应用天然产物 ›› 2018, Vol. 8 ›› Issue (2): 131-135.DOI: 10.1007/s13659-018-0159-9
• SHORT COMMUNICATION • 上一篇
Yuan-Liang Ma1,2, Xiao-Han Tang1, Wen-Juan Yuan1,3, Xiao Ding1, Ying-Tong Di1, Xiao-Jiang Hao1
收稿日期:
2018-02-26
修回日期:
2018-03-13
出版日期:
2018-04-24
发布日期:
2018-04-26
通讯作者:
Ying-Tong Di, Xiao-Jiang Hao
基金资助:
Yuan-Liang Ma1,2, Xiao-Han Tang1, Wen-Juan Yuan1,3, Xiao Ding1, Ying-Tong Di1, Xiao-Jiang Hao1
Received:
2018-02-26
Revised:
2018-03-13
Online:
2018-04-24
Published:
2018-04-26
Contact:
Ying-Tong Di, Xiao-Jiang Hao
Supported by:
摘要: A new ent-abietane diterpernoid, named ebracteolata D (1), along with 11 known analogues, was isolated from the roots of Euphorbia ebracteolata Hayata. The structure of 1 was elucidated on the basis of spectroscopic analysis and molecular modeling. Cytotoxicity of compounds 1-12 was evaluated as well as the effect on the NF-κB pathway. Among them, compound 12, jolkinolide B, displayed broad inhibitory effects against proliferation of tumor cell lines. Mechanistic studies indicated that the compound 12 can inhibit TNF-α induced NF-κB activation, thereby inducing tumor cell apoptosis.
Yuan-Liang Ma, Xiao-Han Tang, Wen-Juan Yuan, Xiao Ding, Ying-Tong Di, Xiao-Jiang Hao. Abietane Diterpernoids from the Roots of Euphorbia ebracteolata[J]. 应用天然产物, 2018, 8(2): 131-135.
Yuan-Liang Ma, Xiao-Han Tang, Wen-Juan Yuan, Xiao Ding, Ying-Tong Di, Xiao-Jiang Hao. Abietane Diterpernoids from the Roots of Euphorbia ebracteolata[J]. Natural Products and Bioprospecting, 2018, 8(2): 131-135.
1. M. Karin, Nature 441, 431-436 (2006) 2. M.B. Alj, V. Barbu, M. Fillet, A. Chariot, B. Relic, N. Jacobs, J. Gielen, M.P. Merville, V. Bours, Oncogene 22, 90-97 (2003) 3. A.S. Baldwin, J. Clin. Invest. 107, 241-246 (2001) 4. H.M. Shen, V. Tergaonkar, Apoptosis 14, 348-363 (2009) 5. J.M. Barret, A. Bouchou, M.L. Marionneau, V. Offrete, N. Cabrol, C. Bailly, Can. Res. 64, 460-460 (2004) 6. A. Vasas, J. Hohmann, Chem. Rev. 114, 8579-8612 (2014) 7. C.S. Huang, S.H. Luo, Y.L. Li, C.H. Li, J. Hua, Y. Liu, S.X. Jing, Y. Wang, M.J. Yang, S.H. Li, Nat. Prod. Bioprospect. 4, 91-92 (2014) 8. Y.F. Yang, J.Q. Peng, L. Shi, Z.R. Li, M.H. Qiu, Nat. Prod. Bioprospect. 3, 99-102 (2013) 9. Chinese Pharmacopoeia Commission, Pharmacopoeia of the People's Republic of China. I (China Medical Science Press, Beijing, 2010) 10. W.J. Yuan, G.P. Yang, J.H. Zhang, Y. Zhang, D.Z. Chen, S.L. Li, Y.T. Di, X.J. Hao, Phytochem. Lett. 18, 176-179 (2016) 11. W.J. Yuan, W.F. Gao, J.H. Zhang, P. Cao, Y. Zhang, D.Z. Chen, S.L. Li, Y.T. Di, X.J. Hao, Nat. Prod. Commun. 12, 63-65 (2017) 12. W.J. Yuan, X. Ding, Z. Wang, B.J. Yang, X.N. Li, Y. Zhang, D.Z. Chen, S.L. Li, Q. Chen, Y.T. Di, H.A. Aisa, X.J. Hao, Sci. Rep. 7, e14507 (2017) 13. Y. Li, M. Xu, X. Ding, C. Yan, Z.Q. Song, L.W. Chen, X.H. Huang, X. Wang, Y.L. Jian, G.H. Tang, C.Y. Tang, Y.T. Di, S.Z. Mu, X.Z. Liu, K. Liu, T. Li, Y.C. Wang, L. Miao, W.X. Guo, X.J. Hao, C.L. Yang, Nat. Cell. Biol. 18, 1065-1077 (2016) 14. A.R. Lal, R.C. Cambie, P.S. Rutledge, P.D. Woodgate, Phytochemistry 29, 2239-2246 (1990) 15. W.X. Wang, X.B. Ding, Acta. Pharm. Sin. 33, 128-131 (1998) 16. H.M. Shi, L.D. Williams, H.H. Sung, H.X. Zhu, Y.I. Nancy, Z.D. Min, Planta Med. 71, 349-354 (2005) 17. Z.G. Liu, Z.L. Li, D.H. Li, N. Li, J. Bai, F. Zhao, D.L. Meng, H.M. Hua, Bioorg. Med. Chem. Lett. 26, 1-5 (2016) 18. D. Uemura, Y. Hirata, Tetrahedron Lett. 15, 1387-1390 (1972) 19. X.Z. Kuang, W. Li, Y. Kanno, N. Yamashita, S. Kikkawa, I. Azumaya, K. Nemoto, Y. Asada, K. Koike, J. Nat. Med. 70, 412-422 (2016) 20. T. Morgenstern, M. Bittner, M. Silva, P. Aqueveque, J. Jakupovica, Phytochemistry 41, 1149-1153 (1996) 21. P.W. Wang, S.M. Henning, D. Herbe, PLoS ONE 5, e10202 (2010) 22. C. Lv, X.H. Yan, Q. Tu, Y.T. Di, C.M. Yuan, X. Fang, Y. BenDavid, L. Xia, J.X. Gong, Y.M. Shen, Z. Yang, X.J. Hao, Angew. Chem. Int. Ed. 55, 7539-7543 (2016) 23. Y. Yan, J.X. Zhang, T. Huang, X.Y. Mao, W. Gu, H.P. He, Y.T. Di, S.L. Li, D.Z. Chen, Y. Zhamg, X.J. Hao, J. Nat. Prod. 78, 811-821 (2015) 24. X.H. Yan, Y.T. Di, X. Fang, S.Y. Yang, H.P. He, S.L. Li, Y. Lu, X.J. Hao, Phytochemistry 72, 508-513 (2011) 25. F.G. Zeng, Q. Su, Y.T. Di, X.J. Hao, Nat. Prod. Res. Dev. 28, 1171-1175 (2016) |
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