Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/3413
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dc.contributor.authorShah, Ujala N.-
dc.date.accessioned2012-06-20T07:29:33Z-
dc.date.available2012-06-20T07:29:33Z-
dc.date.issued2012-
dc.identifier.urihttp://10.1.7.181:1900/jspui/123456789/3413-
dc.description.abstractOxidation is a chain of chemical reactions generating free radicals by transferring electrons from a substrate to an oxidizing agent. Oxygen is a highly reactive molecule that damages living organisms by producing free radicals like reactive oxygen species (ROS) and reactive nitrogen species (RNS). An excess of these free radicals leads to diseases like aging, diabetes, cancer, atherosclerosis, Parkinson’s disease, Alzheimer, inflammation, etc. An antioxidant is a molecule capable of inhibiting the oxidation of other molecules by maintaining the balance between the processes generating and utilizing the free radicals. Literature survey revealed that more than 1300 coumarins have been identified from natural sources and they exhibited good antioxidant activity. Also natural antioxidants like curcumin and resveratrol contain stilbene moiety giving antioxidant activity. Extensive survey also revealed that 2-amino benzothiazole moiety shows better antioxidant activity. Hence two series of compounds were designed and synthesized as potential antioxidants. Structure elucidation of the synthesized compounds was done by spectral analysis. The antioxidant activity of the synthesized compounds was determined by Nitric oxide, Superoxide, DPPH and Hydrogen peroxide radical scavenging activity using ascorbic acid as the reference standard.en_US
dc.publisherInstitute of Pharmacy, Nirma University, A'baden_US
dc.relation.ispartofseriesPDR00194en_US
dc.subjectDissertation Reporten_US
dc.subjectMedicinal Chemistryen_US
dc.subject10MPHen_US
dc.subject10MPH409en_US
dc.subjectPDR00194en_US
dc.titleSynthesis of Chalcone Derivatives of Coumarin and 2-amino Bezothiazole as Antioxidantsen_US
dc.typeDissertationen_US
Appears in Collections:M.Pharm. Research Reports, Department of Medicinal Chemistry

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