Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]2O[C@H]2C[C@@H](O)[C@@]3(C)[C@H]4[C@H](O)C[C@]5(C)[C@@H](C[C@@H]6OC(CCC(=C)CO[C@@H]7O[C@H](CO)[C@H](O)[C@H](O)[C@H]7O)=C(C)[C@H]56)[C@@H]4CC=C3C2)[C@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=GWNCJTZKIAESFW-VVGMGORKSA-N

Formula

C45H70O19

Mass

915.036

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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 - Diterpene glycoside - Diterpenoid - 1-hydroxysteroid - 11-hydroxysteroid - 11-alpha-hydroxysteroid - Hydroxysteroid - Terpene glycoside - Delta-5-steroid - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - O-glycosyl compound - Glycosyl compound - Disaccharide - Fatty acyl - Oxane - Dihydrofuran - 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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