Structure Information
Structure

Compound Identification

SMILES

COC(=O)[C@H]1CC(=O)N2C3=C(C=C(Cl)C=C3)C3=C2[C@H]1NCC3

InChIKey

InChIKey=UUBIPWORYDNUGD-FZMZJTMJSA-N

Formula

C16H15ClN2O3

Mass

318.76

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Indolonaphthyridine alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Indolonaphthyridine alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Aryl chloride - Aryl halide - Benzenoid - Heteroaromatic compound - Methyl ester - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Lactam - Secondary amine - Carboxylic acid derivative - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Azacycle - Organochloride - Hydrocarbon derivative - Amine - Organohalogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as indolonaphthyridine alkaloids. These are a numerous and relatively straightforward subgroup of the b-carbolines, e.g. Canthin-6-one, in which an additional C3 unit is attached between C-1 and the indole nitrogen to form an additional ring. The group includes a few dimeric examples, such as Haplophytine.

External Descriptors

Not available

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