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Comparative Study
. 2010 Feb 1;20(3):1040-4.
doi: 10.1016/j.bmcl.2009.12.045. Epub 2009 Dec 16.

Design and synthesis of some new quinoline-3-carbohydrazone derivatives as potential antimycobacterial agents

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Comparative Study

Design and synthesis of some new quinoline-3-carbohydrazone derivatives as potential antimycobacterial agents

Sumesh Eswaran et al. Bioorg Med Chem Lett. .

Abstract

A series of 26 new quinoline derivatives carrying active pharmacophores has been synthesized and evaluated for their in vitro antituberculosis activity against Mycobacterium tuberculosis H37Rv (MTB), Mycobacterium smegmatis (MC(2)), and Mycobacterium fortuitum following the broth micro dilution assay method. Compounds 13e, 13i, 13k, 14a, 14c, 14i, and 14k exhibited significant minimum inhibition concentrations, when compared with first line drugs isoniazid (INH) and rifampicin (RIF) and could be ideally suited for further modifications to obtain more efficacious compounds in the fight against multi-drug resistant tuberculosis.

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