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Last Updated: November 24, 2024

Claims for Patent: 4,738,974

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Summary for Patent: 4,738,974

Title:	Base addition salts of omeprazole
Abstract:	Novel salts of omeprazole with Li.sup.+, Na.sup.+, K.sup.+, Mg.sup.2+, Ca.sup.2+, Ti.sup.4+, N.sup.+ (R.sup.1).sub.4 or ##STR1## as cation; processes for their preparation thereof, pharmaceutical compositions containing such salts and their use in medicine.
Inventor(s):	Brandstrom; Arne E. (Gothenburg, SE)
Assignee:	Aktiebolaget Hassle (SE)
Application Number:	06/854,739
Patent Claims:	1. A compound of the formula ##STR9## wherein n is 1, 2, or 4; and A.sup.n+ is Li.sup.+, Na.sup.+, K.sup.+, Mg.sup.2+, or Ca.sup.2+. 2. A compound according to claim 1 wherein A.sup.n+ is Na.sup.+, K.sup.+, Mg.sup.2+ or Ca.sup.2+. 3. A compound according to claim 1 wherein A.sup.n+ is Na.sup.+. 4. A compound according to claim 1 wherein A.sup.n+ is Mg.sup.2+. 5. A pharmaceutical composition for inhibiting gastric acid secretion comprising a compound according to claim 1 in an amount effective to inhibit gastric acid secretion and a pharmaceutically acceptable carrier. 6. A pharmaceutical composition for inhibiting gastric acid secretion comprising a compound according to claim 2 in an amount effective to inhibit gastric acid secretion and a pharmaceutically acceptable carrier. 7. A pharmaceutical composition for inhibiting gastric acid secretion comprising a compound according to claim 3 in an amount effective to inhibit gastric acid secretion and a pharmaceutically acceptable carrier. 8. A pharmaceutical composition for inhibiting gastric acid secretion comprising a compound according to claim 4 in an amount effective to inhibit gastric acid secretion and a pharmaceutically acceptable carrier. 9. A method for inhibiting gastric acid secretion by administering to mammals an amount of a compound as defined in claim 1 sufficient to inhibit gastric acid secretion. 10. A method for inhibiting gastric acid secretion by administering to mammals an amount of a compound as defined in claim 2 sufficient to inhibit gastric acid secretion. 11. A method for inhibiting gastric acid secretion by administering to mammals an amount of a compound as defined in claim 3 sufficient to inhibit gastric acid secretion. 12. A method for inhibiting gastric acid secretion by administering to mammals an amount of a compound as defined in claim 4 sufficient to inhibit gastric acid secretion. 13. A method for the treatment of gastrointestinal inflammatory diseases in mammals by administering to mammals an amount of a compound as defined in claim 1 sufficient to treat gastrointestinal inflammatory disease. 14. A method for the treatment of gastrointestinal inflammatory diseases in mammals by administering to mammals an amount of a compound as defined in claim 2 sufficient to treat gastrointestinal inflammatory disease. 15. A method for the treatment of gastrointestinal inflammatory diseases in mammals by administering to mammals an amount of a compound as defined in claim 3 sufficient to treat gastrointestinal inflammatory disease. 16. A method for the treatment of gastrointestinal inflammatory diseases in mammals by administering to mammals an amount of a compound as defined in claim 4 sufficient to treat gastrointestinal inflammatory disease. 17. A method for providing gastrointestinal cytoprotective effects in mammals by administering to mammals an amount of a compound as defined in claim 1 sufficient to provide gastrointestinal cytoprotective effects. 18. A method for providing gastrointestinal cytoprotective effects in mammals by administering to mammals an amount of a compound as defined in claim 2 sufficient to provide gastrointestinal cytoprotective effects. 19. A method for providing gastrointestinal cytoprotective effects in mammals by administering to mammals an amount of a compound as defined in claim 3 sufficient to provide gastrointestinal cytoprotective effects. 20. A method for providing gastrointestinal cytoprotective effects in mammals by administering to mammals an amount of a compound as defined in claim 4 sufficient to provide gastrointestinal cytoprotective effects.

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