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Nine New Farnesylphenols from the Basidiomycete Albatrellus Caeruleoporus |
Liang-Yan Liu1,2, Zheng-Hui Li1, Gang-Qiang Wang1, Kun Wei1, Ze-Jun Dong1, Tao Feng1, Gen-Tao Li1, Yan Li1, Ji-Kai Liu1 |
1. State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China; 2. University of the Chinese Academy of Sciences, Beijing 100049, China |
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Abstract Nine previously-unreported farnesylphenols, involving eight neogrifolin derivatives(1-8) and one grifolin analogue(9), together with three known compounds, were isolated from the fruiting bodies of the mushroom Albatrellus caeruleoporus. Their structures were elucidated as(S)-17-hydroxy-18, 20-ene-neogrifolin(1),(S)-18, 19-dihydroxyneogrifolin(2),(S)-9-hydroxy-10, 22-ene-neogrifolin(3),(9S, 10R)-6, 10-epoxy-9-hydroxyneo grifolin(4),(9S, 10R)-6, 9-epoxy-10-hydroxyneogrifolin(5),(-)-13, 14-dihydroxyneogrifolin(6), albatrelin G(7), albatrelin H(8), and one grifolin analogue,(S)-10-hydroxygrifolin(9), grifolin(10), neogrifolin(11), and albatrellin(12) by extensive spectroscopic analyses and chemical methods. Compounds 7 and 8 showed weak cytotoxic activity to cell lines HL-60, SMMC-7721, A-549, and MCF-7, in vitro.
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Keywords
Albatrellus caeruleoporus
Mushroom
Polyporaceae
Farnesylphenols
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Fund:This project was supported by the National Natural Sciences Foundation of China(U1132607). |
Issue Date: 11 February 2018
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1. Z.H. Ding, Z.J. Dong, J.K. Liu, Helv. Chim. Acta 84, 259-262 (2001) 2. B. Koch, W. Steglich, Eur. J. Org. Chem. 2007, 1631-1635 (2007) 3. M. Nukata, T. Hashimoto, I. Yamamoto, N. Iwasaki, M. Tanaka, Y. Asakawa, Phytochemistry 59, 731-737 (2002) 4. D.N. Quang, T. Hashimoto, Y. Arakawa, C. Kohchi, T. Nishizawa, G.I. Soma, Y. Asakawa, Bioorg. Med. Chem. 14, 164-168 (2006) 5. X.L. Yang, C. Qin, F. Wang, Z.J. Dong, J.K. Liu, Chem. Biodivers. 5, 484-489 (2008) 6. L. Zhang, Z.J. Dong, J.K. Liu, Acta Bot. Yunn. 31, 187-189 (2009) 7. T. Hashimoto, D.N. Quan, M. Nukada, M. Nukada, Y. Asakawa, Heterocycles 65, 2431-2439 (2005) 8. D.Q. Luo, H.J. Shao, H.J. Zhu, J.K. Liu, Z. Naturforschung C60, 50-56 (2005) 9. H. Kawagishi, A. Tanaka, K. Sugiyama, H. Mori, H. Sakamoto, Y. Ishoguro, K. Kobayashi, M. Uramoto, Phytochemistry 42, 547-548 (1996) 10. V. Hellwig, R. Nopper, F. Mauler, J. Freitag, J.K. Liu, Z.H. Ding, M. Stadler, Arch. Pharm. 336, 119-126 (2003) 11. M. Ye, J.K. Liu, Z.X. Lu, Y. Zhao, S.F. Liu, L.L. Li, M. Tan, X.X. Weng, W. Li, Y. Cao, FEBS Lett. 579, 3437-3443 (2005) 12. H.D. Zheng, P.G. Liu, Microbiol. China 33, 104-107 (2006) 13. S. Jones, D. Valette, Org. Lett. 11, 5358-5361 (2009) 14. M. Nakata, M. Arai, K. Tomooka, N. Ohsawa, M. Kinoshita, Bull. Chem. Soc. Jpn. 62, 2618-2635 (1989) 15. H. Ziffer, K.I. Kawai, M. Kasai, M. Imuta, C. Froussios, J. Org. Chem. 48, 3017-3021 (1983) 16. T. Mukaiyama, T. Shintou, K. Fukumoto, J. Am. Chem. Soc. 125, 10538-10539 (2003) 17. L.J. Reed, H. Muench, Am. J. Hyg. 27, 493-497 (1938) |
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