Structure Information
Structure

Compound Identification

SMILES

[H]C(C)(CCC1(O)OC2([H])CC3([H])C4([H])CCC5([H])CC([H])(CCC5(C)C4([H])CCC3(C)C2([H])C1([H])C)OC1([H])OC([H])(CO)C([H])(O)C([H])(O)C1([H])O)COC1([H])OC([H])(CO)C([H])(O)C([H])(O)C1([H])O

InChIKey

InChIKey=DJKIYSUAUHFEBC-UHFFFAOYSA-N

Formula

C39H66O14

Mass

758.943

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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 - Furostane-skeleton - 22-hydroxysteroid - Diterpenoid - Hydroxysteroid - Terpene glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Fatty acyl - Monosaccharide - Oxane - Oxolane - Secondary alcohol - Hemiacetal - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Primary alcohol - 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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