CNC(=O)C1=C(CNC(=O)C2=C(O)C3=C(C=CC=N3)C(=N2)N2CCCN(C)S2(=O)=O)C=CC(F)=C1

InChIKey=GWOOXRGXRXFABB-UHFFFAOYSA-N

C22H23FN6O5S

502.52

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

3-halobenzoic acids and derivatives Benzamides Pyridinecarboxylic acids and derivatives 2-heteroaryl carboxamides Benzoyl derivatives Hydroxypyridines Fluorobenzenes Imidolactams Thiadiazinanes Aryl fluorides Sulfuric acid diamides Heteroaromatic compounds Vinylogous acids Secondary carboxylic acid amides Azacyclic compounds Organooxygen compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Naphthyridine - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Pyridine carboxylic acid or derivatives - Benzamide - Benzoic acid or derivatives - 2-heteroaryl carboxamide - Benzoyl - Hydroxypyridine - Halobenzene - Fluorobenzene - Imidolactam - Benzenoid - Aryl halide - Thiadiazinane - Pyridine - Aryl fluoride - Sulfuric acid diamide - Monocyclic benzene moiety - Vinylogous acid - Organic sulfuric acid or derivatives - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organofluoride - Organohalogen 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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