Bioorganic and Medicinal Chemistry p. 101 - 113 (1997)
Update date:2022-08-03
Topics:
Njoroge, F. George
Doll, Ronald J.
Vibulbhan, Bancha
Alvarez, Carmen S.
Bishop, W. Robert
Petrin, Joanne
Kirschmeier, Paul
Carruthers, Nicholas I.
Wong, Jesse K.
Albanese, Margaret M.
Piwinski, John J.
Catino, Joseph
Girijavallabhan
Ganguly, Ashit K.
A comprehensive structure-activity relationship (SAR) study of novel tricyclic amides has been undertaken. The discovery of compounds that are potent FPT inhibitors in the nanomolar range has been achieved. These compounds are nonpeptidic and do not contain sulfhydryl groups. They selectively inhibit farnesyl protein transferase (FPT) and not geranylgeranyl protein transferase-1 (GGPT-1). They also inhibit H-Ras processing in Cos monkey kidney cells.
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