Compound Identification
SMILES
CC(C)[C@@H]1[C@H]2[C@H]3O[C@H](\C=C(C)/[C@@H](O)CC[C@@]3(C)OC(C)=O)[C@H]2[C@](C)(OC(C)=O)[C@@H](OC(C)=O)[C@H]1OC(C)=O
InChIKey
InChIKey=NZXPVYKFJWQKJS-HEZYZENASA-N
Formula
C28H42O10
Mass
538.634
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
- Subclass Diterpenoids
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Class
Prenol lipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Prenol lipids
Subclass
Diterpenoids
Intermediate Tree Nodes
Not available
Direct Parent
Eunicellane and asbestinane diterpenoids
Alternative Parents
Cladiellane diterpenoids Tetracarboxylic acids and derivatives Cyclitols and derivatives Tetrahydrofurans Secondary alcohols Carboxylic acid esters Oxacyclic compounds Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Cladiellane diterpenoid - Eunicellane-type diterpenoid - Tetracarboxylic acid or derivatives - Cyclitol or derivatives - Tetrahydrofuran - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton.
External Descriptors
Not available