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Synthesis of 2-[[(4-fluoroalkoxy-2-pyridyl)methyl]sulfinyl]-1H- benzimidazoles as antiulcer agents.
Kubo, K; Oda, K; Kaneko, T; Satoh, H; Nohara, A.
Affiliation
  • Kubo K; Research and Development Division, Takeda Chemical Industries, Ltd., Osaka, Japan.
Chem Pharm Bull (Tokyo) ; 38(10): 2853-8, 1990 Oct.
Article in En | MEDLINE | ID: mdl-2076571
ABSTRACT
Many 2-[[(4-fluoroalkoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazoles were synthesized and tested for anti-secretory, antiulcer, and cytoprotective activities. Most of these compounds were superior to omeprazole in anti-secretory and antiulcer potencies, and especially in protecting the gastric mucosa from ethanol-induced damage. Among these compounds, 2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl] - 1H-benzimidazole, AG-1749 (lansoprazole) (6f), was selected for further development and clinical evaluation.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Stomach Ulcer / Omeprazole / Anti-Ulcer Agents Type of study: Etiology_studies Limits: Animals Language: En Journal: Chem Pharm Bull (Tokyo) Year: 1990 Document type: Article Affiliation country: Japan
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Collection: 01-internacional Database: MEDLINE Main subject: Stomach Ulcer / Omeprazole / Anti-Ulcer Agents Type of study: Etiology_studies Limits: Animals Language: En Journal: Chem Pharm Bull (Tokyo) Year: 1990 Document type: Article Affiliation country: Japan