Synthesis and In Vitro Anti-Tubercular Activity of a Series of N- (Disubstitutedbenzoyl)Isoniazid Derivatives

Author(s): Ivan Neves Junior, Maria C.S. Lourenco, Guilherme de B.P. de Miranda, Thatyana R.A. Vasconcelos, Karla C. Pais, Jose dos P. de A. Junior, M. S.V. Wardell, James L. Wardell, V. N. de Souza.

Journal Name: Letters in Drug Design & Discovery

Volume 3 , Issue 6 , 2006

Submit Manuscript
Submit Proposal

Abstract:

A series of eight N-(disubstitutedbenzoyl)isoniazid derivatives have been synthesized and evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis H37Rv using the alamar blue susceptibility test and the activity expressed as the minimum inhibitory concentration (MIC) in μg/mL. Compounds 15 and 16 exhibited a significant activity (0.5 μg/mL) when compared with first line drugs such as isoniazid (INH) and rifampicin (RIP) and could be a good starting point to develop new lead compounds in the fight against multi-drug resistant tuberculosis.

Keywords: Isoniazid, analogs, anti-tubercular activity

Rights & PermissionsPrintExport Cite as


Article Details

VOLUME: 3
ISSUE: 6
Year: 2006
Page: [424 - 428]
Pages: 5
DOI: 10.2174/157018006777805549
Price: $58

Article Metrics

PDF: 10