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Journal of Medicinal Chemistry|March 2, 2018
Covalent Allosteric Probe for the Metabotropic Glutamate Receptor 2: Design, Synthesis, and Pharmacological CharacterizationMaarten L J Doornbos, Xuesong Wang, Sophie C Vermond, et al.Science (New York, N.Y.)|July 17, 2012
Structural basis for allosteric regulation of GPCRs by sodium ionsWei Liu, Eugene Chun, Aaron A Thompson, et al.Molecular Pharmacology|July 16, 2014
Discovery and mapping of an intracellular antagonist binding site at the chemokine receptor CCR2Annelien J M Zweemer, Julia Bunnik, Margo Veenhuizen, et al.Nature Communications|August 18, 2025
Molecular basis of ligand binding and receptor activation at the human A3 adenosine receptorLiudi Zhang, Jesse I Mobbs, Felix M Bennetts, et al.Journal of Chemical Information and Modeling|November 12, 2025
Combining AlphaFold with Focused Virtual Library Design in the Development of Novel CCR2 and CCR5 AntagonistsKhaled Essa, Kian Noorman van der Dussen, Yao Yao, et al.Chemmedchem|May 29, 2009
Discovery of selective luteinizing hormone receptor agonists using the bivalent ligand methodKimberly M Bonger, Richard J B H N van den Berg, Annemiek D Knijnenburg, et al.Arthritis & Rheumatology (Hoboken, N.J.)|December 25, 2024
Absence of Functional Autoantibodies Targeting Angiotensin II Receptor Type 1 and Endothelin-1 Type A Receptor in Circulation and Purified IgG From Patients With Systemic SclerosisWieke M van Oostveen, Eva M Hoekstra, E W Nivine Levarht, et al.Neurobiology of Disease|January 31, 2026
Impedance-based phenotypic profiling of metabotropic glutamate receptor ligand responses in SCA1 human iPSC-derived neuronal culturesLaurie M C Kerkhof, Ronald A M Buijsen, Stefan Hartman, et al.Structure (London, England : 1993)|November 12, 2013
The role of a sodium ion binding site in the allosteric modulation of the A(2A) adenosine G protein-coupled receptorHugo Gutiérrez-de-Terán, Arnault Massink, David Rodríguez, et al.Bioorganic & Medicinal Chemistry|February 20, 2008
Synthesis and evaluation of homodimeric GnRHR antagonists having a rigid bis-propargylated benzene coreKimberly M Bonger, Richard J B H N van den Berg, Annemiek D Knijnenburg, et al.Pageof 16