7-Methyl bile acids: Effects of chenodeoxycholic acid, cholic acid, and their 7β-methyl analogues on the formation of cholesterol gallstones in the prairie dog

Author:

Matoba Naoyuki,Cohen Bertram I.,Mosbach Erwin H.,Stenger Richard J.,Kuroki Syoji,Une Mizuho,McSherry Charles K.

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference28 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. Metabolism of 3α,7α-dihydroxy-7β-methyl-5β-cholanoic acid and 3α,7β-dihydroxy-7β-methyl-5β-cholanoic acid in hamsters;Une;Biochim Biophys Acta,1985

4. Metabolism of the bile acid analogues, 7β-methyl-cholic acid and 7α-methyl-ursocholic acid;Kuroki;J Lipid Res,1987

5. 7-Methyl bile acids: 7β-methyl-cholic acid inhibits bacterial 7-dehydroxylation of cholic acid and chenodeoxycholic acid in the hamster;Kuroki;J Lipid Res,1987

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