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Chemistry & Biology
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November 21, 2007
Structural proof of a dimeric positive modulator bridging two identical AMPA receptor-binding sites
Birgitte H Kaae, Kasper Harpsøe, Jette S Kastrup, et al.
Molecular Pharmacology
|
August 18, 2012
Pharmacological characterization and modeling of the binding sites of novel 1,3-bis(pyridinylethynyl)benzenes as metabotropic glutamate receptor 5-selective negative allosteric modulators
Christina Mølck, Kasper Harpsøe, David E Gloriam, et al.
Bioorganic & Medicinal Chemistry
|
January 18, 2005
Selective inhibitors of GABA uptake: synthesis and molecular pharmacology of 4-N-methylamino-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-ol analogues
Rasmus P Clausen, Ejner K Moltzen, Jens Perregaard, et al.
FEBS Letters
|
May 18, 2011
Enzyme kinetic studies of histone demethylases KDM4C and KDM6A: towards understanding selectivity of inhibitors targeting oncogenic histone demethylases
Jan B L Kristensen, Anders L Nielsen, Lars Jørgensen, 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.
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.
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.
ACS Chemical Neuroscience
|
January 19, 2017
Radiosynthesis and Evaluation of [<sup>11</sup>C]3-Hydroxycyclopent-1-enecarboxylic Acid as Potential PET Ligand for the High-Affinity γ-Hydroxybutyric Acid Binding Sites
Claus H Jensen, Hanne D Hansen, Tina Bay, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 4, 2012
α4βδ GABA(A) receptors are high-affinity targets for γ-hydroxybutyric acid (GHB)
Nathan Absalom, Laura F Eghorn, Inge S Villumsen, et al.
Neurochemical Research
|
May 24, 2014
Pharmacological identification of a guanidine-containing β-alanine analogue with low micromolar potency and selectivity for the betaine/GABA transporter 1 (BGT1)
Anas Al-Khawaja, Jette G Petersen, Maria Damgaard, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 83) with videos related to
Sort By:
Page
of 9
Chemistry & Biology
|
November 21, 2007
Structural proof of a dimeric positive modulator bridging two identical AMPA receptor-binding sites
Birgitte H Kaae, Kasper Harpsøe, Jette S Kastrup, et al.
Molecular Pharmacology
|
August 18, 2012
Pharmacological characterization and modeling of the binding sites of novel 1,3-bis(pyridinylethynyl)benzenes as metabotropic glutamate receptor 5-selective negative allosteric modulators
Christina Mølck, Kasper Harpsøe, David E Gloriam, et al.
Bioorganic & Medicinal Chemistry
|
January 18, 2005
Selective inhibitors of GABA uptake: synthesis and molecular pharmacology of 4-N-methylamino-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-ol analogues
Rasmus P Clausen, Ejner K Moltzen, Jens Perregaard, et al.
FEBS Letters
|
May 18, 2011
Enzyme kinetic studies of histone demethylases KDM4C and KDM6A: towards understanding selectivity of inhibitors targeting oncogenic histone demethylases
Jan B L Kristensen, Anders L Nielsen, Lars Jørgensen, 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.
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.
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.
ACS Chemical Neuroscience
|
January 19, 2017
Radiosynthesis and Evaluation of [<sup>11</sup>C]3-Hydroxycyclopent-1-enecarboxylic Acid as Potential PET Ligand for the High-Affinity γ-Hydroxybutyric Acid Binding Sites
Claus H Jensen, Hanne D Hansen, Tina Bay, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 4, 2012
α4βδ GABA(A) receptors are high-affinity targets for γ-hydroxybutyric acid (GHB)
Nathan Absalom, Laura F Eghorn, Inge S Villumsen, et al.
Neurochemical Research
|
May 24, 2014
Pharmacological identification of a guanidine-containing β-alanine analogue with low micromolar potency and selectivity for the betaine/GABA transporter 1 (BGT1)
Anas Al-Khawaja, Jette G Petersen, Maria Damgaard, et al.
Page
of 9