Compound Identification
SMILES
C[C@H]1C[C@@H](C=C(C)C)[C@@]23[C@@H]1CC[C@H](C)[C@@]2(O)C(=O)C(OC(C)=O)=C(C)C3=O
InChIKey
InChIKey=VKFQFGWXKKFZLB-QFMPVXEGSA-N
Formula
C22H30O5
Mass
374.477
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Diterpenoids
- Level 5 Elisabethane diterpenoids
-
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
Elisabethane diterpenoids
Alternative Parents
Cyclohexenones Tertiary alcohols Enol esters Cyclic alcohols and derivatives Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic homopolycyclic compounds
Substituents
Elisabethane diterpenoid - Cyclohexenone - Cyclic alcohol - Enol ester - Tertiary alcohol - Carboxylic acid ester - Ketone - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Carbonyl group - Organooxygen compound - Aliphatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as elisabethane diterpenoids. These are diterpenoids with a structure based on the elisabethane skeleton, a tricyclic serrulatane derivative that is formed by connecting the C1 and C9 atom of serrulatane. This class of compounds also includes seco-elisabethane derivatives, nor-elisabethanes (resulting from the loss of one carbon atom), and bisnor-elisabethanes (resulting from the loss of two carbon atoms).
External Descriptors
Not available