Inoscavin A

Inoscavin A
Names
	IUPAC name 2-(3,4-Dihydroxyphenyl)-6-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-5'-methylspiro[2H-furo[3,2-c]pyran-3,2'-furan]-3',4-dione
Identifiers
CAS Number	250124-03-9 [[1]];
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:200360;
ChEMBL	ChEMBL487596;
ChemSpider	8609895;
PubChem CID	10434469;
CompTox Dashboard (EPA)	DTXSID301045779 ;
	InChI InChI=1S/C25H18O9/c1-12-8-21(30)25(34-12)22-20(33-23(25)14-4-7-17(27)19(29)10-14)11-15(32-24(22)31)5-2-13-3-6-16(26)18(28)9-13/h2-11,23,26-29H,1H3/b5-2+ Key: ZGKUEJPXTILOCD-GORDUTHDSA-N;
	SMILES CC1=CC(=O)C2(O1)C(OC3=C2C(=O)OC(=C3)/C=C/C4=CC(=C(C=C4)O)O)C5=CC(=C(C=C5)O)O;
Properties
Chemical formula	C25H18O9
Molar mass	462.410 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

Inoscavin A is an antioxidant isolated from the mushroom Inonotus xeranticus.^[2]

References

^ "KNApSAcK Metabolite Information - C00030513". www.knapsackfamily.com.
^ Kim, Jong-Pyung; Yun, Bong-Sik; Shim, Young Key; Yoo, Ick-Dong (1999). "Inoscavin A, a new free radical scavenger from the mushroom Inonotus xeranticus". Tetrahedron Letters. 40 (36): 6643. doi:10.1016/S0040-4039(99)01406-9.

Lee, YS; Kang, YH; Jung, JY; Lee, S; Ohuchi, K; Shin, KH; Kang, IJ; Park, JH; Shin, HK; Lim, SS (2008). "Protein glycation inhibitors from the fruiting body of Phellinus linteus". Biological & Pharmaceutical Bulletin. 31 (10): 1968–72. doi:10.1248/bpb.31.1968. PMID 18827365.

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.