Cl.Cl.COC1=NC2=C(CCN3CCC(CC3)NCC3=NN=C4SCC(=O)NC4=C3)C(F)=CN=C2C=C1

InChIKey=BZRUWWVDSGIZFK-UHFFFAOYSA-N

C23H28Cl2FN7O2S

556.48

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

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

Aromatic heteropolycyclic compounds

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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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