Structure Information
Structure

Compound Identification

SMILES

CC(C)=C[C@@H]1C[C@](C)(O)[C@H]2[C@@H](C[C@@]3(C)[C@@H]4CC=C5[C@@H](C=C(O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(=O)C5(C)C)[C@]4(C)C(=O)C[C@]23C)O1

InChIKey

InChIKey=MJHZIBPAZLJXHU-HBFZBQDJSA-N

Formula

C36H52O10

Mass

644.802

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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

Steroidal saponins

Direct Parent

Cucurbitacin glycosides

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Cucurbitacin glycoside skeleton - Diterpene glycoside - 20-hydroxysteroid - Diterpenoid - 3-oxo-delta-1-steroid - 3-oxosteroid - 14-alpha-methylsteroid - Hydroxysteroid - Oxosteroid - 11-oxosteroid - Delta-1-steroid - Terpene glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Cyclohexenone - Monosaccharide - Oxane - Tertiary alcohol - Cyclic ketone - Ketone - Secondary alcohol - Acetal - Oxacycle - Dialkyl ether - Organoheterocyclic compound - Ether - Polyol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Alcohol - Organic oxygen compound - Aldehyde - Primary alcohol - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.

External Descriptors

Not available

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