Journal of Natural Products · 2021 · 15 citations · 21 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryAntifungal AgentsAntifungal PharmacologyChemical Library DesignMedicinal PlantsNatural Product Drug DiscoveryStructure-activity Relationship AnalysisHydrogen BondingIntramolecular Hydrogen BondingMedicinal Aromatic PlantsMolecular NetworkingNew Antifungal AgentsPlant Alkaloids
Voatriafricanines A and B (1 and 2), the first examples of vobasine-aspidosperma-aspidosperma monoterpene trisindole alkaloids, were isolated from the stem barks of Voacanga africana, guided by a molecular networking strategy. Their structures, including absolute configurations, were elucidated by spectroscopic methods and ECD calculations. Compounds 1 and 2 possess intramolecular hydrogen bonding, sufficiently robust to transfer homonuclear and heteronuclear magnetizations. Compound 1 exhibited potent antimycobacterial activity with no discernible cytotoxic activity.
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