COC1=NC2=C(CCN3CCC(NCC4=NC5=C(SCC(=O)N5)C=C4)C(O)C3)C(F)=CN=C2C=C1

InChIKey=XNIMUFKTMYBCGE-UHFFFAOYSA-N

C24H27FN6O3S

498.58

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

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

Aromatic heteropolycyclic compounds

Naphthyridine - 2-pyridylmethylamine - Aryl thioether - Alkyl aryl ether - 4-aminopiperidine - Aralkylamine - Alkylarylthioether - Para-thiazine - Aryl halide - Aryl fluoride - Imidolactam - Piperidine - Pyridine - Heteroaromatic compound - Secondary carboxylic acid amide - Secondary alcohol - Tertiary aliphatic amine - Amino acid or derivatives - Carboxamide group - 1,2-aminoalcohol - Lactam - Tertiary amine - Secondary amine - Thioether - Azacycle - Carboxylic acid derivative - Ether - Secondary aliphatic amine - Organic nitrogen compound - Organohalogen compound - Carbonyl group - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Amine - Organic oxide - Alcohol - Organic oxygen compound - 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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