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dc.contributor.authorVirsodia, Sumit R.-
dc.date.accessioned2011-08-27T06:20:33Z-
dc.date.available2011-08-27T06:20:33Z-
dc.date.issued2010-
dc.identifier.urihttp://hdl.handle.net/123456789/2619-
dc.description.abstract(E)-4-chloro-N-((2-(4-nitrostyryl)-1H-benzo[d]imidazol-1-yl) methyl) aniline analogs (SV – 1 to SV - 13) were synthesized from 2-styryl benzimidazole [27] and substituted phenyl amine derivatives in presence of DMF and formaldehyde. 2-styryl benzimidazoles [27] have been synthesized from 2-methyl benzimidazole through the condensation reaction with various aromatic aldehydes. The structure of synthesize compounds has been established on the basis of their spectral data (IR, 1H NMR and Mass). The purity of the compounds was confirmed by TLC. The synthesized compounds were evaluated for antibacterial activity against several bacteria using cup plate method. Compounds SV-3, SV-4, SV-7, SV-9 and SV-13 were exhibited good antibacterial activity against E. coli, B. subtilis, S. aureus and K. pneumonia and comparable with standard streptomycin.en_US
dc.publisherInstitute of Pharmacy, Nirma University, A'baden_US
dc.relation.ispartofseriesPDR00111en_US
dc.subjectDissertation Reporten_US
dc.subjectMedicinal Chemistryen_US
dc.subject08MPHen_US
dc.subject08MPH409en_US
dc.subjectPDR00111en_US
dc.titleSynthesis and Pharmacololgical Evaluataion of substituted Styral Benzimidazole Derivattivesen_US
dc.typeDissertationen_US
Appears in Collections:M.Pharm. Research Reports, Department of Medicinal Chemistry

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