Molecular Modelling for Enzyme Inhibition: A Search for a New Treatment for Cataract and New Antimicrobials and Herbicides

dc.contributor.authorStuart, Blair Gibb
dc.date.accessioned2010-09-29T01:17:53Z
dc.date.available2011-09-28T11:20:06Z
dc.date.issued2010en
dc.description.abstractThere have been several reports that cataract development results from unregulated Ca2+ mediated degradation of lens crystallins. The calpain isoform m-calpain, a cysteine protease, is known to be a major player in cataract formation in rodent lenses and recent evidence indicates that over-activation by Ca2+ causes cataractogenesis in other mammals. Molecular modelling studies of seventeen analogues of compound SJA6017 (our lead compound) in a calpain model are compared to measured IC50 values against ovine calpain. The studies validated the potential of the ‘model’, method and defined activity criteria that could be used as a tool to select molecules to synthesize as potential calpain inhibitors. Using this screening methodology and two virtual libraries of potential inhibitory molecules led to the synthesis of several inhibitors including macrocyclic 811. In vitro sheep eye lens culture experiments showed that macrocycle 811 possessed the characteristics to slow cataractogenesis.en
dc.identifier.urihttp://hdl.handle.net/10092/4551
dc.identifier.urihttp://dx.doi.org/10.26021/5721
dc.language.isoen
dc.publisherUniversity of Canterbury. Chemistryen
dc.relation.isreferencedbyNZCUen
dc.rightsCopyright Blair Gibb Stuarten
dc.rights.urihttps://canterbury.libguides.com/rights/thesesen
dc.subjectCataracten
dc.subjectmolecular modelingen
dc.subjectcalpainen
dc.titleMolecular Modelling for Enzyme Inhibition: A Search for a New Treatment for Cataract and New Antimicrobials and Herbicidesen
dc.typeTheses / Dissertations
thesis.degree.disciplineBiochemistryen
thesis.degree.grantorUniversity of Canterburyen
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophyen
uc.bibnumber1480449
uc.collegeFaculty of Scienceen
uc.embargo12en
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