1.
Bioorg Med Chem Lett
; 15(10): 2679-84, 2005 May 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15863341
RESUMO
We describe the synthesis and structure/activity relationship of RGD mimetics that are potent inhibitors of the integrin alpha(v)beta3. Indol-1-yl propionic acids containing a variety of basic moieties at the 5-position, as well as substitutions alpha and beta to the carboxy terminus were synthesized and evaluated. Novel compounds with improved potency have been identified.