Natural Products and Bioprospecting · 2019 · 18 citations · 13 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryPlant BiochemistryStructure-activity RelationshipsMedicinal PlantsNatural Product Drug DiscoveryStructure-activity Relationship AnalysisDisaggregationDisaggregation MechanismsNuclear Magnetic Resonance StudiesPlant Alkaloids
Abstract Diterpenoid alkaloids have neroprotective activity. Herein, three napelline-type diterpenoid alkaloids 1 – 3 , two aconitine-type diterpenoid alkaloids 4 – 5 , and one isoquinline-type alkaloid 6 , as well as one lignan glycoside 7 , have been isolated from the roots of Aconitum pendulum Busch. Compounds 1 and 7 were new compounds, and their chemical structures were determined on the basis of nuclear magnetic resonance (NMR) spectra and mass spectrometry analysis. A ThT assay revealed that compound 2 showed significant disaggregation potency on the A β 1−42 aggregates. Graphical Abstract
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Further New Gypenosides from Jiaogulan (<i>Gynostemma pentaphyllum</i>)
Jun Wang, Jun‐Li Yang, Panpan Zhou et al. · Journal of Agricultural and Food Chemistry · 2017 · 56 citations