Cirsilineol

Cirsilineol
Names
	IUPAC name 5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxychromen-4-one
	Other names Eupatrin; 4',5-Dihydroxy-3',6,7-trimethoxyflavone
Identifiers
CAS Number	41365-32-6 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:3718 ;
ChemSpider	142644;
PubChem CID	162464;
UNII	08DZZ529FE ;
CompTox Dashboard (EPA)	DTXSID20194314 ;
	InChI InChI=1S/C18H16O7/c1-22-13-6-9(4-5-10(13)19)12-7-11(20)16-14(25-12)8-15(23-2)18(24-3)17(16)21/h4-8,19,21H,1-3H3 Key: VKOSQMWSWLZQPA-UHFFFAOYSA-N; InChI=1S/C18H16O7/c1-22-13-6-9(4-5-10(13)19)12-7-11(20)16-14(25-12)8-15(23-2)18(24-3)17(16)21/h4-8,19,21H,1-3H3 Key: VKOSQMWSWLZQPA-UHFFFAOYSA-N;
	SMILES COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O;
Properties
Chemical formula	C18H16O7
Molar mass	344.319 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Cirsilineol is a bioactive flavone isolated from Artemisia[1] and from Teucrium gnaphalodes.[2]

References

Sheng, X; Sun, Y; Yin, Y; Chen, T; Xu, Q (2008). "Cirsilineol inhibits proliferation of cancer cells by inducing apoptosis via mitochondrial pathway". The Journal of Pharmacy and Pharmacology. 60 (11): 1523–9. doi:10.1211/jpp/60.11.0014. PMID 18957174.
Flavonoid Aglycones and Glycosides from Teucrium gnaphalodes. F. A. T. Barberán, M. I. Gil, F. Tomás, F. Ferreres and A. Arques, J. Nat. Prod., 1985, 48 (5), pages 859–860, doi:10.1021/np50041a040

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