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121 related items for PubMed ID: 3393143

  • 1. Differential inhibition of hepatic ferrochelatase by regioisomers of N-butyl-, N-pentyl-, N-hexyl-, and N-isobutylprotoporphyrin IX.
    McCluskey SA, Marks GS, Whitney RA, Ortiz de Montellano PR.
    Mol Pharmacol; 1988 Jul; 34(1):80-6. PubMed ID: 3393143
    [Abstract] [Full Text] [Related]

  • 2. Evidence for the stereoselective inhibition of chick embryo hepatic ferrochelatase by N-alkylated porphyrins.
    McCluskey SA, Whitney RA, Marks GS.
    Mol Pharmacol; 1989 Oct; 36(4):608-14. PubMed ID: 2811858
    [Abstract] [Full Text] [Related]

  • 3. Ferrochelatase-inhibitory activity and N-alkylprotoporphyrin formation with analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine (DDC) containing extended 4-alkyl groups: implications for the active site of ferrochelatase.
    McCluskey SA, Marks GS, Sutherland EP, Jacobsen N, Ortiz de Montellano PR.
    Mol Pharmacol; 1986 Oct; 30(4):352-7. PubMed ID: 3762522
    [Abstract] [Full Text] [Related]

  • 4. Evidence for the stereoselective inhibition of chick embryo hepatic ferrochelatase by N-alkylated porphyrins. II.
    Kimmett SM, Whitney RA, Marks GS.
    Mol Pharmacol; 1992 Aug; 42(2):307-10. PubMed ID: 1513328
    [Abstract] [Full Text] [Related]

  • 5. Isolation of regioisomers of N-alkylprotoporphyrin IX from chick embryo liver after treatment with porphyrinogenic xenobiotics.
    Kobus SM, Wong SG, Marks GS.
    Can J Physiol Pharmacol; 2001 Sep; 79(9):814-21. PubMed ID: 11599783
    [Abstract] [Full Text] [Related]

  • 6. Isolation of N-vinylprotoporphyrin IX after hepatic cytochrome P450 inactivation by 3-[(arylthio)ethyl]sydnone in chick embryos pretreated with phenobarbital, glutethimide, dexamethasone, and beta-naphthoflavone: differential inhibition of ferrochelatase by N-vinylprotoporphyrin regioisomers.
    Kimmett SM, Whitney RA, Marks GS.
    Mol Pharmacol; 1996 Apr; 49(4):676-82. PubMed ID: 8609896
    [Abstract] [Full Text] [Related]

  • 7. Suicidal destruction of cytochrome P-450 and reduction of ferrochelatase activity by 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine and its analogues in chick embryo liver cells.
    Marks GS, Allen DT, Johnston CT, Sutherland EP, Nakatsu K, Whitney RA.
    Mol Pharmacol; 1985 Apr; 27(4):459-65. PubMed ID: 3982391
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. Isolation of an N-alkylprotoporphyrin IX from chick embryo livers following the administration of 3,5-diethoxycarbonyl-1,4-dihydro-4-ethyl-2,6-dimethylpyridine.
    McCluskey SA, Sutherland EP, Racz WJ, Marks GS.
    Can J Physiol Pharmacol; 1987 Jul; 65(7):1500-2. PubMed ID: 3664364
    [Abstract] [Full Text] [Related]

  • 11. 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; 70(8):1069-74. PubMed ID: 1473038
    [Abstract] [Full Text] [Related]

  • 12. Thin-layer chromatographic separation of the ferrochelatase-inhibitory ring A and ring B regioisomers of N-ethylprotoporphyrin from a mixture of the four regioisomers.
    Kimmett SM, Marks GS.
    J Pharmacol Toxicol Methods; 1992 Sep; 28(2):113-7. PubMed ID: 1482786
    [Abstract] [Full Text] [Related]

  • 13. The apoprotein of cytochrome P450 3A2 does not selectively direct alkylation to one of four pyrrole rings of N-vinylprotoporphyrin IX.
    McNamee JP, Kobus SM, Marks GS.
    Can J Physiol Pharmacol; 1996 Aug; 74(8):996-1000. PubMed ID: 8960390
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Comparison of the effects of 3-ethoxycarbonyl-1,4-dihydro-2,4-dimethylpyridine and 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine on ferrochelatase activity and heme biosynthesis in chick embryo liver cells in culture.
    Marks GS, Allen DT, Sutherland EP, McCluskey SA, Whitney RA.
    Can J Physiol Pharmacol; 1986 Apr 01; 64(4):483-6. PubMed ID: 3730932
    [Abstract] [Full Text] [Related]

  • 16. Ferrochelatase-inhibitory and porphyrin-inducing properties of 3,5-diethoxycarbonyl-1, 4-dihydro-2,4,6-trimethylpyridine and its analogues in chick embryo liver cells.
    Cole SP, Whitney RA, Marks GS.
    Mol Pharmacol; 1981 Sep 01; 20(2):395-403. PubMed ID: 7300820
    [No Abstract] [Full Text] [Related]

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  • 18. Gender differences in N-alkyl protoporphyrin IX production in rats after the administration of porphyrinogenic xenobiotics.
    Wong SG, Kobus SM, McNamee JP, Marks GS.
    Drug Metab Dispos; 1998 Aug 01; 26(8):739-44. PubMed ID: 9698287
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