245
    • Wrighton, S.A.1    Stevens, J.C.2    Becker, G.W.3    Vandenbranden, M.4
  • 9
  • 10
    • 0025841777 scopus 로고
    • Purification and characterization of human liver microsomal cytochrome P450 2A6
    • C. H. Yun, T. Shimada, and F. P. Guengerich: Purification and characterization of human liver microsomal cytochrome P450 2A6. Mol. Pharmacol. 40, 679-685 (1991).
    • (1991) Mol. Pharmacol. , vol.40 , pp. 679-685
    • Yun, C.H.1    Shimada, T.2    Guengerich, F.P.3
  • 13
    • 0027366623 scopus 로고
    • Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S- Mephenytoin 4′-hydroxylation
    • K. Chiba, K. Kabayashi, K. Manabe, M. Tani, and T. Ishizaki: Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytoin 4′-hydroxylation. Pharmacol. Exp. Ther. 266, 52-59 (1993).
    • (1993) Pharmacol. Exp. Ther. , vol.266 , pp. 52-59
    • Chiba, K.1    Kabayashi, K.2    Manabe, K.3    Tani, M.4    Ishizaki, T.5
  • 14
    • 0026035519 scopus 로고
    • Role of human cytochrome P450 2E1 in the oxidation of many low molecular weight cancer suspects
    • F. P. Guengrich, D. Kim, and M. Iwasaki: Role of human cytochrome P450 2E1 in the oxidation of many low molecular weight cancer suspects. Chem. Res. Toxicol. 4, 168-179 (1991).
    • (1991) Chem. Res. Toxicol. , vol.4 , pp. 168-179
    • Guengrich, F.P.1    Kim, D.2    Iwasaki, M.3
  • 15
    • 0020665350 scopus 로고
    • Inactivation of cytochrome P450 by a troleandomycin metabolite: Protective role of glutathione
    • D. Pessaye, M. Tinel, D. Larrey, B. Colbert, and G. Babany: Inactivation of cytochrome P450 by a troleandomycin metabolite: Protective role of glutathione. J. Pharmacol. Exp. Ther. 224, 685-691 (1983).
    • (1983) J. Pharmacol. Exp. Ther. , vol.224 , pp. 685-691
    • Pessaye, D.1    Tinel, M.2    Larrey, D.3    Colbert, B.4    Babany, G.5
  • 16
    • 0026702860 scopus 로고
    • Metabolism of nicotine by human liver microsomes: Stereoselective formation of trans-nicotine N′-oxide
    • J. R. Cashman, S. B. Park, Z. C. Yang, S. A. Wrighton, P. Jacob, and N. L. Benowitz: Metabolism of nicotine by human liver microsomes: Stereoselective formation of trans-nicotine N′-oxide. Chem. Res. Toxicol. 5, 639-646 (1992).
    • (1992) Chem. Res. Toxicol. , vol.5 , pp. 639-646
    • Cashman, J.R.1    Park, S.B.2    Yang, Z.C.3    Wrighton, S.A.4    Jacob, P.5    Benowitz, N.L.6
  • 17
    • 0030077735 scopus 로고    scopus 로고
    • Identification of the human cytochromes P450 responsible for the in vitro formation of the major oxidative metabolites of the antipsychotic agent olanzapine
    • B. J. Ring, J. Catlow, T. J. Lindsay, T. Gillespie, L. K. Roskos, B. J. Cerimele, S. P. Swanson, M. A. Hamman, and S. A. Wrighton: Identification of the human cytochromes P450 responsible for the in vitro formation of the major oxidative metabolites of the antipsychotic agent olanzapine. J. Pharmacol. Exp. Ther. 276, 658-666 (1996).
    • (1996) J. Pharmacol. Exp. Ther. , vol.276 , pp. 658-666
    • Ring, B.J.1    Catlow, J.2    Lindsay, T.J.3    Gillespie, T.4    Roskos, L.K.5    Cerimele, B.J.6    Swanson, S.P.7    Hamman, M.A.8    Wrighton, S.A.9
  • 19
    • 0023894686 scopus 로고
    • Flavin-containing monooxygenase catalytic mechanism and substrate specificities
    • D. M. Ziegler: Flavin-containing monooxygenase catalytic mechanism and substrate specificities. Drug Metab. Rev. 19, 1-32 (1988).
    • (1988) Drug Metab. Rev. , vol.19 , pp. 1-32
    • Ziegler, D.M.1
  • 21
    • 0031012608 scopus 로고    scopus 로고
    • Substituent elimination from p-substituted phenols by cytochrome P450, ipso-substitution of the oxygen atom of the active species
    • T. Ohe, T. Mashino, and M. Hirobe: Substituent elimination from p-substituted phenols by cytochrome P450, ipso-substitution of the oxygen atom of the active species. Drug Metab. Dispos. 25, 116-122 (1997).
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 116-122
    • Ohe, T.1    Mashino, T.2    Hirobe, M.3
  • 23
    • 0025316330 scopus 로고
    • Flavin-containing monooxygenases: Enzymes adapted for multisubstrate specificity
    • D. M. Ziegler: Flavin-containing monooxygenases: enzymes adapted for multisubstrate specificity. Trends Pharmacol. Sci. 11, 321-324 (1990).
    • (1990) Trends Pharmacol. Sci. , vol.11 , pp. 321-324
    • Ziegler, D.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.