Compound Identification
SMILES
COC(=O)C12COC34C5CC1\C(CN5CCC23C1=CC=CC=C1N4C)=C\C
InChIKey
InChIKey=HAGBWVNSVWLTKY-LNKIKWGQSA-N
Formula
C22H26N2O3
Mass
366.461
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Corynanthean-type alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Corynanthean-type alkaloids
Alternative Parents
Beta carbolines Carbazoles Quinolizidines Dialkylarylamines Aralkylamines Oxepanes Piperidines Benzenoids Methyl esters Oxolanes Trialkylamines Amino acids and derivatives Monocarboxylic acids and derivatives Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Corynanthean skeleton - Beta-carboline - Carbazole - Pyridoindole - Quinolizidine - Indole or derivatives - Dialkylarylamine - Oxepane - Aralkylamine - Piperidine - Benzenoid - Oxolane - Methyl ester - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group.
External Descriptors
Not available