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Structure Information
Structure

Compound Identification

SMILES

CC1OC(OC2C(O)C(O)C(CO)OC2OC2C[C@@]3(C)C(C[C@H](O)[C@H]4[C@@H](CCC34C)C3(C)CCC(O3)C(C)(C)O)[C@]3(C)CC[C@@H](O)C(C)(C)C23)C(O)C(O)C1O.CC(C)=CCCC(C)(OC1OC(CO)C(O)C(O)C1O)C1CCC2(C)[C@H]1[C@@H](O)CC1[C@]3(C)CC[C@@H](O)C(C)(C)C3C(C[C@]21C)OC1OC(CO)C(O)C(O)C1O

InChIKey

InChIKey=MVCNDBCNAOAFGD-YAZVVNPJSA-N

Formula

C84H144O28

Mass

1602.048

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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

Not available

Substituents

Triterpene saponin - Triterpenoid - 3-alpha-hydroxysteroid - Hydroxysteroid - 12-hydroxysteroid - 3-hydroxysteroid - Steroid - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - O-glycosyl compound - Glycosyl compound - Disaccharide - Fatty acyl - Oxane - Tetrahydrofuran - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Ether - Dialkyl ether - 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 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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