Journal of Medicinal Chemistry · 2003 · 60 citations · 7 references
MedicineOncologyPharmacologyCancer PharmacologyEnzymologyMolecular OncologyEnzyme InhibitionEnzyme KineticsRas Family OncogenesSynthetic LethalityInhibitor ScreeningRas Structure-function Relationships
A series of novel diaryl ether lactams have been identified as very potent dual inhibitors of protein farnesyltransferase (FTase) and protein geranylgeranyltransferase I (GGTase-I), enzymes involved in the prenylation of Ras. The structure of the complex formed between one of these compounds and FTase has been determined by X-ray crystallography. These compounds are the first reported to inhibit the prenylation of the important oncogene Ki-Ras4B in vivo. Unfortunately, doses sufficient to achieve this endpoint were rapidly lethal.
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Sequence dependence of protein isoprenylation
Sheri L. Moores, Michael D. Schaber, S.D. Mosser et al. · Journal of Biological Chemistry · 1991 · 582 citations · Full text