Structure Information
Structure

Compound Identification

SMILES

CCO[C@@H]1C[C@H]2C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]3[C@@]4(C)CC=C[C@@H](C)[C@@H]4C[C@@H](O1)[C@@]23CO

InChIKey

InChIKey=NIZGNEILAYIBLR-FSWMOUKGSA-N

Formula

C27H46O4Si

Mass

462.746

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 - Naphthopyran - Naphthalene - Oxane - Pyran - Trialkylheterosilane - Organic metalloid salt - Organoheterocyclic compound - Organoheterosilane - Acetal - Oxacycle - Organosilicon compound - Alcohol - Primary alcohol - Organooxygen compound - Organic metalloid moeity - Organic oxygen compound - Hydrocarbon derivative - 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