Peptide inhibitors of farnesyl-protein transferase

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

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530330, A61K 3800

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active

056611285

ABSTRACT:
The present invention is directed to tetrapeptides which inhibit farnesyl-protein transferase (FPTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to a method of treating cancer with tetrapeptide inhibitors of farnesyl protein transferase, as well as pharmaceutical formulations useful for this method of treatment.

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James, G.L. et al., "Benzodiazepine Peptidomimetic BZA-5B Interrupts the MAP Kinase Activation Pathway in H-Ras-transformed Rat-1 Cells, but Not in Untransformed Cells", The Journal of Biological Chemistry, vol. 269, No. 44, pp. 27705-27714 (1994).
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Kohl, N.E. et al., "Protein Farnesyltransferase Inhibitors Block the Growth of Ras-Dependent Tumors in Nude Mice", Proc. Natl. Acad. Sci. USA Med. Sci., vol. 91 pp. 9141-9145 (1994).
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