The effects of diminishing albumin binding to some Endothelin receptor antagonists by Szczepankiewicz, Bruce G., Bal, Radhika B., von Geldern, Thomas W., Wu-Wong, Jinshyun R., Chiou, William J., Dixon, Douglas B., Opgenorth, Terry J., Hoffman, Daniel J., Borre, Anthony J., Marsh, Kennan C., Nguyen, Bach N.

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Discovery of PH-797804, a highly selective and potent inhibitor of p38 MAP kinase by Selness, Shaun R, Devraj, Rajesh V, Devadas, Balekudru, Walker, John K, Boehm, Terri L, Durley, Richard C, Shieh, Huey, Xing, Li, Rucker, Paul V, Jerome, Kevin D, Benson, Alan G, Marrufo, Laura D, Madsen, Heather M, Hitchcock, Jeff, Owen, Tom J, Christie, Lance, Promo, Michele A, Hickory, Brian S, Alvira, Edgardo, Naing, Win, Blevis-Bal, Radhika, Messing, Dean, Yang, Jerry, Mao, Michael K, Yalamanchili, Gopi, Vonder Embse, Richard, Hirsch, Jeffrey, Saabye, Matthew, Bonar, Sheri, Webb, Elizabeth, Anderson, Gary, Monahan, Joseph B

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Discovery of N-substituted pyridinones as potent and selective inhibitors of p38 kinase by Selness, Shaun R., Devraj, Rajesh V., Monahan, Joseph B., Boehm, Terri L., Walker, John K., Devadas, Balekudru, Durley, Richard C., Kurumbail, Ravi, Shieh, Huey, Xing, Li, Hepperle, Michael, Rucker, Paul V., Jerome, Kevin D., Benson, Alan G., Marrufo, Laura D., Madsen, Heather M., Hitchcock, Jeff, Owen, Tom J., Christie, Lance, Promo, Michele A., Hickory, Brian S., Alvira, Edgardo, Naing, Win, Blevis-Bal, Radhika

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Identification, synthesis and SAR of amino substituted pyrido[3,2b]pyrazinones as potent and selective PDE5 inhibitors by Owen, Dafydd R., Walker, John K., Jon Jacobsen, E., Freskos, John N., Hughes, Robert O., Brown, David L., Bell, Andrew S., Brown, David G., Phillips, Christopher, Mischke, Brent V., Molyneaux, John M., Fobian, Yvette M., Heasley, Steve E., Moon, Joseph B., Stallings, William C., Joseph Rogier, D., Fox, David N.A., Palmer, Michael J., Ringer, Tracy, Rodriquez-Lens, Margarita, Cubbage, Jerry W., Blevis-Bal, Radhika M., Benson, Alan G., Acker, Brad A., Maddux, Todd M., Tollefson, Michael B., Bond, Brian R., MacInnes, Alan, Yu, Yung

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Design, synthesis and activity of a potent, selective series of N-aryl pyridinone inhibitors of p38 kinase by Selness, Shaun R, Boehm, Terri L, Walker, John K, Devadas, Balekudru, Durley, Richard C, Kurumbail, Ravi, Shieh, Huey, Xing, Li, Hepperle, Michael, Rucker, Paul V, Jerome, Kevin D, Benson, Alan G, Marrufo, Laura D, Madsen, Heather M, Hitchcock, Jeff, Owen, Tom J, Christie, Lance, Promo, Michele A, Hickory, Brian S, Alvira, Edgardo, Naing, Win, Blevis-Bal, Radhika, Devraj, Rajesh V, Messing, Dean, Schindler, John F, Hirsch, Jeffrey, Saabye, Matthew, Bonar, Sheri, Webb, Elizabeth, Anderson, Gary, Monahan, Joseph B

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Li–X-type zeolite mediated Michael addition of thiols to cyclic enones and its application in the synthesis of 13-thiaprostaglandins by Shinde, Popat D, Mahajan, Vishal A, Borate, Hanumant B, Tillu, Vasudha H, Bal, Rajaram, Chandwadkar, Asha, Wakharkar, Radhika D

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2,4-Diarylpyrrolidine-3-carboxylic AcidsPotent ETA Selective Endothelin Receptor Antagonists. 1. Discovery of A-127722 by Winn, Martin, von Geldern, Thomas W, Opgenorth, Terry J, Jae, Hwan-Soo, Tasker, Andrew S, Boyd, Steven A, Kester, Jeffrey A, Mantei, Robert A, Bal, Radhika, Sorensen, Bryan K, Wu-Wong, Jinshyun R, Chiou, William J, Dixon, Douglas B, Novosad, Eugene I, Hernandez, Lisa, Marsh, Kennan C

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Azole Endothelin Antagonists. 2. Structure−Activity Studies by von Geldern, Thomas W, Kester, Jeffrey A, Bal, Radhika, Wu-Wong, Jinshyun R, Chiou, William, Dixon, Douglas B, Opgenorth, Terry J

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Torsional Low-Frequency Reorganization Energy of Biphenyl Anion in Electron Transfer Reactions by Miller, John R, Paulson, Basil Pavlatos, Bal, Radhika, Closs, Gerhard L

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Azole endothelin antagonists. II: Structure-activity studies by VON GELDERN, T. W, KESTER, J. A, RADHIKA BAL, WU-WONG, J. R, CHIOU, W, DIXON, D. B, OPGENORTH, T. J

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