Search Results - "Norton, Monica B"

Biochemical, cellular, and anti-inflammatory properties of a potent, selective, orally bioavailable benzamide inhibitor of Rho kinase activity by Rajagopalan, Lakshman E, Davies, Michael S, Kahn, Larry E, Kornmeier, Christine M, Shimada, Hideaki, Steiner, Toni A, Zweifel, Ben S, Wendling, Jay M, Payne, Maria A, Loeffler, Richard F, Case, Brenda L, Norton, Monica B, Parikh, Mihir D, Nemirovskiy, Olga V, Mourey, Robert J, Masferrer, Jaime L, Misko, Thomas P, Kolodziej, Stephen A

“…Rho kinase, is the most widely studied downstream effector of the small Rho GTPase RhoA. Two Rho kinase isoforms have been described and are frequently…”
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Discovery of a Simple Picomolar Inhibitor of Cholesteryl Ester Transfer Protein by Reinhard, Emily J, Wang, Jane L, Durley, Richard C, Fobian, Yvette M, Grapperhaus, Margaret L, Hickory, Brian S, Massa, Mark A, Norton, Monica B, Promo, Michele A, Tollefson, Michael B, Vernier, William F, Connolly, Daniel T, Witherbee, Bryan J, Melton, Michele A, Regina, Karen J, Smith, Mark E, Sikorski, James A

“…A novel series of substituted N-[3-(1,1,2,2-tetrafluoroethoxy)benzyl]-N-(3-phenoxyphenyl)-trifluoro-3-amino-2-propanols is described which potently and…”
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Novel Terphenyls as Selective Cyclooxygenase-2 Inhibitors and Orally Active Anti-inflammatory Agents by Li, James J, Norton, Monica B, Reinhard, Emily J, Anderson, Gary D, Gregory, Susan A, Isakson, Peter C, Koboldt, Carol M, Masferrer, Jaime L, Perkins, William E, Seibert, Karen, Zhang, Yan, Zweifel, Ben S, Reitz, David B

“…A novel series of terphenyl methyl sulfones and sulfonamides have been shown to be highly potent and selective cyclooxygenase-2 (COX-2) inhibitors. The…”
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Selective Cyclooxygenase Inhibitors: Novel 1,2-Diarylcyclopentenes Are Potent and Orally Active COX-2 Inhibitors by Reitz, David B., Li, James J., Norton, Monica B., Reinhard, Emily J., Collins, Joe T., Anderson, Gary D., Gregory, Susan A., Koboldt, Carol M., Perkins, William E.

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1,2-Diarylcyclopentenes as Selective Cyclooxygenase-2 Inhibitors and Orally Active Anti-inflammatory Agents by Li, James J, Anderson, Gary D, Burton, Earl G, Cogburn, J. Nita, Collins, Joe T, Garland, Danny J, Gregory, Susan A, Huang, Horng-Chih, Isakson, Peter C

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The N-Boc Group as an Activator for the a-Lithiation of Carbamates: Synthesis of 11-Substituted Dibenzoxazepines by J. Hagen, Timothy, F. Rafferty, Michael, T. Collins, Joe, J. Garland, Danny, J. Li, James, B. Norton, Monica, B. Reitz, David, Tsymbalov, Sofya, S. Pitzele, Barnett, Ann Hallinan, E.

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Lithiation and electrophilic substitution of 8-chlorodibenz[b,f][1,4]-oxazepine-10-tert-butylcarbamate: The preparation of novel fused heterocyclic derivatives of 8-chlorodibenzoxazepine by Li, James J., Chrusciel, R. Alan, Norton, Monica B., Reitz, David B., Hagen, Timothy J., Tsymbalov, Sofya, Hallinan, E. Ann

“…Lithiation of 8‐chlorodibenz[b,f][1,4]oxazepine‐10‐tert‐butylcarbamate (1) is described. Electrophilic substitution of the resulting N‐Boc dibenzoxazepine α‐…”
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The N-Boc group as an activator for the α-lithiation of carbamates: synthesis of 11-substituted dibenzoxazepines by HAGEN, T. J, RAFFERTY, M. F, COLLINS, J. T, GARLAND, D. J, LI, J. J, NORTON, M. B, REITZ, D. B, TSYMBALOV, S, PITZELE, B. S, HALLINAN, E. A

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