Compound Identification
SMILES
COC1=C(OC)C=C2C(=C1)N1C3=C2C=CN=C3C=CC1=O
InChIKey
InChIKey=VKMIBFAQYHUWCU-UHFFFAOYSA-N
Formula
C16H12N2O3
Mass
280.283
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 Naphthyridines Indolizines Indoles Anisoles Pyridinones Alkyl aryl ethers Pyrroles Heteroaromatic compounds Lactams Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - Indole - Indole or derivatives - Indolizine - Pyrrolopyridine - Phenol ether - Anisole - Alkyl aryl ether - Pyridinone - Benzenoid - Pyridine - Heteroaromatic compound - Pyrrole - Lactam - Azacycle - Organoheterocyclic compound - Ether - Organooxygen compound - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxygen 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