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Bioorganic & Medicinal Chemistry Letters|April 10, 2007
Metabolic activation of indole-containing prostaglandin D2 receptor 1 antagonists: impacts of glutathione trapping and glucuronide conjugation on covalent bindingJean-François Lévesque, Stephen H Day, Nathalie Chauret, et al.Journal of the American Chemical Society|July 12, 2024
High-Throughput Covalent Modifier Screening with Acoustic Ejection Mass SpectrometryXiujuan Wen, Chang Liu, Kiersten Tovar, et al.Molecular Cell|March 5, 2013
The E3 ligase parkin maintains mitochondrial integrity by increasing linear ubiquitination of NEMOAnne Kathrin Müller-Rischart, Anna Pilsl, Patrick Beaudette, et al.Bioorganic & Medicinal Chemistry Letters|January 12, 2010
The discovery of MK-0674, an orally bioavailable cathepsin K inhibitorElise Isabel, Kevin P Bateman, Nathalie Chauret, et al.Journal of Medicinal Chemistry|February 16, 2007
Discovery of a potent and selective prostaglandin D2 receptor antagonist, [(3R)-4-(4-chloro-benzyl)-7-fluoro-5-(methylsulfonyl)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl]-acetic acid (MK-0524)Claudio F Sturino, Gary O'Neill, Nicolas Lachance, et al.Pageof 6