3α,7α,12α-Trihydroxy-5β-cholest-24-enoyl-CoA hydratase
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-540-85707-5_29.pdf
Reference5 articles.
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2. Xu, R.; Cuebas, D.A.: The reactions catalyzed by the inducible bifunctional enzyme of rat liver peroxisomes cannot lead to the formation of bile acids. Biochem. Biophys. Res. Commun., 221, 271–278 (1996)
3. Novikov, D.K.; Kamps, M.E.: Characterization of the promoter region of the human peroxisomal multifunctional enzyme type 2 gene. Biochem. Biophys. Res. Commun., 284, 226–231 (2001)
4. Kinoshita, T.; Miyata, M.; Ismail, S.M.; Fujimoto, Y.; Kakinuma, K.; Ikekawa, N.; Morisaki, M.: Synthesis and determination of stereochemistry of four diastereoisomers at the C-24 and C-25 position of 3α,7α,12α,24-tetrahydroxy-5β-cholestan-26-oic acid. Chem. Pharm. Bull., 36, 134–141 (1988)
5. Fujimoto, Y.; Kinoshita, T.M Oya, I.; Kakinuma, K.; Ikekawa, N.; Sonoda, Y.; Sato, Y.; Morisaki, M.: Non-stereoselective conversion of the four diastereomers at the C-24 and c-25 positions of 3α,7α,12α,24-tetrahydroxy-5β-cholestan-26-oic acid into cholic acid. Chem. Pharm. Bull., 36, 142–145 (1988)
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