Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol

Includes bibliographical references.

Saved in:
Bibliographic Details
Main Author: Watermeyer, Nicholas D
Other Authors: Gammon, David W
Format: Thesis
Language:English
Published: Department of Chemistry 2015
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613244720414720
access_status_str Open Access
author Watermeyer, Nicholas D
author2 Gammon, David W
author_browse Gammon, David W
Watermeyer, Nicholas D
author_facet Gammon, David W
Watermeyer, Nicholas D
author_sort Watermeyer, Nicholas D
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/12674
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:33:04.194Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2015
publishDateRange 2015
publishDateSort 2015
publisher Department of Chemistry
publisherStr Department of Chemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/12674 Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol Watermeyer, Nicholas D Gammon, David W Steenkamp, Daniel Chemistry Includes bibliographical references. This thesis describes the synthesis of several naphthoquinone- and carbazole-1,4-quinone-derived conjugates of a mycothiol-like scaffold designed to act as redox cycling subversive substrates of the enzyme, Mtr, or potentially inhibit other mycothiol-dependent or biosynthetic enzymes, in order to develop novel antitubercular lead compounds. The expression and purification of Mtr, as well as the attempts made towards the cloning and expression of active Mycobacterial glyoxalase I, in order to generate enzymes on which to assay the synthesised molecules, are also described. Linking of the quinone functionalities to the mycothiol-like scaffold, phenyl-1-thio-Dglucosamine, was envisaged to facilitate delivery of this class of redox active molecules to the active-site of the mycothiol enzymes. Successful completion of the synthesis of naphthoquinone conjugates of this scaffold was not achieved due to a persistent side reaction that took place during an N-tert-butoxycarbonyl deprotection step. However, this unexpected result led to the discovery of a new synthetic route to benzo[g]indoles and benzo[h]quinolines. This route differs from traditional quinoline and indole syntheses in that the aromatic C-N bond is generated by a condensation reaction between a quinone carbonyl and an aliphatic amine, rather than via the traditional condensation of an aromatic amine with a distal carbonyl group. 2015-04-02T14:18:19Z 2015-04-02T14:18:19Z 2012 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/12674 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Watermeyer, Nicholas D
Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol
thesis_degree_str Doctoral
title Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol
title_full Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol
title_fullStr Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol
title_full_unstemmed Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol
title_short Design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol
title_sort design and synthesis of potential inhibitors of enzymes involved in the biosynthesis and utilisation of mycothiol
topic Chemistry
url http://hdl.handle.net/11427/12674
work_keys_str_mv AT watermeyernicholasd designandsynthesisofpotentialinhibitorsofenzymesinvolvedinthebiosynthesisandutilisationofmycothiol