Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Chalcones from the Flowers of Rosa Rugosa and Their Anti-tobacco Mosaic Virus Activities

  • Du, Gang (Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan University of Nationalities) ;
  • Han, Jing-Mei (Key Laboratory of Tobacco Chemistry of Yunnan Province, Yunnan Academy of Tobacco Science) ;
  • Kong, Wei-Song (Key Laboratory of Tobacco Chemistry of Yunnan Province, Yunnan Academy of Tobacco Science) ;
  • Zhao, Wei (Key Laboratory of Tobacco Chemistry of Yunnan Province, Yunnan Academy of Tobacco Science) ;
  • Yang, Hai-Ying (Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan University of Nationalities) ;
  • Yang, Guang-Yu (Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan University of Nationalities) ;
  • Gao, Xue-Mei (Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan University of Nationalities) ;
  • Hu, Qiu-Fen (Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan University of Nationalities)
  • Received : 2012.12.24
  • Accepted : 2013.01.17
  • Published : 2013.04.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Zhang, X. H.; Xie, Z. Z. Chin. J. Shandong. Forest. Sci. Tech. 2012, 42, 5.
  2. Lu, J. L. China. Flowers. Horticul. 2012, 11, 26.
  3. Shibata, K. A Cyclopedia of Useful Plant and Plant Products; Enlarged and Revised Edition, The Hokuryukan: Tokyo, 1957; p 612.
  4. Jiang, Y. Flora of China; Chinese Science Press: Beijing, 1977; Vol 63, p 289.
  5. Ochir, S.; Park, B.; Nishizawa, M.; Kanazawa, T.; Funaki, M.; Yamagishi, T. J. Nat. Med. 2010, 64, 383. https://doi.org/10.1007/s11418-010-0418-5
  6. Park, K. H.; Sung, K.; Choi, S. E.; Kwon, J. H.; Myung, H.; Lee, M. W. Chem. Pharm. Bull. 2010, 58, 1227. https://doi.org/10.1248/cpb.58.1227
  7. Porter, E. A.; van den Bos, A. A.; Kite, G. C.; Veitch, N. C.; Simmonds, M. S. Phytochemistry 2012, 81, 90. https://doi.org/10.1016/j.phytochem.2012.05.006
  8. Kwon, E.; Lee, K. D. Y.; Lee, H.; Kim, D. O.; Baek, N.; Kim, Y. E.; Kim, H. Y. J. Agric. Food. Chem. 2010, 58, 882. https://doi.org/10.1021/jf903515f
  9. Gao, X. M.; Yang, L. Y.; Shu, L. D.; Shen, Y. Q.; Zhang, Y. J.; Hu, Q. F. Heterocycles 2012, 85, 1925. https://doi.org/10.3987/COM-12-12505
  10. Yuan, J. Q.; Yang, X. Z.; Miao, J. H.; Tang, C. P.; Ke, C. Q.; Zhang, J. B.; Ma, X. J.; Ye, Y. Molecules 2008, 13, 2229. https://doi.org/10.3390/molecules13092229
  11. Zeng, N.; Shen, Y.; Li, L. Z.; Jiao, W. H.; Gao, P. Y.; Song, S. J.; Chen, W. S.; Lin, H. W. J. Nat. Prod. 2011, 74, 732. https://doi.org/10.1021/np1007922
  12. Gao, X. M.; Shu, L. D.; Yang, L. Y.; Shen, Y. Q.; Zhang, Y. J.; Hu, Q. F. Bull. Korean Chem. Soc. 2013, 34, in press.
  13. Gao, X. M.; Liying Yang, L. Y.; Shen, Y. Q.; Shu, L. D.; Li, X. M.; Hu, Q. F. Bull. Korean Chem. Soc. 2012, 33, 2447. https://doi.org/10.5012/bkcs.2012.33.7.2447
  14. Geng, Z. L.; Shang, S. H.; Chen, X. J.; Cao, Y. Chin. Tob. Sci. 2011, 32, 84.
  15. Gao, X. M.; Li, X. S.; Yang, X. Z.; Mu, H. X.; Chen, Y. K.; Yang, G. Y.; Hu, Q. F. Heterocycles 2012, 85, 147. https://doi.org/10.3987/COM-11-12349
  16. Hu, Q. F.; Zhou, B.; Gao, X. M.; Yang, L. Y.; Shu, L. D.; Shen, Y. Q.; Li, G. P.; Che, C. T.; Yang, G. Y. J. Nat. Prod. 2012, 75, 1909. https://doi.org/10.1021/np300395m
  17. Huang, L.; Wall, M. E.; Wani, M. C.; Navarro, H.; Santisuk, T.; Reutrakul, V.; Seo, E. K.; Farnsworth, N. R.; Kinghorn, A. D. J. Nat. Prod. 1998, 61, 446. https://doi.org/10.1021/np9703609
  18. Panichpol, K.; Waterman, P. G. Phytochemistry 1978, 17, 1363. https://doi.org/10.1016/S0031-9422(00)94590-4
  19. Matsumoto, J.; Fujimoto, T.; Takino, C.; Saitoh, M.; Hano, Y.; Fukai, T.; Nomura, T. Chem. Pharm. Bull. 1985, 33, 3250. https://doi.org/10.1248/cpb.33.3250
  20. delle Monache, G.; Derosa, M. C.; Scurria, R.; Vitali, A.; Cuteri, A.; Monacelli, B.; Pasqua, G.; Botta, B. Phytochemistry 1995, 39, 575. https://doi.org/10.1016/0031-9422(94)00971-U
  21. Bhakuni, D. S.; Chaturvedi, R. J. Nat. Prod. 1984, 47, 585. https://doi.org/10.1021/np50034a003
  22. Yang, Y.; Zhang, T.; Xiao, L.; Yang, L. X.; Chen, R. Y. Fitoterapia 2010, 81, 614. https://doi.org/10.1016/j.fitote.2010.03.005
  23. Yan, X. H.; Chen, J.; Di, Y. T.; Fang, X.; Dong, J. H.; Sang, P.; Wang, Y. H.; He, H. P.; Zhang, Z. K.; Hao, X. J. J. Agric. Food Chem. 2010, 58, 1572. https://doi.org/10.1021/jf903434h
  24. Song, B. A.; Zhang, H. P.; Wang, H.; Yang, S.; Jin, L. H.; Hu, D. Y.; Pang, L. L.; Xue, W. J. Agric. Food Chem. 2005, 53, 7886. https://doi.org/10.1021/jf051050w
  25. Gooding, G. V. J.; Hebert, T. T. Phytopathology 1967, 57, 1285.

Cited by

  1. Design, Synthesis, and Antiviral Activity of Novel Chalcone Derivatives Containing a Purine Moiety vol.35, pp.5, 2017, https://doi.org/10.1002/cjoc.201600568
  2. -Ferulic Acid Derivatives Containing a Chalcone Moiety as Potential Activator for Plant Resistance Induction vol.65, pp.22, 2017, https://doi.org/10.1021/acs.jafc.7b00958
  3. Three New C-Alkylated Flavones from the Flower of Rosa rugosa and Their Bioactivity vol.94, pp.11, 2017, https://doi.org/10.3987/COM-17-13799
  4. Anti-Inflammatory Activity of Rugchalcone Derivative on Lipopolysaccharides-Stimulated RAW264.7 Cells vol.17, pp.1, 2021, https://doi.org/10.3923/ijp.2021.48.56