C[C@@H]1O[C@@H](OC(=O)[C@]23CCC(C)(C)CC2C2=CCC4[C@@]5(C)CC[C@H](O[C@@H]6O[C@@H](CO)[C@H](O)[C@H]6O)[C@@](C)(CO)C5CC[C@@]4(C)[C@]2(C)CC3)[C@H](O)[C@H](O)[C@H]1O

InChIKey=ZKRAHHRFZSYFBS-MKJNJNLASA-N

C41H66O12

750.967

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Terpene glycosides

Triterpene glycosides

Triterpene saponins

Triterpenoids Steroids and steroid derivatives O-glycosyl compounds Monosaccharides Oxanes Tetrahydrofurans Secondary alcohols Carboxylic acid esters Acetals Monocarboxylic acids and derivatives Polyols Oxacyclic compounds Carbonyl compounds Primary alcohols Hydrocarbon derivatives Organic oxides

Aliphatic heteropolycyclic compounds

Triterpene saponin - Triterpenoid - Steroid - Glycosyl compound - O-glycosyl compound - Oxane - Monosaccharide - Tetrahydrofuran - Secondary alcohol - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Polyol - Acetal - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Alcohol - Organooxygen compound - Primary alcohol - Organic oxygen compound - Carbonyl group - Organic oxide - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.

Not available