COC1=NC2=C(CCN3C[C@H](O)[C@@H](C3)NCC3=NC4=C(SCC(=O)N4)C=C3)C=CN=C2C=C1

InChIKey=AVGGIIBQBYPUHU-MSOLQXFVSA-N

C23H26N6O3S

466.56

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

2-pyridylmethylamines Alkyl aryl ethers Alkylarylthioethers Aralkylamines 1,4-thiazines N-alkylpyrrolidines Imidolactams Heteroaromatic compounds 1,2-aminoalcohols Trialkylamines Secondary carboxylic acid amides Secondary alcohols Amino acids and derivatives Lactams Azacyclic compounds Dialkylamines Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Naphthyridine - 2-pyridylmethylamine - Aryl thioether - Alkyl aryl ether - Aralkylamine - Alkylarylthioether - Para-thiazine - Pyridine - Imidolactam - N-alkylpyrrolidine - Heteroaromatic compound - Pyrrolidine - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Ether - Secondary aliphatic amine - Carboxylic acid derivative - Azacycle - Secondary amine - Thioether - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Amine - Organic nitrogen compound - Carbonyl group - 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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