Li Ke, Li Xiao-Ming, Ji Nai-Yun, Wang Bin-Gui
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, PR China.
Bioorg Med Chem. 2007 Nov 1;15(21):6627-31. doi: 10.1016/j.bmc.2007.08.023. Epub 2007 Aug 22.
Three new natural occurring bromophenols, 3-(3-bromo-4,5-dihydroxyphenyl)-2-(3,5-dibromo-4-hydroxyphenyl)propionic acid (1), (E)-4-(3-bromo-4,5-dihydroxyphenyl)-but-3-en-2-one (2), and (3,5-dibromo-4-hydroxyphenyl) acetic acid butyl ester (3), together with one known bromophenol, 1,2-bis(3-bromo-4,5-dihydroxyphenyl)ethane (4), were isolated and identified from the marine red alga Polysiphonia urceolata. The structures of these compounds were elucidated by extensive analysis of 1D and 2D NMR and IR spectra and MS data. Each of the isolated compounds was evaluated for scavenging alpha, alpha-diphenyl-beta-picrylhydrazyl (DPPH) radical activity and all of them exhibited significant activity with IC(50) values ranging from 9.67 to 21.90 microM, compared to the positive control, a well-known antioxidant butylated hydroxytoluene (BHT), with IC(50) 83.84 microM.
从海洋红藻多管藻中分离并鉴定出三种新的天然存在的溴酚,即3-(3-溴-4,5-二羟基苯基)-2-(3,5-二溴-4-羟基苯基)丙酸(1)、(E)-4-(3-溴-4,5-二羟基苯基)丁-3-烯-2-酮(2)和(3,5-二溴-4-羟基苯基)乙酸丁酯(3),以及一种已知的溴酚1,2-双(3-溴-4,5-二羟基苯基)乙烷(4)。通过对一维和二维核磁共振谱、红外光谱以及质谱数据的广泛分析阐明了这些化合物的结构。对每种分离得到的化合物进行了清除α,α-二苯基-β-苦基肼基(DPPH)自由基活性的评估,与阳性对照、一种著名的抗氧化剂丁基化羟基甲苯(BHT,IC50为83.84 μM)相比,所有这些化合物均表现出显著活性,IC50值在9.67至21.90 μM之间。