甘杰, 韦微, 谭锦妮, 沈梦如, 谭钦刚*. 壮药红花青藤中抑制NO生成的活性成分研究J. 药学学报, 2022,57(6): 1849-1854. doi: 10.16438/j.0513-4870.2022-0035
引用本文: 甘杰, 韦微, 谭锦妮, 沈梦如, 谭钦刚*. 壮药红花青藤中抑制NO生成的活性成分研究J. 药学学报, 2022,57(6): 1849-1854. doi: 10.16438/j.0513-4870.2022-0035
GAN Jie, WEI Wei, TAN Jin-ni, SHEN Meng-ru, TAN Qin-gang*. The NO inhibitory constituents from Illigera rhodanthaJ. Acta Pharmaceutica Sinica, 2022,57(6): 1849-1854. doi: 10.16438/j.0513-4870.2022-0035
Citation: GAN Jie, WEI Wei, TAN Jin-ni, SHEN Meng-ru, TAN Qin-gang*. The NO inhibitory constituents from Illigera rhodanthaJ. Acta Pharmaceutica Sinica, 2022,57(6): 1849-1854. doi: 10.16438/j.0513-4870.2022-0035

壮药红花青藤中抑制NO生成的活性成分研究

The NO inhibitory constituents from Illigera rhodantha

  • 摘要: 采用硅胶、ODS柱色谱、Sephadex LH-20等分离方法对红花青藤藤茎醇提物的化学成分进行分离纯化,通过其理化性质及波谱数据对分离得到的化合物进行结构表征。从红花青藤藤茎醇提物中共分离得到16个化合物:(2R,3R)-2,3-dihydroxy-2-methylbutane-1,4-diyldibenzoate (1)、反式-阿魏酸对羟基苯乙酯(2)、4-O-benzoyl-2-C-methyl-D-erythritol (3)、N-反式阿魏酰基-3-甲基多巴胺(4)、tribulusamide A (5)、柳杉二醇(6)、teuclatriol (7)、齐墩果酸(8)、icario A29)、香草酸(10)、对羟基苯甲酸(11)、没食子酸(12)、没食子酸乙酯(13)、大黄酚(14)、D-1-O-甲基-肌醇(15)和十六烷酸(16)。其中1为新化合物,其绝对构型采用Mosher法并结合ROESY法确定;除101114外,其他化合物均是首次从青藤属中分离得到。与阳性对照药吲哚美辛相比,化合物4689对LPS诱导RAW264.7细胞生成NO均有显著的抑制作用。

     

    Abstract: Sixteen compounds were isolated from the ethanol extract of Illigera rhodantha by silica gel, ODS, and Sephadex LH-20 column chromatographies. These compounds were identified as (2R,3R)-2,3-dihydroxy-2-methylbutane-1,4-diyldibenzoate (1), p-hydroxyphenethyl trans-ferulate (2), 4-O-benzoyl-2-C-methyl-D-erythritol (3), N-trans feruloyl-3-methyldopamine (4), tribulusamide A (5), cryptomeridiol (6), teuclatriol (7), oleanolic acid (8), icario A2 (9), vanillic acid (10),p-hydroxybenzoic acid (11), gallic acid (12), ethyl gallate (13), chrysophanol (14), D-1-O-methyl-inositol (15), and hexadecanoic acid (16) based on their spectral data and physico-chemical properties. Compound 1 is an undescribed compound, of which its absolute configurations were determined by Mosher and ROESY methods; all the compounds except 10, 11 and 14 were isolated from Illigera genus for the first time. Compared with the positive control indomethacin, compounds 4-6, 8 and 9 inhibited significantly against the NO production in LPS-induced RAW 264.7 cells.

     

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