| Literature DB >> 33217195 |
Mélanie Fonte1, Natália Tassi1, Diana Fontinha2, Inés Bouzón-Arnáiz3,4, Ricardo Ferraz1,5, Maria J Araújo1, Xavier Fernàndez-Busquets3,4, Miguel Prudêncio2, Paula Gomes1, Cátia Teixeira1.
Abstract
Multi-stage drugs have been prioritized in antimalarial drug discovery, as targeting more than one process in the Plasmodium life cycle is likely to increase efficiency, while decreasing the chances of emergence of resistance by the parasite. Herein, we disclose two novel acridine-based families of compounds that combine the structural features of primaquine and chloroquine. Compounds prepared and studied thus far retained the in vitro activity displayed by the parent drugs against the erythrocytic stages of chloroquine-sensitive and -resistant Plasmodium falciparum strains, and against the hepatic stages of Plasmodium berghei, hence acting as dual-stage antiplasmodial hits.Entities:
Keywords: Plasmodium; acridines; antimalarial activity; blood-stage; liver-stage; malaria; synthesis
Year: 2020 PMID: 33217195 DOI: 10.1002/cmdc.202000740
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466