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
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Indolonaphthyridine alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Indolonaphthyridine alkaloids
Alternative Parents
Beta carbolines Isoquinolones and derivatives 3-alkylindoles Naphthyridines Indolizines Phenol ethers Pyridinones Alkyl aryl ethers Substituted pyrroles Heteroaromatic compounds Lactams Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboximidic acids Organic oxides Organonitrogen compounds Hydrocarbon derivatives
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