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http://dx.doi.org/10.5012/bkcs.2012.33.3.953

Synthesis of Biologically Active Chalcones and their Anti-inflammatory Effects  

Jeon, Jae-Ho (Institute of Natural Medicine, Hallym University)
Kim, Si-Jun (Department of Chemistry and Institute of Applied Chemistry, Hallym University)
Kim, Cheol-Gi (Department of Chemistry and Institute of Applied Chemistry, Hallym University)
Kim, Jin-Kyung (Department of Biomedical Science, College of Natural Science, Catholic University of Daegu)
Jun, Jong-Gab (Institute of Natural Medicine, Hallym University)
Publication Information
Abstract
Chalcones have been reported to have various biological activities including antitumor, antiparasitic, antileishmanial, antioxidative, superoxide scavenging, antibacterial, and PTP1B activity. Due to the limited natural resources, we had to prepare sizable quantities of biologically active chalcones for bio-tests. Therefore, Claisen-Schmidt condensation between substituted acetophenones and corresponding aldehydes enabled us to prepare chalcones for inflammatory studies. Chalcones thus prepared showed significant suppression of nitric oxide (NO) production at $10{\mu}M$.
Keywords
Chalcones; Claisen-Schmidt condensation; Anti-inflammatory studies; EDDA; NO production;
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1 Ruffin, B.; Castellan, A.; Grelier, S.; Nourmamode, A.; Riela, S.; Trichet, V. J. Appl. Poly. Sci. 1998, 69, 2517.   DOI
2 Kharazmi, A.; Christensen, S. B.; Ming, C.; Theander, T. G. US 5,985,935, 1999.
3 Claisen, L.; Eisleb, O. Justus Liebigs Ann. Chem. 1913, 401, 21.   DOI
4 Cushine, T. P. T.; Lamb, A. J. Int. J. Antimicrob. Ag. 2005, 26, 343.   DOI   ScienceOn
5 Shibata, S. Stem Cells 1994, 12, 44.   DOI   ScienceOn
6 Liu, X. L.; Xu, Y. J.; Go, M. L. Eur. J. Med. Chem. 2008, 43, 1681.   DOI   ScienceOn
7 Kwon, H. S.; Park, J. H.; Kim, D. H.; Kim, Y. H.; Park, J. H.; Shin, H. K.; Kim, J. K. J. Mol. Med. (Berl) 2008, 86, 1287.   DOI   ScienceOn
8 Jeon, J.-H.; Kim, M. R.; Jun, J.-G. Synthesis 2011, 370.
9 Liu, M.; Wilarirat, P.; Go, M.-L. J. Med. Chem. 2001, 44, 4443.   DOI   ScienceOn
10 Nagai, H.; He, J.-X.; Tani, T.; Akao, T. J. Pharm. Pharmacol. 2007, 59, 1421.   DOI   ScienceOn
11 Nielsen, S. F.; Christensen, S. B.; Cruciani, G.; Kharazmi, A.; Liljefors, T. J. Med. Chem. 1998, 41, 4819.   DOI
12 Chen, M.; Christensen, S. B.; Zhai, L.; Rasmussen, M. H.; Theander, T. G.; Frokjaer, S.; Steffansen, S.; Davidsen, J.; Khrazmi, A. J. Infec. Dis. 1997, 176, 1327.   DOI
13 Nicolaou, K. C.; Pfefferkorn, J. A.; Cao, G.-Q. Angew. Chem. Int. Ed. 2000, 39, 734.   DOI
14 Nicolaou, K. C.; Pfefferkorn, J. A.; Roecker, A. J.; Cao, G.-Q.; Barluenga, S.; Mitchell, H. J. J. Am. Chem. Soc. 2000, 122, 9939.   DOI
15 Lee, Y. R.; Wang, X.; Xia, L. Molecules 2007, 12, 1420.   DOI
16 Claisen, L.; Claparede, A. Ber. 1881, 14, 2460.   DOI
17 Scmidt, J. G. Ber. 1881, 14, 1459.   DOI
18 Vermooy, J. H.; Dentener, M. A.; Suylen, R. J. van.; Buurman, W. A.; Wouters, E. F. Am. J. Respir Cell Mol. Biol. 2002, 26,152.   DOI   ScienceOn
19 Nabaei-Bidhendi, G.; Bannerjee, N. R. J. Ind. Chem. Soc. 1990, 67, 43.