Structure Information
Structure

Compound Identification

SMILES

CC(=O)O[C@H]1[C@@H]2C(=C)[C@H](CC[C@@]2(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)C2=C(C)C(=O)C[C@]1(O)C2(C)C)OC(=O)\C=C\C1=CC=CC=C1

InChIKey

InChIKey=VBLNERPSGWCFQJ-NINUBRFRSA-N

Formula

C35H42O10

Mass

622.711

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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

Aromatic homopolycyclic compounds

Substituents

Taxane diterpenoid - Tetracarboxylic acid or derivatives - Cinnamic acid or derivatives - Cinnamic acid ester - Styrene - Fatty acid ester - Cyclohexenone - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Tertiary alcohol - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Ketone - Carboxylic acid ester - Cyclic ketone - Carboxylic acid derivative - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Aromatic 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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