CC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(=O)C[C@H]2C1=CC[C@H]1[C@@]3(C)C[C@@H](O)[C@H]([C@](C)(O)[C@@H](O)\C=C\C(C)(C)O)[C@]3(C)CC(=O)[C@]21C

InChIKey=MZQDGZPGEPGUFS-GDBUQWTOSA-N

C35H52O12

664.789

Organic compounds

Lipids and lipid-like molecules

Steroids and steroid derivatives

Steroidal glycosides

Not available

Steroidal glycosides

Diterpene glycosides 16-alpha-hydroxysteroids 11-oxosteroids Diterpenoids Hexoses O-glycosyl compounds Cyclohexenones Oxanes Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Polyols Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Diterpene glycoside - Steroidal glycoside - 25-hydroxysteroid - 20-hydroxysteroid - Diterpenoid - 16-hydroxysteroid - 16-alpha-hydroxysteroid - 2-oxosteroid - Oxosteroid - 11-oxosteroid - Hydroxysteroid - Terpene glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Cyclohexenone - Oxane - Monosaccharide - Tertiary alcohol - Cyclic alcohol - Cyclic ketone - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.

Not available