Pyridone compounds as inhibitors of bacterial type III...

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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C546S297000

Reexamination Certificate

active

07087622

ABSTRACT:
In accordance with the present invention, compounds that inhibit Type III protein section have been identified, and methods for their use provided. In one aspect of the invention, compounds useful in the inhibition of Type III protein section and/or in the treatment and prevention of bacterial infections, particularly Gram-negative bacterial infections, are provided. In another aspect of the invention, methods are provided for the inhibition of Type III protein secretion and/or the treatment and prevention of bacterial infections, particularly Gram-negative bacterial infections using the compounds of the invention.

REFERENCES:
patent: WO 98/13043 (1998-04-01), None
patent: WO 99/26926 (1999-06-01), None
patent: WO 01/40189 (2001-06-01), None
patent: WO 03/103668 (2003-12-01), None
Dragovich, P.S. et al., “Structure-Based Design, Synthesis and Biological Evaluatin of Irreversible Human Rhinovirus 3C Protease Inhibitors. 6. Structure-Activity Studies of Orally Bioavailable, 2-Pyridone-Cntaining Peptidomimetics”, J. Med. Chem vol. 45, 2002, pp. 1607-1623.
PCT International Search Report, dated Oct. 5, 2005, for PCT Int'l. Appln. No. PCT/US2005/015811.

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