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Chromones from the Flowers of Rosa rugosa and Their Cytotoxicity
Corresponding Author(s) : Xuemei Gao
Asian Journal of Chemistry,
Vol. 25 No. 15 (2013): Vol 25 Issue 15
Abstract
A new chromone, 2,2-dimethyl-4-oxo-8-(2-oxopropyl)-chroman-6-yl acetate (1), together with five known chromones (2-6), were isolated from the flowers of Rosa rugosa. The structures of 1-6 were elucidated by spectroscopic methods including extensive 1D and 2D NMR techniques. Compounds 1 were evaluated for their cytotoxicity against five human tumor cell lines and it showed high cytotoxicity against A549 and MCF7 cell with IC50 values of 3.6 and 5.0 μM, respectively.
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- X.M. Gao, L.Y. Yang, L.D. Shu, Y.Q. Shen, Y.J. Zhang and Q.F. Hu, Heterocycles, 85, 1925 (2012).
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- F.M. Dean and M.L. Robinson, Phytochemistry, 10, 3221 (1971).
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- L. Liu, S.C. Liu, S.B. Niu, L.D. Guo, X.L. Chen and Y.S. Che, J. Nat. Prod., 72, 1482 (2009).
- D.R. Mou, W. Zhao, Tao Zhang, L. Wan, G.Y. Yang, Y.K. Chen, Q.F. Hu and M.M. Miao, Heterocycles, 85, 1251 (2012).
- A. Lazarenkow, J. Nawrot-Modranka, E. Brzezinska, U. Krajewska and M. Rozalski, Med. Chem. Res., 21, 1861 (2012).
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References
S.M. Gault and P.M. Synge, The Dictionary of Roses in Colour, Ebury Press, London (1971).
J.L. Lu, China Flowers Horticult., 11, 26 (2012).
L. Putian and Y. Jiang, Flora of China, Chinese Science Press, Beijing (1977).
S. Ochir, B. Park, M. Nishizawa, T. Kanazawa, M. Funaki and T.J. Yamagishi, Nat. Med., 64, 383 (2010).
Y. Hashidoko, S. Tahara and J. Mizutani, Phytochemistry, 32, 387 (1993).
Y. Hashidoko, Phytochemistry, 43, 535 (1996).
H.J. An, I.T. Kim, H.J. Park, H.M. Kim, J.H. Choid and K.T. Lee, Int. Immunopharm., 11, 504 (2011).
Z.P. Xiao, H.K. Wu, T. Wu, H. Shi, B. Hang and H.A. Aisa, Chem. Nat. Comp., 42, 736 (2006).
X.M. Gao, L.Y. Yang, L.D. Shu, Y.Q. Shen, Y.J. Zhang and Q.F. Hu, Heterocycles, 85, 1925 (2012).
M.H. Ma, B. Cui, H.F. Yu and C.Z. Yuan, J. Shandong Inst. Light. Ind., 22, 38 (2008).
S. Thadaniti, W. Archakunakorn, P. Tuntiwachwuttikul and J.B. Bremner, J. Sci. Soc. Thailand, 20, 183 (1994).
T. Fukai, Y. Hano, K. Hirakura, T. Nomura and J. Uzawa, Chem. Pharm. Bull., 33, 4288 (1985).
F.M. Dean and M.L. Robinson, Phytochemistry, 10, 3221 (1971).
N.T. Dat, X.J. Jin, Y.S. Hong and J.J. Lee, J. Nat. Prod., 73, 1167 (2010).
L. Liu, S.C. Liu, S.B. Niu, L.D. Guo, X.L. Chen and Y.S. Che, J. Nat. Prod., 72, 1482 (2009).
D.R. Mou, W. Zhao, Tao Zhang, L. Wan, G.Y. Yang, Y.K. Chen, Q.F. Hu and M.M. Miao, Heterocycles, 85, 1251 (2012).
A. Lazarenkow, J. Nawrot-Modranka, E. Brzezinska, U. Krajewska and M. Rozalski, Med. Chem. Res., 21, 1861 (2012).
T. Mosmann, J. Immunol. Methods, 65, 55 (1983)