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Ferrocenic metal chelators : synthesis, biological and electrochemical studies

Includes bibliographical references.

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Bibliographic Details
Main Author: Muganza, Freddy Munyololo
Other Authors: Chibale, Kelly
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Muganza, Freddy Munyololo
author2 Chibale, Kelly
author_browse Chibale, Kelly
Muganza, Freddy Munyololo
author_facet Chibale, Kelly
Muganza, Freddy Munyololo
author_sort Muganza, Freddy Munyololo
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/6345
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:08.355Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
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:11427/6345 Ferrocenic metal chelators : synthesis, biological and electrochemical studies Muganza, Freddy Munyololo Chibale, Kelly Hutton, Allan T Chemistry Includes bibliographical references. Resistance of Plasmodium falciparum (P. falciparum) to well-established drugs throughout the world has necessitated urgent alternative treatment for malaria. Iron chelation therapy was considered as a possible approach since iron has been found crucial in the metabolic pathways of P. falciparum. A series of novel iron chelators were designed and synthesized based on thiosemicarbazone and/or ferrocenyl moieties. The novel compounds were characterized by NMR, infrared (IR) and mass spectroscopy as well as microanalysis and subjected to biological evaluation. All the N-substituted ferrocenic thiosemicarbazones were evaluated against a chloroquine resistant W2 strain of the malaria parasite P. falciparum and enzymes (falcipains 2 & 3) derived from the same parasite. The intermediate thiosemicarbazone thioesters were also tested against different malaria parasite including chloroquine resistant (K1) and chloroquine sensitive (307) strains as well as against the causative agent of African trypanosomiasis, Trypanosoma brucei (T. brucei). Of the intermediate thiosemicarbazone thioesters, compound 44y a bipyridyl compound was the most active against both K1 and 307 strains with ED50 values of 0.18 /lg/ml (0.625 /lM) and 0.021 /lg/ml (0.072 /lM), respectively. However, this compound 44y also showed similar toxicity to mammalian cells. A number of thiosemicarbazone thioesters displaying preferential potency against a chloroquine resistant (K1) strain were noted. For example, compounds 44a-h, 44k-m, 445, 44u-v were found to be more active against K1 than against the chloroquine sensitive (307) strain. 2014-08-13T14:27:30Z 2014-08-13T14:27:30Z 2006 Master Thesis Masters MSc http://hdl.handle.net/11427/6345 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Muganza, Freddy Munyololo
Ferrocenic metal chelators : synthesis, biological and electrochemical studies
thesis_degree_str Master's
title Ferrocenic metal chelators : synthesis, biological and electrochemical studies
title_full Ferrocenic metal chelators : synthesis, biological and electrochemical studies
title_fullStr Ferrocenic metal chelators : synthesis, biological and electrochemical studies
title_full_unstemmed Ferrocenic metal chelators : synthesis, biological and electrochemical studies
title_short Ferrocenic metal chelators : synthesis, biological and electrochemical studies
title_sort ferrocenic metal chelators synthesis biological and electrochemical studies
topic Chemistry
url http://hdl.handle.net/11427/6345
work_keys_str_mv AT muganzafreddymunyololo ferrocenicmetalchelatorssynthesisbiologicalandelectrochemicalstudies