首页> 外国专利> SPIRONOLACTONE AND ANGIOTENSIN II ANTAGONIST COMBINATION FOR TREATMENT OF CONGESTIVE HEART FAILURE

SPIRONOLACTONE AND ANGIOTENSIN II ANTAGONIST COMBINATION FOR TREATMENT OF CONGESTIVE HEART FAILURE

机译:螺内酯和血管紧张素II拮抗剂联合治疗充血性心力衰竭

摘要

A combination therapy comprising a therapeutically-effective amount of an epoxy-free spirolactone-type aldosterone receptor antagonist and a therapeutically-effective amount of an angiotensin II receptor antagonist is described for treatment of circulatory disorders, including cardiovascular disorders such as hypertension, congestive heart failure, cirrhosis and ascites. Preferred angiotensin II receptor antagonists are those compounds having high potency and bioavailability and which are characterized in having an imidazole or triazole moiety attached to a biphenylmethyl or pyridinyl/phenylmethyl moiety. A preferred epoxy-free spirolactone-type aldosterone receptor antagonist is spironolactone. A preferred combination therapy includes the angiotensin II receptor antagonist 5-[2-[5-[(3,5-dibutyl-1H-1,2,4-triazol-1-yl)methyl]-2-pyridinyl]phenyl-1H-tetrazole and the aldosterone receptor antagonist spironolactone.
机译:描述了包含治疗有效量的无环氧螺内酯型醛固酮受体拮抗剂和治疗有效量的血管紧张素II受体拮抗剂的联合疗法,其用于治疗循环系统疾病,包括心血管疾病,例如高血压,充血性心力衰竭。 ,肝硬化和腹水。优选的血管紧张素II受体拮抗剂是那些具有高效能和生物利用度的化合物,其特征在于具有与联苯甲基或吡啶基/苯甲基部分连接的咪唑或三唑部分。优选的无环氧螺内酯型醛固酮受体拮抗剂是螺内酯。优选的组合疗法包括血管紧张素II受体拮抗剂5- [2- [5-[(3,5-二丁基-1H-1,2,4-三唑-1-基)甲基] -2-吡啶基]苯基-1H -四唑和醛固酮受体拮抗剂螺内酯。

著录项

  • 公开/公告号IL122246A

    专利类型

  • 公开/公告日2004-06-01

    原文格式PDF

  • 申请/专利权人 G.D. SEARLE & CO.;

    申请/专利号IL19960122246

  • 发明设计人

    申请日1996-06-05

  • 分类号A61K45/06;A61K31/585;A61K31/41;A61P9/00;

  • 国家 IL

  • 入库时间 2022-08-21 23:10:44

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