Compound Identification
SMILES
CC(C)(C)C1=CC2=C(C1)C(C)(C)C1=C(CC(=C1)C(C)(C)C)C2(C)C
InChIKey
InChIKey=CKXRJQCSUXMADP-UHFFFAOYSA-N
Formula
C24H36
Mass
324.552
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
Ileabethane, pseudopterane or nor-sandresane diterpenoids
Alternative Parents
Polycyclic hydrocarbons Branched unsaturated hydrocarbons Cyclic olefins Unsaturated aliphatic hydrocarbons
Molecular Framework
Aliphatic homopolycyclic compounds
Substituents
Ileabethane, pseudopterane or nor-sandresane diterpenoid - Branched unsaturated hydrocarbon - Polycyclic hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aliphatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as ileabethane, pseudopterane or nor-sandresane diterpenoids. These are diterpenoids with a structure based on either the ileabethane, the pseudopterane, or the nor-sandresane skeleton. Ileabethane is a tricyclic carbon skeleton arising from the C8-C14 of serrulatane. In the nor-sandresane skeleton, a cyclohexane ring is fused to a seven-membered saturated aliphatic carbocycle, which could stem from the rearrangement of an amphilectane-based precursor involving loss of a carbon atom and a 1,2-alkyl shift with ring expansion.
External Descriptors
Not available