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Identification of GSK3186899/DDD853651 as a Preclinical Development Candidate for the Treatment of Visceral Leishmaniasis.

Michael G ThomasManu De RyckerMyriam AjakaneSébastian AlbrechtAna Isabel Álvarez-PedraglioMarkus BoescheStephen BrandLorna CampbellJuan Cantizani-PerezLaura A T CleghornRoyston C B CopleySabrinia D CrouchAlain DauganGerard DrewesSantiago FerrerSonja Ghidelli-DisseSilvia GonzalezStephanie L GreshamAlan P HillSean J HindleyRhiannon M LoweClaire J MacKenzieLorna MacLeanSujatha ManthriFranck MartinJuan Miguel-SilesVan Loc NguyenSuzanne NorvalMaria Osuna-CabelloAndrew WoodlandStephen PattersonImanol PenaMaria Teresa Quesada-CamposIain H ReidCharlotte RevillJennifer RileyJose Ramon Ruiz-GomezYoko ShishikuraFrederick R C SimeonsAlasdair SmithVictoria C SmithDaniel SpinksLaste StojanovskiJohn ThomasStephen ThompsonTim UnderwoodDavid W GrayJose M FiandorIan H GilbertPaul G WyattKevin D ReadTimothy J Miles
Published in: Journal of medicinal chemistry (2018)
The leishmaniases are diseases that affect millions of people across the world, in particular visceral leishmaniasis (VL) which is fatal unless treated. Current standard of care for VL suffers from multiple issues and there is a limited pipeline of new candidate drugs. As such, there is a clear unmet medical need to identify new treatments. This paper describes the optimization of a phenotypic hit against Leishmania donovani, the major causative organism of VL. The key challenges were to balance solubility and metabolic stability while maintaining potency. Herein, strategies to address these shortcomings and enhance efficacy are discussed, culminating in the discovery of preclinical development candidate GSK3186899/DDD853651 (1) for VL.
Keyphrases
  • healthcare
  • signaling pathway
  • pi k akt
  • small molecule
  • high throughput
  • combination therapy
  • chronic pain