Compound Identification
SMILES
O=CC[C@H]1C[C@@H]2CC(=O)N3C4=CC=CC=C4C4=C3[C@H]2N(CC4)C1
InChIKey
InChIKey=VDZMRKXTAFYZTI-JCGVRSQUSA-N
Formula
C19H20N2O2
Mass
308.381
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 Naphthyridines 3-alkylindoles Aralkylamines Piperidines Benzenoids Pyrroles Heteroaromatic compounds Alpha-hydrogen aldehydes Trialkylamines Lactams Azacyclic compounds 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 - Aralkylamine - Piperidine - Benzenoid - Alpha-hydrogen aldehyde - Heteroaromatic compound - Pyrrole - Lactam - Tertiary amine - Tertiary aliphatic amine - Azacycle - Organoheterocyclic compound - Amine - Aldehyde - Organooxygen compound - Organonitrogen compound - 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 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