ACS Medicinal Chemistry Letters · 2013 · 42 citations · 24 references
Medicinal ChemistryPharmaceutical ChemistryBioorganic ChemistryBiochemistryAntiparasitic AgentBlood-schizontocidal ActivitiesMedicineMalariaNatural SciencesHepatotoxicityHybrid CompoundsEffective CompoundsPharmacologyAntiviral CompoundAmide LinkerDrug Discovery
In a search for effective compounds against both the blood- and liver-stages of infection by malaria parasites with the ability to block the transmission of the disease to mosquito vectors, a series of hybrid compounds combining either a 1,2,4-trioxane or 1,2,4,5-tetraoxane and 8-aminoquinoline moieties were synthesized and screened for their antimalarial activity. These hybrid compounds showed high potency against both exoerythrocytic and erythrocytic forms of malaria parasites, comparable to representative trioxane-based counterparts. Furthermore, they efficiently blocked the development of the sporogonic cycle in the mosquito vector. The tetraoxane-based hybrid 5, containing an amide linker between the two moieties, effectively cleared a patent blood-stage P. berghei infection in mice after i.p. administration. Overall, these results indicate that peroxide-8-aminoquinoline hybrids are excellent starting points to develop an agent that conveys all the desired antimalarial multistage activities in a single chemical entity and, as such, with the potential to be used in malaria elimination campaigns.
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Imaging of <i>Plasmodium</i> Liver Stages to Drive Next-Generation Antimalarial Drug Discovery
Stephan Meister, David Plouffe, Kelli Kuhen et al. · Science · 2011 · 347 citations · Full text
Visualisation and Quantitative Analysis of the Rodent Malaria Liver Stage by Real Time Imaging
Ivo Ploemen, Miguel Prudêncio, Bruno Douradinha et al. · PLoS ONE · 2009 · 238 citations · Full text