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Lead Optimization of Second-Generation Acridones as Broad-Spectrum Antimalarials.

Papireddy KancharlaRozalia A DodeanYuexin LiSovitj PouBrandon PybusVictor MelendezLisa ReadCharles E BaneBrian VeselyMara Kreishman-DeitrickChad BlackQigui LiRichard J SciottiRaul OlmedaThu-Lan LuongHeather GaonaBrittney PotterJason SousaSean MarcsisinDiana CaridhaLisa XieChau VuongQiang ZengJing ZhangPing ZhangHsiuling LinKirk ButlerNorma RoncalLacy Gaynor-OhnstadSusan E LeedChristina NolanFrida G CejaStephanie A RasmussenPatrick K TumwebazePhilip J RosenthalJianbing MuBrett R BaylesRoland A CooperKevin A ReynoldsMartin J SmilksteinMichael K RiscoeJane Xu Kelly
Published in: Journal of medicinal chemistry (2020)
The global impact of malaria remains staggering despite extensive efforts to eradicate the disease. With increasing drug resistance and the absence of a clinically available vaccine, there is an urgent need for novel, affordable, and safe drugs for prevention and treatment of malaria. Previously, we described a novel antimalarial acridone chemotype that is potent against both blood-stage and liver-stage malaria parasites. Here, we describe an optimization process that has produced a second-generation acridone series with significant improvements in efficacy, metabolic stability, pharmacokinetics, and safety profiles. These findings highlight the therapeutic potential of dual-stage targeting acridones as novel drug candidates for further preclinical development.
Keyphrases
  • plasmodium falciparum
  • emergency department
  • cell therapy
  • quality improvement
  • drug delivery
  • smoking cessation
  • replacement therapy