Structure Information
Structure

Compound Identification

SMILES

CC1=C2[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C)[C@]3(C)CCC=C(C[Si](C)(C)C)[C@H]3C[C@H](C[C@@H]1O[Si](C)(C)C(C)(C)C)C2(C)C

InChIKey

InChIKey=LNJVMKLJNWIZHA-IAZOLHQISA-N

Formula

C38H76O3Si4

Mass

693.363

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Diterpenoids

Intermediate Tree Nodes

Not available

Direct Parent

Taxanes and derivatives

Alternative Parents

Molecular Framework

Aliphatic homopolycyclic compounds

Substituents

Taxane diterpenoid - Trialkylheterosilane - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organosilicon compound - Alkylsilane - Organooxygen compound - Organic metalloid moeity - Aliphatic homopolycyclic compound

Description

This compound belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] propellane ring system.

External Descriptors

Not available

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