应用天然产物 ›› 2020, Vol. 10 ›› Issue (1): 45-49.DOI: 10.1007/s13659-020-00233-5
Xin-Yu Jia1, Yong-Mei Wu2, Jing-Ya Li2, Chun Lei1, Ai-Jun Hou1
收稿日期:
2020-01-14
修回日期:
2020-02-06
出版日期:
2020-02-24
发布日期:
2020-02-29
通讯作者:
Chun Lei, Ai-Jun Hou
基金资助:
Xin-Yu Jia1, Yong-Mei Wu2, Jing-Ya Li2, Chun Lei1, Ai-Jun Hou1
Received:
2020-01-14
Revised:
2020-02-06
Online:
2020-02-24
Published:
2020-02-29
Contact:
Chun Lei, Ai-Jun Hou
Supported by:
摘要: Four new alkaloids, ficuhismines A-D (1-4), together with three known ones, were isolated from Ficus hispida. Their structures were elucidated by spectroscopic analysis and chemical method. The new compounds represent the first amine alkaloids with a rhamnosyl moiety (1-2) or with a N-oxide motif (2-4) from the genus Ficus. Compound 2 showed potent inhibitory effect in nuclear factor-κB (NF-κB) pathway luciferase assay with IC50 value of 0.52±0.11 μM.
Xin-Yu Jia, Yong-Mei Wu, Jing-Ya Li, Chun Lei, Ai-Jun Hou. Alkaloid Constituents of Ficus hispida and Their Antiinflammatory Activity[J]. 应用天然产物, 2020, 10(1): 45-49.
Xin-Yu Jia, Yong-Mei Wu, Jing-Ya Li, Chun Lei, Ai-Jun Hou. Alkaloid Constituents of Ficus hispida and Their Antiinflammatory Activity[J]. Natural Products and Bioprospecting, 2020, 10(1): 45-49.
1. Z. Zhou, M.G. Gilbert, Flora China 5, 37-71 (2003) 2. M. Shahriar, S. Islam, S. Parvin, S. Hoque, J. Sci. Res. 5, 393-397 (2013) 3. L.X. Zhang, Z.B. Guan, Subtrop. Plant Sci. 33, 60-62 (2004) 4. M.S.I. Howlader, M.A. Siraj, S.K. Dey, A. Hira, A. Ahmed, M.H. Hossain, Evid-Based Compl. Alt. 7390359 (2017) 5. P. Deepa, K. Sowndhararajan, S. Kim, S.J. Park, J. Ethnopharmacol. 215, 210-232 (2018) 6. B. Pratumvinit, T. Srisapoomi, P. Worawattananon, N. Opartkiattikul, W. Jiratchariyakul, T. Kummalue, J. Med. Plants Res. 3, 255-261 (2009) 7. S.C. Mandal, B. Saraswathi, C.K. Kumar, S.M. Lakshmi, B.C. Maiti, Phytother. Res. 14, 457-459 (2000) 8. J.X. Cheng, B.D. Zhang, W.F. Zhu, C.F. Zhang, Y.M. Qin, M. Abe, T. Akihisa, W.Y. Liu, F. Feng, J. Zhang, J. Ethnopharmacol. 248, 112204 (2020) 9. V.A. Yap, B.J. Loong, K.N. Ting, S.H. Loh, K.T. Yong, Y.Y. Low, T.S. Kam, K.H. Lim, Phytochemistry 109, 96-102 (2015) 10. J. Zhang, W.F. Zhu, J. Xu, W. Kitdamrongtham, A. Manosroi, J. Manosroi, H. Tokuda, M. Abe, T. Akihisa, F. Feng, J. Ethnopharmacol. 214, 37-46 (2018) 11. Z.F. Shi, C. Lei, B.W. Yu, H.Y. Wang, A.J. Hou, Chem. Biodivers. 13, 445-450 (2016) 12. R.G. Baker, M.S. Hayden, S. Ghosh, Cell Metab. 13, 11-22 (2011) 13. K. Nishimura, T. Miyase, H. Noguchi, J. Nat. Prod. 62, 1128-1133 (1999) 14. Z.Q. Cao, H.G. Li, Y.J. Tian, F.F. Mu, J.P. Yang, M.L. Wang, N.N. Zhao, Chin. Tradit. Herbal Drugs 16, 386-388 (1985) 15. W. Xu, P. Wang, S.Z. Li, Q.S. Song, Nat. Prod. Res. Dev. 22, 1003-1005 (2010) 16. Y.M. Peng, J.B. Zheng, Y.B. Zhou, J. Li, Acta Pharmacol. Sin. 34, 939-950 (2013) 17. X. Jia, Y. Wu, C. Lei, Y. Yu, J. Li, J. Li, A. Hou, Chin. Chem. Lett. (2019). https://doi.org/10.1016/j.cclet.2019.10.014 |
[1] | Wei-Ye Wu, Xun Wei, Qiong Liao, Yi-Fan Fu, Lei-Ming Wu, Lei Li, Shu-Qi Wu, Qing-Ren Lu, Fang-Yu Yuan, Dong Huang, Zhang-Hua Sun, Tao Yuan, Gui-Hua Tang. Structurally diverse polyketides and alkaloids produced by a plant-derived fungus Penicillium canescens L1[J]. 应用天然产物, 2025, 15(3): 22-22. |
