Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1[C@@H](O)[C@H](O)CO[C@H]1OC[C@@H]1O[C@@H](O[C@@H](CC[C@@H](C)[C@H]2C[C@@H](O)[C@@H]3[C@]2(C)CC[C@@H]2[C@@]4(C)CC[C@H](O[C@@H]5OC[C@@H](O)[C@H](O)[C@H]5OC)[C@H](O)C4[C@@H](O)[C@@H](O)[C@@]32O)C(C)C)[C@H](O)[C@H]1O

InChIKey

InChIKey=VLRBSKQGHGCGRD-RTWKHRBESA-N

Formula

C44H76O19

Mass

909.073

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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

Tetrahydroxy bile acid, alcohol, or derivatives - Steroidal glycoside - Hydroxy bile acid, alcohol, or derivatives - Bile acid, alcohol, or derivatives - 7-hydroxysteroid - 4-hydroxysteroid - 6-hydroxysteroid - 15-hydroxysteroid - Hydroxysteroid - Disaccharide - Glycosyl compound - O-glycosyl compound - Oxane - Cyclic alcohol - Tetrahydrofuran - Tertiary alcohol - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Ether - Dialkyl ether - Acetal - Polyol - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organooxygen 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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