首页> 外国专利> compound, pharmaceutical composition. methods of inhibiting the binding of endogenous ligands to the crth-2 receptor in a cell, treating, ameliorating or preventing a disorder responsive to inhibiting the binding of endogenous ligands to the crth-2 receptor in an animal and preparing a compound, and kit

compound, pharmaceutical composition. methods of inhibiting the binding of endogenous ligands to the crth-2 receptor in a cell, treating, ameliorating or preventing a disorder responsive to inhibiting the binding of endogenous ligands to the crth-2 receptor in an animal and preparing a compound, and kit

机译:化合物,药物组合物。抑制细胞中内源性配体与crth-2受体结合的方法,治疗,改善或预防动物中抑制内源性配体与crth-2受体结合的疾病并制备化合物和试剂盒的方法

摘要

"COMPOSITION, PHARMACEUTICAL COMPOSITION, METHOD OF INHIBITING THE CONDUCTION OF ENDOGENAL LIGANDS TO THE CRTH-2 RECEIVER IN A CELL, TO TREAT, IMPROVE OR PREVENT A DISTURBANCE RESPONSIBLE TO THE RECYGEN AND ALLOUND LIGO 2 INJECTION A COMPOUND, AND, KIT ". The invention relates to benzimidazole acetic acid compounds which function as antagonists of the homologous T-helper T-receptor receptor (CRTH2) homologous receptor molecule. The invention also relates to the use of such compounds to inhibit the binding of protaglandin D2-2 and its metabolites or certain thromboxane metabolites to the CRTH2 receptor and to treat disorders in response to such inhibition.
机译:“组成,药物成分,抑制内源性配体对细胞中CRTH-2受体的传导的方法,以治疗,改善或预防与RECYGEN和异体LIGO 2注射化合物有关的干扰,”本发明涉及苯并咪唑乙酸化合物,其作为同源T-辅助T受体受体(CRTH2)同源受体分子的拮抗剂。本发明还涉及此类化合物在抑制前列腺素D2-2及其代谢物或某些血栓烷代谢物与CRTH2受体结合以及治疗响应于这种抑制作用的疾病中的用途。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号