Purine and Pyrimidine Pathways as Antimalarial Targets

Malaria continues to plague the endemic regions of sub-Saharan Africa and Southeast Asia. With the current development of artemisinin resistance and a risk of failure of the current first line therapies, there is a growing need for novel antimalarials. Purine and pyrimidine metabolism in Plasmodium...

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Autores principales: Minnow, Yacoba V. T., Schramm, Vern L.
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Lenguaje:inglés
Publicado: IntechOpen 2022
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Acceso en línea:https://www.intechopen.com/chapters/83000
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author Minnow, Yacoba V. T.
Schramm, Vern L.
author_browse Minnow, Yacoba V. T.
Schramm, Vern L.
author_facet Minnow, Yacoba V. T.
Schramm, Vern L.
author_sort Minnow, Yacoba V. T.
building IntechOpen
collection Acceso abierto
description Malaria continues to plague the endemic regions of sub-Saharan Africa and Southeast Asia. With the current development of artemisinin resistance and a risk of failure of the current first line therapies, there is a growing need for novel antimalarials. Purine and pyrimidine metabolism in Plasmodium is distinctly different from the human host, making these pathways valid targets for the development of novel antimalarials. Targeting key enzymes in these pathways with transition state analogs has provided high affinity inhibitors. Transition state mimicry can also provide selectivity for the parasite enzymes over the homologous enzymes of the human host. Resistance of Plasmodium parasites to current antimalarials will be compared to resistance development induced by transition state analogs inhibitors, a feature that may contribute to decreased resistance development. Tight binding and specificity of transition state analog inhibitors provide important features for novel antimalaria therapy with low toxicity and prevention of antibiotic resistance.
doi_str_mv 10.5772/intechopen.106468
first_indexed 2026-10-15T21:39:54Z
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spelling intech-830002022-08-16 Purine and Pyrimidine Pathways as Antimalarial Targets Yacoba V. T. Minnow Vern L. Schramm Health Sciences Malaria continues to plague the endemic regions of sub-Saharan Africa and Southeast Asia. With the current development of artemisinin resistance and a risk of failure of the current first line therapies, there is a growing need for novel antimalarials. Purine and pyrimidine metabolism in Plasmodium is distinctly different from the human host, making these pathways valid targets for the development of novel antimalarials. Targeting key enzymes in these pathways with transition state analogs has provided high affinity inhibitors. Transition state mimicry can also provide selectivity for the parasite enzymes over the homologous enzymes of the human host. Resistance of Plasmodium parasites to current antimalarials will be compared to resistance development induced by transition state analogs inhibitors, a feature that may contribute to decreased resistance development. Tight binding and specificity of transition state analog inhibitors provide important features for novel antimalaria therapy with low toxicity and prevention of antibiotic resistance. IntechOpen 2022-08-16 Chapter, Part Of Book https://www.intechopen.com/chapters/83000 doi:10.5772/intechopen.106468 en ISBN:978-1-80356-791-4 https://creativecommons.org/licenses/by/3.0/ https://www.intechopen.com/books/11576 ; Malaria - Recent Advances and New Perspectives
spellingShingle Health Sciences
Minnow, Yacoba V. T.
Schramm, Vern L.
Purine and Pyrimidine Pathways as Antimalarial Targets
title Purine and Pyrimidine Pathways as Antimalarial Targets
title_full Purine and Pyrimidine Pathways as Antimalarial Targets
title_fullStr Purine and Pyrimidine Pathways as Antimalarial Targets
title_full_unstemmed Purine and Pyrimidine Pathways as Antimalarial Targets
title_short Purine and Pyrimidine Pathways as Antimalarial Targets
title_sort purine and pyrimidine pathways as antimalarial targets
topic Health Sciences
url https://www.intechopen.com/chapters/83000
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