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AMIDES AS NPY5 RECEPTOR ANTAGONISTS

机译:酰胺作为N​​PY5受体拮抗剂

摘要

alpha -alkoxy and alpha -thioalkoxyamide compounds of formula (I) and methods of administering the compositions to mammals to treat disorders such as obesity that are mediated by NPY and especially those mediated by NPY via the Y5 receptor, or pharmaceutically acceptable salts thereof wherein R1-R5 are each individually selected from the group of substituents including hydrogen, halogen, hydroxyl, thiol, lower alkyl, substituted lower alkyl, alkenyl, alkynyl, alkylalkenyl, alkyl alkynyl, alkoxy, alkylthio, acyl, aryloxy, amino, amido, carboxyl, aryl, substituted aryl, heterocycle, heteroaryl, substituted heterocycle, heteroalkyl, cycloalkyl, substituted cycloalkyl, alkylcycloalkyl, alkylcycloheteroalkyl, phenyl, substituted phenyl, benzothiophene, furan, fluoride, nitro, cyano, naphthyl, substituted naphthyl, fluorene, substituted fluorene and dibenzofuran, and wherein X is oxygen or sulfur.
机译:式(I)的α-烷氧基和α-硫代烷氧基酰胺化合物以及将所述组合物给予哺乳动物以治疗诸如由NPY介导的肥胖症,尤其是经由NPY经由Y5受体介导的肥胖症的疾病,或其药学上可接受的盐,其中R1 -R 5各自独立地选自取代基,包括氢,卤素,羟基,硫醇,低级烷基,取代的低级烷基,烯基,炔基,烷基烯基,烷基炔基,烷氧基,烷硫基,酰基,芳氧基,氨基,酰胺基,羧基,芳基,取代的芳基,杂环,杂芳基,取代的杂环,杂烷基,环烷基,取代的环烷基,烷基环烷基,烷基环杂烷基,苯基,取代的苯基,苯并噻吩,呋喃,氟,硝基,氰基,萘基,取代的萘基,芴,取代的芴和二苯并呋喃并且其中X是氧或硫。

著录项

  • 公开/公告号EP0927166A1

    专利类型

  • 公开/公告日1999-07-07

    原文格式PDF

  • 申请/专利权人 BAYER CORPORATION;

    申请/专利号EP19980904909

  • 申请日1998-02-05

  • 分类号C07D233/42;C07D239/38;C07D257/04;C07D235/28;C07D473/18;A61K31/415;C07D239/78;C07D277/16;C07D487/04;C07D213/89;C07D263/58;C07D277/72;C07D213/70;C07D285/125;C07D249/12;C07D271/07;C07D307/64;

  • 国家 EP

  • 入库时间 2022-08-22 02:18:30

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