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Discovery of selective irreversible inhibitors for Bruton's tyrosine kinase.
ChemMedChem. 2007 Jan;2(1):58-61. doi: 10.1002/cmdc.200600221.
ChemMedChem. 2007.
PMID: 17154430
No abstract available.
Optimization of subsite binding to the beta5 subunit of the human 20S proteasome using vinyl sulfones and 2-keto-1,3,4-oxadiazoles: syntheses and cellular properties of potent, selective proteasome inhibitors.
Rydzewski RM, Burrill L, Mendonca R, Palmer JT, Rice M, Tahilramani R, Bass KE, Leung L, Gjerstad E, Janc JW, Pan L.
Rydzewski RM, et al.
J Med Chem. 2006 May 18;49(10):2953-68. doi: 10.1021/jm058289o.
J Med Chem. 2006.
PMID: 16686537
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Design and synthesis of tri-ring P3 benzamide-containing aminonitriles as potent, selective, orally effective inhibitors of cathepsin K.
Palmer JT, Bryant C, Wang DX, Davis DE, Setti EL, Rydzewski RM, Venkatraman S, Tian ZQ, Burrill LC, Mendonca RV, Springman E, McCarter J, Chung T, Cheung H, Janc JW, McGrath M, Somoza JR, Enriquez P, Yu ZW, Strickley RM, Liu L, Venuti MC, Percival MD, Falgueyret JP, Prasit P, Oballa R, Riendeau D, Young RN, Wesolowski G, Rodan SB, Johnson C, Kimmel DB, Rodan G.
Palmer JT, et al. Among authors: burrill lc.
J Med Chem. 2005 Dec 1;48(24):7520-34. doi: 10.1021/jm058198r.
J Med Chem. 2005.
PMID: 16302794
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