1.
Bioorg Med Chem Lett
; 17(17): 4929-33, 2007 Sep 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17590332
RESUMO
Highly potent, selective, and bioavailable inhibitors of human, mouse, or rat cathepsin S are described. The key structural features combine a sulfonyl moiety attached to a large group in P2 and a small substituent in P3.