Design and synthesis of beta-strand conformationally constrained calpain inhibitors for cataract treatment via metathesis ring closure
| dc.contributor.author | Klanchantra, Mutita | en |
| dc.date.accessioned | 2008-09-22T00:55:29Z | |
| dc.date.available | 2008-09-22T00:55:29Z | |
| dc.date.issued | 2006 | en |
| dc.description.abstract | This thesis summarises the progress made in the design and synthesis of conformationally constrained β-strand peptidomimetic compounds using ring closing metathesis methodology under microwave irridation conditions. The best macrocycle were elaborated into an inhibitor for a specific protease target. Calpain was used as an example of protease targeting cataract disease. Chapter One introduces proteases in general centring on the general context of protease inhibitor design. The significant of the β-strand 'bioactive' conformation is discussed in details in particular the exploitation of conformationally constrained to potential lock the 'bioactive' conformation. Chapter Two illustrates in silico methods used to design a series of β-strand macrocycle 2.1-2.7. The analysis of these is performed using molecular modelling software Schrodinger suite (2005). A brief discussion of ring closing metathesis methodology is also included. Chapter Three describes the synthesis of the precursor required for RCM reactions (tripeptides dienes). Various types of allylated amino acid side chains were synthesised. The tripeptides were obtained using standard peptide coupling methodology utilising reagents such as HATU, EDC and HOAT. Chapter Four describes the application of ring closing metathesis for the synthesis of β-strand macrocycles. The development of a new reaction conditions to optimise the ring closing metathesis reaction is discussed. In particular the effect of the use of a Lewis acid (chlorodicyclohexylborane) additive in RCM reactions is investigated. Chapter Five discusses the mechanism of cataract formation, cataract treatment and the potential development of calpain inhibitors. One of the macrocycles synthesised in chapter 4 is elaborated into a calpain inhibitor. The in-vitro assay result of this is presented and this compound is currently undergoing in vivo evaluation. | en |
| dc.identifier.uri | http://hdl.handle.net/10092/1609 | |
| dc.identifier.uri | http://dx.doi.org/10.26021/8857 | |
| dc.language.iso | en | |
| dc.publisher | University of Canterbury. Chemistry | en |
| dc.relation.isreferencedby | NZCU | en |
| dc.rights | Copyright Mutita Klanchantra | en |
| dc.rights.uri | https://canterbury.libguides.com/rights/theses | en |
| dc.subject | RCM | en |
| dc.subject | Cataract | en |
| dc.subject | Calpain | en |
| dc.title | Design and synthesis of beta-strand conformationally constrained calpain inhibitors for cataract treatment via metathesis ring closure | 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 | 1032490 | en |
Files
Original bundle
1 - 1 of 1