Compound Identification
SMILES
C[C@@H]1CC[C@]2(C)[C@@H](CCCC2=C)[C@@]1(C)CC[C@]1(C)CCN2C(C)=NC3=C2C(=NC=N3)N1O
InChIKey
InChIKey=PZPVZLOTCXXZBE-SUNKJPIHSA-N
Formula
C26H39N5O
Mass
437.632
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 1,4-diazepines Pyrimidines and pyrimidine derivatives N-substituted imidazoles Imidolactams Heteroaromatic compounds N-organohydroxylamines Azacyclic compounds Organic oxygen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Clerodane diterpenoid - Pyrimidodiazepine - 6-alkylaminopurine - Imidazopyrimidine - Purine - Para-diazepine - N-substituted imidazole - Pyrimidine - Imidolactam - Heteroaromatic compound - Imidazole - Azole - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen 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