| Literature DB >> 29107811 |
Wan-Ping Wang1, Kun Jiang2, Ping Zhang3, Kai-Kai Shen4, Shi-Jin Qu2, Xiao-Ping Yu3, Chang-Heng Tan5.
Abstract
A phytochemical investigation on the aerial part of Euphorbia helioscopia (Euphorbiaceae) led to the isolation of 22 highly oxygenated diterpenoids with structural types of ent-abietane, ent-kaurane, lathyrane, ent-atisane and ingenane. 17 of them, named euphelionolides A - N, 16-epi-18-hydroxy-abbeokutone, as well as eupheliotriols A and B, were identified to be previously undescribed compounds by extensive analysis of spectroscopic data. The stereostructures of euphelionolides A - K were determined by single crystal X-ray diffraction combined with analysis of substituent effects and comparison of optical characteristics. Eupheliotriol B is the first example of natural occurring lathyrol with 12Z-ene, while ent-atisanes are the first reported from the title plant. Furthermore, euphelionolides F and L exhibited significant cytotoxicity against MCF-7 and PANC-1 cell lines.Entities:
Keywords: Diterpenoids; Ent-abietane; Ent-kaurane; Euphorbia helioscopia; Euphorbiaceae; Lathyrane; Substituent effects
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Year: 2017 PMID: 29107811 DOI: 10.1016/j.phytochem.2017.10.012
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072