Date published: 2025-9-29

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Hyodeoxycholic acid methyl ester (CAS 2868-48-6)

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Alternate Names:
3α,6α-Dihydroxy-5β-cholan-24-oic acid methyl ester
Application:
CAS Number:
2868-48-6
Molecular Weight:
406.60
Molecular Formula:
C25H42O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Hyodeoxycholic acid methyl ester is a methylated derivative of hyodeoxycholic acid, a bile acid involved in the emulsification and absorption of dietary fats. In research, this compound is primarily used to study bile acid metabolism, lipid digestion, and the regulatory mechanisms of cholesterol homeostasis. By incorporating hyodeoxycholic acid methyl ester into experimental setups, researchers can investigate the enzymatic activities responsible for bile acid synthesis and conjugation, particularly the roles of bile acid methyltransferases and hydroxylases. One of the key areas of study involving this compound is its impact on the solubilization and transport of lipids within the digestive system. Hyodeoxycholic acid methyl ester serves as a model compound to examine the interactions between bile acids and dietary fats, providing insights into the mechanisms of fat absorption and the formation of micelles. These studies help explain how modifications in bile acid structure influence their physicochemical properties and biological functions. Additionally, hyodeoxycholic acid methyl ester is used in research to explore its effects on the modulation of gene expression related to lipid metabolism. Researchers utilize this compound to study its interactions with nuclear receptors such as FXR (farnesoid X receptor), which play crucial roles in regulating bile acid synthesis and maintaining lipid and cholesterol homeostasis. These investigations contribute to a deeper understanding of bile acid biochemistry and its broader implications in metabolic regulation and lipid transport.


Hyodeoxycholic acid methyl ester (CAS 2868-48-6) References

  1. Selective activation of liver X receptor alpha by 6alpha-hydroxy bile acids and analogs.  |  Song, C., et al. 2000. Steroids. 65: 423-7. PMID: 10936612
  2. [Synthesis of sterols oxygenated in the terminal fragment of their side chains].  |  Antonchik, AV., et al. 2008. Bioorg Khim. 34: 437-50. PMID: 18695715
  3. Synthesis and antimicrobial evaluation of bile acid tridentate conjugates.  |  Huang, L., et al. 2009. Steroids. 74: 701-6. PMID: 19463693
  4. Hydroxylation of taurolithocholate by isolated human liver microsomes. I. Identification of metabolic product.  |  Trülzsch, D., et al. 1974. Biochem Med. 9: 158-66. PMID: 4150758
  5. The synthesis and characterization of analogs of the antimicrobial compound squalamine: 6 beta-hydroxy-3-aminosterols synthesized from hyodeoxycholic acid.  |  Jones, SR., et al. 1996. Steroids. 61: 565-71. PMID: 8910969
  6. Characterization of bile acid methyl ester acetate derivatives of rat bile using solventless glass capillary gas chromatography and electron impact and ammonia chemical ionization mass spectrometry.  |  Murata, Takeshi,. 1982. Journal of Chromatography A. 239: 571-583.
  7. The first stereoselective synthesis of orostanal, a novel abeo-sterol inducing apoptosis in leukemia cells.  |  Liu, Bo, and Weishan Zhou. 2002. Tetrahedron letters. 43.23: 4187-4189.
  8. The first stereoselective synthesis of orostanal isolated from a marine sponge Stelletta hiwasaensis[J].  |  Liu B, Zhou W S. 2003. Tetrahedron,., 59(18):: 3379-338.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hyodeoxycholic acid methyl ester, 1 g

sc-215162
1 g
$36.00