Compound Identification
SMILES
COC(=O)[C@@H]1C[C@H]2CC(=CN3CCC4=C([C@H]23)N1C1=CC=CC=C41)C(C)=O
InChIKey
InChIKey=SDLCLIJNRMIPBV-VMDGZTHMSA-N
Formula
C21H22N2O3
Mass
350.418
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 Alpha amino acid esters Beta carbolines 3-alkylindoles Naphthyridines Tetrahydropyridines Aralkylamines Benzenoids Heteroaromatic compounds Vinylogous amides Pyrroles Methyl esters Ketones Trialkylamines Monocarboxylic acids and derivatives Enamines Azacyclic compounds Allylamines Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Tacaman alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Alpha-amino acid ester - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Tetrahydropyridine - Benzenoid - Heteroaromatic compound - Pyrrole - Vinylogous amide - Methyl ester - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Ketone - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Allylamine - Enamine - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Amine - Organooxygen 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