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Neuropharmacology|August 25, 2019
Modulation of thalamo-cortical activity by the NMDA receptor antagonists ketamine and phencyclidine in the awake freely-moving ratMaria Amat-Foraster, Pau Celada, Ulrike Richter, et al.Bioorganic & Medicinal Chemistry|October 18, 2012
Design, synthesis and pharmacological characterization of coumarin-based fluorescent analogs of excitatory amino acid transporter subtype 1 selective inhibitors, UCPH-101 and UCPH-102Tri H V Huynh, Bjarke Abrahamsen, Karsten K Madsen, et al.Antioxidants & Redox Signaling|July 24, 2010
Improving the stability of α-conotoxin AuIB through N-to-C cyclization: the effect of linker length on stability and activity at nicotinic acetylcholine receptorsChristopher J Armishaw, Anders A Jensen, Lena D Balle, et al.Journal of Medicinal Chemistry|May 19, 2012
Structure-activity relationship study of selective excitatory amino acid transporter subtype 1 (EAAT1) inhibitor 2-amino-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (UCPH-101) and absolute configurational assignment using infrared and vibrational circular dichroism spectroscopy in combination with ab initio Hartree-Fock calculationsTri H V Huynh, Irene Shim, Henrik Bohr, et al.The Journal of Biological Chemistry|January 10, 2009
Rational design of alpha-conotoxin analogues targeting alpha7 nicotinic acetylcholine receptors: improved antagonistic activity by incorporation of proline derivativesChristopher Armishaw, Anders A Jensen, Thomas Balle, et al.ACS Chemical Neuroscience|August 27, 2016
5-HT2A/5-HT2C Receptor Pharmacology and Intrinsic Clearance of N-Benzylphenethylamines Modified at the Primary Site of MetabolismSebastian Leth-Petersen, Ida N Petersen, Anders A Jensen, et al.European Journal of Medicinal Chemistry|July 20, 2014
Synthesis and pharmacological evaluation of 6-aminonicotinic acid analogues as novel GABA(A) receptor agonistsJette G Petersen, Troels Sørensen, Maria Damgaard, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 5, 2014
Probing α4βδ GABAA receptor heterogeneity: differential regional effects of a functionally selective α4β1δ/α4β3δ receptor agonist on tonic and phasic inhibition in rat brainKirsten Hoestgaard-Jensen, Nils Ole Dalby, Jacob Krall, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 18, 2013
Allosteric modulation of an excitatory amino acid transporter: the subtype-selective inhibitor UCPH-101 exerts sustained inhibition of EAAT1 through an intramonomeric site in the trimerization domainBjarke Abrahamsen, Nicole Schneider, Mette N Erichsen, et al.Bioorganic & Medicinal Chemistry Letters|November 26, 2008
Carbamoylcholine analogs as nicotinic acetylcholine receptor agonists--structural modifications of 3-(dimethylamino)butyl dimethylcarbamate (DMABC)Camilla P Hansen, Anders A Jensen, Thomas Balle, et al.Pageof 16