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IMIDAZO1,5A PYRIDINE DERIVATIVES AND METHODS FOR TREATING ALDOSTERONE MEDIATED DISEASES

机译:咪达唑[1,5A]吡啶衍生物和醛固酮介导的疾病的治疗方法

摘要

Compounds of the formula (I) provide pharmacological agents which are inhibitors of the P450 enzyme, aldosterone synthase, and thus may be employed for the treatment of aldosterone mediated conditions. Accordingly, the compounds of formula (I) may be employed for prevention, delay of progression, or treatment of hypokalemia, hypertension, congestive heart failure, renal failure, in particular, chronic renal failure, restenosis, atherosclerosis, syndrome X, obesity, nephropathy, post-myocardial infarction, coronary heart diseases, increased formation of collagen, fibrosis and remodeling following hypertension and endothelial dysfunction. Preferred are the compounds of formula (I) which are selective inhibitors of aldosterone synthase devoid of undesirable side effects due to general inhibition of cytochrome P450 enzymes.
机译:式(I)的化合物提供了作为P450酶,醛固酮合酶的抑制剂的药理剂,因此可以用于治疗醛固酮介导的病症。因此,式(I)化合物可用于预防,延缓病情发展或治疗低血钾,高血压,充血性心力衰竭,肾衰竭,特别是慢性肾衰竭,再狭窄,动脉粥样硬化,X综合征,肥胖症,肾病,心肌梗塞后,冠心病,高血压和内皮功能障碍后胶原蛋白形成增加,纤维化和重塑。优选的是式(I)化合物,其为醛固酮合酶的选择性抑制剂,由于细胞色素P450酶的一般抑制而没有不良副作用。

著录项

  • 公开/公告号EP1565463B1

    专利类型

  • 公开/公告日2008-06-11

    原文格式PDF

  • 申请/专利权人 NOVARTIS AG;NOVARTIS PHARMA GMBH;

    申请/专利号EP20030767563

  • 发明设计人 FIROOZNIA FARIBORZ;

    申请日2003-11-17

  • 分类号C07D471/04;A61P9;

  • 国家 EP

  • 入库时间 2022-08-21 19:58:48

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