Date published: 2025-10-8

1-800-457-3801

SCBT Portrait Logo
Seach Input

Cholesteryl Linolenate (CAS 2545-22-4)

0.0(0)
Write a reviewAsk a question

Alternate Names:
LINOLEIC ACID CHOLESTEROL ESTER
CAS Number:
2545-22-4
Purity:
≥99%
Molecular Weight:
647.10
Molecular Formula:
C45H74O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Cholesteryl linolenate is a compound that functions as a substrate in lipid metabolism studies. It is involved in the synthesis of lipoproteins and plays a role in the transportation of cholesterol in cellular membranes. Cholesteryl linolenate is also known to interact with enzymes involved in lipid metabolism, influencing their activity and the production of lipid-derived signaling molecules. At the molecular level, Cholesteryl Linolenate can modulate the expression of genes related to lipid metabolism and inflammation. Its mechanism of action involves incorporation into cellular membranes and the regulation of lipid composition, which can impact cellular signaling pathways. Cholesteryl linolenate may influence the function of membrane-bound receptors and ion channels, contributing to the overall regulation of cellular processes.


Cholesteryl Linolenate (CAS 2545-22-4) References

  1. Thioredoxin reductase reduces lipid hydroperoxides and spares alpha-tocopherol.  |  May, JM., et al. 2002. Biochem Biophys Res Commun. 292: 45-9. PMID: 11890669
  2. Uptake and interconversion of cholesterol and cholesteryl esters byPhytophthora cactorum.  |  Elliott, CG. and Knights, BA. 1981. Lipids. 16: 1-7. PMID: 27521017
  3. Cholesteryl ester cycle in cultured hepatoma cells.  |  Glick, JM., et al. 1987. Atherosclerosis. 64: 223-30. PMID: 3606720
  4. The ternary phase diagram of lecithin, cholesteryl linolenate and water: phase behavior and structure.  |  Janiak, MJ., et al. 1974. J Mol Biol. 86: 325-39. PMID: 4472397
  5. Evaluation of a high-performance liquid chromatography method for isolation and quantitation of cholesterol and cholesteryl esters.  |  Carroll, RM. and Rudel, LL. 1981. J Lipid Res. 22: 359-63. PMID: 7240962
  6. beta-Carotene as a probe of lipid domains of reconstituted human plasma low-density lipoprotein: induced circular dichroism.  |  Chen, GC., et al. 1980. Biochemistry. 19: 4706-12. PMID: 7426623
  7. Phase behavior and crystalline structures of cholesteryl ester mixtures: a C-13 MASNMR study.  |  Guo, W. and Hamilton, JA. 1995. Biophys J. 68: 2376-86. PMID: 7647242
  8. Toxicity of polyunsaturated fatty acid esters for human monocyte-macrophages: the anomalous behaviour of cholesteryl linolenate.  |  Hardwick, SJ., et al. 1997. Free Radic Res. 26: 351-62. PMID: 9167940
  9. Micellar solubilization of cholesteryl esters of C18 fatty acids by a nonionic surfactant  |  Fakrul A.A Sayeed 1, Hans Schott. 1986. Journal of Colloid and Interface Science. 109: 140-149.
  10. Cholesteryl oleate: Mounting sex pheromone of the hard tick Dermacentor variabilis (Say) (Acari: Ixodidae)  |  J.G.C Hamilton 1, Daniel E Sonenshine 1, William R Lusby 2. 1989. Journal of Insect Physiology. 35: 873-879.
  11. Influence of steroid structure on the pyrolytic formation of polycyclic aromatic hydrocarbons  |  Phillip F. Britt, A.C. Buchanan III, Michelle K. Kidder, Clyde V. Owens Jr. 2003. Journal of Analytical and Applied Pyrolysis. 66: 71-95.
  12. Thermal Characterization of Induced Mesomorphism in Binary Mixture of Cholesteryl and Poly Ethylene Glycol  |  T. N. Govindaiah, H. R. Sreepad & Nagappa. 2013. Molecular Crystals and Liquid Crystals. 575: 22-29.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cholesteryl Linolenate, 100 mg

sc-294020
100 mg
$70.00