All Stories

  1. Shining Light on an mGlu5 Photoswitchable NAM: A Theoretical Perspective
  2. New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III
  3. Allosteric modulation of metabotropic glutamate receptors by chloride ions
  4. Synthesis and studies on the mGluR agonist activity of FAP4 stereoisomers
  5. Therapeutic potential of group III metabotropic glutamate receptor ligands in pain
  6. Determination of the absolute configuration of phosphinic analogues of glutamate
  7. Overlapping binding sites drive allosteric agonism and positive cooperativity in type 4 metabotropic glutamate receptors
  8. Exploring the Active Conformation of Cyclohexane Carboxylate Positive Allosteric Modulators of the Type 4 Metabotropic Glutamate Receptor
  9. An allosteric modulator to control endogenous G protein-coupled receptors with light
  10. S.24.01 mGluR4 ligands and pain
  11. α-Amino-β-fluorocyclopropanecarboxylic acids as a new tool for drug development: Synthesis of glutamic acid analogs and agonist activity towards metabotropic glutamate receptor 4
  12. Metabotropic Receptors for Glutamate and GABA
  13. Dimers and beyond: The functional puzzles of class C GPCRs
  14. Class C receptor activation mechanisms illustrated by mGlu and GABAB receptors. A review.
  15. Chapter 11. Metabotropic Glutamate Receptors: A Paradigm of Structural and Functional Receptor Complexity
  16. A critical pocket close to the glutamate binding site of mGlu receptors opens new possibilities for agonist design
  17. The complexity of their activation mechanism opens new possibilities for the modulation of mGlu and GABAB class C G protein-coupled receptors
  18. Integrated Synthetic, Pharmacological, and Computational Investigation of cis-2-(3,5-Dichlorophenylcarbamoyl)cyclohexanecarboxylic Acid Enantiomers As Positive Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 4
  19. A Virtual Screening Hit Reveals New Possibilities for Developing Group III Metabotropic Glutamate Receptor Agonists
  20. Metabotropic receptors for glutamate and GABA in pain
  21. Group III metabotropic glutamate receptors inhibit hyperalgesia in animal models of inflammation and neuropathic pain
  22. l -(+)-2-Amino-4-thiophosphonobutyric Acid ( l -thioAP4), a New Potent Agonist of Group III Metabotropic Glutamate Receptors:  Increased Distal Acidity Affords Enhanced Potency
  23. Synthesis and Biological Evaluation of 1-Amino-2-Phosphonomethylcyclopropanecarboxylic Acids, New Group III Metabotropic Glutamate Receptor Agonists
  24. d-myo-Inositol 1-phosphate as a surrogate of d-myo-inositol 1,4,5-tris phosphate to monitor G protein-coupled receptor activation
  25. Asymmetric Functioning of Dimeric Metabotropic Glutamate Receptors Disclosed by Positive Allosteric Modulators
  26. Evidence for a single heptahelical domain being turned on upon activation of a dimeric GPCR
  27. Allosteric modulators of class-C G-protein-coupled receptors open new possibilities for therapeutic application
  28. An overview of toxins and genes from the venom of the Asian scorpion Buthus martensi Karsch
  29. Characterization of two Bunodosoma granulifera toxins active on cardiac sodium channels
  30. Electrophysiological characterization of Bm K M1, an α-like toxin from Buthus martensi Karsch venom
  31. Cluster Organization and Pore Structure of Ion Channels Formed by Beticolin 3, a Nonpeptidic Fungal Toxin
  32. Magnesium ions promote assembly of channel‐like structures from beticolin 0, a non‐peptide fungal toxin purified from Cercospora beticola
  33. Electrophysiological properties of the hypokalaemic periodic paralysis mutation (R528H) of the skeletal muscle α 1S subunit as expressed in mouse L cells