143202-57-7
Chemical Structure
Juniperonic acid ethyl ester
Synonym(s): Ethyl 20:4BSO
- CAS No.: 143202-57-7
- Formula:C22H36O2
- Molecular Weight:332.53
IUPAC Name: ethyl (5Z,11Z,14Z,17Z)-icosa-5,11,14,17-tetraenoate
InChIKey: OMJMEJQTYAELIJ-LYBCEPMBSA-N
SMILES: C(=C\CCCC/C=C\C/C=C\C/C=C\CC)\CCCC(OCC)=O
Biological Activity: Juniperonic acid ethyl ester (Ethyl 20:4BSO) is an orally active non-methylene-interrupted ω-3 polyunsaturated fatty acid ethyl ester. Juniperonic acid ethyl ester exists in Platycladus orientalis seed oil. Juniperonic acid ethyl ester reduces the ratio of 20:3n-9 to arachidonic acid in hepatic phosphatidylcholine of rats with essential fatty acid deficiency. Juniperonic acid ethyl ester is applicable to the research of hypertension and hepatic reperfusion injury[1][2].
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Juniperonic acid ethyl ester | Juniperonic acid ethyl ester (Ethyl 20:4BSO) is an orally active non-methylene-interrupted ω-3 polyunsaturated fatty acid ethyl ester. Juniperonic acid ethyl ester exists in Platycladus orientalis seed oil. Juniperonic acid ethyl ester reduces the ratio of 20:3n-9 to arachidonic acid in hepatic phosphatidylcholine of rats with essential fatty acid deficiency. Juniperonic acid ethyl ester is applicable to the research of hypertension and hepatic reperfusion injury. | |||||||||||||||||||||
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- [1]. Ikeda I, et al. 5c,11c,14c-eicosatrienoic acid and 5c,11c,14c,17c-eicosatetraenoic acid of Biota orientalis seed oil affect lipid metabolism in the rat. Lipids. 1992 Jul;27(7):500-4. [Content Brief]
- [2]. Montañés F, et al. Isolation of non-methylene interrupted or acetylenic fatty acids from seed oils using semi-preparative supercritical chromatography[J]. Journal of the American Oil Chemists' Society, 2017, 94(7): 981-991.
Keywords
