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Rheadinin, a New Bis(styrylpyrone) from Mycelium of Inonotus rheades

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A new bis(styrylpyrone) was isolated from mycelium of Inonotus rheades (Pers.) P. Karst. (Hymenochaetaceae, strain 0186) and identified using UV, IR, MS, and NMR spectroscopy as 3,3-ethylidene-bis[4-hydroxy-6-(4-hydroxystyryl)-2H-pyran-2-one] (rheadinin). In addition, 11 known compounds were found. HPLC showed that mycelium of I. rheades contained more styrylpyrones than fruiting bodies.

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References

  1. R. L. Edwards, D. G. Lewis, and D. V. Wilson, J. Chem. Soc., 4995 (1961).

  2. I. K. Lee, Y. S. Kim, Y. W. Jang, J. Y. Jung, and B. S. Yun, Bioorg. Med. Chem. Lett., 17, 6678 (2007).

    Article  CAS  PubMed  Google Scholar 

  3. I. K. Lee and B. S. Yun, Bioorg. Med. Chem. Lett., 16, 2376 (2006).

    Article  CAS  PubMed  Google Scholar 

  4. I. K. Lee and B. S. Yun, J. Antibiot., 64, 349 (2011).

    Article  CAS  PubMed  Google Scholar 

  5. D. N. Olennikov, A. V. Rokhin, and S. V. Agafonova, Chem. Nat. Compd., 47, 847 (2011).

    Google Scholar 

  6. D. N. Olennikov, L. M. Tankhaeva, A. V. Rokhin, and S. V. Agafonova, Chem. Nat. Compd., 48, 396 (2012).

    Article  CAS  Google Scholar 

  7. T. G. Gornostay, T. A. Penzina, V. A. Chkhenkeli, M. S. Polyakova, S. N. Osipenko, G. B. Borovski, and D. N. Olennikov, Basic Clin. Pharmacol. Toxicol., 115, 10 (2014).

    Google Scholar 

  8. J.-L. Fiasson, Biochem. Syst. Ecol., 10, 289 (1982).

    Article  CAS  Google Scholar 

  9. H. V. K. Wangun and C. Hertweck, Eur. J. Org. Chem., 2007, 3292 (2007).

  10. J.-J. Han, L. Bao, L.-W. He, X.-Q. Zhang, X.-L. Yang, S.-J. Li, Y.-J. Yao, and H.-W. Liu, J. Nat. Prod., 76, 1448 (2013).

    Article  CAS  PubMed  Google Scholar 

  11. I. K. Lee, J. Y. Jung, Y. S. Kim, and B. S. Yun, J. Antibiot., 62, 635 (2009).

    Article  CAS  PubMed  Google Scholar 

  12. K. V. Purtov, V. N. Petushkov, M. S. Baranov, K. S. Mineev, N. S. Rodionova, Z. M. Kaskova, A. S. Tsarkova, A. I. Petunin, V. S. Bondar, E. K. Rodicheva, S. E. Medvedeva, Y. Oba, Y. Oba, A. S. Arseniev, S. Lukyanov, J. I. Gitelson, and I. V. Yampolsky, Angew. Chem., Int. Ed., 54, 8124 (2015).

    Article  CAS  Google Scholar 

  13. M. Klaar and W. Steglich, Chem. Ber., 110, 1058 (1977).

    Article  CAS  Google Scholar 

  14. J.-L. Fiasson, K. Gluchoff-Fiasson, and W. Steglich, Chem. Ber., 110, 1047 (1977).

    Article  CAS  Google Scholar 

Download references

Acknowledgment

The work was supported financially by RFBR Project No. 15-44-04335.

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Authors and Affiliations

  1. Institute of General and Experimental Biology, Siberian Branch, Russian Academy of Sciences, 6 Sakhyanovoi St., Ulan-Ude, 670047, Russia

    D. N. Olennikov

  2. Siberian Institute of Plant Physiology and Biochemistry, Siberian Branch, Russian Academy of Sciences, 132 Lermontova St., Irkutsk, 664033, Russia

    T. G. Gornostai & T. A. Penzina

Authors
  1. D. N. Olennikov
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  2. T. G. Gornostai
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  3. T. A. Penzina
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Correspondence to D. N. Olennikov.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 4, July–August, 2017, pp. 535–537.

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Olennikov, D.N., Gornostai, T.G. & Penzina, T.A. Rheadinin, a New Bis(styrylpyrone) from Mycelium of Inonotus rheades . Chem Nat Compd 53, 629–631 (2017). https://doi.org/10.1007/s10600-017-2076-2

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  • DOI: https://doi.org/10.1007/s10600-017-2076-2

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