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SUBSTITUTED IMIDAZOLE NEUROPEPTIDE Y Y5 RECEPTOR ANTAGONISTS

机译:取代的咪唑神经肽Y Y5受体拮抗剂

摘要

COPOUND OF THE FORMULA IOR A PHARMACEUTICALLY ACCETABLE SALT, SOLVATE OR N-OXIDE THREOF, WHREIN X IS =CH- OR =N-Y IS H, HALOGEN, TRIHALOALKYL, ALKYL, ALKENYL, CYCLOALKYL, CYCLOAKUL, SH, -S-ALKYL, OR -CN.R IS ALKYL, -CF3, CYCLOALKYL, HETEROCYCLOALKYL, HETEROCYCLOALKYL-ALKYL, HETEROARYALKYL OR ADANMANTYL OR OPTIONALLY SUBSITUTES PHENYL, PHENOXYALKYL, PHENYLTHIOALKYL, PYRIDYL, THIENYL, THIAZOLYL, PYRAZIYL, 1,2,5,6-TETRAHYDROPYRIDINE OR , WHEREIN R10 AND R11 ARE HYDROGEN, ALKYL OR TOGETHER FORM A CYCLOALKYL, ARE DISCLOSED, AS WELL AS PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING SAOD COMPOUNDS IN THE TREATMENT OF EATING DISORDERS AND DIABETES.
机译:配方的化合物或药学上可接受的盐,溶剂化物或N氧化物的分子量,其中X为= CH-或= NY为H,卤素,三卤代烷基,烷基,烯基,环烷基,环氯基,SH,-S-烷基或- CN.R是烷基,-CF 3,环烷基,杂环烷基,杂环烷基或腺嘌呤或任选的取代基,苯基,苯氧基烷基,苯硫基烷基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基,吡啶基和R11是氢,烷基或其他形式的环烷基,以及用于治疗饮食失调和糖尿病的药物成分和使用盐化合物的方法。

著录项

  • 公开/公告号MY138524A

    专利类型

  • 公开/公告日2009-06-30

    原文格式PDF

  • 申请/专利权人 SCHERING CORPORATION;

    申请/专利号MY2000PI05922

  • 申请日2000-12-15

  • 分类号C07D233/64;A61K31/415;A61K31/4164;A61K31/4178;A61K31/427;A61K31/4439;A61K31/454;A61K31/4725;A61K31/496;A61K31/506;A61K31/5377;A61P3;A61P3/04;A61P3/10;C07D233/54;C07D233/88;C07D401/04;C07D401/06;C07D401/10;C07D401/12;C07D401/14;C07D403/12;C07D405/12;C07D413/10;C07D417/12;

  • 国家 MY

  • 入库时间 2022-08-21 19:25:13

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