Synthesis and evaluation of CA clan cysteine inhibitors
dc.contributor.author | Millar, Tarek Lawson | en |
dc.date.accessioned | 2008-12-08T20:20:55Z | |
dc.date.available | 2008-12-08T20:20:55Z | |
dc.date.issued | 2008 | en |
dc.description.abstract | This investigation involved the synthesis of potential CA clan cysteine inhibitors of m-calpain and cathepsin B. Inhibitors 2.1.3a-j were based on the SJA-6017 construct containing the N-(4-fluorobenzenesulfonyl) moiety at the P₃ address region. The inhibitor 2.1.3k was based on CAT-0059 a novel dipeptide dialdehyde inhibitor containing the 5-formyl pyrrole moiety at the P₃ address region. Chapter 1 introduces proteases in particular m-calpain and cathepsin B implicated in human pathologies cataract and tumour metastasis respectably. Structure, disease processes and known inhibitors for m-calpain and cathepsin B are presented and described. The chapter also describes drug design and rational including the requirement of the β-strand conformation for enzyme substrate binding. Chapter 2 details the synthesis of m-calpain and cathepsin B inhibitors, N-(4-fluorobenzenesulfonyl) peptide aldehyde 2.1.3a-j and the dipeptide dialdehyde 2.1.3k. The synthesis involved the preparation of the N-(4-fluorobenzenesulfonyl) α-amino acids 2.1.8a-f, the N-(4-fluorobenzenesulfonyl) peptide esters of 2.1.10a-g, the peptide alcohols 2.1.11a-k and the peptide aldehydes 2.1.3a-k. Specific coupling reagents for amide bond formation are also discussed. The oxidation of the alcohols 2.1.11a-k with sulfur trioxide and pyridine complex are also addressed. The results from molecular modelling and enzymatic assays of the inhibitors 2.1.3a-k with m-calpain and cathepsin B are presented and discussed. | en |
dc.identifier.uri | http://hdl.handle.net/10092/1911 | |
dc.identifier.uri | http://dx.doi.org/10.26021/7603 | |
dc.language.iso | en | |
dc.publisher | University of Canterbury. Chemistry | en |
dc.relation.isreferencedby | NZCU | en |
dc.rights | Copyright Tarek Lawson Millar | en |
dc.rights.uri | https://canterbury.libguides.com/rights/theses | en |
dc.title | Synthesis and evaluation of CA clan cysteine inhibitors | en |
dc.type | Theses / Dissertations | |
thesis.degree.discipline | Chemistry | en |
thesis.degree.grantor | University of Canterbury | en |
thesis.degree.level | Masters | en |
thesis.degree.name | Master of Science | en |
uc.bibnumber | 1112800 | en |
uc.college | Faculty of Science | en |
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