Tricyclic imidazopyridines

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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Details

C546S079000

Reexamination Certificate

active

10485515

ABSTRACT:
The invention provides compounds of the formula (I), in which the substituents and symbols are as defined in the description. The compounds inhibit the secretion of gastric acid.

REFERENCES:
patent: 4468400 (1984-08-01), Gold et al.
patent: WO 95/27714 (1995-10-01), None
patent: WO 98/42707 (1998-10-01), None
patent: WO 98/54188 (1998-12-01), None
patent: WO01/72757 (2001-10-01), None
Kaminski, J.J. et al. “Antiulcer Agents. 5. Inhibition of Gastric H+/K+-ATPase by Substituted Imidazo [1, 2-a] pyridines and Related Analogues and Its Implication in Modeling the High Affinity Potassium Ion Binding Site of the Gastric Proton Pump Enzyme”, J. Med. Chem., vol. 34 pp. 533-541, 1991.
Kaminski, J.J. et al. “Antiulcer Agents. 4. Conformational Considerations and the Antiulcer Activity Substituted Imidazo [1, 2-a] pyridines and Related Analogues”,J.Med.Chem.,vol. 32 pp. 1686-1700, 1989.

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