Helvetica Chimica Acta · 2011 · 37 citations · 14 references
PharmacyBiochemistryMedicinal ChemistryDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryAntioxidant DefenseAromatic PlantsFood AntioxidantsMedicinal PlantsStructure-activity Relationship AnalysisAlkaloid GlycosidesBioactive Plant CompoundsIndole AlkaloidsIndole ChemistryMedicinal Aromatic PlantsPharmacological ScreeningPlant AlkaloidsPlant Extract Antioxidants
Abstract Two alkaloids, oleraceins F and G, were isolated from Portulaca oleracea L., and their structures were determined as methyl (2 S )‐6‐[( β ‐ D ‐glucopyranosyl)oxy]‐2,3‐dihydro‐5‐hydroxy‐1‐[(2 E )‐3‐(4‐hydroxy‐3‐methoxyphenyl)prop‐2‐enoyl]‐1 H ‐indole‐2‐carboxylate and methyl (2 S )‐6‐[( β ‐ D ‐glucopyranosyl)oxy]‐2,3‐dihydro‐5‐hydroxy‐1‐[(2 E )‐3‐(4‐hydroxyphenyl)prop‐2‐enoyl]‐1 H ‐indole‐2‐carboxylate, based on their spectroscopic data. Oleraceins F and G exhibited scavenging activity against 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) radical, with EC 50 values of 21.00 and 37.69 μ M , respectively.
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The analgesic and anti-inflammatory effects of Portulaca oleracea L. subsp. sativa (Haw.) Celak
K Chan, M.W. Islam, M. Kamil et al. · Journal of Ethnopharmacology · 2000 · 298 citations
Medicine, Pharmacology, Inflammation +12
Phenolic alkaloids as a new class of antioxidants in <i>Portulaca oleracea</i>
Zijuan Yang, Cejia Liu, Lan Xiang et al. · Phytotherapy Research · 2009 · 167 citations