Sterol Synthesis. Chemical syntheses, spectral properties, and metabolism of 5alpha-cholest-8(14)-en-3beta,15beta-diol and 5alpha-cholest-8(14)-en-3beta,15alpha-diol.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference57 articles.
1. Enzymatic conversion of ‡8(14)-cholesten-3β-ol to cholesterol
2. 5α-Cholest-8(14)-en-3β-ol, a Possible Intermediate in the Biosynthesis of Cholesterol
3. Recent investigations on the nature of sterol intermediates in the biosynthesis of cholesterol
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1. Initial separation methods;Analysis of Sterols;1997
2. Inhibitors of sterol synthesis. Submicromolar 14 alpha-ethyl-5 alpha-cholest-7-ene-3 beta, 15 alpha-diol causes a major modification of the sterol composition of CHO-K1 cells and a marked change in cell morphology.;Journal of Lipid Research;1994-07
3. Inhibitors of sterol synthesis. Chemical synthesis of 7α-ethyl and 16α-ethyl derivatives of Δ8(14)-15-oxygenated sterols and their effects on 3-hydroxy-3-methylglutaryl coenzyme A reductase in CHO-K1 cells;Chemistry and Physics of Lipids;1992-07
4. Inhibitors of sterol synthesis. Chemical synthesis and spectral properties of (25R)-5α-cholest-8(14)-ene-3β,15β,26-triol, a potential metabolite of 3β-hydroxy-5α-cholest-8(14)-en-15-one and its effects on 3-hydroxy-3-methylglutaryl-coenzyme A reductase in CHO-K1 cells;Chemistry and Physics of Lipids;1992-05
5. Inhibitors of sterol synthesis. Chromatography of acetate derivatives of oxygenated sterols.;Journal of Lipid Research;1989-07
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