Inhibitors of sterol biosynthesis. Synthesis and activities of ring C oxygenated sterols
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Organic Chemistry,Molecular Biology,Biochemistry
Reference35 articles.
1. Inhibition of sterol biosynthesis in L cells and mouse liver cells by 15-oxygenated sterols.
2. 14.alpha.-Ethyl-5.alpha.-cholest-7-ene-3.beta.,15.alpha.-diol, an extraordinarily potent inhibitor of sterol biosynthesis in animal cells
3. Inhibition of sterol synthesis in L cells by 14α-ethyl-5α-cholest-7-en-15α-ol-3-one at nanomolar concentrations
4. Inhibition of sterol synthesis in animal cells by 15-oxygenated sterols with the unnatural cis-c-d ring junction—5α, 14β-Cholest-7-en-15α-ol-3-one and 5α, 14β-Cholest-7-en-15β-ol-3-one
5. Inhibition of sterol biosynthesis in animal cells by 14 alpha-alkyl-substituted 15-oxygenated sterols.
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2. Photochemistry and Photophysics of Cholesta-5,7,9(11)-trien-3β-ol in Ethanol;Molecules;2023-05-14
3. Syntheses of Ring C Oxysterols: Inhibitors of Sterol Biosynthesis;Lipids;2007-01-16
4. Oxysterols: Modulators of Cholesterol Metabolism and Other Processes;Physiological Reviews;2000-01-01
5. Review of progress in sterol oxidations: 1987–1995;Lipids;1996-05
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