Potent, non-thiol inhibitors of farnesyltransferase
M J Breslin1, S J deSolms, E A Giuliani
1Department of Medicinal Chemistry, Merck Research Laboratories, West Point, PA 19486, USA.
Bioorganic & Medicinal Chemistry Letters
|January 5, 1999
Abstract:
The structure-activity relationship of a series of non-thiol CaaX analogs, which are inhibitors of farnesyltransferase, is described. These inhibitors contain a substituted phenyl group at the N terminus, which may occupy a novel binding domain on the Ras protein.
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