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