Methyl jacarate

CATALOG # 1234
Amount 25 mg
Price $325.00
Qty
 
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:Application Notes:

    Jacaric acid is a conjugated linolenic acid (CLnA) that is found in high amounts in several natural oils, including Jacaranda mimosofilia seed oil. CLnAs contain 3 or 4 double bonds (which can be any combination of cis or trans) and predominantly 9,11,13- and 8,10,12-octadecatrienoic acid positional isomers. Research indicates that CLnAs posses strong antidiabetic, antiobesity, antiproliferative, and anticarcinogenic activities as well as a significant affect on lipid metabolism.(1) These physiological effects make CLnAs potential candidates as therapeutic agents, although more research is needed to verify previous findings.(2) Some studies suggest that punicic acid and other CLnAs can reduce adipose tissue in mouse models, making it potentially useful as a weight-controlling lipid.(3) CLnAs, including punicic, jacaric, and α-eleostearic acids, have been shown to suppress tumor cell growth through lipoperoxidation and apoptotic pathways.(4,5,6) It has been found that some CLnAs, such as punicic acid and jacaric acid, exert a potent anti-inflammatory effect through the inhibition of TNFα-induced priming of ROS production and inhibition of cyclooxygenase 1 (COX-1).(7,8)

    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