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Bioorganic & Medicinal Chemistry Letters|March 21, 2006
1,3,5-Trisubstituted aryls as highly selective PPARdelta agonistsRobert Epple, Mihai Azimioara, Ross Russo, et al.Bioorganic & Medicinal Chemistry Letters|January 2, 2007
Bicyclic carbamates as inhibitors of papain-like cathepsin proteasesRobert Epple, Hugo D Urbina, Ross Russo, et al.Bioorganic & Medicinal Chemistry Letters|June 6, 2006
3,4,5-Trisubstituted isoxazoles as novel PPARdelta agonists: Part 1Robert Epple, Ross Russo, Mihai Azimioara, et al.Bioorganic & Medicinal Chemistry Letters|September 27, 2005
Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1Hong Liu, David C Tully, Robert Epple, et al.Bioorganic & Medicinal Chemistry Letters|March 27, 2007
Synthesis and SAR of succinamide peptidomimetic inhibitors of cathepsin SArnab K Chatterjee, Hong Liu, David C Tully, et al.Bioorganic & Medicinal Chemistry Letters|August 26, 2006
3,4,5-Trisubstituted isoxazoles as novel PPARdelta agonists. Part 2Robert Epple, Mihai Azimioara, Ross Russo, et al.Journal of Medicinal Chemistry|November 26, 2009
Novel bisaryl substituted thiazoles and oxazoles as highly potent and selective peroxisome proliferator-activated receptor delta agonistsRobert Epple, Christopher Cow, Yongping Xie, et al.Pageof 1