Compound Identification
SMILES
CON1C2=NC=NC3=C2N(CC[C@]1(C)CC[C@@]1(C)[C@H](C)CC[C@@]2(C)[C@@H]1CCCC2=C)C(=O)N3C
InChIKey
InChIKey=WUJLQYOSWFQWEL-XWPWZHHHSA-N
Formula
C27H41N5O2
Mass
467.658
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
Colensane and clerodane diterpenoids
Alternative Parents
Pyrimidodiazepines 6-alkylaminopurines Purinones 1,4-diazepines Pyrimidines and pyrimidine derivatives N-substituted imidazoles Imidolactams Heteroaromatic compounds Ureas N-organohydroxylamines Azacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Clerodane diterpenoid - 6-alkylaminopurine - Pyrimidodiazepine - Purinone - Imidazopyrimidine - Purine - Para-diazepine - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Urea - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.
External Descriptors
Not available