Metabolism of 7 beta-alkyl chenodeoxycholic acid analogs and their effect on cholesterol metabolism in hamsters.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference14 articles.
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3. Metabolism of 3α,7α-dihy-droxy-7β-methyl-5β-cholanoic acid and 3α,7β-dihydroxy-7α-methyl-5β-cholanoic acid in hamsters;Une;Biochim. Biophys. Acta.,1985
4. 7-Methyl bile acid: effects of chenodeoxycholic acid, cholic acid and their 7β-methyl analogues on the formation of cholesterol gallstones in the prairie dog;Matoba;Gastroenterology.,1989
5. Synthesis of bile acid analogs: 7-alkylated chenodeoxycholic acids;Une;Steroids.,1989
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1. (E)-7-Ethylidene-lithocholic Acid (7-ELCA) Is a Potent Dual Farnesoid X Receptor (FXR) Antagonist and GPBAR1 Agonist Inhibiting FXR-Induced Gene Expression in Hepatocytes and Stimulating Glucagon-like Peptide-1 Secretion From Enteroendocrine Cells;Frontiers in Pharmacology;2021-08-13
2. Structure-activity relationship of bile acids and bile acid analogs in regard to FXR activation;Journal of Lipid Research;2004-01
3. Hypocholesterolemic Effect of Bile Acid Sulfonate Analogs in Hamsters.;Biological and Pharmaceutical Bulletin;2001
4. Metabolism and time-course excretion of murideoxycholic acid, a 6β-hydroxylated bile acid, in humans;Journal of Hepatology;1993
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