Compound Identification
SMILES
CCC1=CN2CCC3=C4[C@H]2[C@H](C1)C=C(N4C1=CC=CC=C31)C(=O)OC
InChIKey
InChIKey=OVLMDKBCINTONY-AUUYWEPGSA-N
Formula
C21H22N2O2
Mass
334.419
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 Alpha amino acids and derivatives Naphthyridines Tetrahydropyridines Aralkylamines Benzenoids Heteroaromatic compounds Enoate esters Pyrroles Methyl esters Trialkylamines Enamines Monocarboxylic acids and derivatives Azacyclic compounds Allylamines Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Tacaman alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Tetrahydropyridine - Aralkylamine - Benzenoid - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Methyl ester - Pyrrole - Heteroaromatic compound - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Monocarboxylic acid or derivatives - Allylamine - Enamine - 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 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