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HETEROCYCLIC COMPOUND HAVING INHIBITORY ACTIVITY ON 11- -HYDROXYSTEROID DEHYDROGENASE TYPE I

机译:具有抑制I型11-羟基甾体脱氢酶活性的杂环化合物

摘要

Disclosed is a compound useful as a type I 11²hydroxysteroid dehydrogenase inhibitor. A compound represented by the formula: a pharmaceutically acceptable salt or solvate thereof, wherein R 1 is optionally substituted alkyl or the like, one of R 2 and R 4 is a group of formula: -Y-R 5 , wherein Y is -O- or the like, R 5 is substituted alkyl (the substituent is optionally substituted cycloalkyl or the like), optionally substituted branched alkyl or the like, the other of R 2 and R 4 is hydrogen or optionally substituted alkyl, R 3 is a group of formula: -C(=O)-Z-R 6 , wherein Z is -NR 7 - or -NR 7 -W-, R 6 is optionally substituted cycloalkyl or the like, R 7 is hydrogen or optionally substituted alkyl, W is optionally substituted alkylene, X is =N- or the like, with the proviso that compounds wherein R 2 is 2-(morphorino)ethoxy, R 3 is N-(1-adamantyl)carbamoyl and R 1 is benzyl are excluded.
机译:公开了可用作I型11 2羟基类固醇脱氢酶抑制剂的化合物。由下式表示的化合物:其药学上可接受的盐或溶剂化物,其中R 1为任选取代的烷基等,R 2和R 4中的一个是下式的基团:-Y-R 5,其中Y为-O-等,R 5为取代的烷基(取代基为任选取代的环烷基等),任选取代的支链烷基等,R 2和R 4中的另一个是氢或任选取代的烷基,R 3为下式的基团:-C(= O)-Z-R 6,其中Z是-NR 7-或-NR 7 -W-,R 6为任选取代的环烷基等,R 7为氢或任选取代的烷基,W是任选取代的亚烷基,X是= N-等,前提是排除其中R 2是2-(吗啉基)乙氧基,R 3是N-(1-金刚烷基)氨基甲酰基和R 1是苄基的化合物。

著录项

  • 公开/公告号EP1953145A4

    专利类型

  • 公开/公告日2011-08-24

    原文格式PDF

  • 申请/专利权人 SHIONOGI & CO. LTD.;

    申请/专利号EP20060832946

  • 申请日2006-11-20

  • 分类号C07D231/18;A61K31/415;A61K31/4152;A61K31/4155;A61K31/4178;A61K31/4439;A61K31/454;A61K31/4709;A61K31/496;A61K31/662;C07D403/06;C07D403/12;C07D405/12;C07D409/12;

  • 国家 EP

  • 入库时间 2022-08-21 17:58:27

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