Chemical synthesis and hepatic biotransformation of 3 alpha,7 alpha-dihydroxy-7 beta-methyl-24-nor-5 beta-cholan-23-oic acid, a 7-methyl derivative of norchenodeoxycholic acid: studies in the hamster.-Reference-Cited by-同舟云学术

Chemical synthesis and hepatic biotransformation of 3 alpha,7 alpha-dihydroxy-7 beta-methyl-24-nor-5 beta-cholan-23-oic acid, a 7-methyl derivative of norchenodeoxycholic acid: studies in the hamster.

Published:1991-11 Issue:11 Volume:32 Page:1729-1740
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Yoshii M,Mosbach EH,Schteingart CD,Hagey LR,Hofmann AF,Cohen BI,McSherry CK

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference50 articles.

1. New bile acid analogs: 3α,7α-dihydroxy-7β-methyl-5β-cholanoic acid, 3α,7β-dihydroxy-7α-methyl-5β-cholanoic acid, and 3α-hydroxy-7ξ-methyl-5β-cholanoic acid;Une;J. Lipid Res.,1984

2. Synthesis of potential cholelitholytic agents: 3α,7α,12α-trihydroxy-7β-methyl-5β-cholanoic acid, 3α,7β,12α-trihydroxy-7α-methyl-5β-cholanoic acid, and 3α,12α-dihydroxy-7ξ–methyl-5β-cholanoic acid;Kuroki;J. Lipid Res.,1985

3. Synthesis of new bile acid analogues and their metabolism in the hamster: 3α,6α-dihydroxy-6β-methyl-5β-cholanoic acid and 3α,6β-dihydroxy-6α-methyl-5β-cholanoic acid;Matoba;J. Lipid Res.,1989

4. Metabolism of 3α,7α-dihydroxy-7β-methyl-5β-cholanoic acid and 3α,7β-dihydroxy-7α-methyl-5β-cholanoic acid in hamsters;Une;Biochim. Biophys. Acta.,1985

5. Metabolism of the bile acid analogues, 7β-methyl-cholic acid and 7α-methyl-ursocholic acid;Kuroki;Gastroenterology.,1987

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