Journal of Natural Products · 2008 · 19 citations · 8 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryEnzymologySynthetic Medicinal ChemistryAntiparasitic PharmacologyEnzyme DiscoveryEnzyme InhibitionEnzyme ScreeningMalariaStructure-activity Relationship AnalysisAntimalarial Drug DevelopmentAntiparasitic Drug DiscoveryGlycoside Natural ProductsHeterocyclic Natural ProductsHigh-throughput Screening LibrariesNovel Antiparasitic Compound Classes
High-throughput screening of a plant and marine invertebrate extract library to find natural products that inhibit the malarial parasite enzyme target hemoglobinase II led to the isolation of two new active prenylated chalcones, bipinnatones A (1) and B (2), from aerial parts of the Queensland shrub Boronia bipinnata. Their structures were assigned from interpretation of 2D NMR and high-resolution ESIMS data. Compounds 1 and 2 inhibited hemoglobinase II with IC 50 values of 64 and 52 microM, respectively.
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