Copyright (c) 2013 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis and Anticoccidial Activities of Quinoline Carboxylate Derivatives with Methyl (E)-2-(3-methoxy)acrylate Moiety
Corresponding Author(s) : Yu-Liang Wang
Asian Journal of Chemistry,
Vol. 25 No. 15 (2013): Vol 25 Issue 15
Abstract
A series of novel quinoline carboxylate derivatives with methyl (E)-2-(3-methoxy) acrylate group were designed and synthesized as anticoccidial medicines. The structures were confirmed by 1H NMR, IR and HR-MS spectra. The biological activities were primarily evaluated according to the anticoccidial index method. The results indicated that these compounds (7c, 7d, 7e, 7g) exhibited anticoccidial activities against Eimeria tenella. In particular, the anticoccidial index of 6-decyloxy-7-ethoxy-4-{6-[2-(2-methoxy-1-methoxycarbonyl-vinyl)phenoxy]pyrimidin-4-yloxy}-quinoline-3-carboxylic acid ethyl ester (7e) was 168.7, which indicated that the compound has a good anticoccidial activity.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- R.B. Williams, Int. J. Parasitol, 29, 1209 (1999).
- C.F. Duffy, G.F. Mathis and R.F. Power, Vet. Parasitol., 130, 185 (2005).
- D. Feng, M. Fisher, G.B. Liang, X.X. Qian, C. Brown, A. Gurnett, P.S. Leavitt, P.A. Liberator, J. Mathew, A. Misura, S. Samaras, T. Tamas, D.M. Schmatz, M. Wyvratt and T. Biftu, Bioorg. Med. Chem. Lett., 16, 5978 (2006).
- H.D. Chapman, Avian. Pathol., 26, 221 (1997).
- G. Greif and B. Stephan, Parasitol. Res., 82, 706 (1996).
- J.J. Xu, J.P. Tao and J.B. Peng, Anim. Husbandry Vet. Med., 40, 18 (2008).
- Y.Y. Zhang and Y.L. Wang, Chinese Chem. Lett., 21, 426 (2010).
- J.N. Hodgson, Br. Vet. J., 124, 209 (1968).
- G.Q. Li, S. Kanu, F.Y. Xiang, S.M. Xiao, L. Zhang, H.W. Chen and H.J. Ye, Vet. Parasitol., 119, 261 (2004).
- J.H. You, C.W. Ye, Y.B. Weng, X.H. Mo and Y.L. Wang, Arkivoc., 1 (2008).
- C.R. Yan, J. Xu, Y.B. Weng, J. Li, Y.L. Wang and H. Chen, Chem. Biol. Drug. Des., 72, 314 (2008).
- J. Xu, C.R. Yan, Y.B. Weng, L.L. Qiu and Y.L. Wang, Chem. Res. Appl., 21, 694 (2009).
- J. Dong, H. Dao, J.S. Lou and H.J. Pi, Fine Chem. Intermed., 37, 25 (2007).
- C.R. Yan, L. Li, K.Q. Wu and Y.L. Wang, J. Yibin Uni., 5 (2012).
- J.J. Xu, J.P. Tao and J.B. Peng, Anim. Husbandry Vet. Med., 40, 18 (2008).
- S.D. Folz, B.L. Lee and L.H. Nowakowski, Int. J. Parasitol., 75, 696 (1989)
References
R.B. Williams, Int. J. Parasitol, 29, 1209 (1999).
C.F. Duffy, G.F. Mathis and R.F. Power, Vet. Parasitol., 130, 185 (2005).
D. Feng, M. Fisher, G.B. Liang, X.X. Qian, C. Brown, A. Gurnett, P.S. Leavitt, P.A. Liberator, J. Mathew, A. Misura, S. Samaras, T. Tamas, D.M. Schmatz, M. Wyvratt and T. Biftu, Bioorg. Med. Chem. Lett., 16, 5978 (2006).
H.D. Chapman, Avian. Pathol., 26, 221 (1997).
G. Greif and B. Stephan, Parasitol. Res., 82, 706 (1996).
J.J. Xu, J.P. Tao and J.B. Peng, Anim. Husbandry Vet. Med., 40, 18 (2008).
Y.Y. Zhang and Y.L. Wang, Chinese Chem. Lett., 21, 426 (2010).
J.N. Hodgson, Br. Vet. J., 124, 209 (1968).
G.Q. Li, S. Kanu, F.Y. Xiang, S.M. Xiao, L. Zhang, H.W. Chen and H.J. Ye, Vet. Parasitol., 119, 261 (2004).
J.H. You, C.W. Ye, Y.B. Weng, X.H. Mo and Y.L. Wang, Arkivoc., 1 (2008).
C.R. Yan, J. Xu, Y.B. Weng, J. Li, Y.L. Wang and H. Chen, Chem. Biol. Drug. Des., 72, 314 (2008).
J. Xu, C.R. Yan, Y.B. Weng, L.L. Qiu and Y.L. Wang, Chem. Res. Appl., 21, 694 (2009).
J. Dong, H. Dao, J.S. Lou and H.J. Pi, Fine Chem. Intermed., 37, 25 (2007).
C.R. Yan, L. Li, K.Q. Wu and Y.L. Wang, J. Yibin Uni., 5 (2012).
J.J. Xu, J.P. Tao and J.B. Peng, Anim. Husbandry Vet. Med., 40, 18 (2008).
S.D. Folz, B.L. Lee and L.H. Nowakowski, Int. J. Parasitol., 75, 696 (1989)