Concerning the chemical synthesis of 3β-hydroxy-5α-cholest-8(14)-en-15-one, a novel regulator of cholesterol metabolism
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Organic Chemistry,Molecular Biology,Biochemistry
Reference55 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, a potent inhibitor of sterol biosynthesis, has two sites of action in cultured mammalian cells.
3. Inhibitors of sterol synthesis. Dietary administration of 5α-cholest-8(14)-en-3β-ol-15-one inhibits the intestinal absorption of cholesterol in lymph-cannulated rats
4. Inhibitors of sterol synthesis. The effects of dietary 5α-cholest-8(14)-en-3β-ol-15-one on the fate of [4-14C]cholesterol and [2,4-3H]5α-cholest-8(14)-en-3β-ol-15-one after intragastric administration to rats
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2. Regulation of cholesterol biosynthesis and metabolism in Hep G2 cells by Δ8(14)-15-ketoergostane derivatives;Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry;2010-08-19
3. (22R,23R)-3β-hydroxy-22,23-epoxy-5α-ergost-8(14)-en-15-one: Improved synthesis and toxicity to MCF-7 cells;Russian Journal of Bioorganic Chemistry;2008-11
4. Novel side chain modified Δ8(14)-15-ketosterols;Steroids;2007-03
5. New Δ8(14)-15-Ketosterols with an Oxygenated Side Chain;Russian Journal of Bioorganic Chemistry;2005-05
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