Structure Information
Structure

Compound Identification

SMILES

CC1C2C(CC3C4CCC5CC(CCC5(C)C4CCC23C)OC2OC(C(O)C(O)C2O)C(O)=O)OC11CCC(CO)CN1N=O

InChIKey

InChIKey=XSMGCTDDJHYMKM-UHFFFAOYSA-N

Formula

C33H52N2O10

Mass

636.783

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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 - Steroid-glucuronide-skeleton - Diterpene glycoside - Spirosolane skeleton - Diterpenoid - Steroidal alkaloid - Terpene glycoside - Azasteroid - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Glycosyl compound - Azaspirodecane - Alkaloid or derivatives - 1-nitrosopiperidine - Beta-hydroxy acid - Pyran - Piperidine - Oxane - Monosaccharide - Hydroxy acid - Tetrahydrofuran - Organic n-nitroso compound - Secondary alcohol - Organic nitroso compound - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen 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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