Synthesis and biological evaluation of trisubstituted imidazole derivatives as inhibitors of p38α mitogen-activated protein kinase
DK Kim, JH Lim, JA Lee, PM Dewang
Index: Kim, Dae-Kee; Lim, Jin-Hwi; Lee, Jung A.; Dewang, Purushottam M. Bioorganic and Medicinal Chemistry Letters, 2008 , vol. 18, # 14 p. 4006 - 4010
Full Text: HTML
Citation Number: 12
Abstract
A series of trisubstituted imidazole derivatives containing a 4-fluorophenyl group, a pyrimidine ring, and a CN-or CONH2-substituted benzyl moiety have been synthesized and evaluated for p38α MAP kinase inhibitory activity. Among them, compounds 22c, 27b, and 28b inhibited p38α MAP kinase with IC50 values 27.6, 28, and 31nM, respectively.
Related Articles:
[Scribner, Andrew; Dennis, Richard; Hong, Jean; Lee, Shuliang; McIntyre, Donald; Perrey, David; Feng, Dennis; Fisher, Michael; Wyvratt, Matthew; Leavitt, Penny; Liberator, Paul; Gurnett, Anne; Brown, Chris; Mathew, John; Thompson, Donald; Schmatz, Dennis; Biftu, Tesfaye European Journal of Medicinal Chemistry, 2007 , vol. 42, # 11-12 p. 1334 - 1357]
[Collis, Alan J; Foster, Martyn L; Halley, Frank; Maslen, Christopher; McLay, Iain M; Page, Kenneth M; Redford; Souness, John E; Wilsher, Nicola E Bioorganic and Medicinal Chemistry Letters, 2001 , vol. 11, # 5 p. 693 - 696]
[Sansebastiano; Mosti; Menozzi; Schenone; Muratore; Petta; Debbia; Pesce Schito; Schito Farmaco, 1993 , vol. 48, # 3 p. 335 - 355]
[Farmaco, , vol. 48, # 3 p. 335 - 355]
[Journal of Organic Chemistry, , vol. 56, # 19 p. 5610 - 5614]