Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/253229
Title: Synthesis characterization and pharmacological studies of 2 5 disubstituted 1 3 4 oxadiazole derivatives
Researcher: Kavitha S
Guide(s): Kannan K
Keywords: Disubstituted
Oxadiazole Derivatives
Pharmacological
Physical Sciences,Chemistry,Chemistry Applied
Synthesis
University: Anna University
Completed Date: 2018
Abstract: Heterocyclic compounds have one or more heteroatom in the nucleus. They are two thirds of organic compounds and accounting for recent publications. Heterocyclic compounds are present in the natural products in the form of alkaloids, flavonoids and bio molecules etc., They are used predominately in pharmaceutics, polymer, dyestuff and agrochemicals. About 90% of the synthesized heterocycles are used as drugs and boundary between biology and chemistry deals new discovery and applications crossed by heterocyclic compounds. Heterocylces have shown considerable biological applications such as anticancer, antimicrobial, antibiotic, antihistaminic and anticonvulsant activities. Among the heterocyclic compounds, 1,3,4-oxadiazole derivatives are most important class of compounds for new drug development. 1,3,4-oxadiazole have been known for about 80 years and their biological activities strengthen only in the last decade. 1,3,4-oxadiazole showed a variety of chemical and pharmacological applications. Particularly, 2,5-disubstituted oxadiazole derivatives were found to possess antitumor, antimicrobial, antioxidant, anti-HIV, anti-inflammatory, antidiabetic and anticonvulsant activities. newline
Pagination: xxvii, 206p.
URI: http://hdl.handle.net/10603/253229
Appears in Departments:Faculty of Science and Humanities

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02_certificates.pdf712.15 kBAdobe PDFView/Open
03_abstract.pdf45.24 kBAdobe PDFView/Open
04_acknowledgement.pdf38.74 kBAdobe PDFView/Open
05_table of contents.pdf80.75 kBAdobe PDFView/Open
06_list_of_symbols and abbreviations.pdf38.61 kBAdobe PDFView/Open
07_chapter1.pdf372.46 kBAdobe PDFView/Open
08_chapter2.pdf315.61 kBAdobe PDFView/Open
09_chapter3.pdf2.54 MBAdobe PDFView/Open
10_chapter4.pdf2.5 MBAdobe PDFView/Open
11_conclusion.pdf72.75 kBAdobe PDFView/Open
12_references.pdf163.16 kBAdobe PDFView/Open
13_list of publications.pdf46.7 kBAdobe PDFView/Open
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