Structure Information
Structure

Compound Identification

SMILES

CC1C2CC(=O)O[C@@H]3C[C@@](C)([C@@H]4OC(=O)C=C4C)C(=C(O)C1=O)[C@@]23CO

InChIKey

InChIKey=SRNFRTSVHROPLE-NXXSFZJESA-N

Formula

C19H22O7

Mass

362.378

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Terpene lactones

Intermediate Tree Nodes

Not available

Direct Parent

Quassinoids

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Quassinoid - Delta valerolactone - Cyclohexenone - Delta_valerolactone - 2-furanone - Dicarboxylic acid or derivatives - Oxane - Dihydrofuran - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Lactone - Ketone - Carboxylic acid ester - Cyclic ketone - Organoheterocyclic compound - Oxacycle - Enol - Carboxylic acid derivative - Primary alcohol - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.

External Descriptors

Not available

Previous Back Next