Lisa M Shewchuk

Novel, potent P2-P3 pyrrolidine derivatives of ketoamide-based cathepsin K inhibitors.

J. A. Ray, L. Shewchuk, A. Hassell, 2006, Bioorganic & medicinal chemistry letters.

P2-P3 conformationally constrained ketoamide-based inhibitors of cathepsin K.

J. A. Ray, L. Shewchuk, A. Hassell, 2005, Bioorganic & medicinal chemistry letters.

Anilinopyrazole as selective CDK2 inhibitors: design, synthesis, biological evaluation, and X-ray crystallographic analysis.

Yoshiaki Washio, L. Shewchuk, M. Hasegawa, 2003, Bioorganic & medicinal chemistry letters.

Design of potent, selective, and orally bioavailable inhibitors of cysteine protease cathepsin k.

L. Shewchuk, A. Hassell, K. Wells-Knecht, 2004, Journal of medicinal chemistry.

Potent and selective P2-P3 ketoamide inhibitors of cathepsin K with good pharmacokinetic properties via favorable P1', P1, and/or P3 substitutions.

David N Deaton, Aaron B Miller, David G Barrett, 2004, Bioorganic & medicinal chemistry letters.