C[C@H](CO)N(CC(=O)N1CCOCC1)C(=O)C1=C(O)C2=C(NC1=O)C=C(CC1=CC=C(F)C=C1)C=N2

InChIKey=IKPXNXKWRHYTPR-OAHLLOKOSA-N

C25H27FN4O6

498.511

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

Alpha amino acids and derivatives Pyridinecarboxylic acids and derivatives Fluorobenzenes Hydroxypyridines Pyridinones Aryl fluorides Morpholines Vinylogous amides Tertiary carboxylic acid amides Heteroaromatic compounds Vinylogous acids Lactams Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary alcohols

Aromatic heteropolycyclic compounds

Alpha-amino acid or derivatives - Naphthyridine - Pyridine carboxylic acid or derivatives - Halobenzene - Hydroxypyridine - Pyridinone - Fluorobenzene - Aryl fluoride - Morpholine - Oxazinane - Aryl halide - Monocyclic benzene moiety - Pyridine - Benzenoid - Heteroaromatic compound - Tertiary carboxylic acid amide - Vinylogous acid - Vinylogous amide - Lactam - Carboxamide group - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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