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Identification and Antifungal Activity of Metabolites from the Mangrove Fungus Phoma sp. L28

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Chemistry of Natural Compounds Aims and scope

A new anthraquinone, 7-(γ,γ)-dimethylallyloxymacrosporin (1), along with five known analogues, macrosporin (2), 7-methoxymacrosporin (3), tetrahydroaltersolanol B (4), altersolanol L (5), and ampelanol (6), were isolated from the mangrove endophytic fungus Phoma sp. L28. All of them were first found in Phoma sp. Their structures were established by comprehensive spectroscopic analyses and comparison with the published data. These compounds displayed in vitro antifungal activities against Colletotrichum musae (Berk. & M. A. Curtis) Arx., Colletotrichum gloeosporioides (Penz) Sacc., Fusarium graminearum Schw., Penicillium italicum Wehme, Fusarium oxysporum Schlecht. f. sp. lycopersici (Sacc.) W.C. Snyder et H. N. Hansen, and Rhizoctonia solani Kuhn at different levels. Notably, compound 2 exhibited potent antifungal activity against Fusarium graminearum Schw. as compared with the positive control carbendazim.

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References

  1. E. Montel, P. D. Bridge, and B. C. Sutton, Mycopathologia, 115, 89 (1991).

    Article  CAS  PubMed  Google Scholar 

  2. E. L. Kim, J. L. Li, H. T. Dang, J. Hong, C. O. Lee, D. K. Kim, W. D. Yoon, E. Kim, Y. H. Liu, and J. H. Jung, Bioorg. Med. Chem. Lett., 22, 3126 (2012).

    Article  CAS  PubMed  Google Scholar 

  3. Y. Kanai, D. Ishiyama, H. Senda, W. Iwatani, H. Takahashi, H. Konno, S. Tokumasu, and S. Kanazawa, J. Antibiot., 53, 863 (2000).

    Article  CAS  PubMed  Google Scholar 

  4. K. Herath, G. Harris, H. Jayasuriya, D. Zink, S. Smith, F. Vicente, G. Bills, J. Collado, A. Gonzalez, B. Jiang, J. N. Kahn, S. Galuska, R. Giacobbe, G. Abruzzo, E. Hickey, P. Liberateor, D. Xu, T. Roemer, and S. B. Singh, Bioorg. Med. Chem., 17, 1361 (2009).

    Article  CAS  PubMed  Google Scholar 

  5. S. Huang, W. J. Ding, C. Y. Li, and D. G. Cox, Pharmacogn. Mag., 10, 410 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  6. W. J. Ding, S. Q. Zhang, B. Gong, C. Y. Li, and X. F. Wang, Guangdong Agric. Sci., 41, 74 (2014).

    CAS  Google Scholar 

  7. A. H. Aly, R. A. E. Ebel, V. Wary, W. E. G. Muller, S. Kozytska, U. Hentschel, P. Proksch, and R. Ebel, Phytochemistry, 69, 1716 (2008).

    Article  CAS  PubMed  Google Scholar 

  8. A. Evidente, R. Rodeva, A. Andolfi, Z. Stoyanova, C. Perrone, and A. Motta, Eur. J. Plant Pathol., 130, 173 (2011).

    Article  CAS  Google Scholar 

  9. N. Okamura, K. Mimura, H. Haraguchi, K. Shingu, K. Miyahara, and A. Yagi, Phytochemistry, 42, 77 (1996).

    Article  CAS  Google Scholar 

  10. A. Debbab, A. H. Aly, R. A. E. Ebel, V. Wray, W. E. G. Muller, F. Totzke, U. Zirrgiebel, C. Schachtele, M. H. G. Kubbutat, W. H. Lin, M. Mosaddak, A. Hakiki, P. Proksch, and R. Ebel, J. Nat. Prod., 72, 626 (2009).

    Article  CAS  PubMed  Google Scholar 

  11. X. M. Zhou, C. J. Zheng, G. Y. Chen, X. P. Song, C. R. Han, G. N. Li, Y. H. Fu, W. H. Chen, and Z. G. Niu, J. Nat. Prod., 77, 2021 (2014).

    Article  CAS  PubMed  Google Scholar 

  12. Y. N. Wang, C. J. Zheng, C. L. Shao, and C. Y. Wang, Chin. J. Mar. Drugs, 34, 10 (2015).

    Google Scholar 

  13. C. J. Zheng, C. L. Shao, Z. Y. Guo, J. F. Chen, D. S. Deng, K. L. Yang, Y. Y. Chen, X. M. Fu, Z. G. She, Y. C. Lin, and C. Y. Wang, J. Nat. Prod., 75, 189 (2012).

    Article  CAS  PubMed  Google Scholar 

  14. J. H. Wang, S. Huang, C. Y. Li, W. J. Ding, Z. G. She, and C. L. Li, Chem. Nat. Compd., 51, 239 (2015).

    Article  Google Scholar 

  15. S. Prachya, S. Wiyakrutta, N. Sriubolmas, N. Ngamrojanavanich, C. Mahidol, S. Ruchirawat, and P. Kittakoop, Planta Med., 73, 1418 (2007).

    Article  CAS  PubMed  Google Scholar 

  16. J. H. Wang, W. J. Ding, R. M. Wang, Y. P. Du, H. L. Liu, X. H. Kong, and C. Y. Li, Mar. Drugs, 13, 4492 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgment

This work was supported by the National Natural Science Foundation of China (21102049), the Natural Science Foundation of Guangdong Province of China (2015A030313405, 9451064201003751), the Science and Technology Project of Guangdong Province (2016A020222019), the Scientific Research Foundation for Returning Overseas Chinese Scholars, State Education Ministry 2015-311, and the Innovation Experiment Program for University students of Guangdong Province (201510564196).

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Correspondence to Chunyuan Li.

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Published in Khimiya Prirodnykh Soedinenii, No. 2, March–April, 2017, pp. 204–206.

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Huang, S., Xu, J., Li, F. et al. Identification and Antifungal Activity of Metabolites from the Mangrove Fungus Phoma sp. L28. Chem Nat Compd 53, 237–240 (2017). https://doi.org/10.1007/s10600-017-1961-z

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  • DOI: https://doi.org/10.1007/s10600-017-1961-z

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