Structure Information
Structure

Compound Identification

SMILES

CC(C)(O)[C@H]1CC[C@](C)(O1)C1[C@@H](O)C[C@@]2(C)C3CCC4[C@]5(C[C@@]35CC[C@]12C)CC1=C(ON=C1)C4(C)C

InChIKey

InChIKey=KVPMNAZNTGOHOJ-VVVXTWPGSA-N

Formula

C31H47NO4

Mass

497.72

Export to:

JSON SDF CSV

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

Aromatic heteropolycyclic compounds

Substituents

Triterpene saponin - Cycloartanol-skeleton - 9b,19-cyclo-lanostane-skeleton - Triterpenoid - Hydroxysteroid - 16-hydroxysteroid - 16-beta-hydroxysteroid - Steroid - Azole - Cyclic alcohol - Heteroaromatic compound - Isoxazole - Tetrahydrofuran - Tertiary alcohol - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Aromatic 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

Previous Back Next