Search Results - Breitenbucher, James G

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  1. 1
    3-[5-(3,4-Dichloro-phenyl)-1-(4-methoxy-phenyl)-1H-pyrazol-3-yl]-2-m-tolyl-propionate (JNJ-17156516), a Novel, Potent, and Selective Cholecystokinin 1 Receptor Antagonist: In Vitro and in Vivo Pharmacological Comparison with Dexloxiglumide

    3-[5-(3,4-Dichloro-phenyl)-1-(4-methoxy-phenyl)-1H-pyrazol-3-yl]-2-m-tolyl-propionate (JNJ-17156516), a Novel, Potent, and Selective Cholecystokinin 1 Receptor Antagonist: In Vitro... by Morton, Magda F, Barrett, Terrance D, Yan, Wen, Freedman, Jamie M, Lagaud, Guy, Prendergast, Clodagh E, Moreno, Veronica, Pyati, Jayashree, Figueroa, Katherine, Li, Lina, Wu, Xiaodong, Rizzolio, Michele, Breitenbucher, James G, McClure, Kelly, Shankley, Nigel P

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  2. 2
    In‐vitro and in‐vivo pharmacology of a novel TRPV1 receptor antagonist: JNJ38748021

    In‐vitro and in‐vivo pharmacology of a novel TRPV1 receptor antagonist: JNJ38748021 by Bhattacharya, Anindya, Hawryluk, Natalie A, Merit, Jeffrey E, Nasser, Nadia, Ao, Hong, Wang, Qi, Tham, Chui‐Se, Maher, Michael P, Kansagara, Mena, Scott, Brian P, Hack, Michael D, Breitenbucher, James G, Chaplan, Sandra R, Wickenden, Alan D

    Published in The FASEB journal
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  3. 3
    Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-directed Serine Protease Inhibitors

    Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-directed Serine Protease Inhibitors by Katz, Bradley A., Elrod, Kyle, Verner, Erik, Mackman, Richard L., Luong, Christine, Shrader, William D., Sendzik, Martin, Spencer, Jeffrey R., Sprengeler, Paul A., Kolesnikov, Aleks, Tai, Vincent W.-F., Hui, Hon C., Guy Breitenbucher, J., Allen, Darin, Janc, James W.

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  4. 4
    Inhibition of fatty acid amide hydrolase produces analgesia by multiple mechanisms

    Inhibition of fatty acid amide hydrolase produces analgesia by multiple mechanisms by Chang, Leon, Luo, Lin, Palmer, James A, Sutton, Steven, Wilson, Sandy J, Barbier, Ann J, Breitenbucher, James Guy, Chaplan, Sandra R, Webb, Michael

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  5. 5
    2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors

    2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors by MACKMAN, Richard L, HUI, Hon C, SPRENGELER, Paul A, TARIO, James, VERNER, Erik, JING WANG, BREITENBUCHER, J. Guy, KATZ, Bradley A, LUONG, Christine, MARTELLI, Arnold, MCGEE, Danny, RADIKA, Kesavan, SENDZIK, Martin, SPENCER, Jeffrey R

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