Planta Medica · 2020 · 30 citations · 17 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryEnzymologyStructure-activity RelationshipsEnzyme InhibitionStructure-activity Relationship AnalysisGlycosidase InhibitionGlycosidase InhibitorsGlycosidases
Abstract Chemical investigation of the lichen Parmotrema tsavoense led to the isolation of 5 new depsidones, parmosidones F – J (1 – 5). These compounds were structurally elucidated using spectroscopic methods including HRESIMS and 2D NMR data. Compounds 1, 3, and 4 were evaluated for their inhibition of α-glucosidase. All exhibited potent α-glucosidase inhibitory activity with IC50 values ranging from 10.7 to 17.6 µM, which was much lower than that of the positive control acarbose (IC50 449 µM).
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Chemical and Botanical Guide to Lichen Products
Mason E. Hale, Chicita F. Culberson · The Bryologist · 1970 · 388 citations
Life Sciences, Botany, Chemistry +14
Lichens—a promising source of bioactive secondary metabolites
Joël Boustié, Martín Grube · Plant Genetic Resources · 2005 · 357 citations