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=CN=CNC1=O
InChIKey
InChIKey=BZZQXQSFBIRQFC-VJEBXGNLSA-N
Formula
C26H36N2O5
Mass
456.583
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
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Subclass
Diterpenoids
- Level 5 Mutilane diterpenoids
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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
Mutilane diterpenoids
Alternative Parents
Pyrimidinecarboxylic acids Hydropyrimidine carboxylic acids and derivatives Pyrimidones Vinylogous amides Heteroaromatic compounds Lactams Cyclic ketones Carboxylic acid esters Dialkyl ethers Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Mutilane diterpenoid - Hydropyrimidine carboxylic acid derivative - Pyrimidine-5-carboxylic acid - Pyrimidine-5-carboxylic acid or derivatives - Pyrimidone - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Carboxylic acid ester - Cyclic ketone - Ketone - Lactam - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Carboxylic acid derivative - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic nitrogen compound - 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