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http://dx.doi.org/10.5012/bkcs.2006.27.11.1861

Synthesis of Piperazinylalkylisoxazoline Analogues and Their Binding Affinities for Dopamine Receptor Subtypes  

Jung, Ji-Young (Department of Chemistry & Institute of Basic Science, Sungshin Women’s University)
Jung, Sun-Ho (Department of Chemistry & Institute of Basic Science, Sungshin Women’s University)
Koh, Hun-Yeong (Department of Chemistry, Inha University)
Pae, Ae-Nim (Biochemicals Research Center, Korea Institute of Science and Technology)
Park, Woo-Kyu (Pharmaceutical Screening Research Team, Korea Research Institute of Chemical Technology)
Kong, Jae-Yang (Pharmaceutical Screening Research Team, Korea Research Institute of Chemical Technology)
Publication Information
Bulletin of the Korean Chemical Society / v.27, no.11, 2006 , pp. 1861-1864 More about this Journal
Keywords
Dopamine receptors; Piperazinylalkylisoxazolines; Combinatorial synthesis; Reductive amination; 1,3-Dipolar cycloaddition;
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1 Bettinetti, L.; Löber, S.; Hubner, H.; Gmeiner, P. J. Comb. Chem. 2005, 7, 309   DOI   ScienceOn
2 Ji, M.; Chen, J.; Ding, K.; Wu, X.; Varady, J.; Levant, B.; Wang, S. Bioorg. Med. Chem. Lett. 2005, 15, 1701   DOI   ScienceOn
3 Padwa, A. 1,3-Dipolar Cycloaddition Chemistry; John-Wiley & Sons: New York, 1984; Vol. 1 and 2
4 Baldino, C. M. J. Comb. Chem. 2000, 2, 89   DOI   ScienceOn
5 Abdel-Magid, A. F.; Carson, K. G.; Harris, B. D.; Maryanoff, C. A.; Shah, R. D. J. Org. Chem. 1996, 61, 3849   DOI   ScienceOn
6 Lober, S.; Hubner, H.; Gmeiner, P. Bioorg. Med. Chem. Lett. 2006, 16, 2955   DOI   ScienceOn
7 Sokoloff, P.; Giros, B.; Martres, M.-P.; Bouthenet, M.-L.; Schwartz, J.-C. Nature 1990, 347, 146   DOI   ScienceOn
8 Van Tol, H. M.; Bunzow, J. R.; Guan, H. C.; Sunahara, R. K.; Seeman, P.; Niznik, H. B.: Civelli, O. Nature 1991, 30, 610
9 Enguehard-Gueiffier, C.; Hubner, H.; El Hakmaoui, A.; Allouchi, H.; Gmeiner, P.; Argiolas, A.; Melis, M. R.; Gueiffier, A. J. Med. Chem. 2006, 49, 3938   DOI   ScienceOn
10 Leopoldo, M.; Lacivita, E.; Colabufo, N. A.; Beradi, F.; Perrone, R. J. Pharm. Pharmacol. 2006, 58, 209   DOI   ScienceOn
11 Lentz, D.; Boeckler, F.; Hubner, H.; Gmeiner, P. Bioorg. Med. Chem. 2005, 13, 4434   DOI   ScienceOn
12 Wang, X.; Bhatia, P. A.; Daanen, J. F.; Latsaw, S. P.; Rhode, J.; Kolsa, T.; Hakeem, A. A.; Matulenko, M. A.; Nakane, M.; Uchic, M. E.; Miller, L. N.; Chang, R.; Moreland, R. B.; Brioni, J. D.; Stewart, A. O. Bioorg. Med. Chem. 2005, 13, 4667   DOI   ScienceOn
13 Cha, M. Y.; Choi, B. C.; Kang, K. H.; Pae, A. N.; Choi, K. I.; Cho, Y. S.; Koh, H. Y.; Lee, H.-Y.; Jung, D.; Kong, J. Y. Bioorg. Med. Chem. Lett. 2002, 12, 1327   DOI   ScienceOn
14 Studer, A.; Curran, D. P. Tetrahedron 1997, 53, 6681   DOI   ScienceOn
15 Grandy, D. K.; Marchinonmi, M. A.; Makam, H.; Stofko, R. E.; Alfano, M.; Frothingham, L.; Fischer, J. B.; Burke-Howie, K. J.; Bunzow, J. R.; Server, A. C.; Civelli, O. Proc. Natl. Acad. Sci. U.S.A. 1989, 86, 9762   DOI   ScienceOn
16 Chu, W.; Tu, Z.; McElveen, E.; Xu, J.; Taylor, M.; Luedtke, R. R.; March, R. H. Bioorg. Med. Chem. 2005, 13, 77   DOI   ScienceOn
17 Ding, K.; Chen, J.; Ji, M.; Wu, X.; Varady, J.; Yang, C. Y.; Lu, Y.; Deschamps, J. R.; Levant, B.; Wang, S. J. Med. Chem. Lett. 2005, 48, 3171   DOI   ScienceOn
18 Chen, J.; Ding, K.; Levant, B.; Wang, S. Bioorg. Med. Chem. Lett. 2006, 16, 443   DOI   ScienceOn
19 Mohr, P.; Decker, M.; Enzensperger, C.; Lehmann, J. J. Med. Chem. 2006, 49, 2110   DOI   ScienceOn
20 Kang, K. H.; Pae, A. N.; Choi, K. I.; Cho, Y. S.; Chung, B. Y.; Lee, J. E.; Jung, S. H.; Koh, H. Y.; Lee, H.-Y. Tetrahedron Lett. 2001, 42, 1057   DOI   ScienceOn