School of Pharmacy, Fudan University, Shanghai, China.
Planta Med. 2013 May;79(8):701-6. doi: 10.1055/s-0032-1328461. Epub 2013 May 13.
Three new sesquiterpenoid derivatives 1, 2, and 3 were isolated from Ferula ferulaeoides. To confirm the structure, compound 2 was also synthesized via a condensation reaction between compound 1 and 2,2-dimethoxypropane. The structures of these three compounds were elucidated by means of spectroscopic and chemical methods. Their antibacterial activity against drug-resistant Staphylococcus aureus strains were evaluated with MIC values in the range of 0.5-128 µg/mL. Compounds 1 and 3 were capable of inhibiting efflux of ethidium bromide using an in vitro assay. The cytotoxicity of the compounds was evaluated on cultured HEK293 cells, and none of them showed toxicity to HEK293 cells at a concentration of 125 µg/mL.
从 Ferula ferulaeoides 中分离得到三个新的倍半萜类衍生物 1、2 和 3。为了确定结构,还通过化合物 1 和 2,2-二甲氧基丙烷之间的缩合反应合成了化合物 2。通过光谱和化学方法阐明了这三个化合物的结构。用 MIC 值在 0.5-128μg/ml 范围内评估了它们对耐药性金黄色葡萄球菌菌株的抗菌活性。化合物 1 和 3 能够使用体外测定抑制溴化乙锭的外排。在培养的 HEK293 细胞上评估了化合物的细胞毒性,在 125μg/ml 的浓度下,它们均对 HEK293 细胞没有毒性。