Structure Information
Structure

Compound Identification

SMILES

C\C=C1/C[N+]2(C)CCC3=C4[C@@H]2C[C@@H]1C(CO)N4C1=CC=CC=C31

InChIKey

InChIKey=HFLUPWJGJPYITM-ILIQZIPWSA-N

Formula

C20H25N2O

Mass

309.432

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Taxonomic Classification

Taxonomy Tree

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 Beta carbolines Naphthyridines 3-alkylindoles Aralkylamines Piperidines Benzenoids Tetraalkylammonium salts Pyrroles Heteroaromatic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives Organic cations

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pleiocarpaman skeleton - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Piperidine - Benzenoid - Tetraalkylammonium salt - Heteroaromatic compound - Pyrrole - Quaternary ammonium salt - Azacycle - Organoheterocyclic compound - Primary alcohol - Amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organic cation - 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

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