메뉴 건너뛰기




Volumn 6, Issue 1, 1996, Pages 81-91

Interaction of human liver cytochromes P450 in vitro with LY307640, a gastric proton pump inhibitor

Author keywords

human liver microsomes; LY307640; P450s; proton pump inhibitor

Indexed keywords

BUFURALOL; COMPLEMENTARY DNA; COUMARIN; CYTOCHROME P450 ISOENZYME; DESMETHYL LY 307640; DIETHYLDITHIOCARBAMIC ACID; DRUG METABOLITE; ENZYME INHIBITOR; FLUNITRAZEPAM; FURAFYLLINE; LY 307640; LY 307640 SULFONE; MEPHENYTOIN; MIDAZOLAM; OMEPRAZOLE; PHENOBARBITAL; PROTON PUMP INHIBITOR; QUINIDINE; RABEPRAZOLE; SULFAPHENAZOLE; TROLEANDOMYCIN; UNCLASSIFIED DRUG;

EID: 0029872402     PISSN: 0960314X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00008571-199602000-00007     Document Type: Article
Times cited : (92)

References (33)
  • 3
    • 0024359553 scopus 로고
    • Effect of quinidine on the dextromethorphan O-demethylase activity of microsomal fractions from human liver
    • Broly F, Libersa C, Lhermitte M, Bechtel P, Dupuis B. Effect of quinidine on the dextromethorphan O-demethylase activity of microsomal fractions from human liver. Br J Clin Pharmacol 1989: 28, 29-36.
    • (1989) Br J Clin Pharmacol , vol.28 , pp. 29-36
    • Broly, F.1    Libersa, C.2    Lhermitte, M.3    Bechtel, P.4    Dupuis, B.5
  • 4
    • 0027366623 scopus 로고
    • Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytoin 4′-hydroxylation
    • Chiba K, Kabayashi K, Manabe K, Tani M, Kamataki T, Ishizaki T. Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytoin 4′-hydroxylation. Pharmacol Exp Ther 1993: 266, 52-59.
    • (1993) Pharmacol Exp Ther , vol.266 , pp. 52-59
    • Chiba, K.1    Kabayashi, K.2    Manabe, K.3    Tani, M.4    Kamataki, T.5    Ishizaki, T.6
  • 6
    • 0027956791 scopus 로고
    • Characterization of dextromethorphan N-demethylation by human liver microsomes
    • Gorski JC, Jones DR, Wrighton SA, Hall SD. Characterization of dextromethorphan N-demethylation by human liver microsomes. Biochem Pharmacol 1994: 47, 173-182.
    • (1994) Biochem Pharmacol , vol.47 , pp. 173-182
    • Gorski, J.C.1    Jones, D.R.2    Wrighton, S.A.3    Hall, S.D.4
  • 7
    • 0022467917 scopus 로고
    • Oxidation of quinidine by human liver cytochrome P-450
    • Guengerich FP, Muller-Enoch D, Blair IA. Oxidation of quinidine by human liver cytochrome P-450. Mol Pharmacol 1986: 30, 287-295.
    • (1986) Mol Pharmacol , vol.30 , pp. 287-295
    • Guengerich, F.P.1    Muller-Enoch, D.2    Blair, I.A.3
  • 8
    • 0026035519 scopus 로고
    • Role of human cytochrome P450 IIE1 in the oxidation of many low molecular weight cancer suspects
    • Guengerich FP, Kim D-H, Iwasaki M. Role of human cytochrome P450 IIE1 in the oxidation of many low molecular weight cancer suspects. Chem Res Toxicol 1991: 4, 168-179.
    • (1991) Chem Res Toxicol , vol.4 , pp. 168-179
    • Guengerich, F.P.1    Kim, D.-H.2    Iwasaki, M.3
  • 10
    • 0027942060 scopus 로고
    • Relevance of in vitro kinetic parameters to in vivo metabolism of xenobiotics
    • Houston JB. Relevance of in vitro kinetic parameters to in vivo metabolism of xenobiotics. Toxicol In Vitro 1994a: 8, 507-512.
