Structure Information
Structure

Compound Identification

SMILES

CN(C)[C@@H]1N2C3=CC=CC=C3C3=C2C(=C[C@]11CCOC1=O)N(CC3)C(C)=O

InChIKey

InChIKey=UWACLXLGGVZUIK-TZIWHRDSSA-N

Formula

C21H23N3O3

Mass

365.433

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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 - Aminopyridine - Gamma butyrolactone - Benzenoid - Heteroaromatic compound - Oxolane - Pyrrole - Tertiary carboxylic acid amide - Acetamide - Carboxamide group - Carboxylic acid ester - Lactone - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Organic oxide - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organonitrogen compound - Carbonyl group - 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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