KR-003048, a potent, orally active inhibitor of p38 mitogen-activated protein kinase von 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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Optimization of α-ketoamide based p38 inhibitors through modifications to the region that binds to the allosteric site von 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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The design and synthesis of novel α-ketoamide-based p38 MAP kinase inhibitors von 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 von 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 von 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 von 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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Morphiceptin and β-casomorphin-5 analogues containing a reduced peptide bond: Selective μ-receptor agonists and a novel μ antagonist, H-Tyr-Proψ(CH2-NH)Phe-Pro-Gly-OH von Delaet, Nancy G. J., Verheyden, Patricia M. F., Tourwe, Dirk, Van Binst, G., Davis, Peg, Burks, Thomas F.

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Comparative study of methods to couple hindered peptides von SPENCER, JEFFREY R., ANTONENKO, VALERY V., DELAET, NANCY G.J., GOODMAN, MURRAY

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Unusual peptide bond cleavage reactions during acidolytic deprotection reactions von Spencer, Jeffrey R, Delaet, Nancy G. J, Toy-Palmer, Anna, Antonenko, Valery V, Goodman, Murray

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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... von 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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Assignment of the 1 H‐nmr resonances of the four rotamers of β‐casomorphin‐5 in DMSO von Delaet, Nancy G. J., Verheyden, Patricia M. F., Tourwé, Dirk, Van Binst, Georges

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Assignment of the 1H-NMR resonances of the four rotamers of beta-casomorphin-5 in DMSO von Delaet, N.G.J. (Vrije Universiteit Brussel, Burssels, Belgium), Verheyden, P.M.F, Tourwe, D, Binst, G. van

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Modulators of calcitonin and amylin receptor activity von DELAET NANCY, SEBO LUBOMIR, URBAN JAN, PRYOR KENT, MILLER STEPHEN

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Modulators of calcitonin and amylin receptor activity von Pryor, Kent, Urban, Jan, Sebo, Lubomir, Miller, Stephen, Delaet, Nancy

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4H-1,2,4-TRIAZOLE-3(2H)-THIONE DERATIVES AS SPHINGOMYELINASE INHIBITORS von OHMAWARI, NAGASHIGE, DELAET, NANCY, NAKAI, HISAO

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THERAPY USING CYTOKINE INHIBITORS von CROWLEY, CONSTANCE, A, GROVE, CARRIE, GAIL, MILLER, STEPHEN, KING, BERNARD, PRYOR, KENT, DELAET, NANCY G., J, ERNST, JUSTIN, HEPBURN, BONNIE, LARSON, CHRISTOPHER, J, SHUSTER, LEWIS, J

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CYTOKINE INHIBITORS von SAIAH, EDDINE, DELAET, NANCY, G., J, ROBERTS, EDWARD, NAKANISHI, HIROSHI, ERNST, JUSTIN, KAHL, JEFFREY, D, BOMAN, ERIK, CONDE-CEIDE, SUSANA, DAHL, RUSSELL, MONTALBAN, ANTONIO, G, MILLER, STEPHEN, SULLIVAN, ROBERT, WANG, ZHIJUN, LARSON, CHRISTOPHER

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THERAPY USING CYTOKINE INHIBITORS von KING, BERNARD, D, DELAET, NANCY, PRYOR, KENT, ALLGREN, ROBIN, LARSON, CHRISTOPHER, HEPBURN, BONNIE

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BISAMIDE CYTOKINE INHIBITORS von MONTALBAN, ANTONIO, GARRIDO, BOMAN, ERIK, SEBO, LUBOMIR, DELAET, NANCY, G.L, PEI, YAZHONG, WANG, ZHIJUN, URBAN, JAN, LARSON, CHRISTOPHER, LUM, CHRISTOPHER

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MODULATORS OF CCR-5 ACTIVITY von BOMAN, ERIK, DAHL, RUSSELL, SEBO, LUBOMIR, DELAET, NANCY, G. J, ERNST, JUSTIN, URBAN, JAN, LUM, CHRISTOPHER

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