Yang Min Cheol, Lee Kyu Ha, Kim Ki Hyun, Choi Sang Un, Lee Kang Ro
Natural Products Laboratory, College of Pharmacy, Sungkyunkwan University, Suwon 440-746, Korea.
Arch Pharm Res. 2007 Sep;30(9):1067-74. doi: 10.1007/BF02980239.
Chromatographic separation of the MeOH extract from the aerial parts of Saussurea pulchella led to the isolation of seven terpenes (1-4, 11-13), and eight phenolics (5-10, 14-15). Their structures were determined by spectroscopic means to be (3S)-3-O-(3',4'-diangeloyl-beta-D-glucopyranosyloxy)-3,7-trimethylocta-1,6-diene (1), 7delta-methoxy- 4(14)- oppositen-1beta-ol (2) 4(15)- eudesmene-1beta, 6alpha-diol (3), 3alpha-hydroxy-5, 6-epoxy-7-megastigmen-9-one (4), (+)-syringaresinol (5), (7S, 8R, 8'R)-5,5'-dimethoxylariciresinol (6), 8alpha-hydroxypinoresinol (7), (7'R, 8'R)-2,2'- dimethoxy-4- (3-hydroxyl-propenyl)-4'-(1,2,3-trihydroxypropyl)-biphenyl ether (8), 4-allyl-2,6- dimethoxyphenyl glucoside (9), 2-methoxy-4-(2-propenyl)phenyl beta-D-glucoside (10), (-)-oplopan-4-one- 10alpha-O-beta-D-glucoside (11), linalyl-O-beta-D-glucoside (12), amarantholidoside IV (13), (+)-1-hydroxypinoresinol 1-O-beta-D-glucoside (14), and syringin (15). Compounds 1-3 and 8-13 were first isolated from the genus Saussurea. The isolated compounds were examined for cytotoxic activity against four human cancer cell lines in vitro using the sulforhodamin B bio assay method.
对美丽风毛菊地上部分的甲醇提取物进行色谱分离,得到了7种萜类化合物(1 - 4、11 - 13)和8种酚类化合物(5 - 10、14 - 15)。通过光谱手段确定它们的结构分别为(3S)-3 - O-(3',4'-二当归酰基-β-D-吡喃葡萄糖氧基)-3,7 - 三甲基辛-1,6 - 二烯(1)、7δ-甲氧基-4(14)-奥波斯汀-1β-醇(2)、4(15)-桉叶二烯-1β,6α-二醇(3)、3α-羟基-5,6 - 环氧-7 - 大柱头酮-9 - 酮(4)、(+)-紫丁香树脂酚(5)、(7S,8R,8'R)-5,5'-二甲氧基落叶松脂醇(6)、8α-羟基松脂醇(7)、(7'R,8'R)-2,2'-二甲氧基-4-(3 - 羟基丙烯基)-4'-(1,2,3 -三羟基丙基)-联苯醚(8)、4 - 烯丙基-2,6 -二甲氧基苯基葡萄糖苷(9)、2 - 甲氧基-4-(2 - 丙烯基)苯基β-D-葡萄糖苷(10)、(-)-奥普洛潘-4 - 酮-10α-O-β-D-葡萄糖苷(11)、芳樟醇-O-β-D-葡萄糖苷(12)、苋色藜糖苷IV(13)、(+)-1 - 羟基松脂醇1 - O-β-D-葡萄糖苷(14)和紫丁香苷(15)。化合物1 - 3和8 - 13首次从风毛菊属植物中分离得到。使用磺基罗丹明B生物测定法对分离得到的化合物进行了体外抗四种人类癌细胞系的细胞毒性活性检测。