    • (1994) Toxicol in Vitro , vol.8 , pp. 507-512
    • Houston, J.B.1
  • 11
    • 0028342648 scopus 로고
    • Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance
    • Houston JB. Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance. Biochem Pharmacol 1994b: 47, 1469-1479.
    • (1994) Biochem Pharmacol , vol.47 , pp. 1469-1479
    • Houston, J.B.1
  • 12
    • 0029114726 scopus 로고
    • Comparison of the interaction potential of a new proton pump inhibitor, E3810, versus omeprazole with diazepam in extensive and poor metabolizers of S-mephenytoin 4′-hydroxylation
    • Ishizaki T, Chiba K, Manabe K, Koyama E, Hayashi M, Yasuda S, Horai Y, Tomono Y, Yamato C, Toyoki T. Comparison of the interaction potential of a new proton pump inhibitor, E3810, versus omeprazole with diazepam in extensive and poor metabolizers of S-mephenytoin 4′-hydroxylation. Clin Pharmacol Ther 1995: 58, 155-164.
    • (1995) Clin Pharmacol Ther , vol.58 , pp. 155-164
    • Ishizaki, T.1    Chiba, K.2    Manabe, K.3    Koyama, E.4    Hayashi, M.5    Yasuda, S.6    Horai, Y.7    Tomono, Y.8    Yamato, C.9    Toyoki, T.10
  • 15
    • 0027462638 scopus 로고
    • Understanding consequences of concurrent therapies
    • Peck CC, Temple R, Collins JM. Understanding consequences of concurrent therapies. JAMA 1993: 269, 1550-1552.
    • (1993) JAMA , vol.269 , pp. 1550-1552
    • Peck, C.C.1    Temple, R.2    Collins, J.M.3
  • 17
    • 0025100774 scopus 로고
    • The pharmacokinetics of omeprazole in humans - A study of single intravenous and oral doses
    • Regardh GG, Andersson T, Lagerstrom PO, Lundborg P, Skanberg I. The pharmacokinetics of omeprazole in humans - a study of single intravenous and oral doses. Ther Drug Monit 1990: 12, 163-172.
    • (1990) Ther Drug Monit , vol.12 , pp. 163-172
    • Regardh, G.G.1    Andersson, T.2    Lagerstrom, P.O.3    Lundborg, P.4    Skanberg, I.5
  • 20
    • 0026795695 scopus 로고
    • Inhibitors of imiprimine metabolism by human liver microsomes
    • Skjelbo E, Brosen K. Inhibitors of imiprimine metabolism by human liver microsomes. Br J Clin Pharmacol 1992: 34, 256-261.
    • (1992) Br J Clin Pharmacol , vol.34 , pp. 256-261
    • Skjelbo, E.1    Brosen, K.2
  • 21
    • 0026459382 scopus 로고
    • Speculations on the substrate structure-activity relationship (SSAR) of cytochrome P450 enzymes
    • Smith DA, Jones BC. Speculations on the substrate structure-activity relationship (SSAR) of cytochrome P450 enzymes. Biochem Pharmacol 1992: 44, 2089-2098.
    • (1992) Biochem Pharmacol , vol.44 , pp. 2089-2098
    • Smith, D.A.1    Jones, B.C.2
  • 22
    • 0027442014 scopus 로고
    • Interaction of the enantiomers of fluoxetine and norfluoxetine with human liver cytochromes P450
    • Stevens JC, Wrighton SA. Interaction of the enantiomers of fluoxetine and norfluoxetine with human liver cytochromes P450. J Pharmacol Exp Ther 1993: 266, 964-971.
    • (1993) J Pharmacol Exp Ther , vol.266 , pp. 964-971
    • Stevens, J.C.1    Wrighton, S.A.2
  • 23
    • 0026677681 scopus 로고
    • The rational selection of drug interaction studies: Implications of recent advances in drug metabolism
