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Molecular Pharmacology
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February 25, 2026
UCM-A86 is a selective positive allosteric modulator of GluN1/GluN3 NMDA receptors
Avery J Benton, Mia R Johns, Emil Diamant, et al.
Journal of Medicinal Chemistry
|
December 23, 2016
Development of Radiolabeled Ligands Targeting the Glutamate Binding Site of the N-Methyl-d-aspartate Receptor as Potential Imaging Agents for Brain
Lucia Tamborini, Ying Chen, Catherine A Foss, et al.
Biorxiv : the Preprint Server for Biology
|
November 26, 2025
UCM-A86 is a selective positive allosteric modulator of GluN1/GluN3 NMDA receptors
Avery J Benton, Mia R Johns, Emil Diamant, et al.
Journal of Medicinal Chemistry
|
April 23, 2010
4-hydroxy-1,2,5-oxadiazol-3-yl moiety as bioisoster of the carboxy function. Synthesis, ionization constants, and molecular pharmacological characterization at ionotropic glutamate receptors of compounds related to glutamate and its homologues
Marco L Lolli, Cecilia Giordano, Darryl S Pickering, et al.
Nature Cardiovascular Research
|
July 17, 2025
The thrombin receptor PAR1 orchestrates changes in lymphatic endothelial cell junction morphology to augment lymphatic drainage during lung injury
Chou Chou, Camila Ceballos Paredes, Barbara Summers, et al.
Journal of Medicinal Chemistry
|
June 27, 2008
N-Hydroxypyrazolyl glycine derivatives as selective N-methyl-D-aspartic acid receptor ligands
Rasmus P Clausen, Caspar Christensen, Kasper B Hansen, et al.
Molecular Pharmacology
|
August 3, 2011
Mechanism for noncompetitive inhibition by novel GluN2C/D N-methyl-D-aspartate receptor subunit-selective modulators
Timothy M Acker, Hongjie Yuan, Kasper B Hansen, et al.
Chemmedchem
|
July 29, 2010
Novel 3-carboxy- and 3-phosphonopyrazoline amino acids as potent and selective NMDA receptor antagonists: design, synthesis, and pharmacological characterization
Paola Conti, Andrea Pinto, Lucia Tamborini, et al.
Journal of Medicinal Chemistry
|
December 6, 2017
Augmentation of Anticancer Drug Efficacy in Murine Hepatocellular Carcinoma Cells by a Peripherally Acting Competitive N-Methyl-d-aspartate (NMDA) Receptor Antagonist
Mikko Gynther, Ilaria Proietti Silvestri, Jacob C Hansen, et al.
Nature Communications
|
October 29, 2010
A subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors
Praseeda Mullasseril, Kasper B Hansen, Katie M Vance, et al.
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Search research articles
Search
Showing results (61-70 of 85) with videos related to
Sort By:
Page
of 9
Molecular Pharmacology
|
February 25, 2026
UCM-A86 is a selective positive allosteric modulator of GluN1/GluN3 NMDA receptors
Avery J Benton, Mia R Johns, Emil Diamant, et al.
Journal of Medicinal Chemistry
|
December 23, 2016
Development of Radiolabeled Ligands Targeting the Glutamate Binding Site of the N-Methyl-d-aspartate Receptor as Potential Imaging Agents for Brain
Lucia Tamborini, Ying Chen, Catherine A Foss, et al.
Biorxiv : the Preprint Server for Biology
|
November 26, 2025
UCM-A86 is a selective positive allosteric modulator of GluN1/GluN3 NMDA receptors
Avery J Benton, Mia R Johns, Emil Diamant, et al.
Journal of Medicinal Chemistry
|
April 23, 2010
4-hydroxy-1,2,5-oxadiazol-3-yl moiety as bioisoster of the carboxy function. Synthesis, ionization constants, and molecular pharmacological characterization at ionotropic glutamate receptors of compounds related to glutamate and its homologues
Marco L Lolli, Cecilia Giordano, Darryl S Pickering, et al.
Nature Cardiovascular Research
|
July 17, 2025
The thrombin receptor PAR1 orchestrates changes in lymphatic endothelial cell junction morphology to augment lymphatic drainage during lung injury
Chou Chou, Camila Ceballos Paredes, Barbara Summers, et al.
Journal of Medicinal Chemistry
|
June 27, 2008
N-Hydroxypyrazolyl glycine derivatives as selective N-methyl-D-aspartic acid receptor ligands
Rasmus P Clausen, Caspar Christensen, Kasper B Hansen, et al.
Molecular Pharmacology
|
August 3, 2011
Mechanism for noncompetitive inhibition by novel GluN2C/D N-methyl-D-aspartate receptor subunit-selective modulators
Timothy M Acker, Hongjie Yuan, Kasper B Hansen, et al.
Chemmedchem
|
July 29, 2010
Novel 3-carboxy- and 3-phosphonopyrazoline amino acids as potent and selective NMDA receptor antagonists: design, synthesis, and pharmacological characterization
Paola Conti, Andrea Pinto, Lucia Tamborini, et al.
Journal of Medicinal Chemistry
|
December 6, 2017
Augmentation of Anticancer Drug Efficacy in Murine Hepatocellular Carcinoma Cells by a Peripherally Acting Competitive N-Methyl-d-aspartate (NMDA) Receptor Antagonist
Mikko Gynther, Ilaria Proietti Silvestri, Jacob C Hansen, et al.
Nature Communications
|
October 29, 2010
A subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors
Praseeda Mullasseril, Kasper B Hansen, Katie M Vance, et al.
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of 9