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pubmed-article:7712129pubmed:abstractTextReplacement of the central amino methylene linkage of C[psi CH2NH]A[psi CH2NH]AX tetrapeptide inhibitors with carbon tethers led to compounds with potency in the nanomolar range. Some of the more potent olefinic compounds inhibit Ras processing in intact v-ras transformed NIH 3T3 cells with IC50 values in the 0.1 to 1 microM range, and inhibit selectively the anchorage-independent growth of H-ras transformed Rat1 cells at 10 microM.lld:pubmed
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pubmed-article:7712129pubmed:articleTitleSynthesis and biological activity of ras farnesyl protein transferase inhibitors. Tetrapeptide analogs with amino methyl and carbon linkages.lld:pubmed
pubmed-article:7712129pubmed:affiliationDepartment of Medicinal Chemistry, Merck Research Laboratories, West Point, PA 19486.lld:pubmed
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