申请人:Shionogi Seiyaku Kabushiki Kaisha
公开号:US05319099A1
公开(公告)日:1994-06-07
The present invention relates to novel 3-benzylidene-1-carbamoyl-2-pyrroridone analogues having advantage anti-inflammatory activities, which is represented by the formula: ##STR1## wherein R.sup.1 and R.sup.2 each is independently hydrogen, alkyl, alkoxy, or halogen; R.sup.3 is hydrogen or acyl; R.sup.4 is hydrogen, alkyl, hydroxy, alkoxy, cyano, or halogen; R.sup.5 and R.sup.6 each is independently hydrogen, alkyl, aryl, aralkyl, heterocyclic group, substituted or unsubstituted amino, or OR.sup.7 wherein R.sup.7 is hydrogen, alkyl, aryl, acyl, or aralkyl, or taken together with the adjacent nitrogen atom may form heterocyclic group which may contain N, O, and/or S, and X and Y each is independently O, S, substituted or unsubstituted imino, or substituted or unsubstituted methylene. In more detail, the present invention provides an anti-inflammatory agent which is useful for the treatment of chronic inflammation and has little side effect, e.g., stomach disease.
本发明涉及具有优势抗炎活性的新型3-苄基亚甲基-1-氨基甲酰基-2-吡咯酮类似物,其化学式如下:其中R1和R2各自独立地为氢、烷基、烷氧基或卤素;R3为氢或酰基;R4为氢、烷基、羟基、烷氧基、氰基或卤素;R5和R6各自独立地为氢、烷基、芳基、芳基烷基、杂环基团、取代或未取代氨基,或OR7,其中R7为氢、烷基、芳基、酰基或芳基烷基,或与相邻氮原子一起形成可能含有N、O和/或S的杂环基团,X和Y各自独立地为O、S、取代或未取代亚胺基,或取代或未取代亚甲基。更详细地说,本发明提供了一种抗炎药物,可用于治疗慢性炎症并且副作用小,例如胃病。