Grifolin

Grifolin
Names
	Preferred IUPAC name 5-Methyl-2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzene-1,3-diol
Identifiers
CAS Number	6903-07-7 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL487804;
ChemSpider	4522608;
PubChem CID	5372312;
CompTox Dashboard (EPA)	DTXSID401044417 ;
	InChI InChI=1S/C22H32O2/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-20-21(23)14-19(5)15-22(20)24/h8,10,12,14-15,23-24H,6-7,9,11,13H2,1-5H3/b17-10+,18-12+ Key: PZHNKNRPGLTZPO-VZRGJMDUSA-N; InChI=1/C22H32O2/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-20-21(23)14-19(5)15-22(20)24/h8,10,12,14-15,23-24H,6-7,9,11,13H2,1-5H3/b17-10+,18-12+ Key: PZHNKNRPGLTZPO-VZRGJMDUBE;
	SMILES CC1=CC(=C(C(=C1)O)C/C=C(\C)/CC/C=C(\C)/CCC=C(C)C)O;
Properties
Chemical formula	C22H32O2
Molar mass	328.496 g·mol−1
Melting point	41 °C (106 °F; 314 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Grifolin is an isolate of the mushroom Albatrellus confluens which upregulates DAPK1 in vitro.^[1]

References

^ Luo, XJ; Li, LL; Deng, QP; Yu, XF; Yang, LF; Luo, FJ; Xiao, LB; Chen, XY; Ye, M; Liu, JK; Cao, Y (2011). "Grifolin, a potent antitumour natural product upregulates death-associated protein kinase 1 DAPK1 via p53 in nasopharyngeal carcinoma cells". European Journal of Cancer. 47 (2): 316–25. doi:10.1016/j.ejca.2010.09.021. PMID 20943371.

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