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宽舌橐吾的化学成分研究 被引量:13

Study on the Chemical Constituents of Ligularia platyglossa (Franch.) Hand .-Mazz.
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摘要 目的:研究宽舌橐吾(Ligulariaplatyglossa (Franch )Hand -Mazz )的化学成分,发现生物活性成分,为其资源开发利用奠定化学基础。方法:采用硅胶柱、SephadexLH 2 0柱和Rp 18反相柱层析法分离、重结晶纯化化合物,根据理化性质和波谱数据鉴定化合物结构。结果:从宽舌橐吾的根和根茎中分得艾里莫芬烷型倍半萜内酯类、黄酮类、苯甲酸类和吡咯里西啶生物碱类等7个已知化合物,分别为:Eremophil 1(10 ) ,7(11) ,8(9)- trien 12 ,8- olide(1) ;8βHydroxy eremophil- 7(11) ,9(10 )- dien 12 ,8α- olide(2 ) ;2 - Oxo eremophil 1(10 ) ,7(11) ,8(9) - trien -12 ,8- olide(3) ;黄颜木素(Fisetin) (4) ;异香草酸(Isovanillicacid ,即3 -Hydroxy- 4 - methoxy benzoicacid) (5 ) ;7- Angelyhe -liotridine(6 ) ;胡萝卜苷(7)。结论:以上化合物均为首次从宽舌橐吾中分得,其中化合物2~6为首次从橐吾属中分得,化合物3为新的天然产物。 AIM:To find out bioactive compounds from Ligula ria pl atyglossa. METHOD: Compounds were isolated by silica gel, Sep hadex LH-20 and Rp-18 column chromatography,and purified by recrystallizati on . Their structures were identified by NMR spectral data and other methods. RESULT: Seven compounds were isolated and identified as Eremophil-1( 10),7(11),8(9) -trien-12,8-olide (1); 8β-Hydroxy-ere mophil-7(11),9(10)) -dien-12,8α-olide (2);2-Oxo-erem ophil-1(10),7(11),8(9) -trien-12,8-olide (3);Fisetin (4); Isovanillic acid (5);7-Angelyhelio tridine (6) and Daucosterol (7), respective ly.CONCLUSION: All of the compounds were isolated from this plant for the first time and compounds 2, 3, 4, 5 and 6 were isolated from Ligularia genus for the first time. Compound 3 was a new natural entity.
出处 《中国药科大学学报》 CAS CSCD 北大核心 2005年第2期114-117,共4页 Journal of China Pharmaceutical University
基金 国家自然科学基金资助项目 (No 3 0 2 70 15 7)~~
关键词 菊科 橐吾属 宽舌橐吾 化学成分 Compositae Ligularia Genus Ligularia platyglossa Chemical constitu ents
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  • 10[10]13C-NMR spectral data of compounds 1-4. (1): C-1 - C-15: 34.1, 30.1, 21.3, 34.7, 43.6, 31.9, 149.3, 151.3, 113.0, 72.9, 122.9, 172.1, 8.4, 15.5, 15.7; (2): C-1 - C-15: 29.8, 29.4, 22.6, 34.0, 43.5, 36.4, 150.8, 147.4, 111.2, 74.0, 122.1, 171.6, 8.3, 14.3, 16.0, (3): C-1 - C-15: 36.5, 30.7, 26.6, 43.7, 45.7, 32.3, 158.7, 100.4, 118.1, 152.1, 122.2, 172.0, 8.0, 15.4, 17.5, (4): C-1 - C-15: 37.2, 27.2, 25.8, 40.8, 41.2, 45.2, 158.7, 103.0, 126.8, 136.6, 123.1, 172.2, 8.1, 15.8, 17.8,1H-NMR spectral data of compounds 1-4. (1): 1.92 m, H-1; 1.58 m, H-1(; 1.36 m, H-2; 1.42 m, H-2(; 1.49 m, H-3; 1.82 m, H-3(; 2.23 m, H-4α; 2.64 br d (13.0), H-6α; 2.59 d (13.0), H-6β; 5.48 br s, H-9; 1.85 d (1.4), H-13; 0.83 s, H-14; 0.85 d (6.6), H-15; 3.76 br, OH. (2):1.82 ddd (13.0, 13.0, 4.2), H-1; 1.62 m, H-1(; 1.28 m, H-2; 1.35 m, H-2(; 1.58 m, H-3; 1.62 m, H-3(; 1.76 m, H-4α; 2.59 br d (13.0), H-6α; 2.57 br d (13.0), H-6β; 5.42 br s, H-9; 1.84 br s, H-13; 1.02 s, H-14; 0.76 d (6.8), H-15; (3): 2.12 m, H-1 & H-1'; 1.35 m, H-2; 1.45 m, H-2(; 1.38 m, H-3; 1.47 m, H-3(; 1.55 m, H-4α; 2.38 br d (12.6), H-6α; 2.69 d (13.0), H-6β; 5.66 br s, H-9; 1.76 d (1.4), H-13; 0.85 s, H-14; 0.90 d (6.8), H-15; (4): 2.52 dd (14.5, 2.6), H-1; 2.15 m, H-1(; 1.45 m, H-2; 2.13 m, H-2(; 1.34 m, H-3; 1.42 m, H-3(; 1.67 m, H-4α; 2.75 d (14.6), H-6α; 2.73 d (14.6), H-6β; 5.58 t (2.5), H-9; 1.81 d (1.4), H-13; 0.80 s, H-14; 0.97 d (6.8), H-15; 3.38 br, OH.

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