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 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:65976 N
ChEMBL	ChEMBL522282 Y
ChemSpider	9721048 Y
PubChem CID	11546269
UNII	84L7S5MVN5 Y
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 Y Key: CBPFOSMNDISZLV-UHFFFAOYSA-N Y 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). N verify (what is YN ?) 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).

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