Structure Information
Structure

Compound Identification

SMILES

C[C@H]([C@@H](O)C\C=C(\C)CO)[C@H]1CC[C@@]2(C)[C@@H]3CCC4[C@]5(C[C@@]35CC[C@]12C)CC[C@H](O[C@@H]1O[C@H](C)[C@H](O[C@@H]2O[C@H](CO[C@@H]3O[C@H](C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)C4(C)C

InChIKey

InChIKey=NEXOJELFRVHFMW-ZHLPLYGGSA-N

Formula

C48H80O16

Mass

913.152

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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 - Triterpene saponin - Triterpene glycoside - Cycloartanol-skeleton - Triterpenoid - Cycloartane-skeleton - 9b,19-cyclo-lanostane-skeleton - 26-hydroxysteroid - Oligosaccharide - Dihydroxy bile acid, alcohol, or derivatives - Hydroxy bile acid, alcohol, or derivatives - 22-hydroxysteroid - Bile acid, alcohol, or derivatives - Hydroxysteroid - Fatty acyl glycoside - Alkyl glycoside - O-glycosyl compound - Glycosyl compound - Fatty alcohol - Fatty acyl - Oxane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - 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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