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Furostanol saponins with inhibitory action against COX-2 production from Tupistra chinensis rhizomes 被引量:3

Furostanol saponins with inhibitory action against COX-2 production from Tupistra chinensis rhizomes
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摘要 Two furostanol saponins were obtained from the n-butanol fraction of methanol extract from Tupistra chinensis rhizomes, a folk medicine of Shennongjia Forest District of Hubei Province. Their structures were determined as (25S)-26-O-(β-D-glucopyranosyl)- furost-1β, 3β, 22α, 26-tetrol-3-O-β-D-glucopyranosyl-(1 → 4)-β-D-glucopyranosyl-(1 → 2)-β-D-glucopyranoside (1) and (25R)- 26-O-(β-D-glucopyranosyl)-furost-1β, 3β 22a, 26-tetrol 3-O-β-D-glucopyranosyl-(1 → 4)-β-D-glucopyranosyl-(1 → 2)-β-D-glu- copyranoside (2), on basis of chemical and spectroscopic evidences. 1 and 2 displayed marked inhibitory action towards COX-2 production in macrophages of the rat abdomen induced by LPS at 20 μg/mL. Two furostanol saponins were obtained from the n-butanol fraction of methanol extract from Tupistra chinensis rhizomes, a folk medicine of Shennongjia Forest District of Hubei Province. Their structures were determined as (25S)-26-O-(β-D-glucopyranosyl)- furost-1β, 3β, 22α, 26-tetrol-3-O-β-D-glucopyranosyl-(1 → 4)-β-D-glucopyranosyl-(1 → 2)-β-D-glucopyranoside (1) and (25R)- 26-O-(β-D-glucopyranosyl)-furost-1β, 3β 22a, 26-tetrol 3-O-β-D-glucopyranosyl-(1 → 4)-β-D-glucopyranosyl-(1 → 2)-β-D-glu- copyranoside (2), on basis of chemical and spectroscopic evidences. 1 and 2 displayed marked inhibitory action towards COX-2 production in macrophages of the rat abdomen induced by LPS at 20 μg/mL.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第10期1239-1242,共4页 中国化学快报(英文版)
基金 financially supported by the National Natural Science Foundation of China(No.30670213) Key Scientific Program of China Three Gorges University(No.2005ZD007).
关键词 Tupistra chinensis Bak. Furostanol saponin COX-2 Folk medicines Tupistra chinensis Bak. Furostanol saponin COX-2 Folk medicines
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  • 1[1]M.Q.Chen,Chin.Bull.Bot.16 (1999) 37 (in Chinese).
  • 2[2]J.B.Zhang,B.Yu,Y.Z.Hui,Chin.J.Org.Chem.20 (2000) 663 (in Chinese).
  • 3[3](a) K.Hostettmann,A.Marston,Saponins (Chemistry and Pharmacology of Natural Products),Cambridge University Press,Cambridge,1995,p.76;(b)K.Hostettmann,A.Marston,Saponins (Chemistry and Pharmacology of Natural Products),Cambridge University Press,Cambridge,1995,p.287.
  • 4[4]P.K.Agrawal,D.C.Jain,R.K.Gupta,et al.Phytochemistry 24 (1985) 2479.
  • 5[5]S.J.Wu,T.Zhao,Y.Q.Qin,Modern Chemistry of Constituents from Traditional Chinese Medicines,China Medical and Pharmaceutical Science and Technology Press,Beijing,2002,p.564 (in Chinese).
  • 6[6]S.G.Sparg,M.E.Light,J.van Staden,J.Ethnopharm.94 (2004) 219.
  • 7[7]M.V.D'Auria,L.Minale,R.Riccio,Chem.Rev.93 (1993) 1839.
  • 8[8]Y.H.Zhan,Resources of Medicinal Plants in Shennongjia of China,Hubei Scientific and Technologic Press,Wuhan,1994 p.16 (in Chinese).
  • 9[9]K.Zou,J.Wu,M.Du,et al.Chin.Chem.Lett.18 (2007) 65.
  • 10[10]X.J.He,F.Qiu,Y.Shoyama,et al.J.Asian Nat.Prod.Res.4 (2002) 189.

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