Compound Identification
SMILES
CC1CCC2(C)C(CCC=C2C)C1(C)CC\C(C)=C\Cn1c[n+](C)c2ncnc(N[O-])c12.CC1CCC2(C)C(CCC=C2C)C1(C)CC\C(C)=C\Cn1c[n+](C)c2[nH+]c[nH+]c(N[O-])c12
InChIKey
InChIKey=AKPJRQQEWLKEPK-BUVCPBHVSA-P
Formula
C52H80N10O2
Mass
877.279
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
Purines and purine derivatives Arylhydroxamates Pyrimidines and pyrimidine derivatives N-substituted imidazoles Imidolactams Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Not available
Substituents
Clerodane diterpenoid - Imidazopyrimidine - Purine - Arylhydroxamate - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic cation - 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