Natural Products and Bioprospecting    2021, Vol. 11 Issue (4) : 459-464     DOI: 10.1007/s13659-021-00310-3
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Tangutidines A-C, Three Amphoteric Diterpene Alkaloids from Aconitum tanguticum
Hao-Yi Li1,2, Bing-Chao Yan1, Li-Xin Wei3, Han-Dong Sun1, Pema-Tenzin Puno1
1 State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, and Yunnan Key Laboratory of Natural Medicinal Chemistry, Kunming 650201, People's Republic of China;
2 University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China;
3 Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety Evaluation, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810008, People's Republic of China
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Abstract  Three new diterpene alkaloids, tangutidines A-C (1-3), and four known alkaloids (4-7) were isolated from the whole plant of Aconitum tanguticum, from which amphoteric diterpene alkaloids (1-3) were obtained for the first time. The structures of 1-3 were elucidated by detailed interpretation of spectroscopic data, including MS and NMR data. All of them were evaluated for their cytotoxic activities.
Keywords Aconitum tanguticum      Amphoteric diterpene alkaloids      Tangutidine      Cytotoxic activity     
Fund:This project was supported financially by the Second Tibetan Plateau Scientific Expedition and Research (STEP) program (2019QZKK0502) and the National Natural Science Foundation of China (No. 81673329). Authors are grateful for Dr. Ming Zhang from northwest institute of plateau biology, Chinese Academy of Sciences, for the assistance for obtaining plant materials.
Corresponding Authors: Han-Dong Sun, Pema-Tenzin Puno     E-mail: hdsun@mail.kib.ac.cn;punopematenzin@mail.kib.ac.cn
Issue Date: 30 July 2021
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Hao-Yi Li,Bing-Chao Yan,Li-Xin Wei, et al. Tangutidines A-C, Three Amphoteric Diterpene Alkaloids from Aconitum tanguticum[J]. Natural Products and Bioprospecting, 2021, 11(4): 459-464.
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http://npb.kib.ac.cn/EN/10.1007/s13659-021-00310-3     OR     http://npb.kib.ac.cn/EN/Y2021/V11/I4/459
1. Y. Shen, W.J. Liang, Y.N. Shi, E.J. Kennelly, D.K. Zhao, Nat. Prod. Rep. 37, 763-796 (2020)
2. J. Wang, X.H. Meng, T. Chai, J.L. Yang, Y.P. Shi, Nat. Prod. Bioprospect. 9, 419-423 (2019)
3. T.P. Yin, L. Cai, Y. Li, Y.S. Fang, L. Peng, Z.T. Ding, Nat. Prod. Bioprospect. 5, 271-275 (2015)
4. D.S. Luo, Chinese Tibetan Herbal Medicine (Nationalities Publishing House, Beijing, 1997), pp. 65-66
5. Z.M. Liu, S.Y. Qin, J.F. Zhao, X. Liu, C.H. Wang, Z.W. Zhang, W.Z. Luo, G.Y. Zhong, J. World Sci. Technol. Mod. Tradit. Chin. Med. Mater. Med. 19, 636-643 (2017)
6. X.R. Fan, L.H. Yang, Z.H. Liu, L.M. Lin, C. Li, S.S. Guo, Z.M. Wang, Z.J. Wang, F. Sui, Phytochemistry 160, 71-77 (2019)
7. B.S. Joshi, Y.L. Bai, D.H. Chen, S.W. Pelletier, W.T. Wang, Tetrahedron Lett. 34, 7525-7528 (1993)
8. J.X. Cao, L.B. Li, J. Ren, S.P. Jiang, R.R. Tian, X.L. Chen, S.L. Peng, J. Zhang, H.J. Zhu, Helv. Chim. Acta 91, 1954-1960 (2008)
9. L. Li, J.F. Zhao, Y.B. Wang, H.B. Zhang, Helv. Chim. Acta. 87, 866-868 (2004)
10. S.J. Qu, C.H. Tian, Z.L. Liu, S.H. Jiang, L. Yu, D.Y. Zhu, J. Phytochem. Lett. 4, 144-146 (2011)
11. L. Lin, D.L. Chen, X.Y. Liu, Q.H. Chen, F.P. Wang, Helv. Chim. Acta. 93, 118-122 (2010)
12. S.W. Pelletier, B.S. Joshi, D.H. Chen, X.L. Zhang, J.K. Snyder, W.T. Wang, Heterocycles 32, 1793-1804 (1991)
13. Y.B. Wang, R. Huang, H.B. Zhang, L. Li, Helv. Chim. Acta. 88, 1081-1084 (2005)
14. H.K. Desai, S.W. Pelletier, J. Nat. Prod. 56, 2193-2197 (1993)
15. L. Xu, M. Luo, L.M. Lin, X. Zhang, C. Li, Z.M. Wang, Y.M. Luo, J. Asian Nat. Prod. Res. 15, 743-749 (2013)
16. Y.R. Li, L. Xu, C. Li, Z.M. Wang, L.X. Yang, J. Asian Nat. Prod. Res. 16, 730-734 (2014)
17. R.F. Wang, X.W. Yang, C.M. Ma, S.Q. Cai, J.N. Li, Y. Shoyama, Heterocycles 63, 1443-1448 (2004)
18. Z.C. He, D.M. Wang, G.C. Li, J.Y. Wu, Chin. Tradit. Herb. Drugs 45, 1526-1531 (2014)
19. Z.H. Gao, L.M. Kong, X.S. Zou, Y.M. Shi, S.Z. Shang, H.R. Luo, C.Q. Liang, X.N. Li, Y. Li, X. Du, W.L. Xiao, H.D. Sun, Nat. Prod. Bioprospect. 2, 249-254 (2013)
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