Literature DB >> 3445290

Synthesis of 3 beta-hydroxy-5 alpha-cholest-8-en-7-one and 3 beta-hydroxy-5 alpha-cholest-8-en-11-one: evaluation as potential hypocholesterolemic agents.

E J Parish1, V B Nanduri, J M Seikel, H H Kohl, K E Nusbaum.   

Abstract

An efficient procedure for the chemical synthesis of 3 beta-hydroxy-5 alpha-cholest-8-en-7-one and 3 beta-hydroxy-5 alpha-cholest-8-en-11-one is described. These ketosterols have been shown to have possible significant hypocholesterolemic effects when fed to normal rats at a level of 0.15% in a laboratory chow diet. The diets containing the steroids caused significant decreases in food consumption which were associated with decreases in the rate of gain in body weight.

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Year:  1986        PMID: 3445290     DOI: 10.1016/0039-128x(86)90027-9

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  2 in total

1.  Syntheses of ring C oxysterols: inhibitors of sterol biosynthesis.

Authors:  Edward J Parish; Chi Luo; Thomas Webb; John D Gorden
Journal:  Lipids       Date:  2007-01-16       Impact factor: 1.880

Review 2.  Side-chain oxysterol regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity.

Authors:  E J Parish; S C Parish; S Li
Journal:  Lipids       Date:  1995-03       Impact factor: 1.880

  2 in total

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