Skip to main content

3α,7α,12α-Trihydroxy-5β-cholest-24-enoyl-CoA hydratase

  • Chapter
Class 4–6 Lyases, Isomerases, Ligases

Part of the book series: Springer Handbook of Enzymes ((HDBKENZYMES,volume S7))

  • 101 Accesses

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Kurosawa, T.; Sato, M.; Inoue, K.; Yoshimura, T.; Tohma, M.; Jiang, L.L.; Hashimoto, T.: Separation of stereoisomers of C27-bile acid CoA esters by liquid chromatography and its application to the study of the stereospecificities of d-and l-bifunctional protein in bile acid biosynthesis. Anal. Chim. Acta, 365, 249–257 (1998)

    Article  CAS  Google Scholar 

  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)

    Article  CAS  PubMed  Google Scholar 

  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)

    Article  CAS  PubMed  Google Scholar 

  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)

    CAS  Google Scholar 

  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)

    CAS  Google Scholar 

Download references

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2010 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

(2010). 3α,7α,12α-Trihydroxy-5β-cholest-24-enoyl-CoA hydratase. In: Schomburg, D., Schomburg, I., Chang, A. (eds) Class 4–6 Lyases, Isomerases, Ligases. Springer Handbook of Enzymes, vol S7. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-85707-5_29

Download citation

Publish with us

Policies and ethics