Compound Identification
SMILES
CCOC(=O)C([C@@H]1C[C@@H]2N(CCC3=C2NC2=CC=CC=C32)C\C1=C/C)C(=O)OCC
InChIKey
InChIKey=UIBKWSWBDFNSCJ-GTWHDPJTSA-N
Formula
C24H30N2O4
Mass
410.514
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 3-alkylindoles Quinolizines Aralkylamines 1,3-dicarbonyl compounds Benzenoids Piperidines Dicarboxylic acids and derivatives Pyrroles Heteroaromatic compounds Carboxylic acid esters Amino acids and derivatives Trialkylamines Azacyclic compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Corynanthean skeleton - Beta-carboline - Pyridoindole - 3-alkylindole - Quinolizine - Indole - Indole or derivatives - Aralkylamine - Dicarboxylic acid or derivatives - Piperidine - Benzenoid - 1,3-dicarbonyl compound - Heteroaromatic compound - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - 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