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DC Field | Value | Language |
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dc.contributor.advisor | Capretta, Alfredo | - |
dc.contributor.author | Johnson, Emma | - |
dc.date.accessioned | 2019-12-02T20:43:13Z | - |
dc.date.available | 2019-12-02T20:43:13Z | - |
dc.date.issued | 2019 | - |
dc.identifier.uri | http://hdl.handle.net/11375/25080 | - |
dc.description.abstract | Abstract The current rise in antibiotic resistance and lack of discovery of new antibiotics in recent years has caused an antibiotic crisis. A strategy for overcoming this crisis is to relook at previously discarded antibiotics and with medicinal chemistry, use their structure as a scaffold for the development of a new antibiotic. Edeines are a group of antimicrobials discovered by Kurylo-Borowska in 1959 that were discarded for toxicity and this work aimed to use edeine for the structural basis in the development of a novel antibiotic. Using both solution phase and solid phase peptide synthesis ꞵ-tyrosine-L-isoseryl-diaminopropionic acid was synthesized to develop a synthetic strategy for the peptide synthesis of Edeine A. Solid phase peptide synthesis techniques were used to synthesize two simplified edeine analogues which demonstrated that the amino acid 2,6-diamino-7-hydroxylazaleic acid was necessary for antimicrobial activity. A synthetic strategy for the synthesis of 2,6-diamino-7-hydroxylazaleic acid (DAHAA) using ring closing metathesis and aminohydroxylation was developed and starting materials were synthesized. Using solid phase synthesis and the strategy for synthesizing DAHAA, a library of edeine analogues could be made using parallel synthesis and assayed for specific antimicrobial activity. This could lead to the development of a lead antibiotic which used edeine as a structural scaffold, therefore a novel antibiotic could be clinically used without large scale resistance present in the environment like the currently used antibiotics. | en_US |
dc.language.iso | en | en_US |
dc.subject | edeine | en_US |
dc.subject | organic chemistry | en_US |
dc.subject | synthesis | en_US |
dc.subject | antibiotic | en_US |
dc.title | SYNTHESIS OF EDEINE DERIVATIVES AS AN APPROACH TO TACKLE THE ANTIBIOTIC CRISIS | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | Chemistry and Chemical Biology | en_US |
dc.description.degreetype | Thesis | en_US |
dc.description.degree | Master of Science (MSc) | en_US |
Appears in Collections: | Open Access Dissertations and Theses |
Files in This Item:
File | Description | Size | Format | |
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Johnson_Emma_S_2019November_MSc.pdf | 2.03 MB | Adobe PDF | View/Open |
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