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Chemical Constituents of Hypericum petiolulatum

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Chemical study on the methanol extract of aerial parts of Hypericum petiolulatum led to the isolation of one new polycyclic polyprenylated acylphloroglucinol (PPAP), dihroxuralodin (1), and one new chromone (2), together with four known PPAPs (3–6) and nine xanthones (7–15). Their structures were established on the basis of spectroscopic data, including IR, MS, 1D, and 2D NMR. All the isolated PPAPs (1, 3–6) were evaluated for their cytotoxicity against human prostate cancer cell line PC-3 and human breast cancer cell line MCF-7. Compounds 2 and 7–15 were tested for their antioxidant activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals. Compounds 1 and 3 exhibited moderate cytotoxicity against MCF-7 tumor cell line with IC50 values of 8.9 and 10.3 μM, respectively. Compounds 2 and 7–15 exhibited potent antioxidant activity with IC50 values ranging from 5.6 to 36.8 μM, when compared to the positive control, butylated hydroxytoluene (BHT, IC50 = 78.8 μM).

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References

  1. J. X. Li, K. Y. Guan, and F. C. Kong, Acta Hort. Sin., 30, 171 (2003).

    Google Scholar 

  2. C. Nor, D. Albring, A. B. F. Ferraz, J. Schripsema, V. Pires, P. Sonnet, D. Guillaume, and G. L. Von Poser, Biochem. Syst. Ecol., 32, 517 (2004).

    Article  CAS  Google Scholar 

  3. J. Sarris, Phytother. Res., 21, 703 (2007).

    Article  PubMed  Google Scholar 

  4. H. Zhu, C. Chen, J. Liu, B. Sun, G. Wei, Y. Li, J. Zhang, G. Yao, Z. Luo, Y. Xue, and Y. Zhang, Phytochemistry, 115, 222 (2015).

    Article  CAS  PubMed  Google Scholar 

  5. M. Ali, A. Latif, K. Zaman, M. Arfan, D. Maitland, H. Ahmad, and M. Ahmad, Fitoterapia, 95, 258 (2014).

    Article  CAS  PubMed  Google Scholar 

  6. R. Ciochina and R. B. Grossman, Chem. Rev., 106, 3963 (2006).

    Article  CAS  PubMed  Google Scholar 

  7. L. Beerhues, Phytochemistry, 67, 2201 (2006).

    Article  CAS  PubMed  Google Scholar 

  8. Q. Zhao, H. L. Zhang, X. Zhang, X. M. Li, Y. Z. Sun, and H. Su, Chin. J. Chin. Mater. Med., 23, 40 (2015).

    Google Scholar 

  9. X. Q. Chen, X. Cheng, K. Wang, J. He, Z. H. Pan, M. M. Li, L. Y. Peng, G. Xu, and Q. S. Zhao, Chem. Biodiv., 7, 196 (2010).

    Article  CAS  Google Scholar 

  10. J. S. A. R. Teixeira and F. G. Cruz, Tetrahedron Lett., 46, 2813 (2005).

    Article  CAS  Google Scholar 

  11. W. Hashida, N. Tanaka, and Y. Takaishi, J. Nat. Med., 61, 371 (2007).

    Article  CAS  Google Scholar 

  12. J. Y. Lee, R. K. Duke, V. H. Tran, J. M. Hook, and C. C. Duke, Phytochemistry, 67, 2550 (2006).

    Article  CAS  PubMed  Google Scholar 

  13. X. W. Yang, M. M. Li, X. Liu, D. Ferreira, Y. Ding, J. J. Zhang, Y. Liao, H. B. Qin, and G. Xu, J. Nat. Prod., 78, 885 (2015).

    Article  CAS  PubMed  Google Scholar 

  14. X. Liu, X. W. Yang, C. Q. Chen, C. Y. Wu, J. J. Zhang, J. Z. Ma, H. Wang, L. X. Yang, and G. Xu, J. Nat. Prod., 76, 1612 (2013).

    Article  CAS  PubMed  Google Scholar 

  15. H. Zhou, Y. L. Liu, G. Blasko, and G. A. Cordell, Phytochemistry, 28, 3569 (1989).

    Article  CAS  Google Scholar 

  16. H. Tosa, M. Iinuma, K. I. Murakami, T. Ito, T. Tanaka, V. Chelladurai, and S. Riswan, Phytochemistry, 45, 133 (1997).

    Article  CAS  Google Scholar 

  17. G. Rath, O. Potterat, S. Mavi, and K. Hostettmann, Phytochemistry, 43, 513 (1996).

    Article  CAS  PubMed  Google Scholar 

  18. S. Ngouela, F. Zelefack, B. N. Lenta, E. T. Ngouamegne, D. N. Tchamo, E. Tsamo, and J. D. Connolly, Nat. Prod. Res., 19, 685 (2005).

    Article  CAS  PubMed  Google Scholar 

  19. F. Della Monache, M. Marquina, G. Delle Monache, G. B. Marini Bettdo, and R. Alves De lima, Phytochemistry, 22, 103 (1983).

  20. Y. Li, Y. Xu, J. Wu, S. Wang, Y. Meng, Y. Ye, H. Yang, X. Gao, and Q. Gao, Heterocycles, 87, 2625 (2013).

    Article  CAS  Google Scholar 

  21. Y. Sugiyama, K. Watanabe, and A. Hirota, Biosci. Biotech. Biochem., 73, 230 (2009).

    Article  CAS  Google Scholar 

Download references

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Correspondence to Li-Yuan Tang or Fei Li.

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Published in Khimiya Prirodnykh Soedinenii, No. 3, May–June, 2017, pp. 389–393.

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Rui, DY., Chen, XQ., Li, Z. et al. Chemical Constituents of Hypericum petiolulatum . Chem Nat Compd 53, 457–462 (2017). https://doi.org/10.1007/s10600-017-2022-3

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  • DOI: https://doi.org/10.1007/s10600-017-2022-3

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