CC(C)=CCC(O)[C@](C)(O)C1[C@H](O)C[C@@]2(C)[C@@H]3CC=C4[C@@H](CC(=O)C(OC5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)=C4C)[C@]3(C)C(=O)C[C@]12C

InChIKey=TVWVPIMEOJKJPZ-KLWAZRTMSA-N

C35H52O11

648.79

Organic compounds

Lipids and lipid-like molecules

Steroids and steroid derivatives

Steroidal glycosides

Not available

Steroidal glycosides

Diterpene glycosides 16-alpha-hydroxysteroids 14-alpha-methylsteroids 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 - 22-hydroxysteroid - 20-hydroxysteroid - Diterpenoid - 14-alpha-methylsteroid - 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