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Chemmedchem
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September 5, 2009
4,4-Dimethyl- and diastereomeric 4-hydroxy-4-methyl- (2S)-glutamate analogues display distinct pharmacological profiles at ionotropic glutamate receptors and excitatory amino acid transporters
Lennart Bunch, Darryl S Pickering, Thierry Gefflaut, et al.
Journal of Medicinal Chemistry
|
April 26, 2013
Development of 2'-substituted (2S,1'R,2'S)-2-(carboxycyclopropyl)glycine analogues as potent N-methyl-d-aspartic acid receptor agonists
Rune Risgaard, Simon D Nielsen, Kasper B Hansen, et al.
Journal of Medicinal Chemistry
|
July 17, 2013
Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(Piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted: design, synthesis, and pharmacological evaluation
Jacob Krall, Claus H Jensen, Troels E Sørensen, et al.
Chemmedchem
|
November 15, 2008
Stereocontrolled synthesis and pharmacological evaluation of azetidine-2,3-dicarboxylic acids at NMDA receptors
Mangaleswaran Sivaprakasam, Kasper B Hansen, Olivier David, et al.
Journal of Medicinal Chemistry
|
September 6, 2002
Selective agonists at group II metabotropic glutamate receptors: synthesis, stereochemistry, and molecular pharmacology of (S)- and (R)-2-amino-4-(4-hydroxy[1,2,5]thiadiazol-3-yl)butyric acid
Rasmus P Clausen, Hans Bräuner-Osborne, Jeremy R Greenwood, et al.
Organic & Biomolecular Chemistry
|
October 22, 2005
Azetidinic amino acids: stereocontrolled synthesis and pharmacological characterization as ligands for glutamate receptors and transporters
Hans Bräuner-Osborne, Lennart Bunch, Nathalie Chopin, et al.
European Journal of Pharmacology
|
September 15, 2004
The respective N-hydroxypyrazole analogues of the classical glutamate receptor ligands ibotenic acid and (RS)-2-amino-2-(3-hydroxy-5-methyl-4-isoxazolyl)acetic acid
Rasmus P Clausen, Kasper B Hansen, Patrizia Calí, et al.
European Journal of Medicinal Chemistry
|
September 18, 2018
4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric γ-aminobutyric acid receptor binding site
Alessandro Giraudo, Jacob Krall, Birgitte Nielsen, et al.
European Journal of Medicinal Chemistry
|
July 25, 2017
Pharmacological characterization and binding modes of novel racemic and optically active phenylalanine-based antagonists of AMPA receptors
Ewa Szymańska, Birgitte Nielsen, Tommy N Johansen, et al.
Bioorganic & Medicinal Chemistry
|
August 31, 2014
Design, synthesis and in vitro pharmacology of GluK1 and GluK3 antagonists. Studies towards the design of subtype-selective antagonists through 2-carboxyethyl-phenylalanines with substituents interacting with non-conserved residues in the GluK binding sites
Niklas Sköld, Birgitte Nielsen, Jacob Olsen, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 111) with videos related to
Sort By:
Page
of 12
Chemmedchem
|
September 5, 2009
4,4-Dimethyl- and diastereomeric 4-hydroxy-4-methyl- (2S)-glutamate analogues display distinct pharmacological profiles at ionotropic glutamate receptors and excitatory amino acid transporters
Lennart Bunch, Darryl S Pickering, Thierry Gefflaut, et al.
Journal of Medicinal Chemistry
|
April 26, 2013
Development of 2'-substituted (2S,1'R,2'S)-2-(carboxycyclopropyl)glycine analogues as potent N-methyl-d-aspartic acid receptor agonists
Rune Risgaard, Simon D Nielsen, Kasper B Hansen, et al.
Journal of Medicinal Chemistry
|
July 17, 2013
Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(Piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted: design, synthesis, and pharmacological evaluation
Jacob Krall, Claus H Jensen, Troels E Sørensen, et al.
Chemmedchem
|
November 15, 2008
Stereocontrolled synthesis and pharmacological evaluation of azetidine-2,3-dicarboxylic acids at NMDA receptors
Mangaleswaran Sivaprakasam, Kasper B Hansen, Olivier David, et al.
Journal of Medicinal Chemistry
|
September 6, 2002
Selective agonists at group II metabotropic glutamate receptors: synthesis, stereochemistry, and molecular pharmacology of (S)- and (R)-2-amino-4-(4-hydroxy[1,2,5]thiadiazol-3-yl)butyric acid
Rasmus P Clausen, Hans Bräuner-Osborne, Jeremy R Greenwood, et al.
Organic & Biomolecular Chemistry
|
October 22, 2005
Azetidinic amino acids: stereocontrolled synthesis and pharmacological characterization as ligands for glutamate receptors and transporters
Hans Bräuner-Osborne, Lennart Bunch, Nathalie Chopin, et al.
European Journal of Pharmacology
|
September 15, 2004
The respective N-hydroxypyrazole analogues of the classical glutamate receptor ligands ibotenic acid and (RS)-2-amino-2-(3-hydroxy-5-methyl-4-isoxazolyl)acetic acid
Rasmus P Clausen, Kasper B Hansen, Patrizia Calí, et al.
European Journal of Medicinal Chemistry
|
September 18, 2018
4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric γ-aminobutyric acid receptor binding site
Alessandro Giraudo, Jacob Krall, Birgitte Nielsen, et al.
European Journal of Medicinal Chemistry
|
July 25, 2017
Pharmacological characterization and binding modes of novel racemic and optically active phenylalanine-based antagonists of AMPA receptors
Ewa Szymańska, Birgitte Nielsen, Tommy N Johansen, et al.
Bioorganic & Medicinal Chemistry
|
August 31, 2014
Design, synthesis and in vitro pharmacology of GluK1 and GluK3 antagonists. Studies towards the design of subtype-selective antagonists through 2-carboxyethyl-phenylalanines with substituents interacting with non-conserved residues in the GluK binding sites
Niklas Sköld, Birgitte Nielsen, Jacob Olsen, et al.
Page
of 12