    • Tucker GT. The rational selection of drug interaction studies: Implications of recent advances in drug metabolism. Internat J Clin Pharmacol Ther Toxicol 1992: 30, 550-553.
    • (1992) Internat J Clin Pharmacol Ther Toxicol , vol.30 , pp. 550-553
    • Tucker, G.T.1
  • 24
    • 0016174577 scopus 로고
    • Preparation and properties of partially purified cytochrome P-450 and reduced nicotinamide adenine dinucleotide phosphate-cytochrome P-450 reductase from rabbit liver microsomes
    • van der Hoeven TA, Coon MJ. Preparation and properties of partially purified cytochrome P-450 and reduced nicotinamide adenine dinucleotide phosphate-cytochrome P-450 reductase from rabbit liver microsomes. J Biol Chem 1974: 249, 6302-6310.
    • (1974) J Biol Chem , vol.249 , pp. 6302-6310
    • Van Der Hoeven, T.A.1    Coon, M.J.2
  • 26
    • 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 Toxicol 1992: 22, 1-21.
    • (1992) Crit Rev Toxicol , vol.22 , pp. 1-21
    • Wrighton, S.A.1    Stevens, J.C.2
  • 27
    • 0028361593 scopus 로고
    • Inhibition of human CYP3A catalyzed 1′-hydroxy midazolam formation by ketoconazole, nifedipine, erythromycin, cimetidine, and nizatidine
    • Wrighton SA, Ring BJ. Inhibition of human CYP3A catalyzed 1′-hydroxy midazolam formation by ketoconazole, nifedipine, erythromycin, cimetidine, and nizatidine. Pharmaceut Res 1994: 11, 921-924.
    • (1994) Pharmaceut Res , vol.11 , pp. 921-924
    • Wrighton, S.A.1    Ring, B.J.2
  • 29
    • 0027445449 scopus 로고
    • Isolation and characterization of human liver cytochrome P450 2C19: Correlation between 2C19 and S-mephenytoin 4′-hydroxylation
    • Wrighton SA, Stevens JC, Becker GW, VandenBranden M. Isolation and characterization of human liver cytochrome P450 2C19: Correlation between 2C19 and S-mephenytoin 4′-hydroxylation. Arch Biochem Biophys 1993a: 306, 240-245.
    • (1993) Arch Biochem Biophys , vol.306 , pp. 240-245
    • Wrighton, S.A.1    Stevens, J.C.2    Becker, G.W.3    VandenBranden, M.4
  • 32
    • 0029083823 scopus 로고
    • Comparison of the kinetic disposition and metabolism of a new proton pump inhibitor, E3810, and omeprazole in relation to S-mephenytoin 4′-hydroxylation status
    • Yasuda S, Horai Y, Tomono Y, Nakai H, Yamato C, Manabe K, Kobayashi K, Chiba K, Ishizaki T. Comparison of the kinetic disposition and metabolism of a new proton pump inhibitor, E3810, and omeprazole in relation to S-mephenytoin 4′-hydroxylation status. Clin Pharmacol Ther 1995: 58, 143-154.
    • (1995) Clin Pharmacol Ther , vol.58 , pp. 143-154
    • Yasuda, S.1    Horai, Y.2    Tomono, Y.3    Nakai, H.4    Yamato, C.5    Manabe, K.6    Kobayashi, K.7    Chiba, K.8    Ishizaki, T.9
  • 33
    • 0025841777 scopus 로고
    • Purification and characterization of human liver microsomal cytochrome P-450 2A6
    • Yun C-H, Shimada T, Guengerich FP. Purification and characterization of human liver microsomal cytochrome P-450 2A6. Molec Pharmacol 1991: 40, 679-685.
    • (1991) Molec Pharmacol , vol.40 , pp. 679-685
    • Yun, C.-H.1    Shimada, T.2    Guengerich, F.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.