Palcernuine, the first [5/6/6/6]-cernuane-type alkaloid from Palhinhaea cernua f. sikkimensis

Yu Tang Juan Xiong Yike Zou Bastien Nay Li-Jun Wang Jin-Feng Hu

引用本文: Yu Tang,  Juan Xiong,  Yike Zou,  Bastien Nay,  Li-Jun Wang,  Jin-Feng Hu. Palcernuine, the first [5/6/6/6]-cernuane-type alkaloid from Palhinhaea cernua f. sikkimensis[J]. Chinese Chemical Letters, 2016, 27(6): 969-973. doi: 10.1016/j.cclet.2016.02.014 shu
Citation:  Yu Tang,  Juan Xiong,  Yike Zou,  Bastien Nay,  Li-Jun Wang,  Jin-Feng Hu. Palcernuine, the first [5/6/6/6]-cernuane-type alkaloid from Palhinhaea cernua f. sikkimensis[J]. Chinese Chemical Letters, 2016, 27(6): 969-973. doi: 10.1016/j.cclet.2016.02.014 shu

Palcernuine, the first [5/6/6/6]-cernuane-type alkaloid from Palhinhaea cernua f. sikkimensis

  • 基金项目:

    The authors gratefully acknowledge Mr. Qiu-Shi Tan (Chongqing Institute of Medicinal Plant Cultivation, China) for the plant collection and identification. This work was supported by NSFC grants (Nos. 21472021, 81273401, 81202420), grants from the Ph.D. Programs Foundation of Ministry of Education (MOE) of China (Nos. 20120071110049, 20120071120049), and the National Basic Research Program of China (973 Program, No. 2013CB530700).

摘要: One novel (named palcernuine, 1) and five known cernuane-type (2-6) alkaloids were isolated from the whole plant of Palhinhaea cernua f. sikkimensis. The structure of 1, possessing an unprecedented [5/6/6/6]-tetracyclic ring system containing two nitrogen atoms, was established on the basis of spectroscopic methods, and its absolute configuration was determined by comparison of the experimental and calculated electronic circular dichroism (ECD) spectra. A plausible biosynthetic pathway to 1 is proposed.

English

    1. [1] Editor Committee for Flora of China of the Chinese Academy of Science, Flora of China, [7_TD$DIF]Vol. 6, Science Press, Beijing, 2004, pp. 69-73.

    2. [2] D.B. Zhang, J.J. Chen, L. Zhang, et al., Bioactive alkaloids from Palhinhaea cernua, Phytochem. Lett. 10 (2014) 76-79.

    3. [3] L.B. Dong, Y.N. Wu, S.Z. Jiang, et al., Isolation and complete structural assignment of Lycopodium alkaloid cernupalhine a: theoretical prediction and total synthesis validation, Org. Lett. 16 (2014) 2700-2703.

    4. [4] L.B. Dong, X. Gao, F. Liu, et al., Isopalhinine A, a unique pentacyclic Lycopodium alkaloid from Palhinhaea cernua, Org. Lett. 15 (2013) 3570-3573.

    5. [5] S. Morel, I. Kerzaon, V. Roumy, et al., A new cernuane-type alkaloid from Lycopodium cernuum, Biochem. Syst. Ecol. 45 (2012) 188-190.

    6. [6] L.B. Dong, J. Yang, J. He, et al., Lycopalhine A, a novel sterically congested Lycopodium alkaloid with an unprecedented skeleton from Palhinhaea cernua, Chem. Commun. 48 (2012) 9038-9040.

    7. [7] F.W. Zhao, Q.Y. Sun, F.M. Yang, et al., Lycopodium alkaloids from Palhinhaea cernua, J. Braz. Chem. Soc. 23 (2012) 349-354.

    8. [8] F.W. Zhao, Q.Y. Sun, F.M. Yang, et al., Palhinine A, a novel alkaloid from Palhinhaea cernua, Org. Lett. 12 (2010) 3922-3925.

    9. [9] H. Morita, Y. Hirasawa, T. Shinzato, et al., New phlegmarane-type, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium, Tetrahedron 60 (2004) 7015-7023.

    10. [10] X.Q. Ma, D.R. Gang, The Lycopodium alkaloids, Nat. Prod. Rep. 21 (2004) 752-772.

    11. [11] J. Yan, L. Sun, X. Zhang, et al., Serratene triterpenoids from Palhinhaea cernua var. sikkimensis, Chem. Pharm. Bull. 57 (2009) 1381-1384.

    12. [12] Y. Tang, Y. Fu, J. Xiong, et al., Casuarinines A-J, lycodine-type alkaloids from Lycopodiastrum casuarinoides, J. Nat. Prod. 76 (2013) 1475-1484.

    13. [13] Y. Tang, J. Xiong, J.F. Hu, Lycopodium alkaloids from Diphasiastrum complanatum, Nat. Prod. Commun. 10 (2015) 2091-2094.

    14. [14] W.A. Ayer, J.K. Jenkins, S. Valverde-Lopez, et al., The alkaloids of Lycopodium cernuum L. I. the structures of cernuine and lycocernuine, Can. J. Chem. 45 (1967) 433-443.

    15. [15] W.X. Wang, J.J. Zhu, Y.K. Zou, et al., Trichotomone, a new cytotoxic dimeric abietane-derived diterpene from Clerodendrum trichotomum, Tetrahedron Lett. 54 (2013) 2549-2552.

    16. [16] J. Wang, W.Z. Zhai, Y.K. Zou, et al., Eucalyptals D and E, new cytotoxic phloroglucinols from the fruits of Eucalyptus globulus and assignment of absolute configuration, Tetrahedron Lett. 53 (2012) 2654-2658.

    17. [17] M.J. Frisch, et al., Gaussian 09, Revision D. 01, Gaussian, Inc., Wallingford, CT, 2009.

    18. [18] W.A. Ayer, J.K. Jenkins, K. Piers, et al., The alkaloids of Lycopodium cernuum L. II. the stereochemistry of cernuine and lycocernuine, Can. J. Chem. 45 (1967) 445-450.

    19. [19] W.A. Ayer, J.K. Jenkins, S. Valverde-Lopez, et al., The alkalcids of Lycopodium cernuum, Tetrahedron Lett. 5 (1964) 2201-2209.

    20. [20] L. Marion, R.H.F. Manske, The alkaloids of Lycopodium species, Can. J. Res. 26B (1948) 1-2.

    21. [21] H. Morita, Y. Hirasawa, N. Yoshida, et al., Senepodine A, a novel C22N2 alkaloid from Lycopodium chinense, Tetrahedron Lett. 42 (2001) 4199-4201.

    22. [22] Y. Nishikawa, M. Kitajima, H. Takayama, First asymmetric total syntheses of cernuane-type Lycopodium alkaloids, cernuine, and cermizine D, Org. Lett. 10 (2008) 1987-1990.

    23. [23] J.C. Braekman, L. Nyembo, P. Bourdoux, et al., Alkaloid distribution in genus Lycopodium, Phytochemistry 13 (1974) 2519-2528.

    24. [24] S.B.Wu, Y.P. Ji, J.J. Zhu, et al., Steroids fromthe leaves of Chinese Melia azedarach and their cytotoxic effects on human cancer cell lines, Steroids 74 (2009) 761-765.

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  • 收稿日期:  2015-11-25
  • 修回日期:  2016-01-25
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