Planta Medica · 2003 · 56 citations · 0 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryEnzyme InhibitionMedicinal Plant KnowledgeMedicinal PlantsNatural Product Drug DiscoveryStructure-activity Relationship AnalysisActive Compound IsolationAntiviral Natural ProductsBioactive Plant CompoundsBotanical BioassaysMedicinal HerbsMedicinal Plant ResourcesPlant-derived Natural ProductsTelomerase Reverse Transcriptase
Three new protostanes, garciosaterpenes A ( 1), B ( 2) and C ( 3), together with a new digeranylbenzophenone, garciosaphenone A ( 4) were isolated from the ethyl acetate fractions obtained from the crude methanol extracts of the trunk bark and stems of Garcinia speciosa. The structures were elucidated by spectroscopic methods and chemical reactions. Compounds 1 and 3 showed significant inhibitory activities (IC (50) 15.5 and 12.2 microg/mL, respectively) against HIV-1 reverse transcriptase and in the syncytium assay (EC (50) 5.8 microg/mL with TI 3.4 and 37.0 microg/mL with TI 1.9, respectively). Compound 4 was active in HIV-1 RT assay (IC (50) 23.9 microg/mL), but toxic in the syncytium assay. This work represents the first report on the anti-HIV-1 activities of the protostane triterpenes.