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A New Dihydrobenzofuran Neolignan from Stem of Flue-Cured Tobacco and its Anti-tobacco Mosaic Virus Activity
Corresponding Author(s) : Zhihua Liu
Asian Journal of Chemistry,
Vol. 27 No. 8 (2015): Vol 27 Issue 8
Abstract
A new dihydrobenzofuran neolignan, tobdihydrofuran A (1), was isolated from the stems of flue-cured tobacco (a variety of Nicotiana tabacum L). Its structure was elucidated by spectroscopic methods, including extensive 1D and 2D NMR techniques. Compound 1 was also tested for its anti-tobacco mosaic virus (anti-TMV) activity and it shows potential anti-tobacco mosaic virus activity with inhibition rates of 28.6 %.
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- The Editorial Committee of the Administration Bureau of Flora of China, Flora of China, Beijing Science and Technology Press, Beijing, 67 vols. (2005).
- T.W. Hu and Z. Mao, Tob. Control, 15(suppl_1), i37 (2006); doi:10.1136/tc.2005.014621.
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References
The Editorial Committee of the Administration Bureau of Flora of China, Flora of China, Beijing Science and Technology Press, Beijing, 67 vols. (2005).
T.W. Hu and Z. Mao, Tob. Control, 15(suppl_1), i37 (2006); doi:10.1136/tc.2005.014621.
A. Rodgman and T.A. Perfetti, The Chemical Components of Tobacco and Tobacco Smoke, CRC Press, Taylor and Francis Group, Boca Raton, Florida (2008)..
A.P. Cavender and M. Alban, J. Ethnobiol. Ethnomed., 5, 3 (2009); doi:10.1186/1746-4269-5-3.
A. Inta, P. Shengji, H. Balslev, P. Wangpakapattanawong and C. Trisonthi, J. Ethnopharmacol., 116, 508 (2008); doi:10.1016/j.jep.2007.12.015.
X. Feng, J.-S. Wang, J. Luo and L.-Y. Kong, J. Asian Nat. Prod. Res., 12, 252 (2010); doi:10.1080/10286020903550947.
Y. Shinozaki, T. Tobita, M. Mizutani and T. Matsuzaki, Biosci. Biotechnol. Biochem., 60, 903 (1996); doi:10.1271/bbb.60.903.
T. Pettersson, A.M. Eklund and I. Wahlberg, J. Agric. Food Chem., 41, 2097 (1993); doi:10.1021/jf00035a052.
X.C. Wei, S.C. Sumithran, A.G. Deaciuc, H.R. Burton, L.P. Bush, L.P. Dwoskin and P.A. Crooks, Life Sci., 78, 495 (2005); doi:10.1016/j.lfs.2005.09.009.
T. Braumann, G. Nicolaus, W. Hahn and H. Elmenhorst, Phytochemistry, 29, 3693 (1990); doi:10.1016/0031-9422(90)85311-3.
Y.K. Chen, X.S. Li, G.Y. Yang, Z.Y. Chen, Q.F. Hu and M.M. Miao, J. Asian Nat. Prod. Res., 14, 450 (2012); doi:10.1080/10286020.2012.669578.
Q.-F. Hu, G. Yang, X. Li, X. Yang, H. Mu, Y. Chen and X.-M. Gao, Heterocycles, 85, 147 (2012); doi:10.3987/COM-11-12349.
Z.Y. Chen, J.L. Tan, G.Y. Yang, M.M. Miao, Z.Y. Chen and T.F. Li, Phytochem. Lett., 5, 233 (2012); doi:10.1016/j.phytol.2012.01.001.
Y. Chen, T. Li, Z.-Y. Chen, G. Yang, M. Miao and J. Tan, Heterocycles, 83, 2381 (2011); doi:10.3987/COM-11-12317.
W. Li, L.B. Zhang, J.H. Peng, N. Li and X.Y. Zhu, Ind. Crops Prod., 27, 341 (2008); doi:10.1016/j.indcrop.2007.11.011.
Q. Hu, M. Miao, W. Zhao, T. Zhang, L. Wan, G. Yang, Y. Chen and D. Mou, Heterocycles, 85, 2485 (2012); doi:10.3987/COM-12-12557.
X.X. Huang, C.C. Zhou, L.Z. Li, Y. Peng, L.L. Lou, S. Liu, D.M. Li, T. Ikejima and S.J. Song, Fitoterapia, 91, 217 (2013); doi:10.1016/j.fitote.2013.09.011.
Q.F. Hu, B. Zhou, X.M. Gao, L.Y. Yang, L.D. Shu, Y.Q. Shen, G.P. Li, C.T. Che and G.Y. Yang, J. Nat. Prod., 75, 1909 (2012); doi:10.1021/np300395m.
G. Lemière, M. Gao, A.D. Groot, R. Dommisse, J. Lepoivre, L. Pieters and V. Buss, J. Chem. Soc. Perkin. Trans., 1775 (1995); doi:10.1039/p19950001775.
N. Matsuda, H. Sato, Y. Yaoita and M. Kikuchi, Chem. Pharm. Bull. (Tokyo), 44, 1122 (1996); doi:10.1248/cpb.44.1122.
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.