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Dimeric polyphenols to pave the way for new antimalarial drugs.
Degotte, Gilles; Pendeville, Hélène; Di Chio, Carla; Ettari, Roberta; Pirotte, Bernard; Frédérich, Michel; Francotte, Pierre.
  • Degotte G; Laboratory of Medicinal Chemistry, CIRM, Department of Pharmacy, University of Liège Quartier Hôpital - B36 Tower 4, +5, Avenue Hippocrate 15 4000 Liège Belgium dgilles@hotmail.be.
  • Pendeville H; Laboratory of Pharmacognosy, CIRM, Department of Pharmacy, University of Liège Quartier Hôpital - B36 Tower 4, +5, Avenue Hippocrate 15 4000 Liège Belgium.
  • Di Chio C; Platform Zebrafish facility & transgenics, GIGA, University of Liège Quartier Hôpital - B34, +2, Avenue de l'Hôpital 11 4000 Liège Belgium.
  • Ettari R; Dipartimento di Scienze chimiche, biologiche, farmaceutiche e ambientali, Università degli Studi di Messina Viale Annunziata 98168 Messina Italy.
  • Pirotte B; Dipartimento di Scienze chimiche, biologiche, farmaceutiche e ambientali, Università degli Studi di Messina Viale Annunziata 98168 Messina Italy.
  • Frédérich M; Laboratory of Medicinal Chemistry, CIRM, Department of Pharmacy, University of Liège Quartier Hôpital - B36 Tower 4, +5, Avenue Hippocrate 15 4000 Liège Belgium dgilles@hotmail.be.
  • Francotte P; Laboratory of Pharmacognosy, CIRM, Department of Pharmacy, University of Liège Quartier Hôpital - B36 Tower 4, +5, Avenue Hippocrate 15 4000 Liège Belgium.
RSC Med Chem ; 14(4): 715-733, 2023 Apr 26.
Article en En | MEDLINE | ID: mdl-37122550
ABSTRACT
Because of the threat of resistant Plasmodium sp., new orally active antimalarials are urgently needed. Inspired by the structure of ellagic acid, exhibiting potent in vivo and in vitro antiplasmodial effects, polyphenolic structures possessing a similar activity-safety profile were synthesized. Indeed, most exhibited a marked in vitro effect (IC50 < 4 µM) on resistant P. falciparum, without any detrimental effects reported during the toxicity assays (hemolysis, cytotoxicity, in vivo). In addition, they possessed a greater hydrosolubility (from 7 µM to 2.7 mM) compared to ellagic acid. Among them, 30 is the most promising for antimalarial purposes since it displayed a significant parasitaemia reduction after oral administration in mice (50 mg kg-1) compared to the orally ineffective ellagic acid. In conclusion, our investigations led to the identification of a promising scaffold, which could bring new insights for malaria treatment.