Compound Identification
SMILES
CC(=O)C1=CN2CCC3=C4[C@@H]2[C@@H](C[C@@H](C#N)N4C2=CC=CC=C32)C1
InChIKey
InChIKey=KITASABMLWRARB-WTANOLMUSA-N
Formula
C20H19N3O
Mass
317.392
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Tacaman alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Tacaman alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Tacaman alkaloids
Alternative Parents
Indolonaphthyridine alkaloids Beta carbolines 3-alkylindoles Naphthyridines Aralkylamines Tetrahydropyridines Benzenoids Heteroaromatic compounds Pyrroles Vinylogous amides Ketones Trialkylamines Enamines Azacyclic compounds Allylamines Nitriles Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Tacaman alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Tetrahydropyridine - Aralkylamine - Benzenoid - Vinylogous amide - Heteroaromatic compound - Pyrrole - Tertiary aliphatic amine - Tertiary amine - Ketone - Azacycle - Organoheterocyclic compound - Enamine - Allylamine - Carbonitrile - Nitrile - Amine - Organonitrogen compound - Organic oxide - Organooxygen compound - Cyanide - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as tacaman alkaloids. These are alkaloids containing the pentacyclic tacaman skeleton, which consists of a pyrido[1,2-a]indole fused to a quinolizine. Tacaman alkaloids are obtained from a precursor to a pseudoaspidospermidine (type II skeleton) derivative, by the formation of new bonds at C-20/C-3 and C-140/C-17.
External Descriptors
Not available