Structure Information
Structure

Compound Identification

SMILES

COC1(CCC(C)CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)OC2CC3C4CCC5(O)C(O)C(O)CC(O)C5(C)C4CCC3(C)C2[C@@H]1C

InChIKey

InChIKey=TZBWWKHBJHUNHR-VOVGGHIMSA-N

Formula

C34H58O12

Mass

658.826

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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 - Furostane-skeleton - 1-hydroxysteroid - Hydroxysteroid - 5-hydroxysteroid - 4-hydroxysteroid - 3-hydroxysteroid - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Hexose monosaccharide - Alkyl glycoside - O-glycosyl compound - Glycosyl compound - Ketal - Fatty acyl - Oxane - Monosaccharide - Cyclitol or derivatives - Tetrahydrofuran - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen 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

Not available

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