Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1CC[C@H]2[C@H](C)[C@H]3CC[C@H]4[C@@H]5CC(=O)[C@H]6C[C@H](CC[C@]6(C)[C@H]5C[C@H]4[C@@H]3CN2C1)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=BSSXNTZKMOAXRA-LMQJZLJXSA-N

Formula

C33H53NO7

Mass

575.787

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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 - Cerveratrum-type alkaloid - Diterpenoid - Steroidal alkaloid - Azasteroid - Terpene glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Quinolizidine - Alkaloid or derivatives - Monosaccharide - Oxane - Piperidine - Tertiary amine - Tertiary aliphatic amine - Secondary alcohol - Ketone - Organoheterocyclic compound - Polyol - Oxacycle - Azacycle - Acetal - Primary alcohol - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Amine - Alcohol - Aldehyde - 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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