1. Ent-abietane diterpenoids and their probable biogenetic precursors from the roots of Euphorbia fischeriana
- Author
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Jun He, Wei-Ku Zhang, Nuan Zhang, Xiao-Xue Wang, Ying-Xue Shi, Bing-Zhi Ma, Jia Zhang, and Jie-Kun Xu
- Subjects
chemistry.chemical_classification ,Circular dichroism ,010405 organic chemistry ,Stereochemistry ,General Chemical Engineering ,General Chemistry ,Ring (chemistry) ,01 natural sciences ,0104 chemical sciences ,010404 medicinal & biomolecular chemistry ,chemistry.chemical_compound ,chemistry ,Euphorbia fischeriana ,Cytotoxicity ,Human cancer ,Lactone ,Abietane - Abstract
Five new ent-abietane diterpenoids (1–5), along with nine known analogues (6–14), were isolated from the roots of Euphorbia fischeriana. Their structures and absolute configurations were determined by the analysis of extensive spectroscopic data (UV, IR, HRESIMS, NMR) and the comparison of the experimental and calculated electronic circular dichroism (ECD). Among the isolates, it's notable that the ent-abietane diterpenoids bearing an additional five-membered lactone ring might be derived from the proposed precursors of fischeriabietane B (2) and C (3), and their plausible biosynthetic relationship was detailed discussed. All the isolates were evaluated for cytotoxicity against three human cancer cell lines (Panc-28, Bel-7402, and HT-29), 2 and 3 exhibited moderate cytotoxicity.
- Published
- 2017