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Proceedings of the National Academy of Sciences of the United States of America|March 31, 2019
Precise small-molecule cleavage of an r(CUG) repeat expansion in a myotonic dystrophy mouse modelAlicia J Angelbello, Suzanne G Rzuczek, Kendra K Mckee, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of Potent and Selective Urea-Based ROCK Inhibitors and Their Effects on Intraocular Pressure in RatsYan Yin, Michael D Cameron, Li Lin, et al.Journal of Medicinal Chemistry|September 11, 2018
Optimization of a Series of Mu Opioid Receptor (MOR) Agonists with High G Protein Signaling BiasNicole M Kennedy, Cullen L Schmid, Nicolette C Ross, et al.Journal of Medicinal Chemistry|April 11, 2013
Synthesis and biological evaluation of urea derivatives as highly potent and selective rho kinase inhibitorsYan Yin, Li Lin, Claudia Ruiz, et al.European Journal of Medicinal Chemistry|July 6, 2024
Synthesis and evaluation of 3,4,5-trisubstituted triazoles as G protein-biased kappa opioid receptor agonistsAshley E Trojniak, Vuong Q Dang, Kerri M Czekner, et al.Bioorganic & Medicinal Chemistry Letters|November 8, 2008
Chroman-3-amides as potent Rho kinase inhibitorsYen Ting Chen, Thomas D Bannister, Amiee Weiser, et al.Frontiers in Molecular Neuroscience|September 30, 2024
SR9883 is a novel small-molecule enhancer of α4β2* nicotinic acetylcholine receptor signaling that decreases intravenous nicotine self-administration in ratsKevin M Braunscheidel, George Voren, Christie D Fowler, et al.Bioorganic & Medicinal Chemistry Letters|March 18, 2018
Design, synthesis, and evaluation of simple phenol amides as ERRγ agonistsHua Lin, Christelle Doebelin, Rémi Patouret, et al.Journal of Medicinal Chemistry|October 7, 2008
Discovery of substituted 4-(pyrazol-4-yl)-phenylbenzodioxane-2-carboxamides as potent and highly selective Rho kinase (ROCK-II) inhibitorsYangbo Feng, Yan Yin, Amiee Weiser, et al.ACS Chemical Biology|April 30, 2020
Hydrocarbon-Stitched Peptide Agonists of Glucagon-Like Peptide-1 ReceptorGregory H Bird, Accalia Fu, Silvia Escudero, et al.Pageof 15