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A New Butyrolactone from the Fermentation Products of Endophytic Fungus Aspergillus versicolor
Corresponding Author(s) : Yanqing Ye
Asian Journal of Chemistry,
Vol. 27 No. 10 (2015): Vol 27 Issue 10
Abstract
A new butyrolactone, asperphenol C (1), was isolated from the fermentation products of an endophytic fungus Aspergillus versicolor. Its structure was elucidated by spectroscopic methods including extensive 1D- and 2D NMR techniques. Compound 1 was also tested for its antitobacco mosaic virus (anti-TMV) activity. The results showed that compound 1 exhibited anti-TMV activity with inhibition rate of 22.1 %.
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- L.-L. Sun, C.-L. Shao, J.-F. Chen, Z.-Y. Guo, X.-M. Fu, M. Chen, Y.-Y. Chen, R. Li, N.J. de Voogd, Z.-G. She, Y.-C. Lin and C.-Y. Wang, Bioorg. Med. Chem. Lett., 22, 1326 (2012); doi:10.1016/j.bmcl.2011.12.083.
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References
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Y. Wang, J.K. Zheng, P.P. Liu, W. Wang and W.M. Zhu, Mar. Drugs, 9, 1368 (2011); doi:10.3390/md9081368.
F. He, Y.L. Sun, K.S. Liu, X.Y. Zhang, P.Y. Qian, Y.F. Wang and S.H. Qi, J. Antibiot., 65, 109 (2012); doi:10.1038/ja.2011.117.
S. Kumar, R. Garg and A. Kabra, World J. Pharm. Res. Technol., 1, 131 (2013).
W. Wang, H. Kim, S.J. Nam, B.J. Rho and H. Kang, J. Nat. Prod., 75, 2049 (2012); doi:10.1021/np300544a.
R.M. Centko, S. Ramon-Garcia, T. Taylor, B.O. Patrick, C.J. Thompson, V.P. Miao and R.J. Andersen, J. Nat. Prod., 75, 2178 (2012); doi:10.1021/np3006277.
D.-H. Li, T.-J. Zhu, H.-B. Liu, Y.-C. Fang, Q.-Q. Gu and W.-M. Zhu, Arch. Pharm. Res., 29, 624 (2006); doi:10.1007/BF02968245.
X.J. Wang, H.W. Xu, L.L. Guo, J.X. Zheng, B. Xu, X. Guo, C.X. Zheng and H.M. Liu, Bioorg. Med. Chem. Lett., 21, 3074 (2011); doi:10.1016/j.bmcl.2011.03.029.
J. Boukouvalas and R.P. Loach, J. Org. Chem., 73, 8109 (2008); doi:10.1021/jo8015924.
S.L. Khokra, J. Monga, A. Husain, M. Vij and R. Saini, Med. Chem. Res., 22, 5536 (2013); doi:10.1007/s00044-013-0511-x.
H.Q. Gao, W.Q. Guo, Q. Wang, L.Q. Zhang, M.L. Zhu, T.J. Zhu, Q.Q. Gu, W. Wang and D.H. Li, Bioorg. Med. Chem. Lett., 23, 1776 (2013); doi:10.1016/j.bmcl.2013.01.051.
H.-J. Zhang, N.V. Hung, N.M. Cuong, D.D. Soejarto, J.M. Pezzuto, H.H. Fong and G.T. Tan, Planta Med., 71, 452 (2005); doi:10.1055/s-2005-864142.
R. Haritakun, P. Rachtawee, R. Chanthaket, N. Boonyuen and M. Isaka, Chem. Pharm. Bull. (Tokyo), 58, 1545 (2010); doi:10.1248/cpb.58.1545.
R.R. Parvatkar, C. D’Souza, A. Tripathi and C.G. Naik, Phytochemistry, 70, 128 (2009); doi:10.1016/j.phytochem.2008.10.017.
X.M. Niu, H.M. Dahse, K.D. Menzel, O. Lozach, G. Walther, L. Meijer, S. Grabley and I. Sattler, J. Nat. Prod., 71, 689 (2008); doi:10.1021/np070341r.
F. He, J. Bao, X.Y. Zhang, Z.C. Tu, Y.M. Shi and S.H. Qi, J. Nat. Prod., 76, 1182 (2013); doi:10.1021/np300897v.
K.V. Rao, A.K. Sadhukhan, M. Veerender, V. Ravikumar, E.V.S. Mohan, S.D. Dhanvantri, M. Sitaramkumar, J. Moses Babu, K. Vyas and G. Om Reddy, Chem. Pharm. Bull. (Tokyo), 48, 559 (2000); doi:10.1248/cpb.48.559.
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