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Pharmacological combinations include an agonist for adenosine AA receptor and an agonist for phenyladrenaline receptor

机译:药理组合包括腺苷AA受体激动剂和苯肾上腺素受体激动剂

摘要

1. It refers to (a) an equation 1 hypnotic agent for adenosine AA receptor, wherein R1 is h, C1-C6 tar and phenyl, northwest Africa; R2 is h, C1-C6 tar; a is C1-C6 tar; R3 is h, C1-C6, coor4, CN, conr4r4r4, cyclo-c8, phenyl, etc.; r4quies h, C1-C6, cyclohexane, C8; R5 is C1-C6, C1-C6, cycloquilo C1-C6, phenyl; R6 is h, C1-C6, cycloquilo c3-c8, phenyl, etc.; R7 is C1-C6, cycloquilo c3-c8, phenyl, naftio, het; m is 0-2. A formula compound 9 - [(2R, 3R, 4S)5 (R) - 3, 4-dihydroxi-5 - (hydroximetyl) - tetrahydro-2-furan] - 6 - [(2, 2-ifniletil) amine] - N - [2 - (1-piserinil) ethyl] - 9h-purina-2-carboxamida or one of the acceptable salts or prescription solutions; (b) as the terminator of a brominated two kidney adenosine receptor of salmeterol. The combination is an effective method for the treatment of respiratory obstructive diseases.
机译:1.一种用于腺苷AA受体的式1的催眠药,其中R1是h,C1-C6焦油和苯基,西北非洲; R2为h,C1-C6焦油; a为C1-C6焦油; R3是h,C1-C6,coor4,CN,conr4r4r4,环-c8,苯基等; r4是h,C1-C6,环己烷,C8; R5是C1-C6,C1-C6,环基C1-C6,苯基; R 6是h,C 1 -C 6,环基c 3 -c 8,苯基等; R 7是C 1 -C 6,环基c 3 -c 8,苯基,萘基,het; m为0-2。式化合物9-[(2R,3R,4S)5(R)-3,4-二氢氧基-5-(氢肟基)-四氢-2-呋喃]-6-[(2,2-ifniletil)胺]- N- [2-(1-吡嗪酮)乙基] -9h-嘌呤-2-羧酰胺或一种可接受的盐或处方溶液; (b)作为沙美特罗的溴化两个肾腺苷受体的终止剂。该组合是治疗呼吸道阻塞性疾病的有效方法。

著录项

  • 公开/公告号PE20030835A1

    专利类型

  • 公开/公告日2003-10-08

    原文格式PDF

  • 申请/专利权人 PFIZER INC.;

    申请/专利号PE2002001166

  • 发明设计人 YEADON MICHAEL;

    申请日2002-12-03

  • 分类号A61K31/70;

  • 国家 PE

  • 入库时间 2022-08-22 00:01:38

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