Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/602956
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dc.date.accessioned2024-11-26T08:32:07Z-
dc.date.available2024-11-26T08:32:07Z-
dc.identifier.urihttp://hdl.handle.net/10603/602956-
dc.description.abstractThe current research work begins with the rational design of novel sulfonamide derivatives based on existing knowledge. The novel target molecules were designed using molecular hybridization techniques, which involve merging different biologically active molecules through chemical modifications within a single framework that enhances the biological properties of the resulting molecule. The different bioactive heterocyclic pharmacophores like benzisoxazole, L-proline, piperazine, piperidine, benzofuran, pyrazole, oxime, imine, and sulfonamide functionality were clubbed in a single framework to enhance the biological activity of the newly synthesized molecules. newline
dc.format.extent27 MB
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleDesign Synthesis and Biological Evaluation of Some Novel Sulfonamide Derivatives
dc.title.alternative
dc.creator.researcherKilbile, J T
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.description.noteFaculty of Basic and Applied Sciences
dc.contributor.guideSapkal, S B
dc.publisher.placeAurangabad
dc.publisher.universityMGM University, Aurangabad
dc.publisher.institutionMGMU Department of Chemistry
dc.date.registered2021
dc.date.completed2024
dc.date.awarded2024
dc.format.dimensions10 FILES
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:MGMU Department of Chemistry

Files in This Item:
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01_title page.pdfAttached File51.81 kBAdobe PDFView/Open
02_prelimanary pages.pdf1.47 MBAdobe PDFView/Open
03_table of contents.pdf123.24 kBAdobe PDFView/Open
04_abstract.pdf674.19 kBAdobe PDFView/Open
05_chapter 1.pdf394.05 kBAdobe PDFView/Open
06_chapter 2.pdf4.55 MBAdobe PDFView/Open
07_chapter 3.pdf6.36 MBAdobe PDFView/Open
08_chapter 4.pdf5.26 MBAdobe PDFView/Open
09_chapter 5.pdf4.87 MBAdobe PDFView/Open
10_chapter 6.pdf3.72 MBAdobe PDFView/Open
12_publications.pdf4.18 MBAdobe PDFView/Open
80_recommendation.pdf1.37 MBAdobe PDFView/Open


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