Structure Information
Structure

Compound Identification

SMILES

C[C@H]1[C@H]2[C@@H](OC11CC[C@@H](C)CO1)[C@@H](O)C1C3CCC4CC(C(O)C[C@]4(C)C3CC[C@]21C)[C@@]1(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=UQXYFHWTJCVQDS-DBXQGTFUSA-N

Formula

C50H82O24

Mass

1067.182

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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 - Triterpenoid - Spirostane skeleton - Oligosaccharide - Prostaglandin skeleton - Eicosanoid - 2-hydroxysteroid - 15-hydroxysteroid - Hydroxysteroid - C-glycosyl compound - Glycosyl compound - O-glycosyl compound - Ketal - Fatty acyl - Oxane - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Primary alcohol - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organooxygen 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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