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Acylated Triterpenoids, Flavonoids, and Lignans Isolated from the Stems of Tetracera loureiri

  • Changon Seo
  • Ji Eun Lee
  • Jung A. Lee
  • Eun-Kyung Ahn
  • Jae-Shin Kang
  • Chang Woo Hyun
  • Seong Su HongEmail author
Article

The genus Tetracera (family Dilleniaceae) contains about 50 species with a pantropical distribution, of which 20 occur in the Neotropical area. In traditional folk medicine, some species have been used as febrifuge, diuretic agent, and antijaundice [1]. Tetracera species has been reported to exhibit a broad range of pharmacological activities such as antidiabetic, analgesic, anti-inflammatory, antipyrexic, anti-HIV and anti-reverse transcriptase, antihyperglycemic, anti-mycobacterial, antioxidant, anti-ulcerogenic, hepatoprotective, DNA polymerase β-inhibitory, glucose-uptake modulating, and xanthine oxidase inhibition activity [2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]. Previous phytochemical investigations of members of this genus have resulted in the isolation of several classes of compounds, including flavonoids and terpenoids [9, 10, 11, 12, 13]. Among them, flavonoids from T. indica induced significant adipogenesis like insulin and enhanced adipogenesis like rosiglitazone [4]....

Notes

Acknowledgment

This study was supported by a grant from the National Institute of Biological Resources (NIBR) under the Ministry of Environment (MOE) of the Republic of Korea (NIBR No.2016-04-202).

References

  1. 1.
    C. C. Lima, R. P. L. Lemos, and L. M. Conserva, J. Pharmacogn. Phytochem., 3, 181 (2014).Google Scholar
  2. 2.
    B. O. Oyebanji, A. B. Saba, and O. A. Oridupa, Afr. J. Trad. Complem. Altern. Med., 11, 30 (2014).CrossRefGoogle Scholar
  3. 3.
    H. S. Kwon, J. A. Park, J. H. Kim, and J. C. You, BMB Rep., 45, 165 (2012).CrossRefGoogle Scholar
  4. 4.
    M. S. Lee, C. H. Kim, D. M. Hoang, B. Y. Kim, C. B. Sohn, M. R. Kim, and J. S. Ahn, Biol. Pharm. Bull., 32, 504 (2009).CrossRefGoogle Scholar
  5. 5.
    A. Umar, Q. U. Ahmed, B. Y. Muhammad, B. B. Dogarai, and S. Z. Soad, J. Ethnopharmacol., 131, 140 (2010).CrossRefGoogle Scholar
  6. 6.
    Q. U. Ahmed, B. B. S. Dogarai, M. Z. A. M. Amiroudine, M. Taher, J. Latip, A. Umar, and B. Y. Muhammad, J. Med. Plants Res., 6, 5912 (2012).Google Scholar
  7. 7.
    F. S. Oluwole, J. A. Ayo, B. O. Omolaso, B. O. Emikpe, and J. K. Adesanwo, Niger. J. Physiol. Sci., 23, 79 (2008).Google Scholar
  8. 8.
    V. Kukongviriyapan, T. Janyacharoen, U. Kukongviriyapan, P. Laupattarakasaem, S. Kanokmedhakul, and P. Chantaranothai, Phytother. Res., 17, 717 (2003).CrossRefGoogle Scholar
  9. 9.
    M. M. Hasan, Q. U. Ahmed, S. Z. M. Soad, J. Latip, M. Taher, T. M. F. Syafiq, M. N. Sarian, A. M. Alhassan, and Z. A. Zakaria, BMC Complem. Altern. Med., 17, 431 (2017).CrossRefGoogle Scholar
  10. 10.
    M. C. Y. Fomogne-Fodjo, D. T. Ndinteh, D. K. Olivier, P. Kempgens, S. van Vuuren, and R. W. Krause, J. Ethnopharmacol., 195, 238 (2016).CrossRefGoogle Scholar
  11. 11.
    J. Ma, S. R. Starck, and S. M. Hecht, J. Nat. Prod., 62, 1660 (1999).CrossRefGoogle Scholar
  12. 12.
    M. T. T. Nguyen and N. T. Nguyen, Nat. Prod. Res., 27, 61 (2008).CrossRefGoogle Scholar
  13. 13.
    L. J. Harrison, G. L. Sia, and K. Y. Sim, Planta Med., 60, 493 (1994).CrossRefGoogle Scholar
  14. 14.
    A. Yili, Mutalipu, H. A. Aisa, and M. I. Isaev, Chem. Nat. Compd., 45, 592 (2009).CrossRefGoogle Scholar
  15. 15.
    A. M. Seca, A. M. Silva, A. J. Silvestre, J. A. Cavaleiro, F. M. Domingues, and C. Pascoal-Neto, Phytochemistry, 56, 759 (2001).CrossRefGoogle Scholar
  16. 16.
    B. S. Siddiqui, Farhat, S. Begum, and S. Siddiqui, Planta Med., 63, 47 (1997).CrossRefGoogle Scholar
  17. 17.
    H. Haberlein and K. P. Tschiersch, Phytochemistry, 35, 765 (1994).CrossRefGoogle Scholar
  18. 18.
    A. Numata, P. Yang, C. Takahashi, R. Fujiki, M. Nabae, and E. Fujita, Chem. Pharm. Bull., 37, 648 (1989).CrossRefGoogle Scholar
  19. 19.
    S. S. Hong, W. Jeong, J. Y. Lee, E. K. Ahn, and J. S. Oh, Chem. Nat. Compd., 52, 1089 (2009).CrossRefGoogle Scholar
  20. 20.
    C. J. Shen, C. K. Chen, and S. S. Lee, J. Chin. Chem. Soc., 56, 1002 (2009).CrossRefGoogle Scholar
  21. 21.
    L. Gao, X. Xu, and J. Yang, Chem. Nat. Compd., 49, 603 (2013).CrossRefGoogle Scholar
  22. 22.
    R. R. Makhmudov, N. G. Abdulladzhanova, and F. G. Kamaev, Chem. Nat. Compd., 47, 288 (2011).CrossRefGoogle Scholar
  23. 23.
    L. Fan, J. Ma, Y. H. Chen, and X. Q. Chen, Chem. Nat. Compd., 50, 433 (2014).CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  • Changon Seo
    • 1
  • Ji Eun Lee
    • 1
  • Jung A. Lee
    • 1
  • Eun-Kyung Ahn
    • 1
  • Jae-Shin Kang
    • 2
  • Chang Woo Hyun
    • 2
  • Seong Su Hong
    • 1
    Email author
  1. 1.Bio-CenterGyeonggido Business & Science Accelerator (GBSA)SuwonRepublic of Korea
  2. 2.Biological Genetic Resources Utilization DivisionNational Institute of Biological Resources (NIBR)IncheonRepublic of Korea

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