首页> 外国专利> n- (4-carbamimidoylbenzyl) -2-alkoxy-2-heterocyclylacet amides as inhibitors of the formation of factor-induced xa, ixa, and thrombin coagulation factors

n- (4-carbamimidoylbenzyl) -2-alkoxy-2-heterocyclylacet amides as inhibitors of the formation of factor-induced xa, ixa, and thrombin coagulation factors

机译:n-(4-氨基甲酰基苄基)-2-烷氧基-2-杂环基乙酰胺作为因子诱导的xa,ixa和凝血酶凝血因子形成的抑制剂

摘要

"N- (4-CARBAMIMIDOYLBENZYL) -2-ALCoxy-2-HETEROCICLILACE TAMIDES AS INHIBITORS OF THE FORMATION OF XA, IXA AND THROMBIN-INDUCED FACTOR FACTORS". The present invention relates to novel heterocyclyl-substituted mandelic acid-derived groups of formula (I), wherein from R 1 to R 6 and A are as defined in the description and claims, as well as their physiologically salts thereof. acceptable. These compounds inhibit the formation of Vila factor and tissue factor-induced coagulation factors Xa, IXa and thrombin and can be used as medicines.
机译:“作为XA,IXA和凝血酶诱导的因子形成的抑制剂的N-(4-氨基甲酰基苄基)-2-烷氧基-2-杂环酰胺”。本发明涉及式(I)的新颖的杂环基取代的扁桃酸衍生的基团,其中R 1至R 6和A如说明书和权利要求中所定义,及其生理盐。可以接受的。这些化合物抑制维拉因子和组织因子诱导的凝血因子Xa,IXa和凝血酶的形成,可以用作药物。

著录项

  • 公开/公告号BRPI0417274A

    专利类型

  • 公开/公告日2007-03-27

    原文格式PDF

  • 申请/专利权人 F. HOFFMANN-LA ROCHE AG;

    申请/专利号BR2004PI17274

  • 申请日2004-12-13

  • 分类号C07D401/04;C07D249/08;C07D231/12;C07D209/48;C07D263/32;C07D235/16;C07D213/76;C07D213/74;C07D413/12;C07D401/12;A61P7/02;

  • 国家 BR

  • 入库时间 2022-08-21 20:59:28

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