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Journal of Medicinal Chemistry
|
February 11, 2016
Tweaking Subtype Selectivity and Agonist Efficacy at (S)-2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propionic acid (AMPA) Receptors in a Small Series of BnTetAMPA Analogues
Shuang-Yan Wang, Younes Larsen, Cristina Vara Navarrete, et al.
ACS Chemical Neuroscience
|
May 22, 2020
Ionotropic Glutamate Receptor GluA2 in Complex with Bicyclic Pyrimidinedione-Based Compounds: When Small Compound Modifications Have Distinct Effects on Binding Interactions
Karla Frydenvang, Darryl S Pickering, Giridhar U Kshirsagar, et al.
Journal of Medicinal Chemistry
|
October 18, 2013
Synthesis, pharmacological and structural characterization, and thermodynamic aspects of GluA2-positive allosteric modulators with a 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide scaffold
Ann-Beth Nørholm, Pierre Francotte, Lars Olsen, et al.
Journal of Medicinal Chemistry
|
February 26, 2013
Studies on an (S)-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid (AMPA) receptor antagonist IKM-159: asymmetric synthesis, neuroactivity, and structural characterization
Lina Juknaitė, Yutaro Sugamata, Kazuya Tokiwa, et al.
Journal of Structural Biology
|
July 14, 2012
Pharmacological and structural characterization of conformationally restricted (S)-glutamate analogues at ionotropic glutamate receptors
Lina Juknaitė, Raminta Venskutonytė, Zeinab Assaf, et al.
Chemmedchem
|
March 3, 2011
Design, synthesis, and pharmacological characterization of novel spirocyclic quinuclidinyl-Δ2-isoxazoline derivatives as potent and selective agonists of α7 nicotinic acetylcholine receptors
Clelia Dallanoce, Pietro Magrone, Carlo Matera, et al.
Journal of Medicinal Chemistry
|
January 9, 2013
Synthesis and biological evaluation of 4-(aminomethyl)-1-hydroxypyrazole analogues of muscimol as γ-aminobutyric acid(a) receptor agonists
Jette G Petersen, Rikke Bergmann, Henriette A Møller, et al.
Organic & Biomolecular Chemistry
|
July 30, 2010
Structure-activity relationships of a small-molecule inhibitor of the PDZ domain of PICK1
Anders Bach, Nicolai Stuhr-Hansen, Thor S Thorsen, et al.
Journal of Medicinal Chemistry
|
September 23, 2010
Structure-activity relationship study of first selective inhibitor of excitatory amino acid transporter subtype 1: 2-Amino-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (UCPH-101)
Mette N Erichsen, Tri H V Huynh, Bjarke Abrahamsen, et al.
Journal of Medicinal Chemistry
|
November 12, 2010
Biostructural and pharmacological studies of bicyclic analogues of the 3-isoxazolol glutamate receptor agonist ibotenic acid
Karla Frydenvang, Darryl S Pickering, Jeremy R Greenwood, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 81) with videos related to
Sort By:
Page
of 9
Journal of Medicinal Chemistry
|
February 11, 2016
Tweaking Subtype Selectivity and Agonist Efficacy at (S)-2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propionic acid (AMPA) Receptors in a Small Series of BnTetAMPA Analogues
Shuang-Yan Wang, Younes Larsen, Cristina Vara Navarrete, et al.
ACS Chemical Neuroscience
|
May 22, 2020
Ionotropic Glutamate Receptor GluA2 in Complex with Bicyclic Pyrimidinedione-Based Compounds: When Small Compound Modifications Have Distinct Effects on Binding Interactions
Karla Frydenvang, Darryl S Pickering, Giridhar U Kshirsagar, et al.
Journal of Medicinal Chemistry
|
October 18, 2013
Synthesis, pharmacological and structural characterization, and thermodynamic aspects of GluA2-positive allosteric modulators with a 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide scaffold
Ann-Beth Nørholm, Pierre Francotte, Lars Olsen, et al.
Journal of Medicinal Chemistry
|
February 26, 2013
Studies on an (S)-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid (AMPA) receptor antagonist IKM-159: asymmetric synthesis, neuroactivity, and structural characterization
Lina Juknaitė, Yutaro Sugamata, Kazuya Tokiwa, et al.
Journal of Structural Biology
|
July 14, 2012
Pharmacological and structural characterization of conformationally restricted (S)-glutamate analogues at ionotropic glutamate receptors
Lina Juknaitė, Raminta Venskutonytė, Zeinab Assaf, et al.
Chemmedchem
|
March 3, 2011
Design, synthesis, and pharmacological characterization of novel spirocyclic quinuclidinyl-Δ2-isoxazoline derivatives as potent and selective agonists of α7 nicotinic acetylcholine receptors
Clelia Dallanoce, Pietro Magrone, Carlo Matera, et al.
Journal of Medicinal Chemistry
|
January 9, 2013
Synthesis and biological evaluation of 4-(aminomethyl)-1-hydroxypyrazole analogues of muscimol as γ-aminobutyric acid(a) receptor agonists
Jette G Petersen, Rikke Bergmann, Henriette A Møller, et al.
Organic & Biomolecular Chemistry
|
July 30, 2010
Structure-activity relationships of a small-molecule inhibitor of the PDZ domain of PICK1
Anders Bach, Nicolai Stuhr-Hansen, Thor S Thorsen, et al.
Journal of Medicinal Chemistry
|
September 23, 2010
Structure-activity relationship study of first selective inhibitor of excitatory amino acid transporter subtype 1: 2-Amino-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (UCPH-101)
Mette N Erichsen, Tri H V Huynh, Bjarke Abrahamsen, et al.
Journal of Medicinal Chemistry
|
November 12, 2010
Biostructural and pharmacological studies of bicyclic analogues of the 3-isoxazolol glutamate receptor agonist ibotenic acid
Karla Frydenvang, Darryl S Pickering, Jeremy R Greenwood, et al.
Page
of 9