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
ChEBI	CHEBI:3718
ChemSpider	142644
Jmol 3D model	Interactive image
PubChem	162464
	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	344.32 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[edit]

^ 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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