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作 者:尹鹏军[1] 汪俊松[1] 王朋然[1] 孔令义[1]
机构地区:[1]中国药科大学天然药物化学教研室,南京210009
出 处:《中国天然药物》2012年第5期383-387,共5页
基 金:supported by the Key Project of National Natural Science Foundation of China (No. 30830116);Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)~~
摘 要:目的:研究野八角果实的化学成分及生物活性。方法:应用硅胶、反相、凝胶色谱及制备 HPLC 对野八角果实的乙醇提取物进行分离纯化, 并且通过光谱方法鉴定化合物结构。进一步用 MTT 法对所分离化合物进行细胞毒活性测试。结果:7 个化合物被分离并鉴定为:veranisatin F (1), anisatin (2), (1S)-minwanenone (3), honokiol (4), macranthol (5), (+)-pinoresinol (6),matairesinol (7)。结论:化合物 1 是一个新的高氧化裂-prezizaane 型倍半萜, 化合物 6 和 7 首次从野八角中分离得到。5-氟脲嘧啶作为阳性对照, 化合物 2 和 3 对人大细胞肺癌细胞株和人肝癌细胞株的增长有较强的的抑制活性, 7 则比较微弱, 其他化合物显示无细胞毒活性。AIM: To study the constituents and bioactivity of Illicium simonsii. METHODS: Compounds were isolated by a com- bination of chromatographic materials, silica gel, ODS, and Sephadex LH-20, and finally purified by preparative HPLC. Their struc- tures were elucidated on the basis of spectroscopic methods, and they were evaluated for their cytotoxic activities by the MTF method. RESULTS: Seven compounds were obtained and were identified as veranisatin F (1), anisatin (2), (1S)-minwanenone (3), honokiol (4), macranthol (5), (+)-pinoresinol (6), and matairesinol (7). CONCLUSIONS: Compound 1 is a new seco-prezizaane-type sesquiterpene, while compounds 6 and 7 were isolated from Illiciurn simonsii for the first time. Compounds 2 and 3 showed strong inhibitory activities against the growth of NCI-H460 and SMMC-7721 cells comparable to 5-fluorouracil, and compound 7 to a lesser extent; the other isolates showed no cytotoxicity.
关 键 词:八角属 野八角 高氧化裂-prezizaane型倍半萜 木脂素 细胞毒
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