Compound Identification
SMILES
C[C@@H]1CC(C=C(C)C)C2=C3[C@H]1CC[C@H](C)C3=C(OCC1=CC=CC=C1)C(O[Si](C)(C)C(C)(C)C)=C2C
InChIKey
InChIKey=SOMRSLBJRWAVIT-UPWDSKRVSA-N
Formula
C33H48O2Si
Mass
504.83
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
Tetralins Phenol ethers Alkyl aryl ethers Benzene and substituted derivatives Trialkylheterosilanes Organic metalloid salts Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Amphilectane, neoamphilectane, cycloamphilectane, or adociane diterpenoid - Tetralin - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Trialkylheterosilane - Organoheterosilane - Organic metalloid salt - Ether - Organic oxygen compound - Organooxygen compound - Organic metalloid moeity - Organosilicon 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