Pages that link to "Q40161379"
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The following pages link to Synthesis and pharmacological characterization of N3-substituted willardiine derivatives: role of the substituent at the 5-position of the uracil ring in the development of highly potent and selective GLUK5 kainate receptor antagonists (Q40161379):
Displaying 15 items.
- ACET is a highly potent and specific kainate receptor antagonist: Characterisation and effects on hippocampal mossy fibre function (Q27652127) (← links)
- Binding site and ligand flexibility revealed by high resolution crystal structures of GluK1 competitive antagonists (Q27662421) (← links)
- Glutamate receptor ion channels: structure, regulation, and function (Q28290774) (← links)
- Novel analogs and stereoisomers of the marine toxin neodysiherbaine with specificity for kainate receptors (Q33552005) (← links)
- Pharmacological activity of C10-substituted analogs of the high-affinity kainate receptor agonist dysiherbaine. (Q33618482) (← links)
- Kainate receptors mediate synaptic input to transient and sustained OFF visual pathways in primate retina (Q33671705) (← links)
- Synaptic pathways that shape the excitatory drive in an OFF retinal ganglion cell (Q35902616) (← links)
- Discovery of a new class of ionotropic glutamate receptor antagonists by the rational design of (2S,3R)-3-(3-carboxyphenyl)-pyrrolidine-2-carboxylic acid (Q36015364) (← links)
- GLUK1 receptor antagonists and hippocampal mossy fiber function (Q37553141) (← links)
- Medicinal chemistry of competitive kainate receptor antagonists (Q38025106) (← links)
- Mapping the Ligand Binding Sites of Kainate Receptors: Molecular Determinants of Subunit-Selective Binding of the Antagonist [3H]UBP310 (Q41452263) (← links)
- Synaptic kainate receptors in CA1 interneurons gate the threshold of theta-frequency-induced long-term potentiation (Q48254235) (← links)
- The Role of Kainate Receptors in the Pathophysiology of Hypoxia-Induced Seizures in the Neonatal Mouse. (Q55187094) (← links)
- Stereoselective Synthesis of New (2S,3R)-3-Carboxyphenyl)pyrrolidine-2-carboxylic Acid Analogues Utilizing a C(sp3)-H Activation Strategy and Structure-Activity Relationship Studies at the Ionotropic Glutamate Receptors (Q89743782) (← links)
- Pharmacological antagonism of kainate receptor rescues dysfunction and loss of dopamine neurons in a mouse model of human parkin-induced toxicity (Q101563969) (← links)