Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1[C@@](O)(CCC(=C)COC2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)OC2CC3C(CCC4C3CCC3C[C@H](C[C@@H](OC5O[C@H](C)[C@@H](O[C@H]6O[C@H](C)[C@H](O)[C@@H](O)[C@H]6O)[C@@H](O)[C@H]5O)[C@]43C)OC3O[C@H](C)C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H](O)[C@H]3O)[C@]12C

InChIKey

InChIKey=OYWZJMOUZKQCFZ-DGYUCRCOSA-N

Formula

C57H94O27

Mass

1211.352

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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 glycosides

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Diterpene glycoside - Steroidal glycoside - 22-hydroxysteroid - Diterpenoid - Hydroxysteroid - Terpene glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Fatty acyl - Oxane - Oxolane - Secondary alcohol - Hemiacetal - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Organooxygen compound - Primary alcohol - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.

External Descriptors

Not available

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