Configuration at C-25 in 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestan-26-oic acid isolated from human bile
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference14 articles.
1. Biosynthesis of chenodeoxycholic acid in man. Stereospecific side-chain hydroxylation of 5β-cholestane-3α,7α-diol;Shefer;J. Clin. Invest.,1978
2. Stereospecific sidechain hydroxylations in the biosynthesis of chenodeoxycholic acid;Shefer;J. Biol. Chem.,1978
3. On the stereospecificity of microsomal “26”-hydroxylation in bile acid biosynthesis;Gustafsson;J. Biol. Chem.,1978
4. Cleavage of the taurine conjugate of 3α,7α,12α-trihydroxy-5β-cholestan-26-oic acid by rat fecal bacteria;Batta;J. Biol. Chem.,1979
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