[2] | Yinling Wei, Hongyan Wen, Lian Yang, Bodou Zhang, Xiaoyu Li, Sheng Li, Jing Dong, Zhenzhen Liang, Yu Zhang. Hypecotumines A-D, new isoquinoline alkaloids with potential PCSK9 inhibition activity from Hypecoum erectum L.[J]. 应用天然产物, 2024, 14(6): 57-57. |
[3] | Ismail Ware, Katrin Franke, Andrej Frolov, Kseniia Bureiko, Elana Kysil, Maizatulakmal Yahayu, Hesham Ali El Enshasy, Ludger A. Wessjohann. Comparative metabolite analysis of Piper sarmentosum organs approached by LC-MS-based metabolic profiling[J]. 应用天然产物, 2024, 14(4): 30-30. |
[4] | Cheng-Yong Tan, Bao-Bao Shi, Mei-Fen Bao, Xiang-Hai Cai. Anti-inflammatory maistemonine-class alkaloids of Stemona japonica[J]. 应用天然产物, 2023, 13(2): 8-8. |
[5] | Ke-Pu Huang, Li-Li Xu, Sheng Li, Yin-Ling Wei, Lian Yang, Xiao-Jiang Hao, Hong-Ping He, Yu Zhang. Uncarialines A-E, new alkaloids from Uncaria rhynchophylla and their anticoagulant activity[J]. 应用天然产物, 2023, 13(2): 13-13. |
[6] | Yue Zhao, Wen-Ke Gao, Xiang-Dong Wang, Li-Hua Zhang, Hai-Yang Yu, Hong-Hua Wu. Phytochemical and pharmacological studies on Solanum lyratum: a review[J]. 应用天然产物, 2022, 12(6): 39-39. |
[7] | Kyu Hwan Shim, Min Ju Kang, Niti Sharma, Seong Soo A.An. Beauty of the beast: anticholinergic tropane alkaloids in therapeutics[J]. 应用天然产物, 2022, 12(5): 33-33. |
[8] | Mei-Ling Xiang, Bin-Yuan Hu, Zi-Heng Qi, Xiao-Na Wang, Tian-Zhen Xie, Zhao-Jie Wang, Dan-Yu Ma, Qi Zeng, Xiao-Dong Luo. Chemistry and bioactivities of natural steroidal alkaloids[J]. 应用天然产物, 2022, 12(4): 23-23. |
[9] | Ghodsi Mohammadi Ziarani, Negar Jamasbi, Fatemeh Mohajer. Recent advances on the synthesis of natural pyrrolizidine alkaloids: alexine, and its stereoisomers[J]. 应用天然产物, 2022, 12(1): 1-15. |
[10] | Pan-Pan Wei, Jia-Cheng Ji, Xu-Jun Ma, Zheng-Hui Li, Hong-Lian Ai, Xin-Xiang Lei, Ji-Kai Liu. Three new pyrrole alkaloids from the endophytic fungus Albifimbria viridis[J]. 应用天然产物, 2022, 12(1): 1-5. |
[11] | Na Zhang, Fan Xia, Song-Yu Li, Yin Nian, Li-Xin Wei, Gang Xu. Diterpenoid Alkaloids from the Aerial Parts of Aconitum flavum Hand. -Mazz[J]. 应用天然产物, 2021, 11(4): 421-429. |
[12] | Hao-Yi Li, Bing-Chao Yan, Li-Xin Wei, Han-Dong Sun, Pema-Tenzin Puno. Tangutidines A-C, Three Amphoteric Diterpene Alkaloids from Aconitum tanguticum[J]. 应用天然产物, 2021, 11(4): 459-464. |
[13] | Zong-Qing Huo, Qian Zhao, Wen-Tao Zhu, Xiao-Jiang Hao, Yu Zhang. Bousmekines A-E, New Alkaloids from Two Bousigonia Species: B.angustifolia and B. mekongensis[J]. 应用天然产物, 2021, 11(2): 207-213. |
[14] | Yun-Li Zhao, Zhong-Ping Gou, Jian-Hua Shang, Wan-Yi Li, Yu Kuang, Ming-Yuan Li, Xiao-Dong Luo. Anti-microbial Effects In Vitro and In Vivo of Alstonia scholaris[J]. 应用天然产物, 2021, 11(1): 127-135. |
[15] | Yuan Huang, Fanglin Xue, Hengmao Liu, Fei Xue, Xiao-Yu Liu, Hao Song, Yong Qin. Asymmetric Total Synthesis of (+)-21-epi-Eburnamonine Via a Photocatalytic Radical Cascade Reaction[J]. 应用天然产物, 2021, 11(1): 99-103. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||