COC1=NC2=C(C=CN=C2C=C1)[C@@H](O)CN1CCC(CC1)NCC1=C(Br)C=C2SCC(=O)NC2=N1

InChIKey=SHVJDPNOVPQBCL-IBGZPJMESA-N

C24H27BrN6O3S

559.48

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

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

Aromatic heteropolycyclic compounds

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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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