Copyright (c) 2014 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
A New Xanthone from the Fermentation Products of Endophytic Fungus of Phomopsis Species
Corresponding Author(s) : Gang Du
Asian Journal of Chemistry,
Vol. 26 No. 15 (2014): Vol 26 Issue 15
Abstract
A new xanthone, 1,3-dihydroxy-4-(1,3,4-trihydroxybutan-2-yl)-8-methoxy-9H-xanthen-9-one (1) was isolated from the fermentation products of a Phomopsis fungus. Their structures were elucidated by spectroscopic methods, including extensive 1D- and 2D- NMR techniques. Compound 1 was also evaluated for their cytotoxicity against five human tumor cell lines and it showed high cytotoxicity against A549 and PC3 cell with IC50 values of 5.8 and 3.6 μM, respectively.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- D. Udayanga, X. Liu, E.H.C. McKenzie, E. Chukeatirote, A.H.A. Bahkali and K.D. Hyde, Fungal Divers., 50, 189 (2011); doi:10.1007/s13225-011-0126-9.
- J.N. Choi, J. Kim, K. Ponnusamy, C. Lim, J.G. Kim, M.J. Muthaiya and C.H. Lee, J. Antibiot., 66, 231 (2013); doi:10.1038/ja.2012.105.
- H. Hussain, M.K. Tchimene, I.K. Ahmed, M. Steinert, S. Draeger, B. Schulz and K. Krohn, Nat. Prod. Commun., 6, 1905 (2011).
- H. Hussain, I. Ahmed, B. Schulz, S. Draeger and K. Krohn, Fitoterapia, 83, 523 (2012); doi:10.1016/j.fitote.2011.12.017.
- H. Hussain, K. Krohn, I. Ahmed, S. Draeger, B. Schulz, S. Di Pietro and G. Pescitelli, Eur. J. Org. Chem., 2012, 1783 (2012); doi:10.1002/ejoc.201101788.
- M. Isaka, A. Jaturapat, K. Rukseree, K. Danwisetkanjana, M. Tanticharoen and Y. Thebtaranonth, J. Nat. Prod., 64, 1015 (2001); doi:10.1021/np010006h.
- C. Hemtasin, S. Kanokmedhakul, K. Kanokmedhakul, C. Hahnvajanawong, K. Soytong, S. Prabpai and P. Kongsaeree, J. Nat. Prod., 74, 609 (2011); doi:10.1021/np100632g.
- E. Adelin, C. Servy, S. Cortial, H. Lévaique, M.-T. Martin, P. Retailleau, G. Le Goff, B. Bussaban, S. Lumyong and J. Ouazzani, Phytochemistry, 72, 2406 (2011); doi:10.1016/j.phytochem.2011.08.010.
- C. Hemtasin, S. Kanokmedhakul, K. Kanokmedhakul, C. Hahnvajanawong, K. Soytong, S. Prabpai and P. Kongsaeree, J. Nat. Prod., 74, 609 (2011); doi:10.1021/np100632g.
- K.S. Masters and S. Brase, Chem. Rev., 112, 3717 (2012); doi:10.1021/cr100446h.
- S. Kaul, S. Gupta, M. Ahmed and M.K. Dhar, Phytochem. Rev., 11, 487 (2012); doi:10.1007/s11101-012-9260-6.
- F. Zhu and Y.C. Lin, Chem. Nat. Comp., 43, 132 (2007); doi:10.1007/s10600-007-0062-9.
- M. Isaka, A. Jaturapat, K. Rukseree, K. Danwisetkanjana, M. Tanticharoen and Y. Thebtaranonth, J. Nat. Prod., 64, 1015 (2001); doi:10.1021/np010006h.
- J.X. Yang, S.X. Qiu, Z.G. She and Y.C. Lin, Chem. Nat. Comp., 49, 31 (2013); doi:10.1007/s10600-013-0498-z.
- X.M. Gao, R.R. Wang, D.Y. Niu, C.Y. Meng, L.M. Yang, Y.T. Zheng, G.Y. Yang, Q.F. Hu, H.D. Sun and W.L. Xiao, J. Nat. Prod., 76, 1052 (2013); doi:10.1021/np400070x.
References
D. Udayanga, X. Liu, E.H.C. McKenzie, E. Chukeatirote, A.H.A. Bahkali and K.D. Hyde, Fungal Divers., 50, 189 (2011); doi:10.1007/s13225-011-0126-9.
J.N. Choi, J. Kim, K. Ponnusamy, C. Lim, J.G. Kim, M.J. Muthaiya and C.H. Lee, J. Antibiot., 66, 231 (2013); doi:10.1038/ja.2012.105.
H. Hussain, M.K. Tchimene, I.K. Ahmed, M. Steinert, S. Draeger, B. Schulz and K. Krohn, Nat. Prod. Commun., 6, 1905 (2011).
H. Hussain, I. Ahmed, B. Schulz, S. Draeger and K. Krohn, Fitoterapia, 83, 523 (2012); doi:10.1016/j.fitote.2011.12.017.
H. Hussain, K. Krohn, I. Ahmed, S. Draeger, B. Schulz, S. Di Pietro and G. Pescitelli, Eur. J. Org. Chem., 2012, 1783 (2012); doi:10.1002/ejoc.201101788.
M. Isaka, A. Jaturapat, K. Rukseree, K. Danwisetkanjana, M. Tanticharoen and Y. Thebtaranonth, J. Nat. Prod., 64, 1015 (2001); doi:10.1021/np010006h.
C. Hemtasin, S. Kanokmedhakul, K. Kanokmedhakul, C. Hahnvajanawong, K. Soytong, S. Prabpai and P. Kongsaeree, J. Nat. Prod., 74, 609 (2011); doi:10.1021/np100632g.
E. Adelin, C. Servy, S. Cortial, H. Lévaique, M.-T. Martin, P. Retailleau, G. Le Goff, B. Bussaban, S. Lumyong and J. Ouazzani, Phytochemistry, 72, 2406 (2011); doi:10.1016/j.phytochem.2011.08.010.
C. Hemtasin, S. Kanokmedhakul, K. Kanokmedhakul, C. Hahnvajanawong, K. Soytong, S. Prabpai and P. Kongsaeree, J. Nat. Prod., 74, 609 (2011); doi:10.1021/np100632g.
K.S. Masters and S. Brase, Chem. Rev., 112, 3717 (2012); doi:10.1021/cr100446h.
S. Kaul, S. Gupta, M. Ahmed and M.K. Dhar, Phytochem. Rev., 11, 487 (2012); doi:10.1007/s11101-012-9260-6.
F. Zhu and Y.C. Lin, Chem. Nat. Comp., 43, 132 (2007); doi:10.1007/s10600-007-0062-9.
M. Isaka, A. Jaturapat, K. Rukseree, K. Danwisetkanjana, M. Tanticharoen and Y. Thebtaranonth, J. Nat. Prod., 64, 1015 (2001); doi:10.1021/np010006h.
J.X. Yang, S.X. Qiu, Z.G. She and Y.C. Lin, Chem. Nat. Comp., 49, 31 (2013); doi:10.1007/s10600-013-0498-z.
X.M. Gao, R.R. Wang, D.Y. Niu, C.Y. Meng, L.M. Yang, Y.T. Zheng, G.Y. Yang, Q.F. Hu, H.D. Sun and W.L. Xiao, J. Nat. Prod., 76, 1052 (2013); doi:10.1021/np400070x.