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) | |
ChemSpider | |
KEGG | |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
| |
| |
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). |
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]
References[edit]
- ^ Leptosidin on metabolomics.jp
- ^ S, Sandeep; V, Priyadarshini; D, Pradhan; M, Munikumar; A, Umamaheswari (2012). "Docking and molecular dynamics simulations studies of human protein kinase catalytic subunit alpha with antagonist". Journal of Clinical and Scientific Research: 15–23. doi:10.15380/2277-5706.JCSR.12.005.