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ID: ALA2401705

Journal: Bioorg Med Chem Lett

Title: Discovery of triazines as potent, selective and orally active PDE4 inhibitors.

Authors: Gewald R, Grunwald C, Egerland U.

Abstract: Expanding on HTS hit 4 afforded a series of [1,3,5]triazine derivatives as novel PDE4 inhibitors. The SAR development and optimization process with the emphasis on ligand efficiency and physicochemical properties led to the discovery of compound 44 as a potent, selective and orally active PDE4 inhibitor.

CiteXplore: 23806553

DOI: 10.1016/j.bmcl.2013.05.099