Journal of the Brazilian Chemical Society · 2002 · 49 citations · 0 references
PharmacyBotanyMedicinal ChemistryDrug DiscoveryPlant BiochemistryStructure-activity RelationshipsAntifungal AgentsAntiparasitic PharmacologyMedicinal Plant KnowledgeMedicinal PlantsStructure-activity Relationship AnalysisBioactivityBioactivity AssessmentBiological Activity FeaturesPlant AlkaloidsQuinoline AlkaloidsQuinoline ChemistryTrypanosoma Cruzi InfectionX-ray Structure Determination
Phytochemical survey of stems and leaves extracts of the South Brazilian endemic plant Raulinoa echinata Cowan, Rutaceae, led to the isolation of known furoquinoline alkaloids: the widespread skimmianine; kokusaginine, maculine, flindersiamine, and also quinolone derivatives: 1-methyl-2-n-nonyl-4-quinolone, 2-n-nonyl-4-quinolone and 1-methyl-2-phenyl-4-quinolone. These alkaloids showed antifungal activity against Leucoagaricus gongylophorus; the symbiotic fungus of leaf-cutting ants (Atta sexdens). They were inactive or displayed weak inhibitory activity when assayed in vitro against trypomastigote forms of Trypanosoma cruzi. In this paper, the isolation, structure elucidation and bioactivity results of these compounds are reported together with the X-ray structure of flindersiamine.