Lactucin
From Wikipedia, the free encyclopedia
| Lactucin | ||
|---|---|---|
 | ||
| IUPAC name (3aR,4R,9aS,9bR)-4-Hydroxy-9-(hydroxymethyl)-6-methyl-3-methylene-4,5,9a,9b-tetrahydro-3aH-azuleno[5,4-d]furan-2,7-dione | ||
| Identifiers | ||
| CAS number | 1891-29-8  | |
| PubChem | 821383 | |
| KEGG | C09489  | |
| Jmol-3D images | Image 1 | |
| ||
| Properties | ||
| Molecular formula | C15H16O5 | |
| Molar mass | 276.28 g/mol | |
| Appearance | White crystalline solid | |
| (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 | ||
Lactucin is a bitter substance that forms a white crystalline solid and belongs to the group of sesquiterpene lactones. It is found in some varieties of lettuce and is an ingredient of lactucarium. It has been shown to have analgesic and sedative properties.[1] It has also shown some antimalarial effects.[2] It is also found in dandelion coffee.
It acts as adenosine receptor agonist.
See also
References
- ↑ Wesołowska A, Nikiforuk A, Michalska K, Kisiel W, Chojnacka-Wójcik E (2006). "Analgesic and Sedative Activities of Lactucin and some Lactucin-Like Guaianolides in Mice". Journal of Ethnopharmacology 107 (2): 254–258. doi:10.1016/j.jep.2006.03.003. PMID 16621374.
- ↑ Bischoff TA, Kelley CJ, Karchesy Y, Laurantos M, Nguyen-Dinh P, Arefi AG (2004). "Antimalarial Activity of Lactucin and Lactucopicrin: Sesquiterpene Lactones Isolated from Cichorium intybus L.". Journal of Ethnopharmacology 95 (2–3): 455–457. doi:10.1016/j.jep.2004.06.031. PMID 15507374.
This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.