Structure Information
Structure

Compound Identification

SMILES

C[C@H]1[C@H]2[C@H](C[C@@]3(O)[C@@H]4CC=C5C[C@H](CC[C@]5(C)[C@H]4CC[C@]23C)O[C@@H]2O[C@H](CO)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]4O)[C@H]3O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)O[C@]11CCC(C)CO1

InChIKey

InChIKey=LNVBVOXSCKNFOD-PARUKXMISA-N

Formula

C50H80O24

Mass

1065.166

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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 - Oligosaccharide - Diterpenoid - 14-hydroxysteroid - Hydroxysteroid - Delta-5-steroid - Terpene glycoside - O-glycosyl compound - Glycosyl compound - Ketal - Oxane - Tetrahydrofuran - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Hemiacetal - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Primary alcohol - Organic oxygen compound - Hydrocarbon derivative - 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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