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Synthesis and pharmacological profile of 1-aryl-3-substituted pyrrolo[3,2-c]quinolines.
Authors:E K Yum  S K Kang  S S Kim  J K Choi  H G Cheon
Institution:Korea Research Institute of Chemical Technology, Yusung, Taejon.
Abstract:A series of 1-aryl-3-substituted pyrrolo3,2-c]quinolines were synthesized and evaluated for their anti-ulcer activity. While 3-substituents of pyrrolo3,2-c]quinolines mostly affected the in vitro H+/K+ ATPase activity, 1-aryl substituents of pyrrolo3,2-c]quinolines affected the in vivo gastric acid secretion. In addition, the compounds with good in vivo activity protected from ethanol-induced ulcer.
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