Quercinol

Quercinol
Names
	Preferred IUPAC name (2S)-2-Methoxy-2-methyl-2H-1-benzopyran-6-ol
Identifiers
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL603950;
ChemSpider	24652783;
PubChem CID	46230832;
	InChI InChI=1S/C11H12O3/c1-11(13-2)6-5-8-7-9(12)3-4-10(8)14-11/h3-7,12H,1-2H3/t11-/m0/s1 Key: DLZKKUHAZDHCSL-NSHDSACASA-N;
	SMILES C[C@]1(C=CC2=C(O1)C=CC(=C2)O)OC;
Properties
Chemical formula	C11H12O3
Molar mass	192.214 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

Quercinol (a chromene derivative), isolated from the mushroom Fomitopsis quercina, has in vitro anti-inflammatory activity, and inhibits the enzymes cyclooxygenase-2, xanthine oxidase, and horseradish peroxidase.^[1]

References

↑ Gebhardt, P.; Dornberger, K.; Gollmick, F.A.; Gräfe, U.; Härtl, A.; Görls, H.; Schlegel, B.; Hertweck, C. (2007-05-01). "Quercinol, an anti-inflammatory chromene from the wood-rotting fungus Daedalea quercina (Oak Mazegill)". Bioorg. Med. Chem. Lett. 17 (9): 2558–60. doi:10.1016/j.bmcl.2007.02.008. PMID 17346963. Retrieved 2024-11-18.

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