Structure Information
Structure

Compound Identification

SMILES

CCC1(C)C(CCC2(C)C1CCC1(C)C2CC=C2C3CC(C)(C)C(OC4OC(CO)C(O)C(O)C4O)C(OC(C)=O)C3(CO)C(O)CC12C)OC1OC(C(OC(=O)C(C)=CC)C(O)C1OC(=O)C(C)=CC)C(O)=O

InChIKey

InChIKey=SYFLRMSFWBXNRJ-UHFFFAOYSA-N

Formula

C55H84O19

Mass

1049.258

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Terpene glycosides

Intermediate Tree Nodes

Triterpene glycosides

Direct Parent

Triterpene saponins

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Triterpene saponin - Triterpenoid - Hydroxysteroid - 16-oxosteroid - Oxosteroid - 7-hydroxysteroid - Steroid - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Tetracarboxylic acid or derivatives - Glycosyl compound - O-glycosyl compound - Fatty acid ester - Fatty acyl - Monosaccharide - Oxane - Pyran - Cyclic alcohol - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Secondary alcohol - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Carboxylic acid - Acetal - Oxacycle - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Carbonyl group - Primary alcohol - Alcohol - Organic oxide - Aliphatic heteropolycyclic compound

Description

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.

External Descriptors

Not available

Previous Back Next