Research Center for Marine Drugs, and Department of Pharmacology, School of Pharmacy, Second Military Medical University, 325 Guo-He Road, Shanghai 200433, China.
Mar Drugs. 2013 May 15;11(5):1565-82. doi: 10.3390/md11051565.
Eighteen new 11,20-epoxy-3Z,5E-dien briaranes, gemmacolides AA-AR (1-18), were isolated together with three known analogs, dichotellides F (19) and I (20), and juncenolide C (21), from the South China Sea gorgonian Dichotella gemmacea. The structures of the compounds were elucidated by detailed spectroscopic analysis and comparison with reported data. The absolute configuration was determined based on the ECD experiment. In the in vitro bioassay, compounds 1-3, 5, 6, 8-12, and 14-19 exhibited different levels of growth inhibition activity against A549 and MG63 cell lines. Preliminary structure-activity analysis suggests that 12-O-isovalerate may increase the activity whereas 13- or 14-O-isovalerate may decrease the activity. Contribution of substitutions at C-2 and C-16 remains uncertain.
从南海柳珊瑚 Dichotella gemmacea 中分离得到了 18 种新的 11,20-环氧-3Z,5E-二烯布里亚烷,即 gemmacolide AA-AR(1-18),以及三个已知的类似物,二切托利德 F(19)和 I(20)以及 juncenolide C(21)。通过详细的光谱分析和与已报道数据的比较,确定了这些化合物的结构。绝对构型是基于 ECD 实验确定的。在体外生物测定中,化合物 1-3、5、6、8-12 和 14-19 对 A549 和 MG63 细胞系表现出不同程度的生长抑制活性。初步的结构-活性分析表明,12-O-异戊酸酯可能会增加活性,而 13-或 14-O-异戊酸酯可能会降低活性。C-2 和 C-16 取代的贡献仍不确定。