Design and synthesis of potent, orally bioavailable dihydroquinazolinone inhibitors of p38 MAP kinase von Stelmach, John E., Liu, Luping, Patel, Sangita B., Pivnichny, James V., Scapin, Giovanna, Singh, Suresh, Hop, Cornelis E.C.A., Wang, Zhen, Strauss, John R., Cameron, Patricia M., Nichols, Elizabeth A., O'Keefe, Stephen J., O'Neill, Edward A., Schmatz, Dennis M., Schwartz, Cheryl D., Thompson, Chris M., Zaller, Dennis M., Doherty, James B.

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Synthesis and biological activity of quinolinone and dihydroquinolinone p38 MAP kinase inhibitors von Chen, Meng-Hsin, Fitzgerald, Patricia, Singh, Suresh B., O’Neill, Edward A., Schwartz, Cheryl D., Thompson, Chris M., O’Keefe, Stephen J., Zaller, Dennis M., Doherty, James B.

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SAR of 3,4-Dihydropyrido[3,2- d]pyrimidone p38 inhibitors von Liu, Luping, Stelmach, John E., Natarajan, Swaminathan R., Chen, Meng-Hsin, Singh, Suresh B., Schwartz, Cheryl D., Fitzgerald, Catherine E., O'Keefe, Stephen J., Zaller, Dennis M., Schmatz, Dennis M., Doherty, James B.

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Hybrid-Designed Inhibitors of p38 MAP Kinase Utilizing N-Arylpyridazinones von Colletti, Steven L, Frie, Jessica L, Dixon, Elizabeth C, Singh, Suresh B, Choi, Bernard K, Scapin, Giovanna, Fitzgerald, Catherine E, Kumar, Sanjeev, Nichols, Elizabeth A, O'Keefe, Stephen J, O'Neill, Edward A, Porter, Gene, Samuel, Koppara, Schmatz, Dennis M, Schwartz, Cheryl D, Shoop, Wesley L, Thompson, Chris M, Thompson, James E, Wang, Ruixiu, Woods, Andrea, Zaller, Dennis M, Doherty, James B

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Pyridazine based inhibitors of p38 MAPK von McIntyre, Charles J, Ponticello, Gerald S, Liverton, Nigel J, O’Keefe, Stephen J, O’Neill, Edward A, Pang, Margaret, Schwartz, Cheryl D, Claremon, David A

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p38MAP kinase inhibitors. Part 1: design and development of a new class of potent and highly selective inhibitors based on 3,4-dihydropyrido[3,2-d]pyrimidone scaffold von Natarajan, Swaminathan R, Wisnoski, David D, Singh, Suresh B, Stelmach, John E, O'Neill, Edward A, Schwartz, Cheryl D, Thompson, Chris M, Fitzgerald, Catherine E, O'Keefe, Stephen J, Kumar, Sanjeev, Hop, Cornelis E C A, Zaller, Dennis M, Schmatz, Dennis M, Doherty, James B

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SAR for MHC class II binding tetrapeptides: Correlation with potential binding site von Cunningham, Barry R, Rivetna, Meheryar, Tolman, Richard L, Flattery, Stacey J, Nichols, Elizabeth A, Schwartz, Cheryl D, Wicker, Linda S, Hermes, Jeffrey D, Jones, A.Brian

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p38 MAP kinase inhibitors. part 1: design and development of a new class of potent and highly selective inhibitors based on 3,4-dihydropyrido[3,2- d]pyrimidone scaffold von Natarajan, Swaminathan R., Wisnoski, David D., Singh, Suresh B., Stelmach, John E., O'Neill, Edward A., Schwartz, Cheryl D., Thompson, Chris M., Fitzgerald, Catherine E., O'Keefe, Stephen J., Kumar, Sanjeev, Hop, Cornelis E.C.A., Zaller, Dennis M., Schmatz, Dennis M., Doherty, James B.

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L-156, 602, A C5a ANTAGONIST WITH A NOVEL CYCLIC HEXADEPSIPEPTIDE STRUCTURE FROM Streptomyces sp. MA6348: FERMENTATION, ISOLATION AND STRUCTURE DETERMINATION von HENSENS, OTTO D., BORRIS, ROBERT P., KOUPAL, LAWRENCE R., CALDWELL, CHARLES G., CURRIE, SARA A., HAIDRI, AKBER A., HOMNICK, CARL F., HONEYCUTT, SUSAN S., LINDENMAYER, SUSAN M., SCHWARTZ, CHERYL D., WEISSBERGER, BARBARA A., WOODRUFF, H. B., ZINK, DEBORAH L., ZITANO, LAURETTA, FIELDHOUSE, JILL M., ROLLINS, THOMAS, SPRINGER, MARTIN S., SPRINGER, JAMES P.

