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ACS Chemical Neuroscience
|
February 18, 2020
Stereoselective Synthesis of New (2<i>S</i>,3<i>R</i>)-3-Carboxyphenyl)pyrrolidine-2-carboxylic Acid Analogues Utilizing a C(sp<sup>3</sup>)-H Activation Strategy and Structure-Activity Relationship Studies at the Ionotropic Glutamate Receptors
Silke Kayser, Jacob C Hansen, Markus Staudt, et al.
Journal of Medicinal Chemistry
|
December 24, 2004
Design, synthesis, and pharmacological characterization of novel, potent NMDA receptor antagonists
Paola Conti, Marco De Amici, Giovanni Grazioso, et al.
International Journal of Molecular Sciences
|
August 12, 2022
Discovery of the First Highly Selective Antagonist of the GluK3 Kainate Receptor Subtype
Paulina Chałupnik, Alina Vialko, Darryl S Pickering, et al.
Chemmedchem
|
January 24, 2012
Structure-activity relationships for negative allosteric mGluR5 modulators
Birgitte H Kaae, Kasper Harpsøe, Trine Kvist, et al.
Journal of Medicinal Chemistry
|
April 4, 2019
Use of the 4-Hydroxytriazole Moiety as a Bioisosteric Tool in the Development of Ionotropic Glutamate Receptor Ligands
Stefano Sainas, Piero Temperini, Jill C Farnsworth, et al.
Journal of Medicinal Chemistry
|
April 26, 2007
A tetrazolyl-substituted subtype-selective AMPA receptor agonist
Stine B Vogensen, Karla Frydenvang, Jeremy R Greenwood, et al.
Bioorganic & Medicinal Chemistry
|
July 20, 2010
A new metabotropic glutamate receptor agonist with in vivo anti-allodynic activity
Nathan J Stanley, Mark R Hutchinson, Trine Kvist, et al.
Journal of Medicinal Chemistry
|
September 18, 2010
Synthesis and antitumor effect in vitro and in vivo of substituted 1,3-dihydroindole-2-ones
Mette K Christensen, Kamille D Erichsen, Christina Trojel-Hansen, et al.
Journal of Medicinal Chemistry
|
January 28, 2016
New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III
Tri H V Huynh, Mette N Erichsen, Amélie S Tora, et al.
Journal of Medicinal Chemistry
|
December 15, 2021
Structure-Activity Studies of 3,9-Diazaspiro[5.5]undecane-Based γ-Aminobutyric Acid Type A Receptor Antagonists with Immunomodulatory Effect
Francesco Bavo, Heleen de-Jong, Jonas Petersen, et al.
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of 12
Search research articles
Search
Showing results (91-100 of 111) with videos related to
Sort By:
Page
of 12
ACS Chemical Neuroscience
|
February 18, 2020
Stereoselective Synthesis of New (2<i>S</i>,3<i>R</i>)-3-Carboxyphenyl)pyrrolidine-2-carboxylic Acid Analogues Utilizing a C(sp<sup>3</sup>)-H Activation Strategy and Structure-Activity Relationship Studies at the Ionotropic Glutamate Receptors
Silke Kayser, Jacob C Hansen, Markus Staudt, et al.
Journal of Medicinal Chemistry
|
December 24, 2004
Design, synthesis, and pharmacological characterization of novel, potent NMDA receptor antagonists
Paola Conti, Marco De Amici, Giovanni Grazioso, et al.
International Journal of Molecular Sciences
|
August 12, 2022
Discovery of the First Highly Selective Antagonist of the GluK3 Kainate Receptor Subtype
Paulina Chałupnik, Alina Vialko, Darryl S Pickering, et al.
Chemmedchem
|
January 24, 2012
Structure-activity relationships for negative allosteric mGluR5 modulators
Birgitte H Kaae, Kasper Harpsøe, Trine Kvist, et al.
Journal of Medicinal Chemistry
|
April 4, 2019
Use of the 4-Hydroxytriazole Moiety as a Bioisosteric Tool in the Development of Ionotropic Glutamate Receptor Ligands
Stefano Sainas, Piero Temperini, Jill C Farnsworth, et al.
Journal of Medicinal Chemistry
|
April 26, 2007
A tetrazolyl-substituted subtype-selective AMPA receptor agonist
Stine B Vogensen, Karla Frydenvang, Jeremy R Greenwood, et al.
Bioorganic & Medicinal Chemistry
|
July 20, 2010
A new metabotropic glutamate receptor agonist with in vivo anti-allodynic activity
Nathan J Stanley, Mark R Hutchinson, Trine Kvist, et al.
Journal of Medicinal Chemistry
|
September 18, 2010
Synthesis and antitumor effect in vitro and in vivo of substituted 1,3-dihydroindole-2-ones
Mette K Christensen, Kamille D Erichsen, Christina Trojel-Hansen, et al.
Journal of Medicinal Chemistry
|
January 28, 2016
New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III
Tri H V Huynh, Mette N Erichsen, Amélie S Tora, et al.
Journal of Medicinal Chemistry
|
December 15, 2021
Structure-Activity Studies of 3,9-Diazaspiro[5.5]undecane-Based γ-Aminobutyric Acid Type A Receptor Antagonists with Immunomodulatory Effect
Francesco Bavo, Heleen de-Jong, Jonas Petersen, et al.
Page
of 12