Methyl jacarate

CATALOG # 1234
Amount 25 mg
Price $325.00
Methyl jacarate
  • Catalog #:1234
  • Scientific Name:Methyl jacarate
  • Common Name:Methyl 8(Z),10(E),12(Z)-Octadecatrienoate; Jacaric acid methyl ester; Conjugated linolenic acid methyl ester; CLnA
  • Empirical Formula:C19H32O2
  • CAS#n/a
  • SDSView Safety Data Sheet
  • Data Sheet:View Data Sheet
  • Formula Weight:293
  • Unit:25 mg
  • Solvent:none
  • Source:Natural
  • Purity:96+%
  • Analytical Methods:GC; TLC; identity confirmed by MS
  • Natural Source:Plant
  • Solubility:hexane, ethanol, methanol, chloroform
  • Physical Appearance:liquid
  • Storage:-20°C
  • Dry Ice:No
  • Hazardous:No
  • Literature References:1. P. Aruna et al. Health Benefits of Punicic Acid: A Review. Comprehensive Reviews in Food Science and Food Safety. Vol. 15 pp. 16-27, 2016
    2. I. Pereira et al. Pomegranate Seed Oil (Punica Granatum L.): A Source of Punicic Acid (Conjugated α-Linolenic Acid). Journal of Human Nutrition and Food Science. Vol. 2(1) pp. 1024, 2014
    3. Koba et al. Genetically Modified Rapeseed Oil Containing cis-9, trans-11, cis-13-Octadecatrienoic Acid Affects Body Fat Mass and Lipid Metabolism in Mice. J. Agric Food Chem. Vol. 55(9) pp. 3741-3748, 2007
    4. T. Tsuzuki et al. Tumor growth suppression by α-eleostearic acid, a linolenic acid isomer with a conjugated triene system, via lipid peroxidation. Carcinogenesis. Vol. 25(8) pp. 1417-1425, 2004
    5. J. Gasmi and J. Sanderson. Jacaric acid and its octadecatrienoic acid geoisomers induce apoptosis selectively in cancerous human prostate cells: a mechanistic and 3-D structure–activity study. Phytomedicine. Vol. 20 pp. 734-742, 2013
    6. Liu, W.N., and Leung, K.N. Jacaric acid inhibits the growth of murine macrophage-like leukemia PU5-1.8 cells by inducing cell cycle arrest and apoptosis. Cancer Cell Int. Vol. 15 pp. 90, 2015
    7. T. Boussetta et al. Punicic Acid a Conjugated Linolenic Acid Inhibits TNFα-Induced Neutrophil Hyperactivation and Protects from Experimental Colon Inflammation in Rats. PLoS One. Vol. 4(7) pp. e6468, 2009
    8. Z. Mashhadi et al. Robust Inhibitory Effects of Conjugated Linolenic Acids on a Cyclooxygenase-related Linoleate 10S-Dioxygenase: Comparison with COX-1 and COX-2. Biochim. Biophys. Acta. Vol. 1851(10) pp. 1346-1352, 2015