Please use this identifier to cite or link to this item: https://idr.l4.nitk.ac.in/jspui/handle/123456789/13282
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dc.contributor.authorHarikrishna, N.
dc.contributor.authorIsloor, A.M.
dc.contributor.authorAnanda, K.
dc.contributor.authorObaid, A.
dc.contributor.authorFun, H.-K.
dc.date.accessioned2020-03-31T08:45:31Z-
dc.date.available2020-03-31T08:45:31Z-
dc.date.issued2016
dc.identifier.citationNew Journal of Chemistry, 2016, Vol.40, 1, pp.73-76en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/13282-
dc.description.abstractA new series of 1?-(4-chlorophenyl)-5-(substituted aryl)-3?-(substituted aryl)-3,4-dihydro-2H,1?H-[3,4?]bipyrazolyl derivatives (6a-e, 8a-e, 10a-e) have been synthesized, characterized and screened for antimicrobial and antitubercular activity. Among the synthesized compounds, the minimum inhibition concentration of 10e was found to be as low as 1.56 ?g ml-1 and that of 10c was 6.25 ?g ml-1 as compared to the standard anti-tb drugs pyrazinamide and streptomycin. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2016.en_US
dc.titleSynthesis, and antitubercular and antimicrobial activity of 1?-(4-chlorophenyl)pyrazole containing 3,5-disubstituted pyrazoline derivativesen_US
dc.typeArticleen_US
Appears in Collections:1. Journal Articles

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