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The critical role of mode of action studies in kinetoplastid drug discovery

Understanding the target and mode of action of compounds identified by phenotypic screening can greatly facilitate the process of drug discovery and development. Here, we outline the tools currently available for target identification against the neglected tropical diseases, human African trypanosom...

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Detalles Bibliográficos
Autores principales: Fairlamb, Alan H., Wyllie, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614965/
https://www.ncbi.nlm.nih.gov/pubmed/37600222
http://dx.doi.org/10.3389/fddsv.2023.1185679
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author Fairlamb, Alan H.
Wyllie, Susan
author_facet Fairlamb, Alan H.
Wyllie, Susan
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description Understanding the target and mode of action of compounds identified by phenotypic screening can greatly facilitate the process of drug discovery and development. Here, we outline the tools currently available for target identification against the neglected tropical diseases, human African trypanosomiasis, visceral leishmaniasis and Chagas’ disease. We provide examples how these tools can be used to identify and triage undesirable mechanisms, to identify potential toxic liabilities in patients and to manage a balanced portfolio of target-based campaigns. We review the primary targets of drugs that are currently in clinical development that were initially identified via phenotypic screening, and whose modes of action affect protein turnover, RNA trans-splicing or signalling in these protozoan parasites.
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spelling pubmed-76149652023-08-20 The critical role of mode of action studies in kinetoplastid drug discovery Fairlamb, Alan H. Wyllie, Susan Front Drug Discov (Lausanne) Article Understanding the target and mode of action of compounds identified by phenotypic screening can greatly facilitate the process of drug discovery and development. Here, we outline the tools currently available for target identification against the neglected tropical diseases, human African trypanosomiasis, visceral leishmaniasis and Chagas’ disease. We provide examples how these tools can be used to identify and triage undesirable mechanisms, to identify potential toxic liabilities in patients and to manage a balanced portfolio of target-based campaigns. We review the primary targets of drugs that are currently in clinical development that were initially identified via phenotypic screening, and whose modes of action affect protein turnover, RNA trans-splicing or signalling in these protozoan parasites. 2023-05-10 /pmc/articles/PMC7614965/ /pubmed/37600222 http://dx.doi.org/10.3389/fddsv.2023.1185679 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Article
Fairlamb, Alan H.
Wyllie, Susan
The critical role of mode of action studies in kinetoplastid drug discovery
title The critical role of mode of action studies in kinetoplastid drug discovery
title_full The critical role of mode of action studies in kinetoplastid drug discovery
title_fullStr The critical role of mode of action studies in kinetoplastid drug discovery
title_full_unstemmed The critical role of mode of action studies in kinetoplastid drug discovery
title_short The critical role of mode of action studies in kinetoplastid drug discovery
title_sort critical role of mode of action studies in kinetoplastid drug discovery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614965/
https://www.ncbi.nlm.nih.gov/pubmed/37600222
http://dx.doi.org/10.3389/fddsv.2023.1185679
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