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New Coumarins from Roots and Fruit of Peucedanum morisonii

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Chemistry of Natural Compounds Aims and scope

Chromatographic separation of constituents from roots and fruit of Peucedanum morisonii Besser (Apiaceae) isolated 30 compounds, including four new coumarins 1–4. UV and NMR spectroscopy and mass spectrometry established that the new compounds were officinalin isovalerate (1), umbelliferone-6-carboxylic acid 7-O-β-D-glucopyranoside (peumoriside I, 2), umbelliferone-6-carboxylic acid 7-O-(6′-O-β-D-apiofuranosyl)-β-D-glucopyranoside (peumoriside II, 3), and bergaptol 7-O-(6′-O-β-D-apiofuranosyl)-β-D-glucopyranoside (peumoriside III, 4). Glycosides 2 and 3 possessed inhibitory activity for cholinesterase, β-secretase 1, and monoamine oxidase.

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References

  1. S. M. Batorova, G. P. Yakovlev, and T. A. Aseeva, Guide to Medicinal Plants of Traditional Tibetan Medicine [in Russian], Nauka, Novosibirsk, 2003, 291 pp.

    Google Scholar 

  2. E. E. Shults, T. N. Petrova, M. M. Shakirov, E. I. Chernyak, L. M. Pokrovskiy, S. A. Nekhoroshev, and G. A. Tolstikov, Chem. Sustainable Dev., 11, 649 (2003).

    Google Scholar 

  3. V. M. Malikov and A. I. Saidkhodzhaev, Chem. Nat. Compd., 34, 517 (1998).

    Article  Google Scholar 

  4. V. M. Malikov and A. I. Saidkhodzhaev, Chem. Nat. Compd., 34, 345 (1998).

    Article  CAS  Google Scholar 

  5. J. Widelski, S. V. Luca, A. Skiba, I. Chinou, L. Marcourt, J.-L. Wolfender, and K. Skalicka-Wozniak, Molecules, 23, 1222 (2018).

    Article  Google Scholar 

  6. A. Czepa and T. Hofmann, J. Agric. Food Chem., 51, 3865 (2003).

    Article  CAS  Google Scholar 

  7. F. Bohlmann and M. Grenz, Chem. Ber., 102, 1673 (1969).

    Article  CAS  Google Scholar 

  8. D. Zhao, M. N. Islam, B. R. Ahn, H. A. Jung, B. W. Kim, and J. S. Choi, Arch. Pharm. Res., 35, 179 (2012).

    Article  CAS  Google Scholar 

  9. Z.-M. Gu, D.-X. Zhang, M. Hattori, and T. Namra, Chem. Pharm. Bull., 38, 2498 (1990).

    Article  CAS  Google Scholar 

  10. D. N. Olennikov and N. K. Chirikova, Chem. Nat. Compd., 56, 628 (2020).

    Article  CAS  Google Scholar 

  11. B. Schuster, M. Winter, and K. Herrmann, Z. Naturforsch., C: J. Biosci., 41, 511 (1986).

  12. D. N. Olennikov, L. M. Tankhaeva, V. V. Partilkhaev, and A. V. Rokhin, Braz. J. Pharmacogn., 22, 490 (2012).

    Article  CAS  Google Scholar 

  13. H. Tesso, W. A. Konig, K. H. Kubeczka, M. Bartnik, and K. Glowniak, Phytochemistry, 66, 707 (2005).

    Article  CAS  Google Scholar 

  14. J. H. Heo, B. H. Eom, H. W. Ryu, M.-G. Kang, J. E. Park, D.-Y. Kim, J.-H. Kim, D. Park, S.-R. Oh, and H. Kim, Sci. Rep., 10, 21695 (2020).

    Article  CAS  Google Scholar 

  15. A. Manayi, S. Saeidnia, S. N. Ostad, A. Hadjiakhoondi, M. R. S. Ardekani, M. Vazirian, Y. Akhtar, and M. Khanavi, Z. Naturforsch., C: J. Biosci., 68, 367 (2013).

  16. R. Bruni, D. Barreca, M. Protti, V. Brighenti, L. Righetti, L. Anceschi, L. Mercolini, S. Benvenuti, G. Gattuso, and F. Pellati, Molecules, 24, 2163 (2019).

    Article  CAS  Google Scholar 

  17. B. Girennavar, G. K. Jayaprakasha, Y. Jadegoud, G. A. N. Gowda, and B. S. Patil, Bioorg. Med. Chem., 15, 3684 (2007).

    Article  CAS  Google Scholar 

  18. T. D. Dai, N. T. Tam, D. D. Thien, N. H. Sa, T. T. Thuy, N. T. H. Anh, and T. D. Quan, Lett. Org. Chem., 15, 1007 (2018).

    Article  CAS  Google Scholar 

  19. A. Caceres, L. Rastrelli, F. De Simone, G. DeMartino, C. Saturnino, P. Saturnino, and R. Aquino, Fitoterapia, 72, 376 (2001).

    Article  CAS  Google Scholar 

  20. Y. Zhao and Z. Yuan, Yaoxue Xuebao, 42, 1070 (2007).

    CAS  Google Scholar 

  21. D. N. Olennikov, I. A. Fedorov, N. I. Kashchenko, N. K. Chirikova, and C. Vennos, Molecules, 24, 2286 (2019).

    Article  CAS  Google Scholar 

  22. D. S. Kruglov, M. J. Kruglova, and D. N. Olennikov, Russ. J. Bioorg. Chem., 46, 1378 (2020).

    Article  CAS  Google Scholar 

  23. D. N. Olennikov and N. K. Chirikova, Chem. Nat. Compd., 55, 1032 (2019).

    Article  CAS  Google Scholar 

  24. D. N. Olennikov, N. K. Chirikova, N. I. Kashchenko, T. G. Gornostai, I. Y. Selyutina, and I. N. Zilfikarov, Int. J. Mol. Sci., 18, 2579 (2017).

    Article  Google Scholar 

  25. M. Akabane, A. Yamamoto, S. Aizawa, A. Taga, and S. Kodama, Anal. Sci., 30, 739 (2014).

    Article  CAS  Google Scholar 

  26. D. N. Olennikov, N. I. Kashchenko, N. K. Chirikova, A. Akobirshoeva, I. N. Zilfikarov, and C. Vennos, Int. J. Mol. Sci., 18, 1685 (2017).

    Article  Google Scholar 

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Acknowledgment

The studies were supported by the Ministry of Education and Science of the Russian Federation (Project No. 121030100227-7).

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Correspondence to D. N. Olennikov.

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Translated from Khimiya Prirodnykh Soedinenii, No. 5, September–October, 2022, pp. 690–694.

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Olennikov, D.N. New Coumarins from Roots and Fruit of Peucedanum morisonii. Chem Nat Compd 58, 816–821 (2022). https://doi.org/10.1007/s10600-022-03805-8

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