Wogonin

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Wogonin[1]
Skeletal formula
Ball-and-stick model
Names
IUPAC name
5,7-Dihydroxy-8-methoxy-2-phenyl-4H-chromen-4-one
Other names
Vogonin
Norwogonin 8-methyl ether
5,7-dihydroxy-8-methoxyflavone
Identifiers
632-85-9 YesY
ChEBI CHEBI:10043 N
ChEMBL ChEMBL16171 N
ChemSpider 4445020 N
Jmol 3D model Interactive image
KEGG C10197 N
PubChem 5281703
  • InChI=1S/C16H12O5/c1-20-15-12(19)7-10(17)14-11(18)8-13(21-16(14)15)9-5-3-2-4-6-9/h2-8,17,19H,1H3 N
    Key: XLTFNNCXVBYBSX-UHFFFAOYSA-N N
  • InChI=1/C16H12O5/c1-20-15-12(19)7-10(17)14-11(18)8-13(21-16(14)15)9-5-3-2-4-6-9/h2-8,17,19H,1H3
    Key: XLTFNNCXVBYBSX-UHFFFAOYAQ
  • COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O
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).
N verify (what is YesYN ?)
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

  1. Wogonin at chemblink.com
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