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Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum

Includes bibliographical references.

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Bibliographic Details
Main Author: October, Natasha
Other Authors: Chibale, Kelly
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author October, Natasha
author2 Chibale, Kelly
author_browse Chibale, Kelly
October, Natasha
author_facet Chibale, Kelly
October, Natasha
author_sort October, Natasha
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/6353
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:51.499Z
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:11427/6353 Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum October, Natasha Chibale, Kelly Chemistry Includes bibliographical references. For many years malaria has been a major cause of human suffering. Despite significant advances in understanding the disease and the parasite, malaria still remains one of the leading causes of morbidity and mortality, particularly in the tropics. Approximately 500 million people are afflicted and almost 3 million people die from the disease annually. Of the four causative species, Plasmodium falciparum is the most lethal. Recent trends indicate rapid emergence of drug-resistent and more virulent strains of the parasite to further intensify the problem. The choice of therapies currently available for the treatment of malaria is highly limited, and several of these may eventually be lost or compromised due to drug resistance. New antimalarial drugs with proven clinical efficacy against current drug-resistance cases of malaria including Plasmodium falciparum infections is critical to combact the disease and cope with the problem of further development or resistance. 2014-08-13T14:28:56Z 2014-08-13T14:28:56Z 2006 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/6353 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
October, Natasha
Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum
thesis_degree_str Doctoral
title Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum
title_full Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum
title_fullStr Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum
title_full_unstemmed Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum
title_short Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum
title_sort design synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite plasmodium falciparum
topic Chemistry
url http://hdl.handle.net/11427/6353
work_keys_str_mv AT octobernatasha designsynthesisandevaluationofpotentialdualdrugstargetingthehaemoglobindegradationpathwayinthemalariaparasiteplasmodiumfalciparum