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- W2022874550 abstract "Certain farnesyl diphosphate (FPP) analogs are potent inhibitors of the potential anticancer drug target protein farnesyltransferase (FTase), but these compounds are not suitable as drug candidates. Thus, phosphoramidate prodrug derivatives of the monophosphate precursors of FPP-based FTase inhibitors have been synthesized. The monophosphates themselves were significantly more potent inhibitors of FTase than the corresponding FPP analogs. The effects of the prodrug 5b (a derivative of 3-allylfarnesyl monophosphate) have been evaluated on prenylation of RhoB and on the cell cycle in a human malignant schwannoma cell line (STS-26T). In combination treatments, 1−3 μM 5b plus 1 μM lovastatin induced a significant inhibition of RhoB prenylation, and a combination of these drugs at 1 μM each also resulted in significant cell cycle arrest in G1. Indeed, combinations as low as 50 nM lovastatin + 1 μM 5c or 250 nM lovastatin + 50 nM 5c were highly cytostatic in STS-26T cell culture." @default.
- W2022874550 created "2016-06-24" @default.
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- W2022874550 date "2007-06-08" @default.
- W2022874550 modified "2023-09-27" @default.
- W2022874550 title "Synthesis, Biochemical, and Cellular Evaluation of Farnesyl Monophosphate Prodrugs as Farnesyltransferase Inhibitors" @default.
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- W2022874550 doi "https://doi.org/10.1021/jm0701829" @default.
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