Alpha v integrin receptor antagonists

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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Details

C514S256000, C514S274000, C514S300000, C514S352000, C540S580000, C544S316000, C544S335000, C546S122000, C546S311000, C546S312000

Reexamination Certificate

active

07056909

ABSTRACT:
The present invention relates to novel chain-fluorinated alkanoic acid derivatives thereof, their synthesis, and their use as αv integrin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors αvβ3 and/or αvβ5 and are useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation, inflammatory arthritis, viral disease, cancer, and metastatic tumor growth.

REFERENCES:
patent: 6048861 (2000-04-01), Askew et al.
Miller et al., Discovery of Orally Active Nonpeptide Vitronectin Receptor Antagonists Based on a 2-Benzazepine Gly-Asp Mimetic, Journal of Medicinal Chemistry, vol. 43, No. 1, pp. 22-26, Jan. 13, 2000.

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