Synthesis of four diastereoisomers at carbons 24 and 25 of 3 alpha,7 alpha,12 alpha,24-tetrahydroxy-5 beta-cholestan-26-oic acid, intermediates of bile acid biosynthesis.-Reference-Cited by-同舟云学术

Synthesis of four diastereoisomers at carbons 24 and 25 of 3 alpha,7 alpha,12 alpha,24-tetrahydroxy-5 beta-cholestan-26-oic acid, intermediates of bile acid biosynthesis.

Published:1983-07 Issue:7 Volume:24 Page:924-929
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Une M,Nagai F,Kihira K,Kuramoto T,Hoshita T

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference13 articles.

1. The Biology of Cholesterol and Related Steroids;Myant,1981

2. Synthesis of 3a,7a, 12a,24£-tetrahydroxy-coprostanic acid;Inai;J. Biochem. (Tokyo).,1964

3. Metabolism of 3a,7a,12a,24-tetrahydroxy-5ß-cholestanoic acid in the guinea pig;Tanaka;Hiroshima J. Med. Sci.,1965

4. The formation of bile acids from cholesterol. The conversion of 5ß-cholestane- 3a,7a,12a-triol-26-oic acid to cholic acid via 5ß-cholestane-3a,7a,12a,24***-tetraol-26-oic acid I by rat liver;Masui;J. Biol. Chem.,1966

5. Reversedphase high-performance liquid chromatographic separation and quantification of individual human bile acids;Mingrone;J. Chromatogr.,1980

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Key discoveries in bile acid chemistry and biology and their clinical applications: history of the last eight decades;Journal of Lipid Research;2014-08

2. A novel varanic acid epimer – (24R,25S)-3α,7α,12α,24-tetrahydroxy-5β-cholestan-27-oic acid – is a major biliary bile acid in two varanid lizards and the Gila monster;Steroids;2012-11

3. Biliary bile acids in birds of the Cotingidae family: Taurine-conjugated (24R,25R)-3α,7α,24-trihydroxy-5β-cholestan-27-oic acid and two epimers (25R and 25S) of 3α,7α-dihydroxy-5β-cholestan-27-oic acid;Steroids;2011-09

4. Identification of intermediates in the bile acid synthetic pathway as ligands for the farnesoid X receptor;Journal of Lipid Research;2004-08

5. Synthesis and anti-HIV activity of a bile acid analog of cosalane;Tetrahedron;2001-11