Leptosidin

Leptosidin
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
CAS Number	486-24-8 ;
3D model (JSmol)	Interactive image;
ChemSpider	4444669 ;
KEGG	C08651 ;
PubChem CID	5281257;
UNII	VE67J9PR82 ;
CompTox Dashboard (EPA)	DTXSID501028834 ;
	InChI InChI=1S/C16H12O6/c1-21-16-11(18)5-3-9-14(20)13(22-15(9)16)7-8-2-4-10(17)12(19)6-8/h2-7,17-19H,1H3/b13-7- Key: PFRGTMTYWMVLMU-QPEQYQDCSA-N ; InChI=1/C16H12O6/c1-21-16-11(18)5-3-9-14(20)13(22-15(9)16)7-8-2-4-10(17)12(19)6-8/h2-7,17-19H,1H3/b13-7- Key: PFRGTMTYWMVLMU-QPEQYQDCBV;
	SMILES COc(c(O)3)c(o1)c(cc3)c(=O)c(=Cc(c2)cc(O)c(O)c2)1;
Properties
Chemical formula	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). verify (what is ?) Infobox references

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]

^ 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.

[1] Leptosidin on metabolomics.jp

[2] 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.

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