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• W2080495265 abstract "Protein farnesyltransferase (FTase) has recently appeared as a new target of parasitic diseases, a field poor in drugs in development. With the aim of creating new bisubstrate inhibitors of FTase, new farnesyl pyrophosphate analogues have been studied. Farnesyl analogues with a malonic acid function exhibited the best inhibitory activity on FTase. This group was introduced into our imidazole-containing model leading to new compounds with submicromolar activities. Kinetic experiments have been realized to determine their binding mode to the enzyme." @default.
• W2080495265 created "2016-06-24" @default.
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• W2080495265 date "2010-01-01" @default.
• W2080495265 modified "2023-10-17" @default.
• W2080495265 title "Towards the synthesis of bisubstrate inhibitors of protein farnesyltransferase: Synthesis and biological evaluation of new farnesylpyrophosphate analogues" @default.
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• W2080495265 doi "https://doi.org/10.1016/j.bmc.2009.12.017" @default.
• W2080495265 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20036564" @default.
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