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Neuropharmacology|February 21, 2017
Reprint of Pharmacological and molecular characterization of the positive allosteric modulators of metabotropic glutamate receptor 2L Lundström, C Bissantz, J Beck, et al.Pharmacology, Biochemistry, and Behavior|March 13, 2002
An investigation of the role of 5-HT(2C) receptors in modifying ethanol self-administration behaviourDenise M Tomkins, N Joharchi, M Tampakeras, et al.British Journal of Pharmacology|April 8, 2011
Structural determinants of allosteric antagonism at metabotropic glutamate receptor 2: mechanistic studies with new potent negative allosteric modulatorsL Lundström, C Bissantz, J Beck, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|June 1, 2001
Effects of Ro 64-6198 in nociceptin/orphanin FQ-sensitive isolated tissuesD Rizzi, R Bigoni, A Rizzi, et al.Psychopharmacology|March 2, 2018
A moderate dose of alcohol selectively reduces empathic accuracyFreya Thiel, Brian D Ostafin, Jana R Uppendahl, et al.Journal of Medicinal Chemistry|August 15, 1997
Novel agonists of 5HT2C receptors. Synthesis and biological evaluation of substituted 2-(indol-1-yl)-1-methylethylamines and 2-(indeno[1,2-b]pyrrol-1-yl)-1-methylethylamines. Improved therapeutics for obsessive compulsive disorderM Bös, F Jenck, J R Martin, et al.European Journal of Medicinal Chemistry|September 28, 2000
Synthesis of (1S,3aS)-8-(2,3,3a,4,5, 6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1,3,8-triaza-spiro[4. 5]decan-4-one, a potent and selective orphanin FQ (OFQ) receptor agonist with anxiolytic-like propertiesJ Wichmann, G Adam, S Röver, et al.Proceedings of the National Academy of Sciences of the United States of America|October 19, 2001
Positive allosteric modulators of metabotropic glutamate 1 receptor: characterization, mechanism of action, and binding siteF Knoflach, V Mutel, S Jolidon, et al.The Journal of Pharmacology and Experimental Therapeutics|July 17, 2001
Pharmacological characterization of the novel nonpeptide orphanin FQ/nociceptin receptor agonist Ro 64-6198: rapid and reversible desensitization of the ORL1 receptor in vitro and lack of tolerance in vivoF M Dautzenberg, J Wichmann, J Higelin, et al.Journal of Medicinal Chemistry|February 7, 2001
High-affinity, non-peptide agonists for the ORL1 (orphanin FQ/nociceptin) receptorS Röver, G Adam, A M Cesura, et al.Pageof 6