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DOI: 10.1055/s-2006-931565
© Georg Thieme Verlag KG Stuttgart · New York
Lignans from Saussurea conica and their NO Production Suppressing Activity
Publikationsverlauf
Received: July 28, 2005
Accepted: January 10, 2006
Publikationsdatum:
24. April 2006 (online)
Abstract
Three new lignan derivatives, conicaols A and B and conicaoside, together with seven known compounds were identified from Saussurea conica. Their structures were elucidated by spectral methods including 1D and 2D NMR techniques. Six 2,3-dibenzylbutyrolactone-type lignans were biologically evaluated, and two of them, arctigenin and matairesinol, showed potent activity to suppress NO production in vitro in LPS-activated macrophages of SD rat.
Key words
Saussurea conica - Asteraceae - conicaols A and B - conicaoside - NO production suppressing activity
References
- 1 Jiangsu New Medical C ollege. Dictionary of Chinese Traditional Medicines. Shanghai; Shanghai Scientific and Technologic Press 1986: p 2087-8
- 2 Fan C Q, Yue J M. Biologically active phenols from Saussureae medusa . Bioorg Med Chem. 2003; 11 703-8
- 3 Fan C Q, Zhan Z J, Li H, Yue J M. Eudesmane type sesquiterpene derivatives from Saussurea conica . Helv Chim Acta. 2004; 87 1446-51
- 4 Fushiya S, Kabe Y, Ikegaya Y, Takano F. (+)-Rhododendrol and epi-rhododendrin suppress the NO production by activated macrophages in vivo . Planta Med. 1998; 64 598-602
- 5 Green L C, Wagner D A, Glogowski J, Skipper P L, Wishnok J S, Tannenbaum S R. Analysis of nitrate, nitrite and 15N nitrate in biological fluids. Anal Biochem. 1982; 126 131-8
- 6 Agrawal P K, Thakur R S. 13C NMR spectroscopy of lignan and neolignan derivatives. Magn Reson Chem. 1985; 23 389-93
- 7 Han B H, Kang Y H, Yang H O, Park M K. A butyrolactone lignan dimer from Actium lappa . Phytochemistry. 1994; 37 1161-3
- 8 Tiwari A K, Srinivas P V, Kumar S P, Rao J M. Free radical scavenging active components from Cedrus deodara . J Agric Food Chem. 2001; 49 4642-5
- 9 Rahman M MA, Dewick P M, Jackson D E, Lucas J A. Lignans of Forsythia intermedia . Phytochemistry. 1990; 29 1971-80
- 10 Nishibe S, Tsukamoto H, Hisada S. Effects of O-methylation and O-glucosylation on 13C NMR chemical shifts of matairesinol, (+)-pinoresinol and (+)-epipinoresinol. Chem Pharm Bull. 1984; 32 4653-7
- 11 Nishibe S, Okabe K, Hisada S. Isolation of phenolic compounds and spectroscopic analysis of a new lignan from Trachelospermum asiaticum . Chem Pharm Bull. 1981; 29 2078-82
- 12 Alberto M J, Sanz-Cervera J F, Garcia-Lliso V, Susanna A, Garcia-Jacas N. Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species. Phytochemistry. 1994; 37 1101-7
- 13 Wang H Y, Yang J S. Chemical components from Arctium lappa . Acta Pharmaceutica Sin. 1993; 28 911-7
- 14 Heiman A S, Ko D H, Chen M Q, Lee H J. New steroidal anti-inflammatory antedrugs: methyl 3,20-dioxo-9α-fluoro-11β,17α,21-trihydroxy-1,4-pregnadiene-16α-carboxylate and methyl 21-acetyloxy-3,20-dioxo-11β,17α-dihydroxy-9α-fluoro-1,4-pregnadiene-16α-carboxylate. Steroids. 1997; 62 491-9
Prof. Jian-Min Yue
State Key Laboratory of Drug Research
Institute of Materia Medica
Shanghai Institute for Biological Sciences
Chinese Academy of Sciences
555 Zu Chong Zhi Road
Zhangjiang Hi-Tech Park
Shanghai 201203
People’s Republic of China
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eMail: jmyue@mail.shcnc.ac.cn