Synthesis Characterization and Antimicrobial Evaluation of Some New 1 3 5 Trisubstituted Pyrazole Derivatives

dc.contributor.guideMayank Gangwar
dc.coverage.spatial
dc.creator.researcherAnupam Sharma
dc.date.accessioned2023-01-20T09:51:41Z
dc.date.available2023-01-20T09:51:41Z
dc.date.awarded2020
dc.date.completed2020
dc.date.registered2017
dc.description.abstractObjective: The objective of the paper was to design, synthesis, and characterization of new 1,3,5-trisubstituted-2- pyrazolines derivative and evaluate for antibacterial activity. Materials and Methods: The 1,3,5-tri-substituted-2- pyrazolines derivatives have been synthesized by the reaction of chalcone derivatives with succinic hydrazide in the environment of pyridine. A total of 20 compounds have been synthesized and characterized by the infrared, 1H -nuclear magnetic resonance, and mass spectral analysis. Antibacterial activity of the compounds carried out on five Gram- positive bacterial strains, that is, Staphylococcus aureus, Staphylococcus faecalis, Bacillus subtilis, Proteus vulgaris, and Bacillus pumilus and two Gram-negative bacterial strains, that is, Escherichia coli and Klebsiella pneumoniae in two different concentrations, that is, 50 and 100 µg/ml by agar diffusion method using cup -plate method. Norfloxacin and ciprofloxacin were used as standard antibacterial drug. Results and Discussion: The data of antibacterial activity against the Gram-positive bacterial strains (S. aureus, S. faecalis, B. subtilis, P. vulgaris, and B. pumilus) suggested the order of activity of compounds: BR-3 gtBR-2gtBR-1gtCL-4gtBR-4gtCL-3gt CL-2gtCL-5gtCL-6gtME-3gtME-2gtME- 4gtME-5gtME-6gtME-7gtCL-7gtCL-8gtCL-1gtME-8gtME-1. The compounds series BR-1 to BR- 4 has shown the highest activity. Compound ME-8, CL-8, CL-7, CL-1, ME-5, ME-6, and ME- 1 have showed mild activity, compounds CL-2, CL-5, ME-4, CL-6, ME-3, ME-2, and ME-7 showed moderate activity, and compounds BR-3, BR-2, BR-1, CL-4, BR-4, and CL-3 have showed good activity against Gram-negative bacteria. The result data of antibacterial activity suggested that Cl, Br, F, and nitro substitution at the third and fifth position may enhance the antibacterial activity of the compounds but the methyl and methoxy substitution may result in reduction of the activity. newline newlineKey words: Agar Diffusion, Antibacterial, Ciprofloxacin, Cup-plate method,
dc.description.note
dc.format.accompanyingmaterialNone
dc.format.dimensions
dc.format.extent
dc.identifier.urihttp://hdl.handle.net/10603/450982
dc.languageEnglish
dc.publisher.institutionPHARMACY
dc.publisher.placeBhopal
dc.publisher.universitySarvepalli Radhakrishnan University
dc.relation
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.titleSynthesis Characterization and Antimicrobial Evaluation of Some New 1 3 5 Trisubstituted Pyrazole Derivatives
dc.title.alternativeSynthesis Characterization and Antimicrobial Evaluation of Some New 1 3 5 Trisubstituted Pyrazole Derivatives
dc.type.degreePh.D.

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