Structure Information
Structure

Compound Identification

SMILES

CC[C@H](C)[C@H](O)C(=O)OC1COC(OC2C[C@H](O)CC3=CC[C@H]4[C@@H]5CC6O[C@]7(CCC(=C)CO7)C(C)C6[C@@]5(C)CC[C@@H]4[C@@]23C)C(OC2OC(C)C(O)C(O)C2O)C1OC(C)=O

InChIKey

InChIKey=GWYMUKPJMPPUTG-AYHPSXDMSA-N

Formula

C46H70O15

Mass

863.051

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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 - 3-beta-hydroxysteroid - 3-beta-hydroxy-delta-5-steroid - Hydroxysteroid - 3-hydroxysteroid - 3-hydroxy-delta-5-steroid - Delta-5-steroid - O-glycosyl compound - Glycosyl compound - Disaccharide - Ketal - Fatty acid ester - Fatty acyl - Oxane - Dicarboxylic acid or derivatives - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - 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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