Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1[C@H](C[C@H]2[C@@H]3CC[C@H]4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)O[C@@H]1OC(CO)[C@H](O[C@@H]2OC(CO)[C@@H](O)[C@H](O[C@@H]3OC(CO)[C@@H](O)[C@H](O)C3O)C2O[C@@H]2OC(CO)[C@@H](O)[C@H](O[C@@H]3OC(C)[C@H](O)C(O)[C@@H]3O)C2O)[C@H](O)C1O)O[C@@]1(C)CC[C@@H](C)CO1

InChIKey

InChIKey=JHSZDVZYOFZGJV-CKCOFUPGSA-N

Formula

C58H98O27

Mass

1227.395

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Subclass

Steroidal glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Steroidal saponins

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Steroidal saponin - Triterpenoid - Spirostane skeleton - Oligosaccharide - Glycosyl compound - O-glycosyl compound - Ketal - Oxane - Secondary alcohol - Polyol - Acetal - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organic oxygen compound - Alcohol - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.

External Descriptors

LIPIDMAPS (LMST01080076) : Spirostanols and derivatives

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