Natural Products and Bioprospecting    2015, Vol. 5 Issue (6) : 271-275     DOI: 10.1007/s13659-015-0075-1
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New Alkaloids from Aconitum stapfianum
Tian-Peng Yin,Le Cai,Ying Li,Yun-Shan Fang, Li Peng,Zhong-Tao Ding
Key Laboratory of Medicinal Chemistry for Nature Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091, China
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Abstract  Nineteen alkaloids, including a new C19-diterpenoid alkaloid stapfianine A(1) and a new benzamide derivative stapfianine B(2) were isolated from the roots of Aconitum stapfianum. Their structures were established on the basis of extensive spectroscopic analyses(IR, HRESIMS, 1D and 2D NMR).
Keywords Aconitum stapfianum      Ranunculaceae      Diterpenoid alkaloid      Benzamide      Stapfianine     
Fund:This project was financially supported by grants from the National Natural Science Foundation of China(No. 81460648), the Program for Changjiang Scholars and Innovative Research Team in University(No. IRT13095) and from the Postgraduate Foundation of Yunnan University(No. YNUY201415).
Issue Date: 11 February 2018
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Tian-Peng Yin,Le Cai,Ying Li, et al. New Alkaloids from Aconitum stapfianum[J]. Natural Products and Bioprospecting, 2015, 5(6): 271-275.
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http://npb.kib.ac.cn/EN/10.1007/s13659-015-0075-1     OR     http://npb.kib.ac.cn/EN/Y2015/V5/I6/271
1. Institute of Botany, Chinese Academy of Science, Institute of Materia Medica and Chinese Academy of Medical Sciences, Flora reipublicae populais sinica, vol. 27 (Science Press, Beijing, 1979), p. 248
2. P.G. Xiao, F.P. Wang, F. Gao, L.P. Yan, D.L. Chen, Y. Liu, Acta Phytotaxon. Sin. 44, 1 (2006)
3. T.P. Yin, L. Cai, H.X. Fang, Y.S. Fang, Z.J. Li, Z.T. Ding, Phytochemistry 116, 314 (2015)
4. T.P. Yin, L. Cai, G. Lei, J.W. Dong, Y.X. Liu, Z.T. Ding, Chin. J. Org. Chem. 33, 2528 (2013)
5. H. Yan, D.L. Chen, X.X. Jian, F.P. Wang, Helv. Chim. Acta 90, 1133 (2007)
6. F.P. Wang, Q.H. Chen, X.Y. Liu, Nat. Prod. Rep. 27, 529 (2010)
7. T.P. Yin, L. Cai, J.M. He, J.W. Dong, H.X. Fang, H. Zhou, Z.T. Ding, J. Asian Nat. Prod. Res. 16, 345 (2014)
8. C.S. Peng, D.L. Chen, Q.H. Chen, F.P. Wang, Chin. J Org. Chem. 25, 1235 (2005)
9. L.M. Sun, H.L. Huang, W.H. Li, Z.D. Nan, G.X. Zhao, C.S. Yuan, Helv. Chim. Acta 92, 1126 (2009)
10. J. Zhang, G.B. Sun, Q.F. Lei, G.Z. Li, J.C. Wang, J.Y. Si, Acta Pharm. Sin. 49, 1150 (2014)
11. J.G. Diaz, J.L. Marapara, F. Valdes, J.G. Sazatornil, W. Herz, Phytochemistry 66, 733 (2005)
12. T.H. Lee, Y.C. Chen, C.K. Lee, C.C. Kuo, H.S. Chang, C.Y. Chao, J.J. Lin, L.C. Lo, Y.H. Kuo, Nat. Prod. Commun. 8, 827 (2013)
13. D. Hüerlander, R. Frohlich, G. Erker, J. Chem. Soc., Dalton Trans., 1513 (2002)
14. Z.B. Li, F.P. Wang, Chin. Chem. Lett. 7, 443 (1996)
15. T.X. Tang, D.L. Chen, F.P. Wang, Chin. J. Org. Chem. 34, 909 (2014)
16. F.P. Wang, Z.B. Li, X.P. Dai, C.S. Peng, Phytochemistry 45, 1539 (1997)
17. D.L. Chen, Q.H. Chen, X.X. Jian, F.P. Wang, Nat. Prod. Res. Dev. 14, 6 (2001)
18. J.B. Hanuman, A. Katz, Phytochemistry 36, 1527 (1994)
19. F.P. Wang, X.T. Liang, Planta Med. 51, 443 (1985)
20. A. EI-Shazly, M. Wink, Z. Naturforsch. 58, 477 (2003)
21. Y. Kashiwada, A. Aoshima, Y. Ikeshiro, Y.P. Chen, H. Furukawa, M. Itoigawa, T. Fujioka, K. Mihashi, L.M. Cosentino, S.L. MorrisNatschke, K.H. Lee, Bioorg. Med. Chem. 13, 443 (2005)
22. E.E. Elgorashi, S.E. Drewes, J. Van Staden, Phytochemistry 56, 637 (2001)
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