Structure Information
Structure

Compound Identification

SMILES

CC1(CCC2C(=C1)C(CC1C(C)(C)C(=O)CCC21C)OC1OC(C(O)C(O)C1O)C(O)=O)C(O)CO

InChIKey

InChIKey=AYWSKAVQDGHBLW-UHFFFAOYSA-N

Formula

C26H40O10

Mass

512.596

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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

Not available

Direct Parent

Diterpene glycosides

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Diterpene glycoside - Pimarane diterpenoid - Abietane diterpenoid - Diterpenoid - Hydrophenanthrene - 1-o-glucuronide - O-glucuronide - Phenanthrene - Glucuronic acid or derivatives - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Beta-hydroxy acid - Monosaccharide - Oxane - Hydroxy acid - Pyran - Ketone - Secondary alcohol - Cyclic ketone - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Primary alcohol - Alcohol - Organooxygen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

External Descriptors

Not available

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