1.
Bioorg Med Chem Lett
; 14(15): 3925-8, 2004 Aug 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15225699
RESUMO
The synthesis of novel aza-1,7-annulated indoles was achieved and these were converted to indolocarbazoles that proved to be potent kinase inhibitors. These compounds were also evaluated in a human colon carcinoma cell line and proved to be good antiproliferative agents.