US2007254924A1PendingUtilityA1
Salts of benzimidazole compound and use thereof
Est. expiryAug 4, 2020(expired)· nominal 20-yr term from priority
A61P 35/00A61P 31/04A61P 25/20C07D 401/12A61P 1/04A61K 31/4439
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Claims
Abstract
A sodium salt, magnesium salt, lithium salt, potassium salt, calcium salt or barium salt of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole, and a pharmaceutical composition comprising the salt. The novel salt is useful as an excellent antiulcer agent.
Claims
exact text as granted — not AI-modified1 - 13 . (canceled)
14 . A method for preventing or treating gastritis, reflux esophagitis, NUD (Non-Ulcer Dyspepsia), gastric cancer, gastricMALT lymphoma, upper gastrointestinal hemorrhage or hyperacidity, which comprises administering an effective amount of at least one selected from the group consisting of a crystalline sodium salt, a crystalline lithium salt, a crystalline potassium salt, a crystalline magnesium salt, a crystalline calcium salt and a crystalline barium salt of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole to a human in need thereof.
15 . A method for eradicating Helicobacter pylori , which comprises administering an effective amount of at least one selected from the group consisting of a crystalline sodium salt, a crystalline lithium salt, a crystalline potassium salt, a crystalline magnesium salt, a crystalline calcium salt or a crystalline barium salt of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole to a human in need thereof.
16 . The method according to claim 14 , wherein said salt is a solvate with water or an alcohol, or a non-solvate.
17 . The method according to claim 14 , wherein said salt is a crystalline sodium salt of (R)-2-[[[3-methyl4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole.
18 . The method according to claim 17 , wherein the crystalline sodium salt has an X-ray diffraction spectrum with the following diffraction peaks:
(i) 15.02, 7.53, 7.05, 5.53, 4.17, 3.96, 3.42, 3.33 Å, (ii) 16.00, 12,65, 7.98, 7.51, 6.35, 5.09, 4.99, 4.92, 4.82, 4.21 Å, or (iii) 8.89, 8.47, 5.64, 5.24, 4.84, 4.23, 4.20, 4.09, 3.60, 3.36 Å.
19 . The method according to claim 14 , wherein said salt is a crystalline potassium salt of (R)-2-[[[3-methyl4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole.
20 . The method according to claim 19 , wherein the potassium has an X-ray diffraction spectrum with the following diffraction peaks:
(i) 16.35, 8.17, 6.81, 5.78, 4.93, 4.50, 4.25, 4.08, 3.65, 3.36, 3.02 Å.
21 . The method according to claim 15 , wherein said salt is a solvate with water or an alcohol, or a non-solvate.
22 . The method according to claim 15 , wherein said salt is a crystalline sodium salt of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole.
23 . The method according to claim 15 , wherein said salt is a crystalline potassium salt of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole.Join the waitlist — get patent alerts
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