Abstract
One new 1,10-secoeudesmanolide (1), two eudesmanolides (2 and 3), together with nine known compounds (4–12) were isolated from the aerial parts of Inula britannica. The structures of the new compounds were elucidated by detailed spectroscopic analysis, including HRESIMS and 2D-NMR spectroscopic method. In addition, compounds 1–4 were tested for their inhibitory effects against LPS-induced NO production in RAW264.7 macrophages.
Similar content being viewed by others
References
Agrawal, P.K. 1989. Carbon- 13 NMR of flavonoids, 102. Elsevier Scientific Publishing Company: Amsterdam.
Ahmed, D., M.I. Choudhary, S. Turkoz, and B. Sener. 1988. Chemical constituents of Buxus sempervirens. Planta Medica 54(2): 173–174.
Bensky, D., A. Gamble, T.J. Kaptchuk, and I.L. Bensky. 1993. Chinese herbal medicine: Materia Medica, 193–194. Seattle: Eastland Press.
Horie, T., Y. Ohtsuru, K. Shibata, K. Yamashita, M. Tsukayama, and Y. Kawamura. 1998. 13C NMR spectral assignment of the A-ring of polyoxygenated flavones. Phytochemistry 47: 865–874.
Jiangsu New Medical College. 1977. Dictionary of Traditional Chinese Materia Medica, vol. 2, 2216–2219. Shanghai: Shanghai People’s Press.
Jin, H.Z., D.H. Lee, J.H. Lee, K. Lee, Y.S. Hong, D.H. Choung, H.Y. Kim, and J.J. Lee. 2006. New sesquiterpene dimers from Inula britannica inhibit NF-κB activation and NO and TNF-production in LPS-stimulated RAW264.7 cells. Planta Medica 72(1): 40–45.
Khan, A.L., J. Hussain, M. Hamayun, S.A. Gilani, S. Ahmad, G. Rehman, Y.-H. Kim, S.-M. Kang, and I.-J. Lee. 2010. Secondary metabolites from Inula britannica L. and their biological activities. Molecules 15: 1562–1577.
Lin, R., D.J. Yu, and Z.Y. Wu. 1989. Flora of China, 263–265. Beijing: Science Press.
Liang, Y.H., M. Ye, J. Han, B.R. Rong, and D.A. Guo. 2011. Lignans and flavonoids from rhizome of Drynaria fortune. Chinese Traditional and Herbal Drugs 42(1): 25–30.
Schmidt, H.H.H.W., and M. Kelm. 1996. Determination of nitrite and nitrate by the Griess reaction. In Methods in Nitric oxide research, Chap. 33, ed. M. Feelisch, and J. Stramler, 491–497. New York: Wiley.
Yang, C., C.M. Wang, and Z.J. Jia. 2003. Sesquiterpenes and other constituents from the aerial parts of Inula japonica. Planta Medica 69: 662–666.
Yuan, J.Q., Y.N. Yan, Y.F. Liu, and J.H. Miu. 2007. Studies on flavonoids of Eupatorium odoratum L. Journal of Chinese Medicinal Materials 30(6): 657–660.
Zhu, J.X., J.J. Qin, H.R. Wang, Y. Zhu, W.D. Zhang, and H.Z. Jin. 2011. Monoterpenes and other chemical constituents from the aerial parts of Inula japonica. Chemistry of Natural Compounds 47(2): 303–305.
Acknowledgments
The work was supported by program NCET Foundation, NSFC (81230090 and 81102778), partially supported by Global Research Network for Medicinal Plants (GRNMP) and King Saud University, Shanghai Leading Academic Discipline Project (B906), FP7-PEOPLE-IRSES-2008 (TCMCANCER Project 230232), Key laboratory of drug research for special environments, PLA, Shanghai Engineering Research Center for the Preparation of Bioactive Natural Products (10DZ2251300) and the Scientific Foundation of Shanghai China (10DZ1971700, 12401900501). National Major Project of China (2011ZX09307-002-03 and 2011ZX09102-006-02). National Key Technology R&D Program of China (2012BAI29B06).
Author information
Authors and Affiliations
Corresponding author
Additional information
Xu-Feng Zhang and Jing-Ling Du have contributed equally to this work.
Rights and permissions
About this article
Cite this article
Zhang, XF., Du, JL., Ren, J. et al. Three new sesquiterpene lactones from Inula britannica . Arch. Pharm. Res. 38, 666–672 (2015). https://doi.org/10.1007/s12272-014-0388-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12272-014-0388-3