Structure Information
Structure

Compound Identification

SMILES

COC1OC\C(=C/C)C2CC3NCCC4=C3N(C3=CC=CC=C43)C12C(=O)OC

InChIKey

InChIKey=GDUAJWBHIGHMEU-YIXHJXPBSA-N

Formula

C22H26N2O4

Mass

382.46

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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 - Delta amino acid or derivatives - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - Diazanaphthalene - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Oxane - Benzenoid - Heteroaromatic compound - Methyl ester - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Secondary amine - Acetal - Azacycle - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Secondary aliphatic amine - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Amine - 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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