Structure Information
Structure

Compound Identification

SMILES

C[C@H]1C2C(CC3C4CC[C@H]5C[C@H](CC[C@]5(C)C4C(=O)C[C@]23C)O[C@@H]2O[C@@H](CO)[C@@H](O[C@@H]3O[C@@H](COC(=O)NCC4=CC=CO4)[C@@H](OC(=O)NCC4=CC=CO4)[C@H](O)[C@@H]3O)[C@H](O)[C@@H]2O)O[C@]11CC[C@@H](C)CO1

InChIKey

InChIKey=BIUDYWZGURLLCF-JAWSIYIGSA-N

Formula

C51H72N2O18

Mass

1001.133

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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

Aromatic heteropolycyclic compounds

Substituents

Steroidal saponin - Triterpenoid - Spirostane skeleton - Oxosteroid - 11-oxosteroid - Disaccharide - Glycosyl compound - O-glycosyl compound - Ketal - Oxane - Furan - Tetrahydrofuran - Heteroaromatic compound - Carbamic acid ester - Carbonic acid derivative - Secondary alcohol - Ketone - Acetal - Oxacycle - Organoheterocyclic compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Primary alcohol - Aromatic 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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