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Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis
[Image: see text] Anti-Wolbachia therapy has been identified as a viable treatment for combating filarial diseases. Phenotypic screening revealed a series of pyrazolopyrimidine hits with potent anti-Wolbachia activity. This paper focuses on the exploration of the SAR for this chemotype, with improve...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436242/ https://www.ncbi.nlm.nih.gov/pubmed/34527179 http://dx.doi.org/10.1021/acsmedchemlett.1c00216 |
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author | McGillan, Paul Berry, Neil G. Nixon, Gemma L. Leung, Suet C. Webborn, Peter J. H. Wenlock, Mark C. Kavanagh, Stefan Cassidy, Andrew Clare, Rachel H. Cook, Darren A. Johnston, Kelly L. Ford, Louise Ward, Stephen A. Taylor, Mark J. Hong, W. David O’Neill, Paul M. |
author_facet | McGillan, Paul Berry, Neil G. Nixon, Gemma L. Leung, Suet C. Webborn, Peter J. H. Wenlock, Mark C. Kavanagh, Stefan Cassidy, Andrew Clare, Rachel H. Cook, Darren A. Johnston, Kelly L. Ford, Louise Ward, Stephen A. Taylor, Mark J. Hong, W. David O’Neill, Paul M. |
author_sort | McGillan, Paul |
collection | PubMed |
description | [Image: see text] Anti-Wolbachia therapy has been identified as a viable treatment for combating filarial diseases. Phenotypic screening revealed a series of pyrazolopyrimidine hits with potent anti-Wolbachia activity. This paper focuses on the exploration of the SAR for this chemotype, with improvement of metabolic stability and solubility profiles using medicinal chemistry approaches. Organic synthesis has enabled functionalization of the pyrazolopyrimidine core at multiple positions, generating a library of compounds of which many analogues possess nanomolar activity against Wolbachia in vitro with improved DMPK parameters. A lead compound, 15f, was selected for in vivo pharmacokinetics (PK) profiling in mice. The combination of potent anti-Wolbachia activity in two in vitro assessments plus the exceptional oral PK profiles in mice puts this lead compound in a strong position for in vivo proof-of-concept pharmacodynamics studies and demonstrates the strong potential for further optimization and development of this series for treatment of filariasis in the future. |
format | Online Article Text |
id | pubmed-8436242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84362422021-09-14 Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis McGillan, Paul Berry, Neil G. Nixon, Gemma L. Leung, Suet C. Webborn, Peter J. H. Wenlock, Mark C. Kavanagh, Stefan Cassidy, Andrew Clare, Rachel H. Cook, Darren A. Johnston, Kelly L. Ford, Louise Ward, Stephen A. Taylor, Mark J. Hong, W. David O’Neill, Paul M. ACS Med Chem Lett [Image: see text] Anti-Wolbachia therapy has been identified as a viable treatment for combating filarial diseases. Phenotypic screening revealed a series of pyrazolopyrimidine hits with potent anti-Wolbachia activity. This paper focuses on the exploration of the SAR for this chemotype, with improvement of metabolic stability and solubility profiles using medicinal chemistry approaches. Organic synthesis has enabled functionalization of the pyrazolopyrimidine core at multiple positions, generating a library of compounds of which many analogues possess nanomolar activity against Wolbachia in vitro with improved DMPK parameters. A lead compound, 15f, was selected for in vivo pharmacokinetics (PK) profiling in mice. The combination of potent anti-Wolbachia activity in two in vitro assessments plus the exceptional oral PK profiles in mice puts this lead compound in a strong position for in vivo proof-of-concept pharmacodynamics studies and demonstrates the strong potential for further optimization and development of this series for treatment of filariasis in the future. American Chemical Society 2021-08-20 /pmc/articles/PMC8436242/ /pubmed/34527179 http://dx.doi.org/10.1021/acsmedchemlett.1c00216 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | McGillan, Paul Berry, Neil G. Nixon, Gemma L. Leung, Suet C. Webborn, Peter J. H. Wenlock, Mark C. Kavanagh, Stefan Cassidy, Andrew Clare, Rachel H. Cook, Darren A. Johnston, Kelly L. Ford, Louise Ward, Stephen A. Taylor, Mark J. Hong, W. David O’Neill, Paul M. Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis |
title | Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis |
title_full | Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis |
title_fullStr | Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis |
title_full_unstemmed | Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis |
title_short | Development of Pyrazolopyrimidine Anti-Wolbachia Agents for the Treatment of Filariasis |
title_sort | development of pyrazolopyrimidine anti-wolbachia agents for the treatment of filariasis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436242/ https://www.ncbi.nlm.nih.gov/pubmed/34527179 http://dx.doi.org/10.1021/acsmedchemlett.1c00216 |
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