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Bioorganic & Medicinal Chemistry Letters|September 29, 2009
Pyrazole-based arylalkyne cathepsin S inhibitors. Part II: optimization of cellular potencyMichael K Ameriks, Hui Cai, James P Edwards, et al.Bioorganic & Medicinal Chemistry Letters|September 3, 2004
The identification and optimization of 2,4-diketobutyric acids as flap endonuclease 1 inhibitorsL Nathan Tumey, Bayard Huck, Elizabeth Gleason, et al.Bioorganic & Medicinal Chemistry Letters|December 18, 2004
The identification and optimization of a N-hydroxy urea series of flap endonuclease 1 inhibitorsL Nathan Tumey, David Bom, Bayard Huck, et al.Bioorganic & Medicinal Chemistry Letters|May 12, 2010
3-Indolyl sultams as selective CRTh2 antagonistsL Nathan Tumey, Michael J Robarge, Elizabeth Gleason, et al.SLAS Discovery : Advancing Life Sciences R & D|May 1, 2026
Repurposing drug screen for the identification of helicase inhibitors from viruses of pandemic concernNicole L Inniss, Margarita Rzhetskaya, Ryan P Kich, et al.Bioorganic & Medicinal Chemistry Letters|March 5, 2005
Isosteric ramatroban analogs: selective and potent CRTH-2 antagonistsMichael J Robarge, David C Bom, L Nathan Tumey, et al.Pageof 1