CN(C)C(=O)CN1CCN(CC1)C1=N\C(=C2\NN=C(CC3=CC=CC=C3)O2)C(=O)C2=C1C=CC=N2

InChIKey=NOCQDVCMIPLLMO-LVWGJNHUSA-N

C25H27N7O3

473.537

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

Alpha amino acids and derivatives N-piperazineacetamides Aryl ketones N-alkylpiperazines Pyridines and derivatives Benzene and substituted derivatives Imidolactams Vinylogous amides Tertiary carboxylic acid amides Heteroaromatic compounds Trialkylamines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Hydrazones Carboximidamides Carboxamidines Azacyclic compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Alpha-amino acid or derivatives - N-piperazineacetamide - Naphthyridine - Aryl ketone - N-alkylpiperazine - Monocyclic benzene moiety - 1,4-diazinane - Piperazine - Pyridine - Benzenoid - Imidolactam - Heteroaromatic compound - Vinylogous amide - Tertiary carboxylic acid amide - Ketone - Carboxamide group - Amino acid or derivatives - Tertiary amine - Tertiary aliphatic amine - Oxacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid amidine - Hydrazone - Carboxylic acid derivative - Azacycle - Amidine - Carboximidamide - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Amine - Aromatic heteropolycyclic compound

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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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.

Not available