Structure Information
Structure

Compound Identification

SMILES

CC[C@@]12CCCN3C[C@@H](Br)[C@]4([C@H]13)C1=C(C=CC(Br)=C1)N=C4[C@](Cl)(C2)C(=O)OC

InChIKey

InChIKey=WPYNQKYQLDTWHR-CRSFFPMXSA-N

Formula

C21H23Br2ClN2O2

Mass

530.69

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Plumeran-type alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Plumeran-type alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Plumeran-type alkaloid - 3-alkylindole - Quinolidine - Indolizidine - Indole or derivatives - Aralkylamine - Aryl halide - Piperidine - N-alkylpyrrolidine - Aryl bromide - Benzenoid - Alpha-halocarboxylic acid or derivatives - Alpha-halocarboxylic acid derivative - Methyl ester - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Ketimine - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organoheterocyclic compound - Alkyl bromide - Organohalogen compound - Organobromide - Imine - Organochloride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Alkyl chloride - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as plumeran-type alkaloids. These are alkaloids with a structure based on the plumeran skeleton. Plumeran is a pentacyclic compound that consists of a pyrrolidine ring shed to the quinoline moiety of pyrido[3,2-c]carbazole ring system.

External Descriptors

Not available

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