Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/150898
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dc.date.accessioned2017-05-23T10:36:07Z-
dc.date.available2017-05-23T10:36:07Z-
dc.identifier.urihttp://hdl.handle.net/10603/150898-
dc.description.abstractOut of all the compounds tested, compound nos. 3h (2-(3-nitro-phenyl)-1,3-bis(1- newlinenaphthylmethyl)-imidazolidine) and 3n (2-(2-chloro-phenyl)-1,3-bis(1-naphthylmethyl)- newlineimidazolidine) showed anti-inflammatory activity (53.43 and 53.02%) comparable with indomethacin (61.45%). These two compounds also exhibited much reduced ulcerogenic activity as compared to standard drug. These compounds showed excellent analgesic action newlinealso when compared with aspirin. newlineIt was encouraging to observe that these compounds did not show any toxic symptoms or mortality given at dose of 1000 mg/kg indicating its wide margin of safety. newlineAll the fourteen compounds were also tested for antimicrobial activity, Compound 3f (2-(4- newlinechloro-phenyl)-1,3-bis(1-naphthylmethyl)-imidazolidine) showed moderate antibacterial and antifungal results. Compound 3f exhibited highest antifungal activity against fungal strain A. newlineniger (70.30%) compared to standard drug fluconazole. newline
dc.format.extent
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleSYNTHESIS CHARACTERIZATION AND BIOLOGICAL EVALUATION OF SOME AZOLES AND TETRAHYDROIMIDAZOLE DERIVATIVES
dc.title.alternative
dc.creator.researcherUmesh Kumar
dc.subject.keywordAzoles, PhenyL, Anti-inflammatory, Ibuprofen, Ulcerogenic activity, Naphthalene
dc.description.note
dc.contributor.guideChawla, Gita , Bawa, Sandhya
dc.publisher.placeDelhi
dc.publisher.universityJamia Hamdard University
dc.publisher.institutionDepartment of Pharmaceutical Chemistry
dc.date.registered2010
dc.date.completed2013
dc.date.awarded2014
dc.format.dimensions
dc.format.accompanyingmaterialDVD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Pharmaceutical Chemistry

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(10) chapter 2 new work.pdfAttached File23.75 kBAdobe PDFView/Open
(11) chapter 2 drug experimental.pdf303.06 kBAdobe PDFView/Open
(12) biological studies, chapter 2.pdf35.32 kBAdobe PDFView/Open
(13) results and discussion, chapter 2.pdf609.49 kBAdobe PDFView/Open
(14) summary chapter 2.pdf25.44 kBAdobe PDFView/Open
(15) introduction, tetrahydroimidazole ch.3.pdf52.99 kBAdobe PDFView/Open
(17) new work, chapter 3.pdf23.53 kBAdobe PDFView/Open
(18) experimental, chapter 3.pdf156.29 kBAdobe PDFView/Open
(19) biological studies, chapter 3.pdf64.47 kBAdobe PDFView/Open
(1) front page thesis.pdf34.37 kBAdobe PDFView/Open
(1) introduction chapter 1.pdf48.81 kBAdobe PDFView/Open
(20) results and discussion, chapter 3.pdf323.51 kBAdobe PDFView/Open
(21) summary chapter 3.pdf25.82 kBAdobe PDFView/Open
(22) bibliography.pdf132.78 kBAdobe PDFView/Open
(23) publication.pdf22.28 kBAdobe PDFView/Open
(2) chapter 1, litarature.pdf187.68 kBAdobe PDFView/Open
(3) certificate copyright.pdf13.49 kBAdobe PDFView/Open
(3) new work, chapter 1.pdf24.57 kBAdobe PDFView/Open
(4) experimental, chapter1.pdf173.85 kBAdobe PDFView/Open
(5) biological studies, chapter 1.pdf60.35 kBAdobe PDFView/Open
(6) result and discussion, chapter 1.pdf302.77 kBAdobe PDFView/Open
(7) contents thesis.pdf5.34 kBAdobe PDFView/Open
(7) summary chapter 1.pdf24.85 kBAdobe PDFView/Open
(8) introction drugs chapter2.pdf44.07 kBAdobe PDFView/Open
(8) preface.pdf28.44 kBAdobe PDFView/Open
(9) chapter 2 literature.pdf142.5 kBAdobe PDFView/Open


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