[1,7]naphthyridines as PDE4 inhibitors

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

C514S300000, C546S122000, C544S362000

Reexamination Certificate

active

07468370

ABSTRACT:
Compounds of formula Iin free or salt form, wherein R1, R2and R3have the meanings as indicated in the specification, are useful for treating conditions mediated by of phosphodiesterase type 4 or the down-regulation or inhibition of TNF-α release, particularly obstructive or inflammatory airways diseases. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.

REFERENCES:
patent: 0 005 232 (1979-11-01), None
patent: 98/18796 (1998-05-01), None
A. Nakata et al., Clinical and Experimental Immunology, 2002, vol. 128, pp. 460-466.
Hersperger et al., “PD-Catalysed Cross-Coupling Reactions for the Synthesis of 6,8-Disubstituted 1.7-Naphtyridines: A Novel Class of Potent and Selective Phosphodiesterase Type 4D Inhibitors”, J. Med. Chem., vol. 43, pp. 675-682 (2000).

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