Copyright (c) 2013 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Study on the Structure-Activity Relations of Brominated Hydroxy Diphenyl Ethers Derivatives with Anilines
Corresponding Author(s) : Kai-Qun Wu
Asian Journal of Chemistry,
Vol. 25 No. 7 (2013): Vol 25 Issue 7
Abstract
In order to study the influence of anilines on antibacterial activity, eight novel brominated hydroxy diphenyl ethers derivatives were designed and synthesized. The antibacterial activities of the new compounds were tested via agar-well diffusion method in vitro under different concentrations. The results showed the derivatives had antibacterial activities at the concentration 50 μg/mL against Staphylococcus aureus SC and Staphylococcus aureus ATCC26112.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- G.M. Sharma, B. Vig and P.R. Burkholder, Marine Technology Society, Washington D.C. (1969).
- G.M. Sharma and B. Vig, Tetrahedron Lett., 13, 1715 (1972).
- B. Carté and D.J. Faulkner, Tetrahedron, 37, 2335 (1981).
- R.S. Norton, K.D. Croft and R.J. Wells, Tetrahedron, 37, 2341 (1981).
- E.N. Segraves, R.R. Shah, N.L. Segraves, T.A. Johnson, S. Whitman, J.K. Sui, V.A. Kenyon, R.H. Cichewicz, P. Crews and T.R. Holman, J. Med. Chem., 47, 4060 (2004).
- J. Salvá and D.J. Faulkner, J. Nat. Prod., 53, 757 (1990).
- D. Handayani, R.A. Edrada, P. Proksch, V. Wray, L. Witte, R.W.M. Van Soest and A. Kunzmann, J. Nat. Prod., 60, 1313 (1997).
- Y.L. Wang, M.L. Ma and S.H. Chen, Youji Huaxue, 25, 734 (2005).
- K.Q. Wu, Y.L. Wang and H. Zheng, CN 1597657 (2005).
- H. Jin, S. Chen and R.T. Hou, Youji Huaxue, 26, 1424 (2006).
- S. Chen, Y. Xin and Y. Zhan, Youji Huaxue, 3, 498 (2008).
- N.K. Utkina, V,A. Denisenko, O.V. Scholokova, M.V. Virovaya, A.V. Gerasimenko, D.Y. Popov, V.B. Krasokhin and A.M. Popov, J. Nat. Prod., 64, 151 (2001).
- N.K. Utkina, V.A. Denisenko, M,V. Virovaya, O,V. Scholokova and N.G. Prokof'eva, J. Nat. Prod., 65, 1213 (2002).
- X. Tang, M. Xie, Y.X. Sun, J.H. Liu, Z.C. Zhong and Y.L. Wang, Chin. Chem. Lett., 20, 435 (2009).
- Y. Zou, J. Wu and R.T. Hou, Youji Huaxue, 1, 111( 2008).
- Z.X. Yang, H. Chen and Y.L. Wang, Youji Huaxue, 3, 432 (2008).
- T. Saitoh and J. Ichikawa, J. Am. Chem. Soc., 127, 9696 (2005)
References
G.M. Sharma, B. Vig and P.R. Burkholder, Marine Technology Society, Washington D.C. (1969).
G.M. Sharma and B. Vig, Tetrahedron Lett., 13, 1715 (1972).
B. Carté and D.J. Faulkner, Tetrahedron, 37, 2335 (1981).
R.S. Norton, K.D. Croft and R.J. Wells, Tetrahedron, 37, 2341 (1981).
E.N. Segraves, R.R. Shah, N.L. Segraves, T.A. Johnson, S. Whitman, J.K. Sui, V.A. Kenyon, R.H. Cichewicz, P. Crews and T.R. Holman, J. Med. Chem., 47, 4060 (2004).
J. Salvá and D.J. Faulkner, J. Nat. Prod., 53, 757 (1990).
D. Handayani, R.A. Edrada, P. Proksch, V. Wray, L. Witte, R.W.M. Van Soest and A. Kunzmann, J. Nat. Prod., 60, 1313 (1997).
Y.L. Wang, M.L. Ma and S.H. Chen, Youji Huaxue, 25, 734 (2005).
K.Q. Wu, Y.L. Wang and H. Zheng, CN 1597657 (2005).
H. Jin, S. Chen and R.T. Hou, Youji Huaxue, 26, 1424 (2006).
S. Chen, Y. Xin and Y. Zhan, Youji Huaxue, 3, 498 (2008).
N.K. Utkina, V,A. Denisenko, O.V. Scholokova, M.V. Virovaya, A.V. Gerasimenko, D.Y. Popov, V.B. Krasokhin and A.M. Popov, J. Nat. Prod., 64, 151 (2001).
N.K. Utkina, V.A. Denisenko, M,V. Virovaya, O,V. Scholokova and N.G. Prokof'eva, J. Nat. Prod., 65, 1213 (2002).
X. Tang, M. Xie, Y.X. Sun, J.H. Liu, Z.C. Zhong and Y.L. Wang, Chin. Chem. Lett., 20, 435 (2009).
Y. Zou, J. Wu and R.T. Hou, Youji Huaxue, 1, 111( 2008).
Z.X. Yang, H. Chen and Y.L. Wang, Youji Huaxue, 3, 432 (2008).
T. Saitoh and J. Ichikawa, J. Am. Chem. Soc., 127, 9696 (2005)