Compound Identification
SMILES
CC(C)(C)C1C2=CC(=C3C=CC4=CC=CC=C4C3=C2C2=C1C=CC1=CC=CC=C21)C(C)(C)C
InChIKey
InChIKey=ZIAXBUZECFNOJW-UHFFFAOYSA-N
Formula
C33H32
Mass
428.619
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
Phenanthrenes and derivatives Fluorenes Naphthalenes Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Amphilectane, neoamphilectane, cycloamphilectane, or adociane diterpenoid - Phenanthrene - Fluorene - Naphthalene - Benzenoid - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - 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