Compound Identification
SMILES
CC[C@@H]1CN2CCC3=C4C2CC1[C@H](N4C1=CC=CC=C31)C(=O)OC
InChIKey
InChIKey=XFAGQYBMGXZIOU-OPKJXMCVSA-N
Formula
C20H24N2O2
Mass
324.424
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Pleiocarpaman alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Pleiocarpaman alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pleiocarpaman alkaloids
Alternative Parents
Indolonaphthyridine alkaloids Alpha amino acid esters Beta carbolines 3-alkylindoles Naphthyridines Aralkylamines Piperidines Benzenoids Heteroaromatic compounds Pyrroles Methyl esters Trialkylamines Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pleiocarpaman skeleton - Indolo[3,2-1de][1,5]naphthyridine - Alpha-amino acid ester - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - 3-alkylindole - Naphthyridine - Indole - Indole or derivatives - Aralkylamine - Benzenoid - Piperidine - Heteroaromatic compound - Methyl ester - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organic oxide - Carbonyl group - Organic oxygen compound - Amine - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pleiocarpaman alkaloids. These are alkaloids with a structure that is based on the pleiocarpaman skeleton. These alkaloids arise from the cyclization of a corynantheine precursor via C-16 to N-1.
External Descriptors
Not available