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Journal Abstract Search

142 related items for PubMed ID: 7923480

  • 41. Inhibitors of sterol synthesis. The effects of dietary 5 alpha-cholest-8(14)-en-3 beta-ol-15-one on the fate of [4-14C]cholesterol and [2,4-3H]5 alpha-cholest-8(14)-en-3 beta-ol-15-one after intragastric administration to rats.
    Brabson JS, Schroepfer GJ.
    Chem Phys Lipids; 1988 May; 47(1):1-20. PubMed ID: 3396132
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  • 42. Inhibition of sterol biosynthesis in animal cells by 14 alpha-alkyl-substituted 15-oxygenated sterols.
    Schroepfer GJ, Parish EJ, Tsuda M, Raulston DL, Kandutsch AA.
    J Lipid Res; 1979 Nov; 20(8):994-8. PubMed ID: 533832
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  • 43. A 15-ketosterol is a liver X receptor ligand that suppresses sterol-responsive element binding protein-2 activity.
    Schmidt RJ, Ficorilli JV, Zhang Y, Bramlett KS, Beyer TP, Borchert K, Dowless MS, Houck KA, Burris TP, Eacho PI, Liang G, Guo LW, Wilson WK, Michael LF, Cao G.
    J Lipid Res; 2006 May; 47(5):1037-44. PubMed ID: 16415294
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  • 44. Synthesis of the marine epoxy sterol 9 alpha,11 alpha-epoxy-5 alpha-cholest-7-ene-3 beta,5,6 beta-triol.
    Migliuolo A, Notaro G, Piccialli V, Sica D.
    Steroids; 1991 Mar; 56(3):154-8. PubMed ID: 2042233
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  • 45. Inhibitors of sterol synthesis. Synthesis and spectral characterization of fatty acids esters of 5 alpha-cholest-8(14)-en-3 beta-ol-15-one.
    St Pyrek J, Schroepfer GJ.
    J Lipid Res; 1987 Nov; 28(11):1308-12. PubMed ID: 3430061
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  • 52. Two new 9,11-secosterols from the marine sponge Spongia officinalis. Synthesis of 9,11-seco-3 beta,6 alpha,11-trihydroxy-5 alpha-cholest-7-en-9-one.
    Migliuolo A, Piccialli V, Sica D.
    Steroids; 1992 Jul; 57(7):344-7. PubMed ID: 1412572
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  • 56. Post-transcriptional regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase by 3 beta-hydroxy-lanost-8-en-32-al, an intermediate in the conversion of lanosterol to cholesterol.
    Leonard DA, Kotarski MA, Tessiatore JE, Favata MF, Trzaskos JM.
    Arch Biochem Biophys; 1994 Apr; 310(1):152-7. PubMed ID: 8161198
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  • 59. Inhibitors of sterol synthesis. Metabolism of 5 alpha-cholest-8(14)-en-3 beta-ol-15-one after intravenous administration to bile duct-cannulated rats.
    Schroepfer GJ, Chu AJ, Needleman DH, Izumi A, Nguyen PT, Wang KS, Little JM, Sherrill BC, Kisic A.
    J Biol Chem; 1988 Mar 25; 263(9):4110-23. PubMed ID: 3346239
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  • 60. Synthesis, properties and reactions of 3 beta-benzoyloxy-7 alpha-15 beta-dichloro-5 alpha-cholest-8(14)-ene.
    Parish EJ, Tsuda M, Schroepfer GJ.
    Chem Phys Lipids; 1979 May 25; 24(2):167-82. PubMed ID: 455568
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