蒋跃平, 刘玉凤, 郭庆兰, 徐成博, 林生, 朱承根, 杨永春, 石建功. 党参水提取物中的木脂素类化学成分J. 药学学报, 2016,51(4): 616-625. doi: 10.16438/j.0513-4870.2015-0874
引用本文: 蒋跃平, 刘玉凤, 郭庆兰, 徐成博, 林生, 朱承根, 杨永春, 石建功. 党参水提取物中的木脂素类化学成分J. 药学学报, 2016,51(4): 616-625. doi: 10.16438/j.0513-4870.2015-0874
JIANG Yue-ping, LIU Yu-feng, GUO Qing-lan, XU Cheng-bo, LIN Sheng, ZHU Cheng-gen, YANG Yong-chun, SHI Jian-gong. Lignanoids from an aqueous extract of the roots of Codonopsis pilosulaJ. Acta Pharmaceutica Sinica, 2016,51(4): 616-625. doi: 10.16438/j.0513-4870.2015-0874
Citation: JIANG Yue-ping, LIU Yu-feng, GUO Qing-lan, XU Cheng-bo, LIN Sheng, ZHU Cheng-gen, YANG Yong-chun, SHI Jian-gong. Lignanoids from an aqueous extract of the roots of Codonopsis pilosulaJ. Acta Pharmaceutica Sinica, 2016,51(4): 616-625. doi: 10.16438/j.0513-4870.2015-0874

党参水提取物中的木脂素类化学成分

Lignanoids from an aqueous extract of the roots of Codonopsis pilosula

  • 摘要: 通过正相硅胶、大孔吸附树脂、MCI树脂、Sephadex LH-20、制备薄层色谱和反相HPLC等多种色谱分离方法相结合,从常用中药党参的水提取物中分离得到16个木脂素类化合物,借助波谱学分析方法鉴定它们的结构分别为:(-)-(7R,7'R,8R,8'S)-4,4-二羟基-3,3',5,5',7-五甲氧基-2,7'-环木脂烷(1)、(-)-(7R,8S)-二氢脱氢双松柏基醇4-O-β-吡喃葡萄糖基-(1"'→2")-β-吡喃葡萄糖苷(2)、(-)-(7R,8S)-二氢脱氢双松柏基醇(3)、(+)-(7S,8R)-脱氢二松柏基醇(4)、(+)-蛇菰脂醛素(5)、(+)-去甲氧基松脂素(6)、(+)-松脂素(7)、(+)-表松脂酚(8)、(-)-丁香脂素(9)、(-)-皮树脂醇(10)、(-)-落叶松脂醇(11)、(-)-开环异落叶松脂醇(12)、(-)-对映-异落叶松脂醇(13)、(+)-(7S,8S)-3-甲氧基-3',7-环氧-8,4'-氧新木脂素-4,9,9'-三醇(14)、(+)-(7S,8R)-3',4-二羟基-3-甲氧基-8,4'-氧新木脂素(15)和(-)-(7R,8R)-3',4-二羟基-3-甲氧基-8,4'-氧新木脂素(16)。以上化合物均为首次从党参中分离得到;其中,化合物1为一个新的2,7'-环木脂烷类天然产物,化合物2为一个新的4',7-环氧-8,3'-新木脂烷类双糖苷。在1×10-5 mol·L-1浓度下,化合物12对半胱氨酸亚铁(Fe2+-Cys)诱导大鼠肝微粒体脂质过氧化的抑制率为(63.4±8.3)%。

     

    Abstract: Sixteen lignanoids were isolated from an aqueous extract of the commonly used Chinese traditional medicine Dangshen, the dried roots of Codonopsis pilosula, by using a combination of various chromatographic techniques, including silica gel, macroporous adsorbent resin, MCI resin, sephadex LH-20, and reversed phase semi-preparative HPLC. On the basis of spectral data analysis, their structures were elucidated and identified as (-)-(7R, 7'R, 8R, 8'S)-4, 4'-dihydroxy-3, 3', 5, 5', 7-pentamethoxy-2, 7'-cyclolignane (1), (-)-(7R, 8S)-dihydrodehydrodiconiferyl alcohol 4-O-β-D-glucopyranosyl-(1"'→2")-β-D-glucopyranoside (2), (-)-(7R, 8S)-dihydrodehydrodiconiferyl alcohol (3), (+)-(7S, 8R)-dehydrodiconiferyl alcohol (4), (+)-balanophonin (5), (+)-demethoxypinoresinol (6), (+)-pinoresinol (7), (+)-epipinoresinol (8), (-)-syringaresinol (9), (-)-medioresinol (10), (-)-lariciresinol (11), (-)-secoisolariciresinol (12), (-)-ent-isolariciresinol (13), (+)-(7S, 8S)-3-methoxy-3', 7-expoxy-8, 4'-neolignan-4, 9, 9'-triol (14), (+)-(7S, 8R)-3', 4-dihydroxy-3-methoxy-8, 4'-neolignan (15), and (-)-(7R, 8R)-3', 4-dihydroxy-3-methoxy-8, 4'-neolignan (16). All these compounds were isolated from C. pilosula for the first time, while compound 1 is a new natural product of 2, 7'-cyclolignan and 2 is a new 4', 7-epoxy-8, 3'-neolignan diglucoside. Compound 12 showed activity against Fe2+-cysteine induced rat liver microsomal lipid peroxidation with an inhibition ratio of (63.4±8.3)% at 1×10-5 mol·L-1.

     

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