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Antimalarials based on the arylpiperazine privileged substructure

Includes bibliographical references (leaves 118-124).

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Bibliographic Details
Main Author: Molyneaux, Carrie-Anne
Other Authors: Chibale, Kelly
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Molyneaux, Carrie-Anne
author2 Chibale, Kelly
author_browse Chibale, Kelly
Molyneaux, Carrie-Anne
author_facet Chibale, Kelly
Molyneaux, Carrie-Anne
author_sort Molyneaux, Carrie-Anne
collection Thesis
description Includes bibliographical references (leaves 118-124).
format Thesis
id oai:open.uct.ac.za:11427/6342
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:45:09.887Z
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:11427/6342 Antimalarials based on the arylpiperazine privileged substructure Molyneaux, Carrie-Anne Chibale, Kelly Chemistry Includes bibliographical references (leaves 118-124). Based on a previous study, arylpiperazines (2-chlorophenylpiperazine, 2-ethoxyphenylpiperazine and phenylpiperazine) were found to be significantly more potent against the chloroquine-resistant (K1) strain than against the chloroquine-sensitive(DIO) strain. In other studies, 8-hydroxy-2-(di-n-propylamino)tetralin (8-0H-DPAT) has been identified as a potential antimalarial agent for the inhibition of the 5-hydroxytryptamine type 1A receptor in Plasmodium falciparum. A number of arylpiperazines are also known to target this receptor in other systems. Coupled with the potential role of arylpiperazines as replacements for the antimalarial 8-OH-OPA T, these results prompted a further investigation into the antiplasmodial properties of a broader range of simple un substituted and substituted arylpiperazines against a broader range of chloroquine-sensitive and chloroquine-resistant strains of PlasmodiumJalciparum. 2014-08-13T14:27:27Z 2014-08-13T14:27:27Z 2005 Master Thesis Masters MSc http://hdl.handle.net/11427/6342 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Molyneaux, Carrie-Anne
Antimalarials based on the arylpiperazine privileged substructure
thesis_degree_str Master's
title Antimalarials based on the arylpiperazine privileged substructure
title_full Antimalarials based on the arylpiperazine privileged substructure
title_fullStr Antimalarials based on the arylpiperazine privileged substructure
title_full_unstemmed Antimalarials based on the arylpiperazine privileged substructure
title_short Antimalarials based on the arylpiperazine privileged substructure
title_sort antimalarials based on the arylpiperazine privileged substructure
topic Chemistry
url http://hdl.handle.net/11427/6342
work_keys_str_mv AT molyneauxcarrieanne antimalarialsbasedonthearylpiperazineprivilegedsubstructure