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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.
Dolman NP, More JC, Alt A, Knauss JL, Pentikäinen OT, Glasser CR, Bleakman D, Mayer ML, Collingridge GL, Jane DE. Dolman NP, et al. Among authors: knauss jl. J Med Chem. 2007 Apr 5;50(7):1558-70. doi: 10.1021/jm061041u. Epub 2007 Mar 10. J Med Chem. 2007. PMID: 17348638