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Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group

Includes bibliographical references.

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Bibliographic Details
Main Author: Kambafwile, Henry Kunda
Other Authors: Chibale, Kelly
Format: Thesis
Language:English
Published: Department of Chemistry 2015
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access_status_str Open Access
author Kambafwile, Henry Kunda
author2 Chibale, Kelly
author_browse Chibale, Kelly
Kambafwile, Henry Kunda
author_facet Chibale, Kelly
Kambafwile, Henry Kunda
author_sort Kambafwile, Henry Kunda
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/11736
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:11427/11736 Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group Kambafwile, Henry Kunda Chibale, Kelly Chemistry Includes bibliographical references. Angiotensin-converting enzyme (ACE) and P. falciparum A M1 (PfA-M1) are both zinc metalloproteases implicated in hypertension and malaria, respectively. Hypertension affects approximately 26 % of the world’s population while each year over 300 million cases of malaria occur worldwide resulting in between 1.5 and 2.7 million deaths annually. Hypertension treatment with current ACE inhibitors is marred by unpleasant side effects, such as cough and angioedema. In malaria, the parasites continuously develop resistance to anti-malarial drugs where the disease is endemic. There is therefore a need for continuous research into the application of new techniques as well as the design of new small molecule chemical entities as probes or chemotherapeutic agents. 2015-01-07T13:45:39Z 2015-01-07T13:45:39Z 2012 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/11736 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Kambafwile, Henry Kunda
Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group
thesis_degree_str Doctoral
title Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group
title_full Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group
title_fullStr Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group
title_full_unstemmed Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group
title_short Synthesis of activity-based protein profiling probes for malaria and hypertension disease models & potential novel ACE inhibitors with an attenuated zinc binding group
title_sort synthesis of activity based protein profiling probes for malaria and hypertension disease models potential novel ace inhibitors with an attenuated zinc binding group
topic Chemistry
url http://hdl.handle.net/11427/11736
work_keys_str_mv AT kambafwilehenrykunda synthesisofactivitybasedproteinprofilingprobesformalariaandhypertensiondiseasemodelspotentialnovelaceinhibitorswithanattenuatedzincbindinggroup