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dc.contributor.advisorRozas, Isabel
dc.contributor.authorCorcoran, Jonathan
dc.date.accessioned2019-04-29T15:06:56Z
dc.date.available2019-04-29T15:06:56Z
dc.date.issued2007
dc.identifier.citationJonathan Corcoran, 'Synthesis, biological evaluation and subsequent SAR of four novel families of alkyliphatic twin drugs', [thesis], Trinity College (Dublin, Ireland). School of Chemistry, 2007, pp 226
dc.identifier.otherTHESIS 8398
dc.identifier.urihttp://hdl.handle.net/2262/86271
dc.description.abstractThe I2-IBS is a well known binding site widely distributed in the body of both animals and humans. It is suspected that they are an allosteric binding site of MAO-B. They have also been linked to several conditions such as Alzheimer’s and neuro protection. Their main physiological function appears to be the ability of I2-IBS ligands to attenuate the tolerance to opiod drugs. This link between the I2-IBS and the u-opioid receptor system has made I2-IBS binding sites of pharmalogical importance.
dc.format1 volume
dc.language.isoen
dc.publisherTrinity College (Dublin, Ireland). School of Chemistry
dc.relation.isversionofhttp://stella.catalogue.tcd.ie/iii/encore/record/C__Rb13330987
dc.subjectChemistry, Ph.D.
dc.subjectPh.D. Trinity College Dublin
dc.titleSynthesis, biological evaluation and subsequent SAR of four novel families of alkyliphatic twin drugs
dc.typethesis
dc.type.supercollectionthesis_dissertations
dc.type.supercollectionrefereed_publications
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (Ph.D.)
dc.rights.ecaccessrightsopenAccess
dc.format.extentpaginationpp 226
dc.description.noteTARA (Trinity's Access to Research Archive) has a robust takedown policy. Please contact us if you have any concerns: rssadmin@tcd.ie


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