Glycyrrhizol

Glycyrrhizol A
Names
	Preferred IUPAC name 1-Methoxy-2,8-bis(3-methylbut-2-en-1-yl)-6H-[1]benzofuro[3,2-c] [1]benzopyran-3,9-diol
Identifiers
CAS Number	877373-00-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:65976 ;
ChEMBL	ChEMBL522282 ;
ChemSpider	9721048 ;
PubChem CID	11546269;
UNII	84L7S5MVN5 ;
CompTox Dashboard (EPA)	DTXSID50468358 ;
	InChI InChI=1S/C26H28O5/c1-14(2)6-8-16-10-18-19-13-30-23-12-21(28)17(9-7-15(3)4)25(29-5)24(23)26(19)31-22(18)11-20(16)27/h6-7,10-12,27-28H,8-9,13H2,1-5H3 Key: CBPFOSMNDISZLV-UHFFFAOYSA-N ; InChI=1/C26H28O5/c1-14(2)6-8-16-10-18-19-13-30-23-12-21(28)17(9-7-15(3)4)25(29-5)24(23)26(19)31-22(18)11-20(16)27/h6-7,10-12,27-28H,8-9,13H2,1-5H3 Key: CBPFOSMNDISZLV-UHFFFAOYAJ;
	SMILES o2c1c(cc(c(O)c1)C\C=C(/C)C)c3c2c4c(OC)c(c(O)cc4OC3)C\C=C(/C)C;
Properties
Chemical formula	C26H28O5
Molar mass	420.50 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Glycyrrhizol A is a prenylated pterocarpan and an isoflavonoid derivative. It is a compound isolated from the root of the Chinese licorice plant (Glycyrrhiza uralensis).^{[citation needed]}

It may has in vitro antibacterial properties.^[1] In one study, the strongest antibacterial activity was observed against Streptococcus mutans, an organism known to cause tooth decay in humans.^[1]

References

^ ^a ^b He J, Chen L, Shi W, Lu Q-Y (2006). "Antibacterial Compounds from Glycyrrhiza uralensis". Journal of Natural Products. 69 (1): 121–124. CiteSeerX 10.1.1.552.7335. doi:10.1021/np058069d. PMID 16441081.

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

[He-1] He J, Chen L, Shi W, Lu Q-Y (2006). "Antibacterial Compounds from Glycyrrhiza uralensis". Journal of Natural Products. 69 (1): 121–124. CiteSeerX 10.1.1.552.7335. doi:10.1021/np058069d. PMID 16441081.

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