Synthesis of Mercapto-(Oxadiazole/Triazole) Carboxylic acid Compounds and their derivatives of Biological interest

dc.contributor.guideChapleen_US
dc.coverage.spatialPharmaceutical Sciencesen_US
dc.creator.researcherRao , Manikrao Anil Madhaven_US
dc.date.accessioned2014-05-20T09:30:54Z
dc.date.available2014-05-20T09:30:54Z
dc.date.awardedn.den_US
dc.date.completed2012en_US
dc.date.issued2014-05-20
dc.date.registeredn.den_US
dc.description.abstractThe research work reported in this dissertation consists of synthesis of newlinepharmacologically active compounds and the modification of their structure according to the result of pharmacological screening. All these synthesized compounds were characterized by satisfactory spectroscopic data. These compounds belongs to the classes of 1,3,4-oxadiazole-2(3H)-thione and 1,2,4- newlinetriazole-3(4H)-thione. All these compounds were screened for different biological newlineactivities including bactericidal, fungicidal, analgesic, anti-inflammatory, newlineanxiolytic and anticonvulsant activities and as expected most of them had exhibited moderate to good activities. Scheme I and Scheme II: Here focus was made mainly on the synthesis of 1,2,4- triazoline-3-thione as the essential pharmacophore and investigation of its combination with various N-substituted carboxamidoalkylthio moiety through sulfur atom and converting them to corresponding sulfoxides and sulfones selectively by solid state green oxidation method using Oxone®. newlineAnalgesic and Anti-inflammatory activity: All the synthesized triazole derivatives (11a-k) were found to exhibit potent anti-inflammatory activity but lower analgesic activity as compared to (6a-k). It might be due to increase in distance between aromatic nucleus and side chain nitrogen by one carbon atom as to exhibit analgesic activity, molecule should contain one aromatic nucleus newlineattached to quaternary carbon then ethylene bridge and tertiary nitrogen. N-Phenyl newlinecarboxamidoethylthio-(4H)-1,2,4-triazole (11a) had exhibited equipotent antiinflammatory newlineand analgesic activity as compared to standard drug. Anxiolytic Activity: All the compounds (6a-k and 11a-k) were tested for their Anxiolytic activity. There was increase in percent time spent and number of entries newlinein the open arm but the Anxiolytic activity was found to be very less as compared newlineto diazepam.en_US
dc.description.noteReferences p. 242-243en_US
dc.format.accompanyingmaterialNoneen_US
dc.format.dimensions-en_US
dc.format.extentP. 249en_US
dc.identifier.urihttp://hdl.handle.net/10603/18477
dc.languageEnglishen_US
dc.publisher.institutionFaculty of Pharmaceutical Sciencesen_US
dc.publisher.placeKukatpallyen_US
dc.publisher.universityJawaharlal Nehru Technological University, Hyderabaden_US
dc.relation-en_US
dc.rightsuniversityen_US
dc.source.inflibnetINFLIBNETen_US
dc.subject.keywordBiologicalen_US
dc.subject.keywordCarboxylicen_US
dc.subject.keywordMercaptoen_US
dc.subject.keywordOxadiazoleen_US
dc.subject.keywordTriazoleen_US
dc.titleSynthesis of Mercapto-(Oxadiazole/Triazole) Carboxylic acid Compounds and their derivatives of Biological interesten_US
dc.title.alternative-en_US
dc.type.degreePh.D.en_US

Files

Original bundle

Now showing 1 - 5 of 18
Loading...
Thumbnail Image
Name:
01_title.pdf
Size:
156.72 KB
Format:
Adobe Portable Document Format
Description:
Attached File
Loading...
Thumbnail Image
Name:
02_dedication.pdf
Size:
46.19 KB
Format:
Adobe Portable Document Format
Loading...
Thumbnail Image
Name:
03_certificate.pdf
Size:
129.61 KB
Format:
Adobe Portable Document Format
Loading...
Thumbnail Image
Name:
04_declaration.pdf
Size:
106.71 KB
Format:
Adobe Portable Document Format
Loading...
Thumbnail Image
Name:
05_acknowledgment.pdf
Size:
92.02 KB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.79 KB
Format:
Plain Text
Description: