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Journal of Medicinal Chemistry|May 31, 2002
Novel class of potent 4-arylalkyl substituted 3-isoxazolol GABA(A) antagonists: synthesis, pharmacology, and molecular modelingBente Frølund, Anne T Jørgensen, Lena Tagmose, et al.Epilepsy Research|February 12, 2008
Inhibition of the betaine-GABA transporter (mGAT2/BGT-1) modulates spontaneous electrographic bursting in the medial entorhinal cortex (mEC)Misty D Smith, Gerald W Saunders, Rasmus P Clausen, et al.Organic & Biomolecular Chemistry|March 8, 2007
Synthesis and pharmacology of glutamate receptor ligands: new isothiazole analogues of ibotenic acidCharlotte G Jørgensen, Rasmus P Clausen, Kasper B Hansen, et al.Journal of Medicinal Chemistry|February 13, 2013
Selective mGAT2 (BGT-1) GABA uptake inhibitors: design, synthesis, and pharmacological characterizationStine B Vogensen, Lars Jørgensen, Karsten K Madsen, et al.Journal of Medicinal Chemistry|July 28, 2007
5-Substituted imidazole-4-acetic acid analogues: synthesis, modeling, and pharmacological characterization of a series of novel gamma-aminobutyric acid(C) receptor agonistsChristian Madsen, Anders A Jensen, Tommy Liljefors, et al.Journal of Medicinal Chemistry|January 22, 2005
Potent 4-aryl- or 4-arylalkyl-substituted 3-isoxazolol GABA(A) antagonists: synthesis, pharmacology, and molecular modelingBente Frølund, Lars S Jensen, Luca Guandalini, et al.Journal of Medicinal Chemistry|January 11, 2013
Design, synthesis, and pharmacological characterization of N- and O-substituted 5,6,7,8-tetrahydro-4H-isoxazolo[4,5-d]azepin-3-ol analogues: novel 5-HT(2A)/5-HT(2C) receptor agonists with pro-cognitive propertiesAnders A Jensen, Niels Plath, Martin H F Pedersen, et al.Organic & Biomolecular Chemistry|January 23, 2004
A stereochemical anomaly: the cyclised (R)-AMPA analogue (R)-3-hydroxy-4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridine-5-carboxylic acid [(R)-5-HPCA] resembles (S)-AMPA at glutamate receptorsStine B Vogensen, Jeremy R Greenwood, Annemarie R Varming, et al.Bioorganic & Medicinal Chemistry|September 18, 2003
Synthesis and in vitro pharmacology at AMPA and kainate preferring glutamate receptors of 4-heteroarylmethylidene glutamate analoguesJon Valgeirsson, Jeppe K Christensen, Anders S Kristensen, et al.The Journal of Pharmacology and Experimental Therapeutics|July 20, 2002
Correlation between anticonvulsant activity and inhibitory action on glial gamma-aminobutyric acid uptake of the highly selective mouse gamma-aminobutyric acid transporter 1 inhibitor 3-hydroxy-4-amino-4,5,6,7-tetrahydro-1,2-benzisoxazole and its N-alkylated analogsH Steve White, Alan Sarup, Tina Bolvig, et al.Pageof 6