C-terminal modifications of histidyl-N-benzylglycinamides to give improved inhibition of Ras farnesyltransferase, cellular activity, and anticancer activity in mice.
Autor: | McNamara DJ; Parke-Davis Pharmaceutical Research, Division of Warner-Lambert Company, Ann Arbor, Michigan 48105, USA. mcnamad@aa.wl.com, Dobrusin E, Leonard DM, Shuler KR, Kaltenbronn JS, Quin J 3rd, Bur S, Thomas CE, Doherty AM, Scholten JD, Zimmerman KK, Gibbs BS, Gowan RC, Latash MP, Leopold WR, Przybranowski SA, Sebolt-Leopold JS |
---|---|
Jazyk: | angličtina |
Zdroj: | Journal of medicinal chemistry [J Med Chem] 1997 Oct 10; Vol. 40 (21), pp. 3319-22. |
DOI: | 10.1021/jm970470c |
Databáze: | MEDLINE |
Externí odkaz: |