Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7521
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dc.contributor.advisorR, Karvembu-
dc.contributor.authorP, HARINI-
dc.date.accessioned2022-12-19T09:15:32Z-
dc.date.available2022-12-19T09:15:32Z-
dc.date.issued2022-12-
dc.identifier.citation48en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7521-
dc.description.abstractThioureas/Thiosemicarbazones are small molecules studied extensively in drug design due to their wide range of biological activities. Selenium is shown to be involved in various metabolic processes in the human body, and low Se levels are observed in the plasma regions of AD patients. Based on this fact, we have synthesized Thiosemicarbazone ligands and Acyl-selenourea ligands as inhibitors of Ađť›˝ aggregation. We hypothesize that the seleno-derivatives will exhibit higher activity than their thio-derivatives. We have also conducted in-silico studies to gain a broader view of the interactions which take place. The docking studies show that there is no considerable difference in the binding abilities and the interactions of the synthesized Acyl-selenourea ligands compared to their corresponding acyl-thiourea counterparts.en_US
dc.language.isoenen_US
dc.subjectSynthesisen_US
dc.subjectAlzheimer'sen_US
dc.titleSynthesis and characterization of Thio/seleno- urea/semicarbazone derivatives for anti-alzheimer studiesen_US
dc.typeThesisen_US
dc.description.embargono embargoen_US
dc.type.degreeBS-MSen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.contributor.registration20171074en_US
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