Date published: 2026-5-1

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20α-Hydroxy Cholesterol (CAS 516-72-3)

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Alternate Names:
5-Cholestene-3β,20α-diol
Application:
20α-Hydroxy Cholesterol is an allosteric activator of the Hedgehog signaling pathway Smoothened (Smo) oncoprotein
CAS Number:
516-72-3
Molecular Weight:
402.65
Molecular Formula:
C27H46O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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20α-Hydroxycholesterol, a cholesterol derivative, has emerged as a key regulator of cellular cholesterol homeostasis and lipid metabolism. Its mechanism of action primarily involves its role as an endogenous agonist for liver X receptors (LXRs), nuclear receptors that play crucial roles in the transcriptional regulation of genes involved in cholesterol metabolism and transport. Upon binding to LXRs, 20α-hydroxycholesterol induces the expression of genes encoding proteins involved in cholesterol efflux, such as ATP-binding cassette transporters ABCA1 and ABCG1, leading to the removal of excess cholesterol from cells. Additionally, 20α-hydroxycholesterol has been shown to modulate the expression of genes involved in fatty acid synthesis and lipid droplet formation, further influencing lipid metabolism. In scientific research, 20α-hydroxycholesterol has been studied extensively to explain its role in cholesterol homeostasis, lipid metabolism, and the pathogenesis of metabolic disorders such as atherosclerosis and non-alcoholic fatty liver disease (NAFLD). Additionally, 20α-hydroxycholesterol serves as a valuable biomarker for assessing cholesterol metabolism and its dysregulation in various physiological and pathological conditions.


20α-Hydroxy Cholesterol (CAS 516-72-3) References

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  2. Nonionic micellar liquid chromatography coupled to immobilized enzyme reactors.  |  Tomer, S., et al. 2001. J Chromatogr A. 923: 7-16. PMID: 11510562
  3. Small Molecule Cocktails Promote Fibroblast-to-Leydig-like Cell Conversion for Hypogonadism Therapy.  |  Yuan, F., et al. 2023. Pharmaceutics. 15: PMID: 37896216
  4. Transformation of labeled cholesterol, 20-alpha-hydroxycholesterol, (22R)-22-hydroxycholesterol, and (22R)-20-alpha, 22-dihydroxycholesterol by adrenal acetone-dried preparations from guinea pigs, cattle and man.  |  Burstein, S., et al. 1970. Steroids. 15: 13-60. PMID: 4905214
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  8. The response of the antioxidant defense system in rat hepatocytes challenged with oxysterols is modified by Covi-ox.  |  Cantwell, H. and Devery, R. 1998. Cell Biol Toxicol. 14: 401-9. PMID: 9879932
  9. Effects of various cooking and re-heating methods on cholesterol oxidation products of beef loin  |  Lee, S. O., et al. 2006. Asian-australasian journal of animal sciences. 19(5): 756-762.
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

20α-Hydroxy Cholesterol, 10 mg

sc-209393
10 mg
$300.00