Artigo Revisado por pares

Synthesis and Anti-Mycobacterial Activity of N-[(E)-(Disubstituted- Phenyl)Methylidene]Isonicotino-Hydrazide Derivatives

2005; Bentham Science Publishers; Volume: 2; Issue: 7 Linguagem: Inglês

10.2174/157018005774479131

ISSN

1875-628X

Autores

Ivan Neves Júnior, Maria Helena Lourenço, Maria das Graças Henriques, B.J.M. Leite Ferreira, T.R.A. Vasconcelos, Mônica A. Peralta, Pedro de Oliveira, J.L. Wardell, Marcus de Souza,

Tópico(s)

Synthesis and Biological Evaluation

Resumo

A series of eight N-[(E)-(disubstituted-phenyl)methylidene]isonicotino-hydrazide derivatives were synthesized and evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis, and the activity expressed as the minimum inhibitory concentration (MIC) in mg/mL. Four compounds 2b-d and 2f exhibited a significant activity (0.6 mg/mL), when compared with first line drugs such as isoniazid (INH) and rifampin (RIP) and could be a good starting point to develop new lead compounds in the fight against multidrug resistant tuberculosis.

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