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NOVEL AND POTENT GASTRIN AND BRAIN CHOLECYSTOKININ ANTAGONISTS FROM Streptomyces olivaceus: TAXONOMY, FERMENTATION, ISOLATION, CHEMICAL CONVERSIONS, AND PHYSICO-CHEMICAL AND BIOCHE... von LAM, Y. K. TONY, BOGEN, DEBRA, CHANG, RAYMOND S., FAUST, KRISTINE A., HENSENS, OTTO D., ZINK, DEBORAH L., SCHWARTZ, CHERYL D., ZITANO, LORETTA, GARRITY, GEORGE M., GAGLIARDI, MAGDA M., CURRIE, SARA A., WOODRUFF, H. BOYD

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p38 MAP kinase inhibitors. Part1: Design and development of a new class of potent and highly selective inhibitors based on 3,4-dihydropyrido[3,2-d]pyrimidone scaffold von NATARAJAN, Swaminathan R, WISNOSKI, David D, HOP, Cornelis E. C. A, ZALLER, Dennis M, SCHMATZ, Dennis M, DOHERTY, James B, SINGH, Suresh B, STELMACH, John E, O'NEILL, Edward A, SCHWARTZ, Cheryl D, THOMPSON, Chris M, FITZGERALD, Catherine E, O'KEEFE, Stephen J, KUMAR, Sanjeev

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Difficidin and oxydifficidin: Novel broad spectrum antibacterial antibiotics produced by Bacillus subtilis. I.Production, taxonomy and antibacterial activity von ZIMMERMAN, SHELDON B., SCHWARTZ, CHERYL D., MONAGHAN, RICHARD L., PELAK, BARBARA ANN, WEISSBERGER, BARBARA, GILFILLAN, EVEMARIE C., MOCHALES, SAGRARIO, HERNANDEZ, SEBASTIAN, CURRIE, SARA A., TEJERA, ENRIQUE, STAPLEY, EDWARD O.

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Tetrapeptide derived inhibitors of complexation of a class II MHC: fully unnatural ligands von Brian Jones, A., Acton, John J., Adams, Alan D., Yuen, Winston, Nichols, Elizabeth A., Schwartz, Cheryl D., Wicker, Linda S., Hermes, Jeffrey D.

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Tetrapeptide derived inhibitors of complexation of a class II MHC: the peptide backbone is not inviolate von Jones, A.Brian, Acton, John J., Rivetna, Meheryar N., Cummings, Richard T., Cubbon, Rose M., Nichols, Elizabeth A., Schwartz, Cheryl D., Wicker, Linda S., Hermes, Jeffrey D.

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DIFFICIDIN AND OXYDIFFICIDIN: NOVEL BROAD SPECTRUM ANTIBACTERIAL ANTIBIOTICS PRODUCED BY BACILLUS SUBTILIS: I. PRODUCTION, TAXONOMY AND ANTIBACTERIAL ACTIVITY von ZIMMERMAN, SHELDON B., SCHWARTZ, CHERYL D., MONAGHAN, RICHARD L., PELAK, BARBARA ANN, WEISSBERGER, BARBARA, GILFILLAN, EVEMARIE C., MOCHALES, SAGRARIO, HERNANDEZ, SEBASTIAN, CURRIE, SARA A., TEJERA, ENRIQUE, STAPLEY, EDWARD O.

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ChemInform Abstract: Pyridazine Based Inhibitors of p38 MAPK von McIntyre, Charles J., Ponticello, Gerald S., Liverton, Nigel J., O'Keefe, Stephen J., O'Neill, Edward A., Pang, Margaret, Schwartz, Cheryl D., Claremon, David A.

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Therapeutic virginiamycin M1 analogs von LAM, YIU-KUEN T, CHANG, RAYMOND S, HENSENS, OTTO D, ZINK, DEBORAH L, SCHWARTZ, CHERYL D

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Fermentation analogs of virginiamycin M1 von LAM, YIU-KUEN T, CHANG, RAYMOND S, HENSENS, OTTO D, ZINK, DEBORAH L, SCHWARTZ, CHERYL D

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Compositions having fermentation analogs of virginiamycin M1 as active ingredient von LAM, YIU-KUEN T, CHANG, RAYMOND S, HENSENS, OTTO D, ZINK, DEBORAH L, SCHWARTZ, CHERYL D

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Therapeutic virginiamycin M1 analogs von LAM, YIU-KUEN T, CHANG, RAYMOND S, HENSENS, OTTO D, ZINK, DEBORAH L, SCHWARTZ, CHERYL D

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