Journal of Natural Products · 2000 · 50 citations · 10 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsAntiviral AgentsAntiviral PharmacologyMedicinal PlantsOncology PharmacologyStructure-activity Relationship AnalysisAnticancer ActivityAnticancer Compound ScreeningAnticancer Marine CompoundsAntiviral Structure-activity RelationshipsBiological Evaluation ReportMarine-derived Anticancer CompoundsMarine-derived Antiviral CompoundsMass Spectral Data Analysis
Two new sesquiterpenes, leitneridanin A (1) and leitneridanin B (2), and seven known compounds, lirioresinol B, (-)-pinoresinal, (+)-lariciresinol, quassimarin (3), simalikalactone D (4), 1-methoxycanthinone (5), and 5-methoxycanthinone (6), were isolated from Leitneria floridana. Their structures were identified on the basis of spectral data. In vitro biological evaluation showed that 5 is a potent anti-HIV agent (EC(50) 0.26 g/mL; TI >39) and that 3-6 suppressed the growth of a panel of human tumor cell lines (KB, A-549, HCT-8, CAKI-1, MCF-7, and SK-MEL-2). Compounds 3 and 4 were significantly active, with ED(50) values in the range of 0.26-0.012 g/mL.
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Medicine, Oncology, Pharmacology +14
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