Synthesis of new bile acid analogues and their metabolism in the hamster: 3 alpha, 6 alpha-dihydroxy-6 beta-methyl-5 beta-cholanoic acid and 3 alpha, 6 beta-dihydroxy-6 alpha-methyl-5 beta-cholanoic acid.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference34 articles.
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3. Efficacy and specificity of chenodeoxycholic acid therapy for dissolving gallstones;Thistle;N. Engl. J. Med.,1973
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5. Chemical therapy of gallbladder and biliary duct stones. Present status and critique;Leuschner;Med. Klin.,1986
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1. GPBAR1 Activation by C6-Substituted Hyodeoxycholane Analogues Protect against Colitis;ACS Medicinal Chemistry Letters;2020-03-02
2. Metabolism, pharmacokinetics, and activity of a new 6-fluoro analogue of ursodeoxycholic acid in rats and hamsters;Gastroenterology;1995-04
3. New 6-substituted bile acids: physico-chemical and biological properties of 6 alpha-methyl ursodeoxycholic acid and 6 alpha-methyl-7-epicholic acid.;Journal of Lipid Research;1994-12
4. 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.;Journal of Lipid Research;1991-11
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