Literature DB >> 6833885

Configuration at C-25 in 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestan-26-oic acid isolated from human bile.

A K Batta, G Salen, S Shefer, B Dayal, G S Tint.   

Abstract

This report describes the isolation of the natural isomer of 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestan-26-oic acid from human bile by a method that retains the configuration at C-25. The stereochemistry at C-25 in this bile acid was defined as 25R by a direct comparison with standard (25R)3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestan-26-oic acid.

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Year:  1983        PMID： 6833885

Source DB:  PubMed          Journal:  J Lipid Res        ISSN： 0022-2275            Impact factor:   5.922


  2 in total

1.  The role of alpha-methylacyl-CoA racemase in bile acid synthesis.

Authors:  Dean A Cuebas; Christopher Phillips; Werner Schmitz; Ernst Conzelmann; Dmitry K Novikov
Journal:  Biochem J       Date:  2002-05-01       Impact factor: 3.857

Review 2.  Bile acids: the role of peroxisomes.

Authors:  Sacha Ferdinandusse; Simone Denis; Phyllis L Faust; Ronald J A Wanders
Journal:  J Lipid Res       Date:  2009-04-08       Impact factor: 5.922
  2 in total

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