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Showing results (61-70 of 70) with videos related to

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Journal of Medicinal Chemistry|February 19, 2013
Chemoenzymatic synthesis of new 2,4-syn-functionalized (S)-glutamate analogues and structure-activity relationship studies at ionotropic glutamate receptors and excitatory amino acid transportersZeinab Assaf, Anja P Larsen, Raminta Venskutonytė, et al.
Journal of Medicinal Chemistry|July 23, 2015
Structure-Activity Relationship Study of Ionotropic Glutamate Receptor Antagonist (2S,3R)-3-(3-Carboxyphenyl)pyrrolidine-2-carboxylic AcidNiels Krogsgaard-Larsen, Morten Storgaard, Charlotte Møller, 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 AntagonistMikko Gynther, Ilaria Proietti Silvestri, Jacob C Hansen, et al.
Chemmedchem|January 13, 2016
New Insight into the Structure-Activity Relationships of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors UCPH-101 and UCPH-102Stinne W Hansen, Mette N Erichsen, Tri H V Huynh, et al.
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 ReceptorsSilke Kayser, Jacob C Hansen, Markus Staudt, 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 IIITri H V Huynh, Mette N Erichsen, Amélie S Tora, et al.
Journal of Medicinal Chemistry|December 23, 2016
Design and Synthesis of a Series of l-trans-4-Substituted Prolines as Selective Antagonists for the Ionotropic Glutamate Receptors Including Functional and X-ray Crystallographic Studies of New Subtype Selective Kainic Acid Receptor Subtype 1 (GluK1) Antagonist (2S,4R)-4-(2-Carboxyphenoxy)pyrrolidine-2-carboxylic AcidNiels Krogsgaard-Larsen, Claudia G Delgar, Karina Koch, et al.
Chemmedchem|January 23, 2016
Bioavailability Studies and in vitro Profiling of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitor UCPH-102Isabell Haym, Tri H V Huynh, Stinne W Hansen, et al.
ACS Chemical Neuroscience|May 25, 2019
Design and Synthesis of 2,3- trans-Proline Analogues as Ligands for Ionotropic Glutamate Receptors and Excitatory Amino Acid TransportersChristian B M Poulie, Anna Alcaide, Mikkel Krell-Jørgensen, et al.
Journal of Medicinal Chemistry|January 23, 2025
Design of (<i>R</i>)-3-(5-Thienyl)carboxamido-2-aminopropanoic Acid Derivatives as Novel NMDA Receptor Glycine Site Agonists: Variation in Molecular Geometry to Improve Potency and Augment GluN2 Subunit-Specific ActivityFabao Zhao, Unai Atxabal, Sofia Mariottini, et al.
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Showing results (61-70 of 70) with videos related to

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Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Journal of Medicinal Chemistry|February 19, 2013
Chemoenzymatic synthesis of new 2,4-syn-functionalized (S)-glutamate analogues and structure-activity relationship studies at ionotropic glutamate receptors and excitatory amino acid transportersZeinab Assaf, Anja P Larsen, Raminta Venskutonytė, et al.
Journal of Medicinal Chemistry|July 23, 2015
Structure-Activity Relationship Study of Ionotropic Glutamate Receptor Antagonist (2S,3R)-3-(3-Carboxyphenyl)pyrrolidine-2-carboxylic AcidNiels Krogsgaard-Larsen, Morten Storgaard, Charlotte Møller, 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 AntagonistMikko Gynther, Ilaria Proietti Silvestri, Jacob C Hansen, et al.
Chemmedchem|January 13, 2016
New Insight into the Structure-Activity Relationships of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors UCPH-101 and UCPH-102Stinne W Hansen, Mette N Erichsen, Tri H V Huynh, et al.
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 ReceptorsSilke Kayser, Jacob C Hansen, Markus Staudt, 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 IIITri H V Huynh, Mette N Erichsen, Amélie S Tora, et al.
Journal of Medicinal Chemistry|December 23, 2016
Design and Synthesis of a Series of l-trans-4-Substituted Prolines as Selective Antagonists for the Ionotropic Glutamate Receptors Including Functional and X-ray Crystallographic Studies of New Subtype Selective Kainic Acid Receptor Subtype 1 (GluK1) Antagonist (2S,4R)-4-(2-Carboxyphenoxy)pyrrolidine-2-carboxylic AcidNiels Krogsgaard-Larsen, Claudia G Delgar, Karina Koch, et al.
Chemmedchem|January 23, 2016
Bioavailability Studies and in vitro Profiling of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitor UCPH-102Isabell Haym, Tri H V Huynh, Stinne W Hansen, et al.
ACS Chemical Neuroscience|May 25, 2019
Design and Synthesis of 2,3- trans-Proline Analogues as Ligands for Ionotropic Glutamate Receptors and Excitatory Amino Acid TransportersChristian B M Poulie, Anna Alcaide, Mikkel Krell-Jørgensen, et al.
Journal of Medicinal Chemistry|January 23, 2025
Design of (<i>R</i>)-3-(5-Thienyl)carboxamido-2-aminopropanoic Acid Derivatives as Novel NMDA Receptor Glycine Site Agonists: Variation in Molecular Geometry to Improve Potency and Augment GluN2 Subunit-Specific ActivityFabao Zhao, Unai Atxabal, Sofia Mariottini, et al.
Pageof 7