Discovery and Characterization of 6-{4-[3-(R)-2-Methylpyrrolidin-1-yl)propoxy]phenyl}-2H-pyridazin-3-one (CEP-26401, Irdabisant): A Potent, Selective Histamine H3 Receptor Inverse... by Hudkins, Robert L, Raddatz, Rita, Tao, Ming, Mathiasen, Joanne R, Aimone, Lisa D, Becknell, Nadine C, Prouty, Catherine P, Knutsen, Lars J. S, Yazdanian, Mehran, Moachon, Gilbert, Ator, Mark A, Mallamo, John P, Marino, Michael J, Bacon, Edward R, Williams, Michael

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Synthesis and discovery of 2,3-dihydro-3,8-diphenylbenzo[1,4]oxazines as a novel class of potent cholesteryl ester transfer protein inhibitors by Wang, Aihua, Prouty, Catherine P., Pelton, Patricia D., Yong, Maria, Demarest, Keith T., Murray, William V., Kuo, Gee-Hong

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Pyridazinodiazepines as a High-Affinity, P2−P3 Peptidomimetic Class of Interleukin-1β-Converting Enzyme Inhibitor by Dolle, Roland E, Prasad, C. V. C, Prouty, Catherine P, Salvino, Joseph M, Awad, Mohamed M. A, Schmidt, Stanley J, Hoyer, Denton, Ross, Tina Morgan, Graybill, Todd L, Speier, Gary J, Uhl, Joanne, Helaszek, Carla T, Ator, Mark A

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First Examples of Peptidomimetic Inhibitors of Interleukin-1β Converting Enzyme by Dolle, Roland E, Prouty, Catherine P, Prasad, C. V. C, Cook, Ewell, Saha, Ashis, Ross, Tina Morgan, Salvino, Joseph M, Helaszek, Carla T, Ator, Mark A

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Discovery and Characterization of 6-{4-[3-( R )-2-Methylpyrrolidin-1-yl)propoxy]phenyl}-2 H -pyridazin-3-one (CEP-26401, Irdabisant): A Potent, Selective Histamine H 3 Receptor Inv... by Hudkins, Robert L., Raddatz, Rita, Tao, Ming, Mathiasen, Joanne R., Aimone, Lisa D., Becknell, Nadine C., Prouty, Catherine P., Knutsen, Lars J. S., Yazdanian, Mehran, Moachon, Gilbert, Ator, Mark A., Mallamo, John P., Marino, Michael J., Bacon, Edward R., Williams, Michael

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Synthesis and discovery of 2,3-dihydro-3,8-diphenylbenzo[1,4]oxazines as a novel class of potent cholestervl ester transfer protein inhibitors by AIHUA WANG, PROUTY, Catherine P, PELTON, Patricia D, MARIA YONG, DEMAREST, Keith T, MURRAY, William V, KUO, Gee-Hong

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Pyridazinodiazepines as a High-Affinity, P 2 −P 3 Peptidomimetic Class of Interleukin-1β-Converting Enzyme Inhibitor by Dolle, Roland E., Prasad, C. V. C., Prouty, Catherine P., Salvino, Joseph M., Awad, Mohamed M. A., Schmidt, Stanley J., Hoyer, Denton, Ross, Tina Morgan, Graybill, Todd L., Speier, Gary J., Uhl, Joanne, Bruce E. Miller, Helaszek, Carla T., Ator, Mark A.

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α-((Tetronoyl)oxy)- and α-((tetramoyl)oxy)methyl ketone inhibitors of the interleukin-1β converting enzyme (ICE) by Graybill, Todd L., Prouty, Catherine P., Speier, Gary J., Hoyer, Denton, Dolle, Roland E., Helaszek, Carla T., Ator, Mark A., Uhl, Joanne, Strastes, Joost

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Structural and stereochemical requirements of time-dependent inactivators of the interleukin-1β converting enzyme by Prasad, C.V.C., Prouty, Catherine P., Hoyer, Denton, Ross, Tina M., Salvino, Joseph M., Awad, Mohamad, Graybill, Todd L., Schmidt, Stanley J., Kelly Osifo, I., Dolle, Roland E., Helaszek, Carla T., Miller, Robert E., Ator, Mark A.

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Synthesis and Discovery of Macrocyclic Polyoxygenated Bis-7-azaindolylmaleimides as a Novel Series of Potent and Highly Selective Glycogen Synthase Kinase-3β Inhibitors by Kuo, Gee-Hong, Prouty, Catherine, DeAngelis, Alan, Shen, Lan, O'Neill, David J, Shah, Chandra, Connolly, Peter J, Murray, William V, Conway, Bruce R, Cheung, Peter, Westover, Lori, Xu, Jun Z, Look, Richard A, Demarest, Keith T, Emanuel, Stuart, Middleton, Steven A, Jolliffe, Linda, Beavers, Mary Pat, Chen, Xin

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Synthesis and Structure−Activity Relationships of Pyrazine-Pyridine Biheteroaryls as Novel, Potent, and Selective Vascular Endothelial Growth Factor Receptor-2 Inhibitors by Kuo, Gee-Hong, Prouty, Catherine, Wang, Aihua, Emanuel, Stuart, DeAngelis, Alan, Zhang, Yan, Song, Fengbin, Beall, Lawrence, Connolly, Peter J, Karnachi, Prahba, Chen, Xin, Gruninger, Robert H, Sechler, Jan, Fuentes-Pesquera, Angel, Middleton, Steven A, Jolliffe, Linda, Murray, William V

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Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors by SHEN, Lan, PROUTY, Catherine, DEMAREST, Keith T, KUO, Gee-Hong, CONWAY, Bruce R, WESTOVER, Lori, XU, Jun Z, LOOK, Richard A, XIN CHEN, BEAVERS, Mary Pat, ROBERTS, Jerry, MURRAY, William V

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Design, Synthesis, and Structure−Activity Relationships of Phthalimide-Phenylpiperazines:  A Novel Series of Potent and Selective α1 a-Adrenergic Receptor Antagonists by Kuo, Gee-Hong, Prouty, Catherine, Murray, William V, Pulito, Virginia, Jolliffe, Linda, Cheung, Peter, Varga, Sally, Evangelisto, Mary, Wang, Jian

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The American public as seen from the circulation desk by Tobitt, Edith, Prouty, Louise, Dyne, Catherine Van, Paine, P M

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