26-Oxygenated derivatives of As04)-15-ketosterols have been synthesized from (25R)-3#,26-diacetoxy-5a-cholest-8( )-en-15-one (IX) as part of a program to prepare potential metabolites and analogs of 3/~-hydroxy-5c~-cholest-8( )-en-15-one (I), a potent regulator of cholesterol metabolism. Partial hyd
โฆ LIBER โฆ
Rates of sterol synthesis and hydroxymethylglutaryl coenzyme a reductase levels, and the effects of cholest-4-en-3-one on these parameters, in the livers of inbred strains of mice
โ Scribed by Robert M. Packie; A. A. Kandutsch
- Publisher
- Springer
- Year
- 1970
- Tongue
- English
- Weight
- 658 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0006-2928
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(25R)-5 alpha-Cholest-8(14)-ene-3 beta,15 beta,26-triol (III) was prepared by reduction of (25R)-3 beta,26-diacetoxy-5 alpha-cholest-8(14)-en-15-one with sodium borohydride followed by treatment of the crude product with lithium aluminium hydride. The trihydroxysterol III, a potential metabolite of