Methyl stearidonate (all cis-6,9,12,15)

CATALOG # 1277
Amount 25 mg
Price $375.00
Methyl stearidonate (all cis-6,9,12,15)
  • Catalog #:1277
  • Scientific Name:Methyl stearidonate (all cis-6,9,12,15)
  • Common Name:C18:4 (all cis-6,9,12,15) Methyl ester; Moroctic acid methyl ester
  • Empirical Formula:C19H30O2
  • CAS#73097-00-4
  • SDSView Safety Data Sheet
  • Data Sheet:View Data Sheet
  • Formula Weight:290
  • Unit:25 mg
  • Solvent:none
  • Source:natural
  • Purity:99%
  • Analytical Methods:GC, TLC, Identity confirmed by MS
  • Natural Source:plant
  • Solubility:chloroform, hexane, ethyl ether
  • Physical Appearance:liquid
  • Storage:-20°C
  • Dry Ice:No
  • Hazardous:No
  • Literature References:Application Notes:

    This product is a high purity polyunsaturated fatty acid methyl ester that is ideal for analysis and biological studies. Recently it has been found that conjugated stearidonic acid can be produced by the bacteria bifidobacteria and propionibacteria from stearidonic acid, suggesting an as yet unexplored pathway of stearidonic acid in mammals through intestinal microbes.1 Stearidonic acid, along with similar polyunsaturated fatty acids, demonstrates inhibitory effects on the 5-lipoxygenase pathway,2 tumor necrosis factor,3 and prostoglandin E2,3 thereby suppressing inflammation. Stearidonic acid is the product of the rate-limiting step in the synthesis of eicosapentaenoic acid from alpha-linolenic acid and is thus more readily converted to eicosapentaenoic than is alpha-linolenic acid.4 Eicosapentaenoic acid has been shown to lower the risk of cardiovascular disease and stearidonic acid is therefore also important in reducing this risk.4 Much research is currently being carried out to try to introduce more stearidonic acid into the human diet.

    1. A. Hennessy et al. “The Production of Conjugated alpha-Linolenic, gamma-Linolenic and Stearidonic Acids by Strains of Bifidobacteria and Propionibacteria” Lipids, Vol. 47:3 pp. 313-327, 2012
    2. M. Guichardant et al. “Stearidonic acid, an inhibitor of the 5-lipoxygenase pathway. A comparison with timnodonic and dihomogammalinolenic acid” Lipids, Vol. 28:4 pp. 321-324, 1993
    3. K. Ishihara et al. “Comparison of the effects of dietary alpha-linolenic, stearidonic, and eicosapentaenoic acids on production of inflammatory mediators in mice” Lipids, Vol. 37:5 pp. 481-486, 2002
    4. S. Lemke et al. “Dietary intake of stearidonic acid–enriched soybean oil increases the omega-3 index: randomized, double-blind clinical study of efficacy and safety” Am J Clin Nutr, Vol. 92:4 pp. 766-775, 2010