Cirsilineol

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Cirsilineol

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
PubChem	162464
ChemSpider	142644
Jmol-3D images	Image 1
SMILES COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O
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
Properties
Molecular formula	C₁₈H₁₆O₇
Molar mass	344.32 g mol⁻¹
Except where noted otherwise, 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]

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.

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