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Journal Abstract Search

97 related items for PubMed ID: 2322893

  • 1. 3,5-Diethoxycarbonyl-2,6-dimethyl-4-ethyl-1,4-dihydropyridine inactivates rat liver cytochrome P-450c, but not its orthologue, rabbit lung form 6.
    Riddick DS, Mackie JE, Massey TE, Marks GS.
    Can J Physiol Pharmacol; 1990 Mar; 68(3):370-3. PubMed ID: 2322893
    [Abstract] [Full Text] [Related]

  • 2. Effects of a series of 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine on the major inducible cytochrome P-450 isozymes of rat liver.
    Riddick DS, Park SS, Gelboin HV, Marks GS.
    Mol Pharmacol; 1989 May; 35(5):626-34. PubMed ID: 2725472
    [Abstract] [Full Text] [Related]

  • 3. Effects of 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine on hepatic cytochrome P-450 heme, apoproteins, and catalytic activities following in vivo administration to rats.
    Riddick DS, Park SS, Gelboin HV, Marks GS.
    Mol Pharmacol; 1990 Jan; 37(1):130-6. PubMed ID: 2405248
    [Abstract] [Full Text] [Related]

  • 4. Inactivation of chick embryo hepatic cytochrome P450 1A, 2H and 3A following in ovo administration of 3,5-diethoxycarbonyl-1,4-dihydro-2,6-dimethyl-4-ethylpyridine and 3-[2-(2,4,6-trimethylphenyl)thioethyl]-4-methylsydnone.
    McNamee JP, Kimmett SM, Marks GS.
    Biochem Pharmacol; 1995 May 17; 49(10):1443-52. PubMed ID: 7763287
    [Abstract] [Full Text] [Related]

  • 5. Irreversible binding of heme to microsomal protein during inactivation of cytochrome P450 by 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine.
    Riddick DS, Marks GS.
    Biochem Pharmacol; 1990 Oct 15; 40(8):1915-21. PubMed ID: 2242024
    [Abstract] [Full Text] [Related]

  • 6. Inactivation of cytochrome P450 and inhibition of ferrochelatase by analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine with 4-nonyl and 4-dodecyl substituents.
    McCluskey SA, Riddick DS, Mackie JE, Kimmett SM, Whitney RA, Marks GS.
    Can J Physiol Pharmacol; 1992 Aug 15; 70(8):1069-74. PubMed ID: 1473038
    [Abstract] [Full Text] [Related]

  • 7. Degradation of rat hepatic cytochrome P-450 heme by 3,5-dicarbethoxy-2,6-dimethyl-4-ethyl-1,4-dihydropyridine to irreversibly bound protein adducts.
    Correia MA, Decker C, Sugiyama K, Caldera P, Bornheim L, Wrighton SA, Rettie AE, Trager WF.
    Arch Biochem Biophys; 1987 Nov 01; 258(2):436-51. PubMed ID: 3674884
    [Abstract] [Full Text] [Related]

  • 8. Dose-dependent, mechanism-based inactivation of cytochrome P450 monooxygenases in vivo by 1-aminobenzotriazole in liver, lung, and kidney of untreated, phenobarbital-treated, and beta-naphthoflavone-treated guinea pigs.
    Knickle LC, Bend JR.
    Can J Physiol Pharmacol; 1992 Dec 01; 70(12):1610-7. PubMed ID: 1301239
    [Abstract] [Full Text] [Related]

  • 9. N-alkylation of the haem moiety of cytochrome P-450 caused by substituted dihydropyridines. Preferential attack of different pyrrole nitrogen atoms after induction of various cytochrome P-450 isoenzymes.
    De Matteis F, Gibbs AH, Hollands C.
    Biochem J; 1983 May 01; 211(2):455-61. PubMed ID: 6870842
    [Abstract] [Full Text] [Related]

  • 10. Mechanism-based inactivation of hepatic cytochrome P450 2C6 and P450 3A1 following in vivo administration of 3,5-diethoxycarbonyl-1,4-dihydro-2,6-dimethyl-4-ethylpyridine to rats: differences from previously observed in vitro results.
    Kimmett SM, McNamee JP, Marks GS.
    Can J Physiol Pharmacol; 1994 Apr 01; 72(4):397-401. PubMed ID: 7922872
    [Abstract] [Full Text] [Related]

