Compound Identification
SMILES
CCCCC\C=C/C=C/C(=O)O[C@@H]1C[C@@H]2[C@]3([C@H](OC(C)=O)O[C@H](OC(C)=O)C3=C1)[C@H](O)C[C@@H](C)[C@]2(C)C[C@@H](OO)C(=C)C=C
InChIKey
InChIKey=HXZWRWDSAJYAQI-VDJNAWDJSA-N
Formula
C34H48O10
Mass
616.748
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
- Subclass Diterpenoids
-
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
Colensane and clerodane diterpenoids
Alternative Parents
Naphthofurans Tricarboxylic acids and derivatives Fatty acid esters Tetrahydrofurans Enoate esters Secondary alcohols Cyclic alcohols and derivatives Peroxols Oxacyclic compounds Alkyl hydroperoxides Acetals Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Clerodane diterpenoid - Naphthofuran - Tricarboxylic acid or derivatives - Fatty acid ester - Fatty acyl - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Hydroperoxide - Carboxylic acid ester - Alkyl hydroperoxide - Oxacycle - Organoheterocyclic compound - Peroxol - Carboxylic acid derivative - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.
External Descriptors
Not available