Wogonin
Names | |
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IUPAC name
5,7-Dihydroxy-8-methoxy-2-phenyl-4H-chromen-4-one
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Other names | |
Identifiers | |
632-85-9 | |
ChEBI | CHEBI:10043 |
ChEMBL | ChEMBL16171 |
ChemSpider | 4445020 |
Jmol 3D model | Interactive image |
KEGG | C10197 |
PubChem | 5281703 |
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Properties | |
C16H12O5 | |
Molar mass | 284.27 g·mol−1 |
Melting point | 203 to 206 °C (397 to 403 °F; 476 to 479 K) |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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verify (what is ?) | |
Infobox references | |
Wogonin is an O-methylated flavone, a flavonoid-like chemical compound which was found in Scutellaria baicalensis.[2] The glycosides of wogonin are known as wogonosides. For example, oroxindin is a wogonin glucuronide isolated from Oroxylum indicum.[3] It is one of the active ingredients of Sho-Saiko-To, a Japanese herbal supplement.
Wogonin has been found in one study to have anxiolytic properties in mice at doses of 7.5 to 30 mg/kg, without exhibiting the sedative and muscle-relaxing properties of benzodiazepines.[2] Preliminary in vitro studies have shown pharmacological effects that indicate wogonin may have anti-tumor properties.[4][5] Wogonin has also been found to possess anticonvulsant effects.[6] It acts as a positive allosteric modulator of the benzodiazepine site of the GABAA receptor.[2][6]
References
- ↑ Wogonin at chemblink.com
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