Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/960
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dc.contributor.authorKumar, Vinod-
dc.date.accessioned2023-04-24T07:29:21Z-
dc.date.available2023-04-24T07:29:21Z-
dc.date.issued2019-
dc.identifier.urihttp://hdl.handle.net/123456789/960-
dc.description.abstractEleven acetohydrazide linked pyrazole derivatives were designed and synthesized via condensation of acetohyadrazide with different substituted formyl pyrazole derivatives under mild reaction conditions. Synthesized compounds were characterized on the basis of IR, NMR (1H & 13C) and mass spectrometry. The antimicrobial activities of all the compounds were screened against four bacterial and two fungal strains. Among the synthesized compounds, three compounds viz. 6b, 6c and 6d were found as efficient antimicrobial agents in reference to the standard drugs viz. ciprofloxacin and amphotericin-B. Further, structure-activity relationship (SAR) study revealed that electron-withdrawing group enhances the antimicrobial potential of synthesized derivatives as compared to other groups present in the ring. Hence, among compounds 6b-c, compound 6d could be explored further against other microbes to prove its vitality.en_US
dc.language.isoenen_US
dc.publisherAsian Journal of Chemistryen_US
dc.subjectAcetohydrazide pyrazoles, Antimicrobial activityen_US
dc.titleNovel acetohydrazide pyrazolederivatives: Design, synthesis,characterization and antimicrobial activityen_US
dc.typeArticleen_US
Appears in Collections:School of Basic Sciences

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