5'-(4-cyclopropanecarbonylpiperazine-1-carbonyl)-5-ethyl-2-methyl-1H-[3,3']bipyridinyl-6-one | 867011-10-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 5'-(4-cyclopropanecarbonylpiperazine-1-carbonyl)-5-ethyl-2-methyl-1H-[3,3']bipyridinyl-6-one
• 英文别名: 5'-(4-Cyclopropanecarbonyl-piperazine-1-carbonyl)-5-ethyl-2-methyl-1H-[3,3']bipyridinyl-6-one；5-[5-[4-(cyclopropanecarbonyl)piperazine-1-carbonyl]pyridin-3-yl]-3-ethyl-6-methyl-1H-pyridin-2-one
• CAS: 867011-10-7
• 化学式: C₂₂H₂₆N₄O₃
• 分子量: 394.473
• InChiKey: WQPZOCSEMHTRGD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  29
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  82.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  5'-ethyl-2'-methyl-6'-oxo-1',6'-dihydro-[3,3']bipyridinyl-5-carboxylic acid 、 1-环丙甲酰基哌嗪 生成 5'-(4-cyclopropanecarbonylpiperazine-1-carbonyl)-5-ethyl-2-methyl-1H-[3,3']bipyridinyl-6-one
  参考文献：
  名称：

  SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP)

  摘要：

  本发明涉及一系列公式I的2,3,5-取代吡啶酮衍生物，其中R、R1、R2、R3和R4如本文所定义。本发明还涉及制备这些化合物的方法。本发明的化合物是聚(腺苷5'-二磷酸核糖)聚合酶（PARP）抑制剂，因此在医药领域中具有广泛的用途，特别是在治疗和/或预防多种疾病，包括与中枢神经系统和心血管疾病相关的疾病方面。

  公开号：

  US20120202795A1

文献信息

• [EN] QUINOLONE CARBOXYLIC ACID DERIVATIVES FOR TREATMENT OF HYPERPROLIFERATIVE CONDITIONS<br/>[FR] DERIVES D'ACIDE CARBOXYLIQUE DE QUINOLONE POUR LE TRAITEMENT DES TROUBLES HYPERPROLIFERATIFS
  申请人：BAYER PHARMACEUTICALS CORP

  公开号：WO2005097752A1

  公开（公告）日：2005-10-20

  Quinolone carboxylic acid derivatives of formula (I) wherein Ar is an optionally substituted phenyl, pyridyl, or pyrimidinyl group and the substituent groups R1, R4, R10, R11, R19, and R20 are as defined in the specification, pharmaceutical compositions containing them, and methods of using them in treatment of hyperproliferative diseases such as cancer are disclosed and claimed.

  公开和声明了式(I)的喹诺酮羧酸衍生物，其中Ar是可选择地取代的苯基、吡啶基或嘧啶基，取代基R1、R4、R10、R11、R19和R20如规范中定义，包含它们的药物组合物，以及在治疗癌症等高增殖性疾病中使用它们的方法。
• [EN] SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP)<br/>[FR] PYRIDONES SUBSTITUES INHIBITEURS DE LA POLY(ADP-RIBOSE) POLYMERASE (PARP)
  申请人：AVENTIS PHARMA INC

  公开号：WO2005097750A1

  公开（公告）日：2005-10-20

  The present invention discloses and claims a series of 2,3,5-substituted pyridone derivatives as defined herein. This invention also relates to methods of making these compounds. The compounds of this invention are inhibitors of poly(adenosine 5'-diphosphate ribose) polymerase (PARP) and are therefore useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases, including diseases associated with the central nervous system and cardiovascular disorders.

  本发明公开并声明了一系列如下定义的2,3,5-取代吡啶酮衍生物。本发明还涉及制备这些化合物的方法。本发明的化合物是多聚腺苷酸二磷酸核糖酶（PARP）的抑制剂，因此在制药剂中特别用于治疗和/或预防各种疾病，包括与中枢神经系统和心血管疾病相关的疾病。
• Substituted pyridones as inhibitors of poly(ADP-ribose) polymerase (PARP)
  申请人：Aventis Pharmaceuticals Inc.

  公开号：US08173682B2

  公开（公告）日：2012-05-08

  The present invention relates to a series of 2,3,5-substituted pyridone derivatives of formula I: wherein R, R1, R2, R3 and R4 are as defined herein. This invention also relates to methods of making these compounds. The compounds of this invention are inhibitors of poly(adenosine 5′-diphosphate ribose) polymerase (PARP) and are therefore useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases, including diseases associated with the central nervous system and cardiovascular disorders.

  本发明涉及一系列式I的2,3,5-取代吡啶酮衍生物，其中R、R1、R2、R3和R4如本文所定义。本发明还涉及制备这些化合物的方法。本发明的化合物是聚腺苷酸二磷酸核糖聚合酶（PARP）的抑制剂，因此在医药领域中具有广泛的应用，特别是在治疗和/或预防多种疾病，包括与中枢神经系统和心血管疾病相关的疾病方面。
• QUINOLONE CARBOXYLIC ACID DERIVATIVES FOR TREATMENT OF HYPERPROLIFERATIVE CONDITIONS
  申请人：Bayer Pharmaceuticals Corporation

  公开号：EP1732897A1

  公开（公告）日：2006-12-20
• US8173682B2
  申请人：——

  公开号：US8173682B2

  公开（公告）日：2012-05-08