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Please use this identifier to cite or link to this item: https://idr.l1.nitk.ac.in/jspui/handle/123456789/10981
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dc.contributor.authorEswaran, S.-
dc.contributor.authorAdhikari, A.V.-
dc.contributor.authorPal, N.K.-
dc.contributor.authorChowdhury, I.H.-
dc.date.accessioned2020-03-31T08:23:31Z-
dc.date.available2020-03-31T08:23:31Z-
dc.date.issued2010-
dc.identifier.citationBioorganic and Medicinal Chemistry Letters, 2010, Vol.20, 3, pp.1040-1044en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/10981-
dc.description.abstractA 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 (MC2), 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. 2009 Elsevier Ltd. All rights reserved.en_US
dc.titleDesign and synthesis of some new quinoline-3-carbohydrazone derivatives as potential antimycobacterial agentsen_US
dc.typeArticleen_US
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