Compound Identification
SMILES
CO[C@@H]1CCC23CC[C@@H](C)[C@](C)(C12)[C@@H](C[C@@](C)(C=C)C(=O)[C@@H]3C)OC(=O)C1=CNC=CC1=O
InChIKey
InChIKey=QUJJCOBHGSKOOR-NYZSHUKYSA-N
Formula
C27H37NO5
Mass
455.595
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Diterpenoids
- Level 5 Mutilane diterpenoids
-
Subclass
Diterpenoids
-
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
Mutilane diterpenoids
Alternative Parents
Pyridinecarboxylic acids Dihydropyridinecarboxylic acids and derivatives Vinylogous amides Heteroaromatic compounds Cyclic ketones Carboxylic acid esters Dialkyl ethers Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Mutilane diterpenoid - Dihydropyridinecarboxylic acid derivative - Pyridine carboxylic acid or derivatives - Pyridine carboxylic acid - Dihydropyridine - Hydropyridine - Pyridine - Heteroaromatic compound - Vinylogous amide - Carboxylic acid ester - Ketone - Cyclic ketone - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as mutilane diterpenoids. These are diterpenoids with a structure based on the mutilane skeleton.
External Descriptors
Not available