Inhibitors of sterol synthesis. Chemical synthesis of 5 beta-cholest-8-ene-3 beta,15 alpha-diol and its effects on 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in CHO-K1 cells.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference46 articles.
1. Inhibition of sterol biosynthesis in L cells and mouse liver cells by 15-oxygenated sterols;Schroepfer;J. Biol. Chem.,1977
2. 14a-Ethyl-5α -cholest-7-en-3β,15a-diol, an extraordinarily potent inhibitor of sterol synthesis in animal cells;Schroepfer;J. Am. Chem. Soc.,1977
3. Inhibition of sterol synthesis in L cells by 14a-ethyl-5α -cholest-7-en-15α -ol-3-one at nanomolar concentrations;Schroepfer;Biochem. Biophys. Res. Common.,1977
4. Inhibition of sterol biosynthesis in animal cells by 14a-alkyl substituted 15- oxygenated sterols;Schroepfer;J. Lipid Res.,1979
5. Inhibition of sterol biosynthesis by 9α-fluoro and 9α-hydroxy derivatives of 5a-cholest-8 (14)-en-3β-ol-15-one;Schroepfer;Biochem. Biophys. Res. Commun.,1979
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Review of progress in sterol oxidations: 1987–1995;Lipids;1996-05
2. 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
3. Inhibitors of sterol synthesis. Characterization of beta,gamma-unsaturated analogs of 3 beta-hydroxy-5 alpha-cholest-8(14)-en-15-one and their effects on 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in CHO-K1 cells.;Journal of Lipid Research;1991-07
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