Optimization of α-ketoamide based p38 inhibitors through modifications to the region that binds to the allosteric site by Montalban, Antonio Garrido, Boman, Erik, Chang, Chau-Dung, Ceide, Susana Conde, Dahl, Russell, Dalesandro, David, Delaet, Nancy G.J., Erb, Eric, Ernst, Justin T., Gibbs, Andrew, Kahl, Jeffrey, Kessler, Linda, Kucharski, Jeff, Lum, Christopher, Lundström, Jan, Miller, Stephen, Nakanishi, Hiroshi, Roberts, Edward, Saiah, Eddine, Sullivan, Robert, Urban, Jan, Wang, Zhijun, Larson, Christopher J.

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KR-003048, a potent, orally active inhibitor of p38 mitogen-activated protein kinase by Montalban, Antonio Garrido, Boman, Erik, Chang, Chau-Dung, Ceide, Susana Conde, Dahl, Russell, Dalesandro, David, Delaet, Nancy G.J., Erb, Eric, Ernst, Justin, Gibbs, Andrew, Kahl, Jeffrey, Kessler, Linda, Lundström, Jan, Miller, Stephen, Nakanishi, Hiroshi, Roberts, Edward, Saiah, Eddine, Sullivan, Robert, Wang, Zhijun, Larson, Christopher J.

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The design and synthesis of novel α-ketoamide-based p38 MAP kinase inhibitors by Montalban, Antonio Garrido, Boman, Erik, Chang, Chau-Dung, Ceide, Susana Conde, Dahl, Russell, Dalesandro, David, Delaet, Nancy G.J., Erb, Eric, Ernst, Justin T., Gibbs, Andrew, Kahl, Jeffrey, Kessler, Linda, Lundström, Jan, Miller, Stephen, Nakanishi, Hiroshi, Roberts, Edward, Saiah, Eddine, Sullivan, Robert, Wang, Zhijun, Larson, Christopher J.

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‘Reverse’ α-ketoamide-based p38 MAP kinase inhibitors by Montalban, Antonio Garrido, Boman, Erik, Chang, Chau-Dung, Ceide, Susana Conde, Dahl, Russell, Dalesandro, David, Delaet, Nancy G.J., Erb, Eric, Gibbs, Andrew, Kahl, Jeff, Kessler, Linda, Lundström, Jan, Miller, Stephen, Nakanishi, Hiroshi, Roberts, Ed, Saiah, Eddine, Sullivan, Robert, Wang, Zhijun, Larson, Christopher J.

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Amino acid derived sulfonamide hydroxamates as inhibitors of procollagen C-Proteinase: solid-Phase synthesis of ornithine analogues by Dankwardt, Sharon M., Martin, Robert L., Chan, Christine S., Van Wart, Harold E., Walker, Keith A.M., Delaet, Nancy G., Robinson, Leslie A.

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Optimization of a-ketoamide based p38 inhibitors through modifications to the region that binds to the allosteric site by Montalban, Antonio Garrido, Boman, Erik, Chang, Chau-Dung, Ceide, Susana Conde, Dahl, Russell, Dalesandro, David, Delaet, Nancy GJ, Erb, Eric, Ernst, Justin T, Gibbs, Andrew, Kahl, Jeffrey, Kessler, Linda, Kucharski, Jeff, Lum, Christopher, Lundstroem, Jan, Miller, Stephen, Nakanishi, Hiroshi, Roberts, Edward, Saiah, Eddine, Sullivan, Robert, Urban, Jan, Wang, Zhijun, Larson, Christopher J

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Corrigendum to “Amino acid derived sulfonamide hydroxamates as inhibitors of procollagen C-proteinase: solid-phase synthesis of ornithine analogues”[Bioorg. Med. Chem. Lett. 11 (20... by Dankwardt, Sharon M, Martin, Robert L, Chan, Christine S, Van Wart, Harold E, Walker, Keith A.M, Delaet, Nancy G, Robinson, Leslie A

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A ?-turn mimic and a thiomethylene dipeptide surrogate employed in the study of cyclic peptide RGD and RCD cell-adhesion inhibitors by Rishton, Gilbert M., Harn, Nancy K., Cripps, Stephan J., Chiang, Shiu-Lan, Mikos, Christy, Cardarelli, Pina, Lobl, Thomas J., Gorcsan, Frank, Moscinski, Mary, Delaet, Nancy G. J., Walker, Sharon M.

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