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A New Phenyl Derivated Butyrolactone from Fermentation Products of Endophytic Fungus Aspergillus terreus
Corresponding Author(s) : Haiying Yang
Asian Journal of Chemistry,
Vol. 27 No. 10 (2015): Vol 27 Issue 10
Abstract
A new phenyl derivated butyrolactone, terrephenol C (1) was isolated from the fermentation products of a fungus Aspergillus terreus. Its structure was elucidated by spectroscopic methods, including extensive 1D NMR and 2D NMR techniques. The antitobacco mosaic virus (anti-TMV) activity of 1 was evaluated and showed anti-TMV activity with inhibition rates of 16.7 %.
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- H. Laatsch, A Data Base for Rapid Structural Determination of Microbial Natural Products and Annual Updates, Chemical Concepts, Weinheim, Germany (2010).
- Z.K. Wang, Y.S. Yang, A.T. Stefka, G. Sun and L.H. Peng, Aliment. Pharmacol. Ther., 39, 751 (2014); doi:10.1111/apt.12665.
- S. Martins, S.I. Mussatto, G. Martinez-Avila, J. Montanez-Saenz, C.N. Aguilar and J.A. Teixeira, Biotechnol. Adv., 29, 365 (2011); doi:10.1016/j.biotechadv.2011.01.008.
- R.M.P. Gutierrez, A.M.N. Gonzalez and A.M. Ramirez, Curr. Med. Chem., 19, 2992 (2012); doi:10.2174/092986712800672111.
- A.S. Awaad, A.J.A. Nabilah and M.E. Zain, Phytother. Res., 26, 1872 (2012); doi:10.1002/ptr.4668.
- Y. Wang, J.K. Zheng, P.P. Liu, W. Wang and W.M. Zhu, Mar. Drugs, 9, 1368 (2011); doi:10.3390/md9081368.
- R.R. Parvatkar, C. D'Souza, A. Tripathi and C.G. Naik, Phytochemistry, 70, 128 (2009); doi:10.1016/j.phytochem.2008.10.017.
- J.A. Joule and K. Mills, Heterocyclic Chemistry, Blackwell Science Publishing: Oxford, UK, edn 4 (2000).
- W. Wang, H. Kim, S.J. Nam, B.J. Rho and H. Kang, J. Nat. Prod., 75, 2049 (2012); doi:10.1021/np300544a.
- R. Haritakun, P. Rachtawee, R. Chanthaket, N. Boonyuen and M. Isaka, Chem. Pharm. Bull. (Tokyo), 58, 1545 (2010); doi:10.1248/cpb.58.1545.
- 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.
- Z.Q. Bai, X.P. Lin, Y.Z. Wang, J.F. Wang, X.F. Zhou, B. Yang, J. Liu, X.W. Yang, Y. Wang and Y.H. Liu, Fitoterapia, 95, 194 (2014); doi:10.1016/j.fitote.2014.03.021.
- 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.
- J.J. Qin, J.X. Zhu, Q. Zeng, X.R. Cheng, Y. Zhu, S.D. Zhang, L. Shan, H.Z. Jin and W.D. Zhang, J. Nat. Prod., 74, 1881 (2011); doi:10.1021/np200319x.
- 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.
- Q.F. Hu, B. Zhou, J.M. Huang, X.M. Gao, L.D. Shu, G.Y. Yang and C.T. Che, J. Nat. Prod., 76, 292 (2013); doi:10.1021/np300727f.
- Q.-F. Hu, B. Zhou, Y.-Q. Ye, Z.-Y. Jiang, X.-Z. Huang, Y.-K. Li, G. Du, G.-Y. Yang and X.-M. Gao, J. Nat. Prod., 76, 1854 (2013); doi:10.1021/np400379u.
References
H. Laatsch, A Data Base for Rapid Structural Determination of Microbial Natural Products and Annual Updates, Chemical Concepts, Weinheim, Germany (2010).
Z.K. Wang, Y.S. Yang, A.T. Stefka, G. Sun and L.H. Peng, Aliment. Pharmacol. Ther., 39, 751 (2014); doi:10.1111/apt.12665.
S. Martins, S.I. Mussatto, G. Martinez-Avila, J. Montanez-Saenz, C.N. Aguilar and J.A. Teixeira, Biotechnol. Adv., 29, 365 (2011); doi:10.1016/j.biotechadv.2011.01.008.
R.M.P. Gutierrez, A.M.N. Gonzalez and A.M. Ramirez, Curr. Med. Chem., 19, 2992 (2012); doi:10.2174/092986712800672111.
A.S. Awaad, A.J.A. Nabilah and M.E. Zain, Phytother. Res., 26, 1872 (2012); doi:10.1002/ptr.4668.
Y. Wang, J.K. Zheng, P.P. Liu, W. Wang and W.M. Zhu, Mar. Drugs, 9, 1368 (2011); doi:10.3390/md9081368.
R.R. Parvatkar, C. D'Souza, A. Tripathi and C.G. Naik, Phytochemistry, 70, 128 (2009); doi:10.1016/j.phytochem.2008.10.017.
J.A. Joule and K. Mills, Heterocyclic Chemistry, Blackwell Science Publishing: Oxford, UK, edn 4 (2000).
W. Wang, H. Kim, S.J. Nam, B.J. Rho and H. Kang, J. Nat. Prod., 75, 2049 (2012); doi:10.1021/np300544a.
R. Haritakun, P. Rachtawee, R. Chanthaket, N. Boonyuen and M. Isaka, Chem. Pharm. Bull. (Tokyo), 58, 1545 (2010); doi:10.1248/cpb.58.1545.
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.
Z.Q. Bai, X.P. Lin, Y.Z. Wang, J.F. Wang, X.F. Zhou, B. Yang, J. Liu, X.W. Yang, Y. Wang and Y.H. Liu, Fitoterapia, 95, 194 (2014); doi:10.1016/j.fitote.2014.03.021.
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.
J.J. Qin, J.X. Zhu, Q. Zeng, X.R. Cheng, Y. Zhu, S.D. Zhang, L. Shan, H.Z. Jin and W.D. Zhang, J. Nat. Prod., 74, 1881 (2011); doi:10.1021/np200319x.
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.
Q.F. Hu, B. Zhou, J.M. Huang, X.M. Gao, L.D. Shu, G.Y. Yang and C.T. Che, J. Nat. Prod., 76, 292 (2013); doi:10.1021/np300727f.
Q.-F. Hu, B. Zhou, Y.-Q. Ye, Z.-Y. Jiang, X.-Z. Huang, Y.-K. Li, G. Du, G.-Y. Yang and X.-M. Gao, J. Nat. Prod., 76, 1854 (2013); doi:10.1021/np400379u.