a The Graduate School of Biotechnology, Institute of Life Sciences & Resources, Kyung Hee University , Yongin 446-701 , Republic of Korea.
Nat Prod Res. 2014;28(11):831-4. doi: 10.1080/14786419.2013.879583. Epub 2014 Feb 5.
In order to identify antioxidant flavonoids from Lindera glauca Blume, we performed phytochemical analysis of L. glauca Blume heartwood and isolated eight flavonoids - lindeglaucol (1), lindeglaucone (2), cilicicone B (3), tamarixetin 3-O-α-L-rhamnoside (4), procyanidin A2 (5), cinnamtannin B1 (6), cinnamtannin D1 (7), and procyanidin A1 (8) - through repeated column chromatography over silica gel (SiO₂), octadecyl silica gel (ODS) and Sephadex LH-20. The chemical structures of compounds 1-8 were elucidated from spectroscopic data (NMR, IR and MS). The low-density lipoprotein oxidation inhibitory activities of the isolated compounds were evaluated in vitro by using the thiobarbituric acid reactive substances assay. Compounds 5-8 exhibited high inhibition activity, comparable to the positive control butyl hydroxyl toluene. Compounds 2 and 3 were slightly less active, while 1 and 4 expressed low activity.
为了从黄瑞木中鉴定出具有抗氧化作用的类黄酮,我们对黄瑞木的心材进行了植物化学分析,并通过反复的硅胶(SiO₂)、十八烷基硅烷(ODS)和葡聚糖 LH-20 柱层析分离出八种类黄酮 - 黄瑞木醇(1)、黄瑞木酮(2)、西利西酮 B(3)、柽柳素 3-O-α-L-鼠李糖苷(4)、原花青素 A2(5)、肉桂单宁 B1(6)、肉桂单宁 D1(7)和原花青素 A1(8)。通过光谱数据(NMR、IR 和 MS)阐明了化合物 1-8 的化学结构。通过硫代巴比妥酸反应物质测定法,在体外评估了分离化合物的低密度脂蛋白氧化抑制活性。化合物 5-8 表现出高抑制活性,与阳性对照丁基羟基甲苯相当。化合物 2 和 3 的活性稍低,而 1 和 4 的活性较低。