Bu Peng-Bin, Li Yan-Ru, Jiang Ming, Wang Xiao-Liang, Wang Fang, Lin Sheng, Zhu Cheng-Gen, Shi Jian-Gong
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Zhongguo Zhong Yao Za Zhi. 2013 Jun;38(11):1740-6.
Eighteen lignans were isolated from an ethanol extract of Machilus robusta by a combination of various chromatographic techniques including column chromatography over silica gel, Sephadex LH-20 and reversed-phase HPLC. Their structures were identified by spectroscopic data analysis as isolariciresinol-9'-O-beta-D-xylopyranoside (1), (+)-5'-methoxy-isolariciresinol-9'-O-beta-D-xylopyranoside(2), lyoniresinol-9'-O-beta-D-xylopyranoside(3), (+)-(8S, 8'S) -4, 4'-dihydroxy-3, 3', 5, 5'-tetramethoxylignan-9, 9'-diol 9-O-beta-D-xylopyranoside (ssioriside, 4), lyoniresinol (5), meso-dihydroguaiaretic acid (6), (+)-(8S, 8'R)-3', 4, 4'-trihydroxy-3'-methoxylignan (7), (8S, 8'R)-4'-hydroxy-3, 3', 4-trimethoxylignan (meso-monomethyl dihydroguaiaretic acid, 8), (+)-guaiacin (9), isoguaiacin (10), (-)-(7'R, 8R, 8'R)-4, 4'-dihydroxy-3, 3', 5-trimethoxy-2, 7'-cyclolignan (11), henricine B (12), (-)-(7S, 7'S, 8R, 8'R)-4, 4'-dihydroxy-3, 3', 5, 5'-tetramethoxy-7, 7'-epoxylignan-9, 9'-dio] (7S, 7'S, 8R, 8'R-icariol A2, 13), (+)-(7R, 8R, 7'E)-4-hydroxy-3, 5'-dimethoxy-7, 4'-epoxy-8, 3'-neolignan-7'-ene (licarin A, 14), nectandrin B (15), machilin-I (16), (-)-pinoresinol (17), and (-)-syringaresinol (18). All compounds were isolated from this plant for the first time. In the preliminary assay, compound 17 showed inhibitory activity against NO secretion of mouse peritoneal macrophages with an inhibition rate of 72.2% at 10 micromol x L(-1).
通过多种色谱技术相结合,包括硅胶柱色谱、葡聚糖凝胶LH - 20柱色谱和反相高效液相色谱,从粗壮润楠的乙醇提取物中分离出18种木脂素。通过光谱数据分析确定它们的结构分别为异落叶松脂醇-9'-O-β-D-吡喃木糖苷(1)、(+)-5'-甲氧基-异落叶松脂醇-9'-O-β-D-吡喃木糖苷(2)、落叶松脂醇-9'-O-β-D-吡喃木糖苷(3)、(+)-(8S,8'S)-4,4'-二羟基-3,3',5,5'-四甲氧基木脂素-9,9'-二醇9 - O-β-D-吡喃木糖苷(ssioriside,4)、落叶松脂醇(5)、内消旋二氢愈创木酸(6)、(+)-(8S,8'R)-3',4,4'-三羟基-3'-甲氧基木脂素(7)、(8S,8'R)-4'-羟基-3,3',4-三甲氧基木脂素(内消旋单甲基二氢愈创木酸,8)、(+)-愈创木脂素(9)、异愈创木脂素(10)、(-)-(7'R,8R,8'R)-4,4'-二羟基-3,3',5-三甲氧基-2,7'-环木脂素(11)、亨利辛B(12)、(-)-(7S,7'S,8R,8'R)-4,4'-二羟基-3,3',5,5'-四甲氧基-7,7'-环氧木脂素-9,9'-二醇(7S,7'S,8R,8'R-淫羊藿苷A2,13)、(+)-(7R,8R,7'E)-4-羟基-3,5'-二甲氧基-7,4'-环氧-8,3'-新木脂素-7'-烯(里卡林A,14)、南烛木脂素B(15)、润楠素-I(16)、(-)-松脂醇(17)和(-)-丁香树脂醇(18)。所有化合物均为首次从该植物中分离得到。在初步试验中,化合物17对小鼠腹腔巨噬细胞的NO分泌表现出抑制活性,在10微摩尔×L(-1)时抑制率为72.2%。