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pubmed-article:10612589pubmed:abstractTextThe design and syntheses of non-thiol inhibitors of farnesyl-protein transferase are described. Optimization of cysteine-substituted diarylethers led to highly potent imidazole-containing diarylethers and diarylsulfones. Polar diaryl linkers dramatically improved potency and gave highly cell active compounds.lld:pubmed
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pubmed-article:10612589pubmed:articleTitleImidazole-containing diarylether and diarylsulfone inhibitors of farnesyl-protein transferase.lld:pubmed
pubmed-article:10612589pubmed:affiliationDepartment of Medicinal Chemistry, Merck Research Laboratories, West Point, PA 19486, USA.lld:pubmed
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