Compound Identification
SMILES
OC(=O)C1=CC=CC=C1N\N=C(/N=NC1=CC=CC=C1C(O)=O)C1=NC2=C(C=CC(=O)N2)C(C=O)=C1
InChIKey
InChIKey=UWNALGDPQAHYOI-MHHQDPAGSA-N
Formula
C24H16N6O6
Mass
484.428
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazanaphthalenes
- Subclass Naphthyridines
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Class
Diazanaphthalenes
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazanaphthalenes
Subclass
Naphthyridines
Intermediate Tree Nodes
Not available
Direct Parent
Naphthyridines
Alternative Parents
Benzoic acids Benzoyl derivatives Phenylhydrazines Pyridine carboxaldehydes Aryl-aldehydes Pyridinones Heteroaromatic compounds Formazans Vinylogous amides Lactams Azo compounds Azacyclic compounds Hydrazones Carboxylic acids Propargyl-type 1,3-dipolar organic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - Benzoic acid or derivatives - Benzoic acid - Benzoyl - 4-pyridine carboxaldehyde - Phenylhydrazine - Aryl-aldehyde - Pyridinone - Monocyclic benzene moiety - Benzenoid - Pyridine - Heteroaromatic compound - Vinylogous amide - Formazan - Azo compound - Lactam - Azacycle - Carboxylic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Hydrazone - Propargyl-type 1,3-dipolar organic compound - Aldehyde - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthyridines. These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.
External Descriptors
Not available