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pmid: 32200067
Ten poly-O-acylated β-dihydroagarofuran sesquiterpenoids, siphonagarofurans A-J, were obtained from the fruits of Siphonodon celastrineus using chromatographic techniques. Their structures were elucidated by extensive use of 2-D NMR spectroscopic methods. The absolute configurations of siphonagarofurans A-J were assigned following analysis of calculated and experimental ECD spectra. The absolute configuration of siphonagarofuran A was also confirmed by X-ray crystallographic analysis. Selected compounds were evaluated for their cytotoxic activity against KB, Vero and Hela cell lines with siphonagarofuran J identified as the most active compound, with IC50 values ranging from 14 to 27 μM.
Fruit, Humans, Biodiversity, Celastraceae, Sesquiterpenes, Taxonomy, HeLa Cells
Fruit, Humans, Biodiversity, Celastraceae, Sesquiterpenes, Taxonomy, HeLa Cells
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