Irigenin
 | |
 | |
| Names | |
|---|---|
| IUPAC name
5,7-dihydroxy-3-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxychromen-4-one | |
| Identifiers | |
| 548-76-5 | |
| 3D model (Jmol) | Interactive image |
| ChEBI | CHEBI:81409  |
| ChemSpider | 4576563 |
| ECHA InfoCard | 100.008.145 |
| PubChem | 5464170 |
| |
| |
| Properties | |
| C18H16O8 | |
| Molar mass | 360.31 g/mol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Irigenin is an O-methylated isoflavone, a type of flavonoid. It can be isolated from the rhizomes of the leopard lily (Belamcanda chinensis),[1] and Iris kemaonensis.[2][3]
Glycosides
Iridin is the 7-glucoside of irigenin.
References
- ↑ Inhibitory effects of Irigenin from the rhizomes of Belamcanda chinensis on nitric oxide and prostaglandin E2 production in murine macrophage RAW 264.7 cells. Kwang Seok Ahn, Eun Jung Noh, Kwang-Hyun Cha, Yeong Shik Kim, Soon Sung Lim, Kuk Hyun Shin and Sang Hoon Jung, 2005
- ↑ Mahmooda, Umar; Kaula, Vijay K.; Jirovetzb, Leopold (December 2002). "Alkylated benzoquinones from Iris kumaonensis". Phytochemistry. 61 (8): 923–926. doi:10.1016/S0031-9422(02)00474-0. Retrieved 3 August 2015.
- ↑ Jiaju Zhou, Guirong Xie and Xinjian Yan Encyclopedia of Traditional Chinese Medicines - Molecular Structures, Pharmalogical Activities, Natural sources and Applications, p. 214, at Google Books
This article is issued from Wikipedia - version of the 8/10/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.