Structure Information
Structure

Compound Identification

SMILES

Cl.C[C@@H]1[C@H]2[C@H](CC3C4CCC5CC(CC[C@]5(C)C4CC[C@]23C)[C@@]2(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[C@@H](CO)[C@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)OC11CCC(C)CN1

InChIKey

InChIKey=GBMIDMBWAJHPIS-UQDWSYJXSA-N

Formula

C50H84ClNO21

Mass

1070.66

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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 - Diterpene glycoside - Spirosolane skeleton - Oligosaccharide - Diterpenoid - Steroidal alkaloid - Azasteroid - Terpene glycoside - C-glycosyl compound - Glycosyl compound - O-glycosyl compound - Azaspirodecane - Alkaloid or derivatives - Ketal - Piperidine - Oxane - Oxolane - Secondary alcohol - Hemiaminal - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Hydrochloride - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - 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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