| 摘要 |
<p>The present invention relates to novel 2-thiazolone derivatives of general formula (I), wherein X stands for -CN, -CONH2, -CO2H or -CO2R group, wherein R is a C1-5 alkyl group; and n is 0, 1 or 2, with the proviso, that when X stands for CO2H, CO2R, n is other than 0. The compounds according to the invention possess advantageous cytoprotective and gastric acid secretion-inhibiting effects and thus, they may be used in the therapy of gastric ulcer.</p> |
