Compound Identification
SMILES
CC1CC(C=C(C)C)C2=C(C)C(=O)C(=O)C3=C2C1=C(O)C=C3C
InChIKey
InChIKey=JVQJPMIBFYBOEO-UHFFFAOYSA-N
Formula
C20H22O3
Mass
310.393
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
- 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
Amphilectane, neoamphilectane, cycloamphilectane, and adociane diterpenoids
Alternative Parents
Naphthoquinones Naphthols and derivatives Tetralins Quinones Aryl ketones 1-hydroxy-2-unsubstituted benzenoids Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Amphilectane, neoamphilectane, cycloamphilectane, or adociane diterpenoid - Naphthoquinone - 2-naphthol - Naphthalene - Tetralin - Quinone - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Cyclic ketone - Ketone - Organic oxide - Carbonyl group - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as amphilectane, neoamphilectane, cycloamphilectane, and adociane diterpenoids. These are diterpenoids with a structure based on the amphilectane or a seco-,neo-, or cyclo- derivative thereof. Amphilectane is a tricyclic structure made up of three cyclohexane fused together, with a methyl group at the C11-, C7-, and C3- positions. Additionally, it carries a 2-methylpropyl group at the C1-position. Amphilectanes are presumably derived from serrulatanes. Cycloamphilectanes represent a further cyclisation.
External Descriptors
Not available