Structure Information
Structure

Compound Identification

SMILES

CC(=O)O[C@H]1C[C@@]2(C)C3CCC4[C@]5(C[C@@]35CC[C@]2(C)C1[C@]1(C)CC[C@@H](O1)C(C)(C)OC(C)=O)CC\C(=N\O)C4(C)C

InChIKey

InChIKey=ZXPNKVBLABPLNE-MZWIEPEVSA-N

Formula

C34H53NO6

Mass

571.799

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Terpene glycosides

Intermediate Tree Nodes

Triterpene glycosides

Direct Parent

Triterpene saponins

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Triterpene saponin - 9b,19-cyclo-lanostane-skeleton - Cycloartane-skeleton - Triterpenoid - Steroid ester - Steroid - Dicarboxylic acid or derivatives - Ketoxime - Tetrahydrofuran - Carboxylic acid ester - Carboxylic acid derivative - Dialkyl ether - Ether - Oxime - Oxacycle - Organoheterocyclic compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.

External Descriptors

Not available

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