Leptosidin
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| IUPAC name
3′,4′,6-Trihydroxy-7-methoxyaurone | |
| Systematic IUPAC name
(2Z)-2-[(3,4-Dihydroxyphenyl)methylidene]-6-hydroxy-7-methoxy-1-benzofuran-3(2H)-one | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C16H12O6 | |
| Molar mass | 300.266 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Leptosidin was the first aurone to be isolated in Coreopsis grandiflora by Geissman T.A. and Heaton C.D. in 1943.[1] Leptosidin blocks the active residues of PRKACA.[2]
