C[C@H](O)C1=C[C@]2(OC1=O)C=C[C@H]1[C@@H]2[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)OC=C1C(O)=O

InChIKey=GGLAWDIODKKBQZ-SZSWQRSVSA-N

C20H24O12

456.4

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Terpene glycosides

Not available

Iridoid O-glycosides

Terpene lactones Hexoses O-glycosyl compounds Bicyclic monoterpenoids Iridoids and derivatives Butenolides Dicarboxylic acids and derivatives Oxanes Vinylogous esters Enoate esters Secondary alcohols Lactones Oxacyclic compounds Polyols Carboxylic acids Acetals Organic oxides Carbonyl compounds Primary alcohols Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Iridoid o-glycoside - Terpene lactone - Hexose monosaccharide - Glycosyl compound - Iridoid-skeleton - O-glycosyl compound - Bicyclic monoterpenoid - Monoterpenoid - 2-furanone - Dicarboxylic acid or derivatives - Monosaccharide - Oxane - Dihydrofuran - Vinylogous ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Secondary alcohol - Carboxylic acid ester - Lactone - Polyol - Carboxylic acid derivative - Carboxylic acid - Acetal - Oxacycle - Organoheterocyclic compound - Primary alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Carbonyl group - Alcohol - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Not available