Tricin
From Self-sufficiency
Revision as of 11:58, 1 September 2010 by Yobot (Talk) (WP:CHECKWIKI error 80 + genfixes + autotagging using AWB (7063))
Not to be confused with Tricine.
| Tricin | |
|---|---|
| File:Tricin.svg | |
| Other names Tricetin 3',5'-dimethyl ether 5,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromen-4-one | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 520-32-1 |
| PubChem | 5281702 |
| SMILES | Script error: No such module "collapsible list". |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C17H14O7 |
| Molar mass | 330.29 g/mol |
| Exact mass | 330.073953 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Tricin is a chemical compound. It is an O-methylated flavone, a type of flavonoid. It can be found in the rice bran[1].
Glycosides
- Tricin 4'-glucoside (Tricin-4'-O-beta-D-glucopyranaoside, CAS number 71855-50-0)
- Tricin 5-glucoside (Tricin 5-O-beta-D-glucopyranoside, CAS number 32769-00-9)
- Tricin 7-O-glucoside (Tricin 7-O-beta-D-glucopyranoside, CAS number 32769-01-0)
Other compounds formed from tricin
Three flavonolignans derived from tricin have been isolated from the herb Avena sativa[2].
External links
References
Cite error: Invalid <references> tag;
parameter "group" is allowed only.
<references />, or <references group="..." />- ↑ The rice bran constituent tricin potently inhibits cyclooxygenase enzymes and interferes with intestinal carcinogenesis in ApcMin mice
- ↑ Flavonolignans from Avena sativa. Eva Wenzig, Olaf Kunert, Daneel Ferreira, Martin Schmid, Wolfgang Schühly, Rudolf Bauer and Alois Hiermann, J. Nat. Prod., 2005, 68 (2), pp 289–292
