Compound Identification
SMILES
C[C@H]1C[C@H](C=C(C)C)C2=C3[C@@H]1CC[C@H](C)C3=C(O)C(OC1OCC(O)C(O)C1O)=C2C
InChIKey
InChIKey=MWZXYPPIOWWIFA-XHSCQTHCSA-N
Formula
C25H36O6
Mass
432.557
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
Phenolic glycosides O-glycosyl compounds Tetralins Pentoses Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Amphilectane, neoamphilectane, cycloamphilectane, or adociane diterpenoid - Phenolic glycoside - Glycosyl compound - O-glycosyl compound - Pentose monosaccharide - Tetralin - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Polyol - Oxacycle - Acetal - Organoheterocyclic compound - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteropolycyclic 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