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Protein Science : a Publication of the Protein Society|September 22, 2001
Crystal structure of Staphylococcus aureus tyrosyl-tRNA synthetase in complex with a class of potent and specific inhibitorsX Qiu, C A Janson, W W Smith, et al.Journal of Medicinal Chemistry|October 10, 1998
Structure-based design of cathepsin K inhibitors containing a benzyloxy-substituted benzoyl peptidomimeticS K Thompson, W W Smith, B Zhao, et al.Bioorganic & Medicinal Chemistry Letters|August 31, 2001
Inhibitors of bacterial enoyl acyl carrier protein reductase (FabI): 2,9-disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as potential antibacterial agentsM A Seefeld, W H Miller, K A Newlander, et al.Bioorganic & Medicinal Chemistry|June 3, 1999
Potent dipeptidylketone inhibitors of the cysteine protease cathepsin KR W Marquis, Y Ru, D S Yamashita, et al.Journal of Medicinal Chemistry|March 23, 2001
Cyclic ketone inhibitors of the cysteine protease cathepsin KR W Marquis, Y Ru, J Zeng, et al.Bioorganic & Medicinal Chemistry Letters|August 22, 2001
1,4-Disubstituted imidazoles are potential antibacterial agents functioning as inhibitors of enoyl acyl carrier protein reductase (FabI)D A Heerding, G Chan, W E DeWolf, et al.Journal of Medicinal Chemistry|February 28, 1997
Structure-based design of substituted diphenyl sulfones and sulfoxides as lipophilic inhibitors of thymidylate synthaseT R Jones, S E Webber, M D Varney, et al.Journal of Medicinal Chemistry|February 16, 1996
Structure-based design of lipophilic quinazoline inhibitors of thymidylate synthaseT R Jones, M D Varney, S E Webber, et al.The Journal of Biological Chemistry|May 24, 2000
Potent and selective nonpeptide inhibitors of caspases 3 and 7 inhibit apoptosis and maintain cell functionalityD Lee, S A Long, J L Adams, et al.Proceedings of the National Academy of Sciences of the United States of America|February 7, 1998
Design of potent and selective human cathepsin K inhibitors that span the active siteS K Thompson, S M Halbert, M J Bossard, et al.Pageof 5