Compound Identification
SMILES
NC1=C(CN2C3=CC=CC=C3C3=C2C1=NC=C3)C(O)=O
InChIKey
InChIKey=VZLJYHNHGLQXQG-UHFFFAOYSA-N
Formula
C15H11N3O2
Mass
265.272
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 Indoles Pyridines and derivatives Benzenoids Vinylogous amides Pyrroles Heteroaromatic compounds Amino acids Azacyclic compounds Monocarboxylic acids and derivatives Enamines Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Diazanaphthalene - Naphthyridine - Indole - Indole or derivatives - Pyridine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Pyrrole - Amino acid - Amino acid or derivatives - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Enamine - Monocarboxylic acid or derivatives - Primary aliphatic amine - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Primary amine - Amine - Hydrocarbon derivative - 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