Development of Pyrazolopyrimidine Anti- Wolbachia Agents for the Treatment of Filariasis

Paul McGillan, Neil G. Berry, Gemma L. Nixon, Suet C. Leung, Peter J.H. Webborn, Mark C. Wenlock, Stefan Kavanagh, Andrew Cassidy, Rachel H. Clare, Darren A. Cook, Kelly L. Johnston, Louise Ford, Stephen A. Ward, Mark J. Taylor, W. David Hong*, Paul M. O'Neill*

*Corresponding author for this work

Research output: Contribution to journalArticle (journal)peer-review

4 Citations (Scopus)
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Abstract

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.

Original languageEnglish
Pages (from-to)1421-1426
Number of pages6
JournalACS Medicinal Chemistry Letters
Volume12
Issue number9
Early online date20 Aug 2021
DOIs
Publication statusPublished - 9 Sept 2021

Keywords

  • Filariasis
  • Onchocerciasis
  • Pyrazolopyrimidine
  • Wolbachia

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