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203633-16-3

203633-16-3 Structure

203633-16-3 Structure
IdentificationBack Directory
[Name]

α-Linolenic acid ethyl ester-d5
[CAS]

203633-16-3
[Synonyms]

α-Linolenic Acid ethyl ester-d5
[Molecular Formula]

C20H34O2
[MOL File]

203633-16-3.mol
[Molecular Weight]

306.49
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Ethanol: soluble
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
Hazard InformationBack Directory
[Description]

α-Linolenic acid ethyl ester-d5 is intended for use as an internal standard for the quantification of α-linolenic acid ethyl ester by GC- or LC-MS. α-Linolenic acid ethyl ester is an esterified form of α-linolenic acid . It increases cyclin E levels and the activity of Cdk2/cyclin E, ERK, and JNK in hepatic stellate cells when used at a concentration of 50 μM.1 α-Linolenic acid ethyl ester (25 μg/ml) inhibits the growth of S. mutans, C. albicans, and P. gingivalis by 98, 72, and 92%, respectively, in vitro.2 It has been found in biodiesel produced from castor oil using ethanol.3 α-Linolenic acid ethyl ester has been used as a substrate in lipid peroxidation assays for antioxidant activity.4
[Uses]

Ethyl linolenate-d5 is the deuterium labeled Ethyl linolenate. Ethyl linolenate is a fatty acid ethyl ester (FAEE). Ethyl linolenate plays an active role in inhibition of the cellular production on melanin with an IC50 of 70 μM. Anti-melanogenesis Effects[1].
[References]

1. Li, J., Hu, W., Baldassare, J.J., et al. The ethanol metabolite, linolenic acid ethyl ester, stimulates mitogen-activated protein kinase and cyclin signaling in hepatic stellate cells Life Sci. 73(9),1083-1096(2003).
2. Huang, C.B., and Ebersole, J.L. A novel bioactivity of omega-3 polyunsaturated fatty acids and their ester derivatives Mol. Oral Microbiol. 25(1),75-80(2010).
3. Concei??o, M.M., Fernandes, V.J., Jr., Bezerra, A.F., et al. Dynamic kinetic calculation of castor oil biodiesel J. Therm. Anal. Calorim. 87(3),865-869(2007).
4. Miyake, T., and Shibamoto, T. Antioxidative activities of natural compounds found in plants J. Agric. Food Chem. 45(5),1819-1822(1997).
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