[Chemical constituents of butyl-phthalides from Ligusticum sinense].

Q3 Pharmacology, Toxicology and Pharmaceutics Zhongguo Zhongyao Zazhi Pub Date : 2025-01-01 DOI:10.19540/j.cnki.cjcmm.20241101.202
Hang Liu, Xue-Ming Zhou, Ting Zheng, Mei-Zhu Wu, Shuo Feng, Ye Lin, Xin-Ming Song, Ji-Ling Yi
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Abstract

Eight butyl-phthalides, senkyunolide K(1), senkyunolide N(2), butylphthalide(3), senkyunolide I(4), senkyunolide H(5),(Z)-butylidenephthalide(6),(Z)-ligustilide(7), and 3-butylidene-7-hydroxyphthalide(8) were isolated from the aerial part of Ligusticum sinense by column chromatography on silica gel column, ODS, Sephadex LH-20 and semi-preparative HPLC. Their structures were elucidated on the basis of spectroscopic and chemical data, especially NMR and MS. Compound 1 was a new butyl-phthalide and compounds 2-8 were isolated from the aerial part of L. sinense for the first time. Furthermore, the inhibitory activities of compounds 1-8 against the nitric oxide(NO) production induced by lipopolysaccharide(LPS) in mouse RAW264.7 macrophages in vitro were evaluated. The results showed that compounds 1-8 exerted inhibitory activities on NO production with IC_(50) of 19.34-42.16 μmol·L~(-1).

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[川芎丁酞的化学成分]。
采用硅胶柱层析、ODS、Sephadex LH-20和半制备高效液相色谱等方法,从Ligusticum sinense的气相部位分离得到8种丁基酞类化合物,分别为仙球内酯K(1)、仙球内酯N(2)、丁基酞(3)、仙球内酯I(4)、仙球内酯H(5)、(Z)-丁基酞(6)、(Z)-藁本内酯(7)和3-丁基酞-7-羟基酞(8)。其中化合物1为新发现的邻丁基化合物,化合物2 ~ 8为首次从L. sinense的地上部分分离得到。进一步研究了化合物1 ~ 8对脂多糖(LPS)诱导的小鼠RAW264.7巨噬细胞一氧化氮(NO)产生的体外抑制活性。结果表明,化合物1 ~ 8具有抑制NO生成的活性,IC_(50)为19.34 ~ 42.16 μmol·L~(-1)。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
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0.00%
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581
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