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Bullington, J.; Argentieri, D.; Averill, K.; Carter, D.; Cavender, D.; Fahmy, B.; Fan, X.; Hall, D.; Heintzelman, G.; Jackson, P.; Leung, W. P.; Li, X.; Ling, P.; Olini, G.; Razler, T.; Reuman, M.; Rupert, K.; Russell, R.; Siekierka, J.; Wadsworth, S.; Wolff, R.; Xiang, B.; Zhanga, Y. M. Inhibitors of unactivated p38 MAP kinase. Bioorg. Med. Chem. Lett., 2006, 16, 6102-6106.
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Structure-activity relationships of triazolopyridine oxazole p38 inhibitors: Identification of candidates for clinical development
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McClure, K. F.; Letavic, M. A.; Kalgutkar, A. S.; Gabel, C. A.; Audoly, L.; Barberia, J. T.; Braganza, J. F.; Carter, D.; Carty, T. J.; Cortina, S. R.; Dombroski, M. A.; Donahue, K. M.; Elliott, N. C.; Gibbons, C. P.; Jordan, C. K.; Kuperman, A. V.; Labasi, J. M.; LaLiberte, R. E.; McCoy, J. M.; Naiman, B. M.; Nelson, K. L.; Nguyen, H. T.; Peese, K. M.; Sweeney, F. J.; Taylor, T. J.; Trebino, C. E.; Abramov, Y. A.; Laird, E. R.; Volberg, W. A.; Zhou, J.; Bach, J.; Lombardo, F. Structure-activity relationships of triazolopyridine oxazole p38 inhibitors: Identification of candidates for clinical development. Bioorg. Med. Chem. Lett., 2006, 16, 4339-4344.
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Bach, J.31
Lombardo, F.32
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Continued exploration of the triazolopyridine scaffold as a platform for p38 MAP kinase inhibition
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Jerome, K. D.; Rucker, P. V.; Xing, L.; Shieh, H. S.; Baldus, J. E.; Selness, S. R.; Letavic, M. A.; Braganza, J. F.; McClure, K. F. Continued exploration of the triazolopyridine scaffold as a platform for p38 MAP kinase inhibition. Bioorg. Med. Chem. Lett., 2010, 20, 469-473.
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Shieh, H.S.4
Baldus, J.E.5
Selness, S.R.6
Letavic, M.A.7
Braganza, J.F.8
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