Structure Information
Structure

Compound Identification

SMILES

C[C@H]1CC[C@@H]2N(C1)C[C@H]1[C@@H]3C[C@H]4[C@@H](CC(=O)[C@@H]5C[C@H](CC[C@]45C)O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H]3CC[C@@H]1[C@]2(C)O

InChIKey

InChIKey=DHQFYEJMFMYGCV-SITYKSBQSA-N

Formula

C33H53NO8

Mass

591.786

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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 alcohol - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Ketone - 1,2-aminoalcohol - Organoheterocyclic compound - Polyol - Oxacycle - Acetal - Azacycle - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Amine - Alcohol - Aldehyde - Organonitrogen 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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