Compound Identification
SMILES
CCC(C)C(O)C(C)CC(C)CCCC(C)CCC1=NC(OC)=C(OC)C(OC(C)=O)=C1C
InChIKey
InChIKey=YDOGKTMWHNVSLQ-UHFFFAOYSA-N
Formula
C27H47NO5
Mass
465.675
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
Diterpenoids
Alternative Parents
Polyhalopyridines O-alkylpyrimidines Methylpyridines Hydroxypyridines Alkyl aryl ethers 2-halopyridines Secondary ketimines Heteroaromatic compounds Enol esters Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Diterpenoid - O-alkylpyrimidine - Polyhalopyridine - 2-halopyridine - Methylpyridine - Hydroxypyridine - Alkyl aryl ether - Pyridine - Heteroaromatic compound - Secondary ketimine - Enol ester - Secondary alcohol - Ketimine - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Imine - Alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.
External Descriptors
Not available