Structure Information
Structure

Compound Identification

SMILES

OC(COC1=CC2=C(C=C1)N1C3=C(N=CC=C23)C2=CC=CC=C2C1=O)=NCCC1=CNC2=CC=CC=C12

InChIKey

InChIKey=SYIMWSFFFRSEHK-UHFFFAOYSA-N

Formula

C30H22N4O3

Mass

486.531

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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 - Isoquinolone - Isoquinoline - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Indolizine - Pyrrolopyridine - Phenol ether - Alkyl aryl ether - Pyridinone - Substituted pyrrole - Benzenoid - Pyridine - Pyrrole - Heteroaromatic compound - Lactam - Propargyl-type 1,3-dipolar organic compound - Carboximidic acid - Carboximidic acid derivative - Ether - Organic 1,3-dipolar compound - Azacycle - Organoheterocyclic compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Organonitrogen 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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