A new sesquiterpene ester (1) has been isolated from the root bark of Tripterygium hypoglaucum. The structure was determined as 1α-acetoxy-6β,9β-dibenzoyloxy-4β-hydroxy-dihydroagarofuran by the extensive analysis of NMR data, and the absolute configurations were established as 1R, 4R, 6S, and 9R by application of the CD excitation chirality method. Compound 1 exhibited weak cytotoxicity against HeLa cells, with an IC₅₀ value of 30.2 μM.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1080/10286020.2013.873410 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!