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British Journal of Pharmacology|February 24, 2025
A bio. tools collection of online resources for GPCR researchTõnis Laasfeld, Friederike Wunsch, Avgi E Apostolakou, et al.The Journal of Biological Chemistry|August 6, 2020
Delineation of molecular determinants for FR900359 inhibition of Gq/11 unlocks inhibition of GαsMichael W Boesgaard, Kasper Harpsøe, Michelle Malmberg, et al.Nature Chemistry|October 22, 2016
Total synthesis and structure-activity relationship studies of a series of selective G protein inhibitorsXiao-Feng Xiong, Hang Zhang, Christina R Underwood, et al.Journal of Medicinal Chemistry|January 11, 2013
Design, synthesis, and pharmacological characterization of N- and O-substituted 5,6,7,8-tetrahydro-4H-isoxazolo[4,5-d]azepin-3-ol analogues: novel 5-HT(2A)/5-HT(2C) receptor agonists with pro-cognitive propertiesAnders A Jensen, Niels Plath, Martin H F Pedersen, et al.European Journal of Pharmacology|February 3, 2023
Pharmacological characterization of novel small molecule agonists and antagonists for the orphan receptor GPR139Lisa Pallareti, Tine F Rath, Boris Trapkov, et al.Nucleic Acids Research|November 18, 2024
GPCRdb in 2025: adding odorant receptors, data mapper, structure similarity search and models of physiological ligand complexesLuis P Taracena Herrera, Søren N Andreassen, Jimmy Caroli, et al.Journal of Medicinal Chemistry|September 11, 2012
Modulation in selectivity and allosteric properties of small-molecule ligands for CC-chemokine receptorsStefanie Thiele, Mikkel Malmgaard-Clausen, Jens Engel-Andreasen, et al.Trends in Pharmacological Sciences|December 27, 2014
Generic GPCR residue numbers - aligning topology maps while minding the gapsVignir Isberg, Chris de Graaf, Andrea Bortolato, 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 modulatorsChristina Mølck, Kasper Harpsøe, David E Gloriam, et al.Neurochemistry International|December 6, 2016
The orphan G protein-coupled receptor GPR139 is activated by the peptides: Adrenocorticotropic hormone (ACTH), α-, and β-melanocyte stimulating hormone (α-MSH, and β-MSH), and the conserved core motif HFRWAnne Cathrine Nøhr, Mohamed A Shehata, Alexander S Hauser, et al.Pageof 11