Tomensides A-D, new antiproliferative phenylpropanoid sucrose esters from Prunus tomentosa leaves

作者：Zhao, Wei; Huang, Xiao-Xiao; Yu, Li-Hong; Liu, Qing-Bo; Li, Ling-Zhi; Sun, Qian; Song, Shao-Jiang^*

来源：Bioorganic & Medicinal Chemistry Letters, 2014, 24(11): 2459-2462.

DOI：10.1016/j.bmcl.2014.04.018

• Prunus tomentosa
• 3-Phenylpropanoid-triacetyl sucrose esters
• Cytotoxicities
• Structure-activity relationships (SAR)

To search for novel cytotoxic constituents against cancer cells as lead structures for drug development, four new 3-phenylpropanoid-triacetyl sucrose esters, named tomensides A-D (1-4), and three known analogs (5-7) were isolated from the leaves of Prunus tomentosa. Their structures were elucidated by spectroscopic analyses (1D, 2D NMR, CD and HRESIMS). The cytotoxic activities of all isolates against four human cancer cell lines (MCF-7, A549, HeLa and HT-29) were assayed, and the results showed that these isolates displayed stronger inhibitory activities compared with positive control 5-fluorouracil. Tomenside A (1) was the most active compound with IC50 values of 0.11-0.62 mu M against the four tested cell lines. The structure-activity relationship (SAR) of the isolates was also discussed. The primary screening results indicated that these 3-phenylpropanoid-triacetyl sucrose esters might be valuable source for new potent anticancer drug candidates.

• 出版日期2014-6-1
• 单位沈阳药科大学