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Bioorganic & Medicinal Chemistry Letters|December 17, 2002
Discovery of a series of (4,5-dihydroimidazol-2-yl)-biphenylamine 5-HT7 agonistsVinod Parikh, Willard M Welch, Anne W SchmidtCNS Drug Reviews|February 22, 2003
The pharmacology of CP-154,526, a non-peptide antagonist of the CRH1 receptor: a reviewPatricia A Seymour, Anne W Schmidt, David W SchulzEuropean Journal of Pharmacology|January 3, 2007
Methylphenidate and atomoxetine increase histamine release in rat prefrontal cortexWeldon E Horner, David E Johnson, Anne W Schmidt, et al.Cytotechnology|November 13, 2008
Cultivation of HEK 293 cell line and production of a member of the superfamily of G-protein coupled receptors for drug discovery applications using a highly efficient novel bioreactorLewis Ho, Cynthia L Greene, Anne W Schmidt, et al.Journal of Medicinal Chemistry|December 4, 2003
Characterization of the 5-HT(7) receptor. Determination of the pharmacophore for 5-HT(7) receptor agonism and CoMFA-based modeling of the agonist binding siteErik S Vermeulen, Anne W Schmidt, Jeffrey S Sprouse, et al.Journal of Medicinal Chemistry|October 16, 2004
Novel 5-HT7 receptor inverse agonists. Synthesis and molecular modeling of arylpiperazine- and 1,2,3,4-tetrahydroisoquinoline-based arylsulfonamidesErik S Vermeulen, Marjan van Smeden, Anne W Schmidt, et al.European Journal of Pharmacology|January 4, 2005
The role of muscarinic receptor antagonism in antipsychotic-induced hippocampal acetylcholine releaseDavid E Johnson, Frank M Nedza, Douglas K Spracklin, et al.Diabetes|April 28, 2005
Inhibitory effects of antipsychotics on carbachol-enhanced insulin secretion from perifused rat islets: role of muscarinic antagonism in antipsychotic-induced diabetes and hyperglycemiaDavid E Johnson, Hanae Yamazaki, Karen M Ward, et al.Bioorganic & Medicinal Chemistry Letters|December 18, 2009
Biaryl piperidines as potent and selective delta opioid receptor ligandsSpiros Liras, Stanton F McHardy, Martin P Allen, et al.Journal of Medicinal Chemistry|February 12, 2008
Synthesis and SAR of 2-aryloxy-4-alkoxy-pyridines as potent orally active corticotropin-releasing factor 1 receptor antagonistsYuhpyng L Chen, John Braselton, James Forman, et al.Pageof 3