Journal of Medicinal Chemistry · 2012 · 46 citations · 13 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsAnthelmintic PharmacologyAntiparasitic AgentsAntiparasitic PharmacologyAntiparasitic TherapyParasitic Disease PathogenesisStructure-activity Relationship AnalysisAnthelmintic Drug DevelopmentAnthelmintic Drug DiscoveryAnthelmintic Drug TherapyDrug Discovery For AnthelminticsIn Vivo StudiesNovel Antiparasitic Compound Classes
Toxoplasma gondii (T. gondii) is an apicomplexan parasite that can cause eye disease, brain disease, and death, especially in congenitally infected and immune-compromised people. Novel medicines effective against both active and latent forms of the parasite are greatly needed. The current study focused on the discovery of such medicines by exploring a family of potential inhibitors whose antiapicomplexan activity has not been previously reported. Initial screening efforts revealed that niclosamide, a drug approved for anthelmintic use, possessed promising activity in vitro against T. gondii. This observation inspired the evaluation of the activity of a series of salicylanilides and derivatives. Several inhibitors with activities in the nanomolar range with no appreciable in vitro toxicity to human cells were identified. An initial structure-activity relationship was explored. Four compounds were selected for evaluation in an in vivo model of infection, and two derivatives with potentially enhanced pharmacological parameters demonstrated the best activity profiles.
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David Plouffe, Achim Brinker, Case W. McNamara et al. · Proceedings of the National Academy of Sciences · 2008 · 452 citations · Full text
Mechanism of Action of Reagents that uncouple Oxidative Phosphorylation
Eugene C. Weinbach, Joel Garbus · Nature · 1969 · 270 citations