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European Journal of Pharmacology|August 24, 2004
Melanin-concentrating hormone-1 receptor antagonism decreases feeding by reducing meal sizeTimothy J Kowalski, Constance Farley, Mary E Cohen-Williams, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 13, 2002
The gerbil elevated plus-maze I: behavioral characterization and pharmacological validationGeoffrey B Varty, Cynthia A Morgan, Mary E Cohen-Williams, et al.
Behavioural Brain Research|August 21, 2007
The effect of caffeine to increase reaction time in the rat during a test of attention is mediated through antagonism of adenosine A2A receptorsGuy A Higgins, Michael E Grzelak, Annamarie J Pond, et al.
Bioorganic & Medicinal Chemistry Letters|June 28, 2005
2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: highly potent, orally active, adenosine A2A antagonists. Part 1Julius J Matasi, John P Caldwell, Hongtao Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2005
2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs as adenosine A2A antagonists: the successful reduction of hERG activity. Part 2Julius J Matasi, John P Caldwell, Hongtao Zhang, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 13, 2002
The gerbil elevated plus-maze II: anxiolytic-like effects of selective neurokinin NK1 receptor antagonistsGeoffrey B Varty, Mary E Cohen-Williams, Cynthia A Morgan, et al.
Pharmacology, Biochemistry, and Behavior|December 3, 2010
Characterization of the selective mGluR1 antagonist, JNJ16259685, in rodent models of movement and coordinationRobert A Hodgson, Lynn A Hyde, Donald H Guthrie, et al.
Bioorganic & Medicinal Chemistry Letters|June 19, 2008
Design, synthesis, and evaluation of fused heterocyclic analogs of SCH 58261 as adenosine A2A receptor antagonistsUnmesh Shah, Claire M Lankin, Craig D Boyle, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2016
Design and synthesis of water soluble β-aminosulfone analogues of SCH 900229 as γ-secretase inhibitorsWen-Lian Wu, Duane A Burnett, John Clader, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 22, 2008
The anxiolytic-like effects of the novel, orally active nociceptin opioid receptor agonist 8-[bis(2-methylphenyl)methyl]-3-phenyl-8-azabicyclo[3.2.1]octan-3-ol (SCH 221510)Geoffrey B Varty, Sherry X Lu, Cynthia A Morgan, et al.
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