Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/10398
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dc.contributor.authorS Raja, A-
dc.contributor.authorK Agarwal, A-
dc.contributor.authorMahajan, N-
dc.contributor.authorN Pandeya, S-
dc.contributor.authorAnanthan, S-
dc.date.accessioned2010-10-12T08:16:10Z-
dc.date.available2010-10-12T08:16:10Z-
dc.date.issued2010-10-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/10398-
dc.description1384-1388en_US
dc.description.abstractCondensation of phenoxy or 4-bromophenoxy acetic acid hydrazide and substituted aryl semicarbazides with appropriate carbonyl compounds yield corresponding hydrazones and semicarbazones, respectively. The chemical structure of the synthesized compounds has been confirmed by UV, IR and 1H NMR spectral data. All the compounds have been investigated for their antibacterial activity against ten pathogenic strains and antitubercular activity against Mycobacterium tuberculosis H37 Rv. Compound 4f, Acetic acid, phenoxy-,[1-(4-chlorophenyl) ethylidene] hydrazide has been found to exhibit 80% inhibition in the preliminary antitubercular screening (MIC >6.25 mg/mL).en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.49B(10) [October 2010]en_US
dc.subjectHydrazonesen_US
dc.subjectsemicarbazonesen_US
dc.subjectsynthesisen_US
dc.subjectantibacterialen_US
dc.subjectantitubercularen_US
dc.titleAntibacterial and antitubercular activities of some diphenyl hydrazones and semicarbazonesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.49B(10) [October 2010]

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