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selective inhibitors of norepinephrine reuptake-serotonin for treating fibromyalgia syndrome, chronic fatigue syndrome and pain

机译:去甲肾上腺素再摄取5-羟色胺的选择性抑制剂治疗纤维肌痛综合征,慢性疲劳综合征和疼痛

摘要

Use of an effective amount of dual reuptake inhibitor of serotonin and norepinephrine NE 5-HT (SNRI NE 5-HT) which is not a tricyclic antidepressant, or a pharmaceutically acceptable salt thereof, as sole Active ingredient in the manufacture of a medicament to treat fibromyalgia syndrome (FMS) and / or the same fisiológicosasociados symptoms in an animal subject; wherein the SNRI NE 5-HT has a inhibition ratio NE: 5-HT in elintervalo 2: 1 to 10: 1, and wherein the SNRI NE 5-HT is an aminocyclopropane compound of the formula I: wherein: R represents hydrogen, halogen, alkyl, alkoxy, hydroxyl, nitro or amino; n represents the value 1 or 2; R1 and R2 are independently selected from the group consisting of hydrogen, alkyl, aryl, substituted aryl, alkaryl, substituted alkaryl and with the adjacent nitrogen atom, a heterocycle, R3 and R4 are independently selected from the group consisting of hydrogen, alkyl, and the adjacent atom denitrógeno, a heterocycle, or a pharmaceutically acceptable salt thereof.
机译:有效量的不是三环抗抑郁药的5-羟色胺和去甲肾上腺素NE> 5-HT(SNRI NE> 5-HT)的双重再吸收抑制剂或其药学上可接受的盐在制造药物中作为唯一的活性成分在动物受试者中治疗纤维肌痛综合征(FMS)和/或相同的fisiológicosasociados症状;其中SNRI NE> 5-HT在elintervalo 2:1至10:1中具有抑制比NE:5-HT,并且其中SNRI NE> 5-HT是式I的氨基环丙烷化合物:其中:R代表氢,卤素,烷基,烷氧基,羟基,硝基或氨基; n表示值1或2; R1和R2独立地选自氢,烷基,芳基,取代的芳基,烷芳基,取代的烷芳基,并且与相邻的氮原子,杂环,R3和R4独立地选自氢,烷基和相邻的原子反硝基,杂环或它们的可药用盐。

著录项

  • 公开/公告号ES2395462T3

    专利类型

  • 公开/公告日2013-02-12

    原文格式PDF

  • 申请/专利权人 CYPRESS BIOSCIENCE INC.;

    申请/专利号ES20020793880T

  • 发明设计人 KRANZLER JAY D.;RAO SRINIVAS G.;

    申请日2002-11-05

  • 分类号A61K45/00;A61K31/00;A61K31/135;A61K31/165;A61P25/00;

  • 国家 ES

  • 入库时间 2022-08-21 16:38:49

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