5-substituted tetralones as inhibitors of ras farnesyl...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C514S397000, C514S399000, C546S275100, C546S178000, C546S146000, C548S315400, C548S264200, C548S341100, C548S315100, C548S236000, C548S312100, C548S314700, C544S405000

Reexamination Certificate

active

06943183

ABSTRACT:
The present invention provides novel 5-substituted tetralones of Formulas I, II, III, and IV and pharmaceutically acceptable salts, esters, amides, and prodrugs thereof, which are useful for treating and preventing uncontrolled or abnormal proliferation of tissues, such as cancer, atherosclerosis, restenosis, and psoriasis. Specifically, the present invention relates to compounds that inhibit the farnesyl transferase enzyme

REFERENCES:
patent: 6265422 (2001-07-01), Bikker et al.
patent: WO 98/34921 (1998-08-01), None
PCT International Search Report PCT/US01/12490, Jan. 16, 2002.

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