Citation: Luo Yunlong, Shen Minggui, Wang Dan, Shang Shibin, Song Zhanqian. Progress in Bioactivities of Dehydroabietic Acid and Its Derivatives[J]. Chemistry, ;2018, 81(2): 122-128. shu

Progress in Bioactivities of Dehydroabietic Acid and Its Derivatives

Luo Yunlong ¹ ,
Shen Minggui ^1,2,, ,
Wang Dan ^1,2 ,
Shang Shibin ^1,2 ,
Song Zhanqian ^1,#

1.
Institute of Chemical Industry of Forest Products, CAF; National Engineering Lab. for Biomass Chemical Utilization; Key and Open Lab. of Forest Chemical Engineering, SFA; Key Lab. of Biomass Energy and Material, Jiangsu Province, Nanjing 210042
2.
Research Institute of Forestry New Technology, CAF, Beijing 100091

Corresponding author: Shen Minggui, shenminggui@sina.com
Received Date: 31 August 2017
Accepted Date: 31 October 2017

Figures(1)

Dehydroabietic acid is a kind of resin acid with tricyclic diterpene structure that separated from rosin. It has a wide range of biological activity and has important applications in the fields of medicine, industry and agriculture. In this paper the activities of dehydroabietic acid and its derivatives in antibacterial, antiviral, BK channel-opening activity, antitumor and other bioactivities are summarized. The research and application prospects of dehydroabietic acid and its derivatives are also previewed.
- Rosin,
- Dehydroabietic acid,
- Derivative,
- Bioactivities
1. [1]
2. [2]
3. [3]
4. [4]
5. [5]
6. [6]
  M A Gonzalez. Eur. J. Med. Chem., 2014, 87: 834~842.
7. [7]
  Y J Cui, X P Rao, S B Shang et al. J. Saudi Chem. Soc., 2017, 21: 258~263.
8. [8]
  W M Zhang, T Yang, X Y Pan et al. Eur. J. Med. Chem., 2017, 127: 917~927.
9. [9]
  M Berger, A Roller, N Maulide. Eur. J. Med. Chem., 2017, 126: 937~943.
10. [10]
  W Gu, S F Wang. Eur. J. Med. Chem., 2010, 45: 4692~4696.
11. [11]
  W Gu, C Qiao, S F Wang et al. Bioorg. Med. Chem. Lett., 2014, 24: 328~331.
12. [12]
  M A Gonzalez, D Perez-Guaita, J Correa-Royero et al. Eur. J. Med. Chem., 2010, 45: 811~816.
13. [13]
  X T Xu, X L Ma, W G Duan et al. Holzforschung, 2013, 67: 107~112.
14. [14]
15. [15]
  J R Tagat, D V Nazarene, M S Puar et al. Bioorg. Med. Chem. Lett., 1994, 4(9): 1101~1104.
16. [16]
  T Fonseca, B Gigante, M M Marques et al. Bioorg. Med. Chem., 2004, 12: 103~112.
17. [17]
  L S Agudelo-Gomez, L A Betancur-Galvis, M A Gonzalez. Pharmacologyonline, 2012, 1: 36~42.
18. [18]
19. [19]
  T Tashima, Y Toriumi, Y Mochizuki et al. Bioorg. Med. Chem., 2006, 14: 8014~8031.
20. [20]
  Y M Cui, E Yasutomi, Y Otani et al. Bioorg. Med. Chem. Lett., 2008, 18: 5201~5205.
21. [21]
  Y M Cui, E Yasutomi, Y Otani et al. Bioorg. Med. Chem. Lett., 2008, 18: 6386~6389.
22. [22]
  Y M Cui, E Yasutomi, Y Otani et al. Bioorg. Med. Chem. Lett., 2010, 18, 8642~8659.
23. [23]
  Y M Cui, X L Liu, W M Zhang et al. Bioorg. Med. Chem. Lett., 2016, 26: 283~287.
24. [24]
  X S Lv, Y M Cui, H Y Wang. Chin. Chem. Lett., 2013, 24: 1023~1026.
25. [25]
  X P Rao, Z Q Song, H Liu et al. Chem. Pharm. Bull., 2008, 56(11): 1575~1578.
26. [26]
  X P Rao, Y Wu, Z Q Song et al. Med. Chem. Res., 2011, 20: 333~338.
27. [27]
  M Ukiya, T Kawaguchi, K Ishii et al. Chem. Biodivers., 2013, 10: 1260~1268.
28. [28]
  X C Huang, M Wang, Y M Pan et al. Eur. J. Med. Chem., 2013, 69: 508~520.
29. [29]
  X C Huang, M Wang, H S Wang et al. Bioorg. Med. Chem. Lett., 2014, 24: 1511~1518.
30. [30]
  X C Huang, M Wang, Y M Pan et al. Bioorg. Med. Chem. Lett., 2013, 23(19): 5283~5289.
31. [31]
  M W Pertino, V Verdugo, C Theoduloz et al. Molecules, 2014, 19: 2523~2535.
32. [32]
  B Sepulveda, L Astudillo, J A Rodriguez et al. Pharm. Res., 2005, 52: 429~437.
33. [33]
  I A Tolmacheva, A V Tarantin, A A Boteva et al. Pharm. Chem. J., 2006, 40(9): 489~493.
34. [34]
1. [1]
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2. [2]
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12. [12]
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15. [15]
  . . Chinese Journal of Inorganic Chemistry, 2024, 40(12): 0-0.
16. [16]
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17. [17]
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19. [19]
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20. [20]
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沈阳化工大学材料科学与工程学院沈阳 110142