  • 11. Inactivation of rat liver microsomal steroid hydroxylations by 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine: evidence for selectivity among steroid-inducible cytochrome P450IIIA forms.
    Riddick DS, McGilvray I, Marks GS.
    Can J Physiol Pharmacol; 1990 Dec 01; 68(12):1533-41. PubMed ID: 2085799
    [Abstract] [Full Text] [Related]

  • 12. Degradation of rat liver cytochromes P450 3A after their inactivation by 3,5-dicarbethoxy-2,6-dimethyl-4-ethyl-1,4-dihydropyridine: characterization of the proteolytic system.
    Correia MA, Davoll SH, Wrighton SA, Thomas PE.
    Arch Biochem Biophys; 1992 Sep 01; 297(2):228-38. PubMed ID: 1497342
    [Abstract] [Full Text] [Related]

  • 13. Evidence for mechanism-based inactivation of rat and chick embryo hepatic cytochrome P4501A and P4503A by dihydropyridines, sydnones, and dihydroquinolines.
    Kimmett SM, McNamee JP, Denofreo RT, Marks GS.
    Biochem Pharmacol; 1994 Jun 01; 47(11):2069-78. PubMed ID: 8010992
    [Abstract] [Full Text] [Related]

  • 14. Inactivation of rat hepatic cytochrome P-450 isozymes by 3,5-dicarbethoxy- 2,6-dimethyl-4-ethyl-1,4-dihydropyridine.
    Sugiyama K, Yao K, Rettie AE, Correia MA.
    Chem Res Toxicol; 1989 Jun 01; 2(6):400-10. PubMed ID: 2519730
    [Abstract] [Full Text] [Related]

  • 15. Effect of the suicide substrate 3,5-diethoxycarbonyl-2,6-dimethyl-4-ethyl-1,4-dihydropyridine on the metabolism of xenobiotics and on cytochrome P-450 apoproteins.
    Tephly TR, Black KA, Green MD, Coffman BL, Dannan GA, Guengerich FP.
    Mol Pharmacol; 1986 Jan 01; 29(1):81-7. PubMed ID: 3080674
    [Abstract] [Full Text] [Related]

  • 16. Olfactory cytochrome P-450. Studies with suicide substrates of the haemoprotein.
    Reed CJ, Lock EA, De Matteis F.
    Biochem J; 1988 Jul 15; 253(2):569-76. PubMed ID: 3263118
    [Abstract] [Full Text] [Related]

  • 17. Synergistic induction of delta-aminolevulinic acid synthase activity by N-ethylprotoporphyrin IX and 3,5-diethoxycarbonyl-1,4-dihydro-2,6-dimethyl-4-isobutylpyridine .
    Mackie JE, Marks GS.
    Biochem Pharmacol; 1989 Jul 01; 38(13):2169-73. PubMed ID: 2735955
    [Abstract] [Full Text] [Related]

  • 18. Differential apoprotein loss of rat liver cytochromes P450 after their inactivation by 3,5-dicarbethoxy-2,6-dimethyl-4-ethyl-1,4-dihydropyridine: a case for distinct proteolytic mechanisms?
    Correia MA, Yao K, Wrighton SA, Waxman DJ, Rettie AE.
    Arch Biochem Biophys; 1992 May 01; 294(2):493-503. PubMed ID: 1567205
    [Abstract] [Full Text] [Related]

  • 19. Bioactivation of arachidonic acid by the cytochrome P450 monooxygenases of guinea pig lung: the orthologue of cytochrome P450 2B4 is solely responsible for formation of epoxyeicosatrienoic acids.
    Knickle LC, Bend JR.
    Mol Pharmacol; 1994 Jun 01; 45(6):1273-80. PubMed ID: 8022420
    [Abstract] [Full Text] [Related]

  • 20. Purification of hepatic microsomal cytochromes P-450 from beta-naphthoflavone-treated Atlantic cod (Gadus morhua), a marine teleost fish.
    Goksøyr A.
    Biochim Biophys Acta; 1985 Jul 05; 840(3):409-17. PubMed ID: 4005295
    [Abstract] [Full Text] [Related]

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