首页> 外国专利> Treating symptoms of chronic pain of neuropathic or psychogenic origin, using 1-benzoyl-4-(pyridinylmethyl-aminomethyl)-piperidine derivatives having both symptomatic and curative analgesic action

Treating symptoms of chronic pain of neuropathic or psychogenic origin, using 1-benzoyl-4-(pyridinylmethyl-aminomethyl)-piperidine derivatives having both symptomatic and curative analgesic action

机译:使用具有症状和治疗镇痛作用的1-苯甲酰基-4-(吡啶基甲基-氨基甲基)-哌啶衍生物治疗神经性或精神性起源的慢性疼痛症状

摘要

The use of 1-benzoyl-4-(((pyridin-2-ylmethyl)-amino)-methyl)-piperidine derivatives (I) for treating the symptoms of chronic pain of neuropathic or psychogenic origin is new. The use of pyridine derivatives of formula (I), or their mineral or organic acid addition salts, is claimed in the production of medicaments for treating the symptoms of chronic pain of neuropathic or psychogenic origin. [Image] U : H; or may also be Me if V = W = H; V : H or Cl; or may also be Me if U = W = H; W : H or F; or may also be Me if U = V = H; X : H or F; Y : Cl or Me; Z : H, F, Cl or Me; A : H, F, Cl, 1-5C alkyl, fluoroalkyl (e.g. CH 2F, CHF 2, CF 3, CHFMe or CF 2Me), 3-5C cycloalkyl, optionally substituted 5-membered aromatic heterocyclyl containing 1-4 of N, O and/or S as heteroatom(s) (provided that not more than one O and/or S is present), OR 1, SR 1, NR 2R 3, azetidino, pyrrolidino or alkoxycarbonyl (preferably COOMe or COOEt); R 11-5C alkyl, CH 2F, CF 3 or 3-5C cycloalkyl; R 2, R 3H, 1-5C alkyl, CF 3 or cyclopropyl. ACTIVITY : Analgesic. In tests for activity against central neuropathic pain induced by spinal column lesions in rats (see Pain, 1996, 66, 279-286), (3-chloro-4-fluorophenyl)-(4-fluoro-(((5-methyl-pyridin-2-ylmethyl)-amino)-methyl)-piperidin-1-yl)-methanone (Ia) was administered (as the fumarate) at a constant rate of 0.63 mg per day for 14 days using an implanted analgesic pump. Statistically significant analgesia was observed from day 10 of the treatment (demonstrating symptomatic analgesic action); and the analgesia remained at the same level from day 15 after cessation of the treatment for a further 14 days (demonstrating curative analgesic action). MECHANISM OF ACTION : 5-HT-1A receptor agonist.
机译:1-苯甲酰基-4-(((吡啶-2-基甲基)-氨基)-甲基)-哌啶衍生物(I)在治疗神经性或精神性起源的慢性疼痛症状中的应用是新的。在制备用于治疗神经性或精神性起源的慢性疼痛症状的药物中,要求保护式(I)的吡啶衍生物或其无机或有机酸加成盐的用途。 [图片] U:H;如果V = W = H,也可能是Me; V:H或Cl;如果U = W = H,也可能是Me; W:H或F;如果U = V = H,也可能是Me; X:H或F; Y:Cl或Me; Z:H,F,Cl或Me; A:H,F,Cl,1-5C烷基,氟代烷基(例如CH 2F,CHF 2,CF 3,CHFMe或CF 2Me),3-5C环烷基,可选取代的含有1-4个N的5元芳族杂环基O和/或S作为杂原子(前提是存在不超过一个的O和/或S),或1,SR 1,NR 2R 3,氮杂环丁烷基,吡咯烷基或烷氧羰基(优选COOMe或COOEt); R 11-5C烷基,CH 2F,CF 3或3-5C环烷基; R 2,R 3H,1-5C烷基,CF 3或环丙基。活动:止痛药。在针对大鼠脊柱病变诱发的中枢神经性疼痛的活性测试中(参见Pain,1996,66,279-286),(3-氯-4-氟苯基)-(4-氟-(((5-甲基-使用植入的止痛泵,以每天0.63 mg的恒定速率(以富马酸酯计)施用吡啶2-(2-甲基甲基)-氨基)-甲基)-哌啶-1-基)-甲酮(Ia),持续14天。从治疗的第10天开始观察到具有统计意义的镇痛效果(证明有症状的镇痛作用);并且在停止治疗后的第15天起,镇痛保持在相同的水平,持续了14天(证明了镇痛作用)。作用机理:5-HT-1A受体激动剂。

著录项

  • 公开/公告号NO334997B1

    专利类型

  • 公开/公告日2014-08-18

    原文格式PDF

  • 申请/专利权人 PIERRE FABRE MEDICAMENT;

    申请/专利号NO20050004673

  • 发明设计人 COLPAERT FRANCIS;VACHER BERNARD;

    申请日2005-10-11

  • 分类号A61K31/445;A61P25;

  • 国家 NO

  • 入库时间 2022-08-21 15:56:51

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