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Biochimica Et Biophysica Acta|November 14, 2002
Novel caged fluorescein diphosphates as photoactivatable substrates for protein tyrosine phosphatasesQingping Wang, John Scheigetz, Bruno Roy, et al.Bioorganic & Medicinal Chemistry|February 26, 2004
Solid phase synthesis of selective caspase-3 peptide inhibitorsErich L Grimm, Bruno Roy, Renee Aspiotis, et al.Bioorganic & Medicinal Chemistry Letters|January 25, 2005
Structure-activity relationship studies on ortho-substituted cinnamic acids, a new class of selective EP(3) antagonistsMichel Belley, Michel Gallant, Bruno Roy, et al.Bioorganic & Medicinal Chemistry Letters|March 15, 2006
Identification of an indole series of prostaglandin D2 receptor antagonistsClaudio F Sturino, Nicolas Lachance, Michael Boyd, et al.Bioorganic & Medicinal Chemistry Letters|January 15, 2011
Difluoroethylamines as an amide isostere in inhibitors of cathepsin KElise Isabel, Christophe Mellon, Michael J Boyd, et al.Bioorganic & Medicinal Chemistry Letters|September 20, 2005
Discovery of a substituted 8-arylquinoline series of PDE4 inhibitors: structure-activity relationship, optimization, and identification of a highly potent, well tolerated, PDE4 inhibitorDwight Macdonald, Anthony Mastracchio, Hélène Perrier, 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 1