[H][C@@]1(O)C[C@@]2(C)[C@@]([H])(CC[C@]3(C)[C@]2([H])CC=C2[C@]4([H])[C@](C)(O)[C@]([H])(C)CC[C@@]4(CC[C@@]32C)C(=O)O[C@]2([H])O[C@]([H])(COC(C)=O)[C@@]([H])(OC(C)=O)[C@]([H])(OC(C)=O)[C@@]2([H])OC(C)=O)C(C)(C)[C@]1([H])O

InChIKey=YQNFQUKKDWYHMX-LIQZXYIUSA-N

C44H66O14

818.998

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Terpene glycosides

Triterpene glycosides

Triterpene saponins

Triterpenoids Pentacarboxylic acids and derivatives Hexoses Oxanes Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Carboxylic acid esters Polyols Oxacyclic compounds Acetals Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

Triterpene saponin - Triterpenoid - Pentacarboxylic acid or derivatives - Hexose monosaccharide - Monosaccharide - Oxane - Cyclic alcohol - Tertiary alcohol - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Alcohol - Organic oxide - Organic oxygen compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - 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