Nervonic acid
Nervonic acid[1] | |
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IUPAC name (Z)-Tetracos-15-enoic acid | |
Other names cis-15-Tetracosenoic acid | |
Identifiers | |
CAS number | 506-37-6 |
PubChem | 5281120 |
ChemSpider | 4444565 |
KEGG | C08323 |
ChEBI | CHEBI:44247 |
ChEMBL | CHEMBL1173379 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C24H46O2 |
Molar mass | 366.62 g/mol |
Melting point | 42–43 °C |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
Nervonic acid is a monounsaturated omega-9 fatty acid. Nervonic acid has been identified as important in the biosynthesis of nerve cell myelin.[2] It is found in the sphingolipids of white matter in human brain.
Nervonic acid is used in the treatment of disorders involving demyelination, such as adrenoleukodystrophy and multiple sclerosis where there is a decreased level of nervonic acid in sphingolipids.[3]
Dietary sources
Nervonic acid is abundant in King Salmon (Chinook) with 140 mg/100g, yellow mustard seed 83 mg/100g, flaxseed 64 mg/100g, Sockeye salmon 40 mg/100g, sesame seed 35 mg/100g, and macademia nuts 18 mg/100g [4]
References
- ↑ Nervonic acid at Sigma-Aldrich
- ↑ US Patent 6664406, Nervonic acid derivatives, their preparation and use
- ↑ WO/1996/005740, Nervonic Acid Compositions
- ↑ http://nutritiondata.self.com/foods-000046000000000000000-w.html
Additional references
- Appelqvist (1976) Lipids in Cruciferae. In: Vaughan JG, Macleod AJ (Eds), The biology and the Chemistry of Cruciferae. Academic Press, London, UK, pp. 221-277.
- Sargent JR, Coupland K, Wilson R (1994). Nervonic Acid and Demyelinating Disease. Medical Hypothesese 42, pp. 237-242.
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