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Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria

Includes abstract.

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Bibliographic Details
Main Author: Krein, Ze-ev
Other Authors: Chibale, Kelly
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Krein, Ze-ev
author2 Chibale, Kelly
author_browse Chibale, Kelly
Krein, Ze-ev
author_facet Chibale, Kelly
Krein, Ze-ev
author_sort Krein, Ze-ev
collection Thesis
description Includes abstract.
format Thesis
id oai:open.uct.ac.za:11427/6320
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:17.361Z
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:11427/6320 Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria Krein, Ze-ev Chibale, Kelly Chemistry Includes abstract. Includes bibliographical references (leaves 151-155). Chloroquine (CQ) was previously identified as a potential anti-HIV agent and reported to inhibit the production of infectious viral particles at concentrations which are non toxic to human cultured cells. It is speculated that this activity is associated with the decreased production of the heavily glycosylated epitope 2G 12 which is found on the gp120 glycoprotein surface. The hypothesized mechanism involves CQ acting on a range of cellular targets. This work identifies CQ as a lead compound for the discovery of potentially inexpensive drugs and its ability to target cellular enzymes as opposed to viral enzymes may endow the compound with the capacity to oppose resistance. This previous work was the basis of this project and prompted a further investigation into whether the quinoline scaffold is the principal cause of CQ's activity and whether other rationally designed compounds which contain this scaffold would be able to maintain similar or even greater anti-HIV activity. In an attempt to achieve greater activity, the dual drug approach was utilized. 2014-08-13T14:26:43Z 2014-08-13T14:26:43Z 2007 Master Thesis Masters MSc http://hdl.handle.net/11427/6320 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Krein, Ze-ev
Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria
thesis_degree_str Master's
title Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria
title_full Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria
title_fullStr Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria
title_full_unstemmed Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria
title_short Utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti-infectives against HIV and malaria
title_sort utilisation of efficient reactions to combine moeities exhibiting biological activity to produce novel anti infectives against hiv and malaria
topic Chemistry
url http://hdl.handle.net/11427/6320
work_keys_str_mv AT kreinzeev utilisationofefficientreactionstocombinemoeitiesexhibitingbiologicalactivitytoproducenovelantiinfectivesagainsthivandmalaria