cis-2-((2-(2-carboxycyclohexanecarbonyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-1,3-dioxoisoindoline-5-carboxylic acid

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 四氢异喹啉
• 英文名称: cis-2-((2-(2-carboxycyclohexanecarbonyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-1,3-dioxoisoindoline-5-carboxylic acid
• 英文别名: 2-[1-[(3-oxo-1H-isoindol-2-yl)methyl]-3,4-dihydro-1H-isoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid
• 化学式: C₂₆H₂₈N₂O₄
• 分子量: 432.519
• InChiKey: CENUFSLZJTXDBJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  32
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  77.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  邻苯二甲酰甘氨酸 在 盐酸 、 tin 、 溶剂黄146 、 三氯氧磷 作用下， 以 5,5-dimethyl-1,3-cyclohexadiene 、 水 、 乙腈 为溶剂， 反应 50.0h， 生成 cis-2-((2-(2-carboxycyclohexanecarbonyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-1,3-dioxoisoindoline-5-carboxylic acid
  参考文献：
  名称：

  DIRECT INHIBITORS OF KEAP1-NRF2 INTERACTION AS ANTIOXIDANT INFLAMMATION MODULATORS

  摘要：

  通过高通量筛选和引物开发的方法，识别化合物作为Keap1-Nrf2相互作用的直接抑制剂。Keap1-Nrf2相互作用的直接抑制剂比现有的间接抑制剂更具特异性，不受各种不良影响，并且是化学预防和治疗各种涉及氧化应激和/或炎症的疾病或症状的潜在药物候选者，包括但不限于癌症、糖尿病、阿尔茨海默病和帕金森病。还公开了识别新化合物以及使用所识别的新化合物或含有这些化合物的组合物来预防或治疗与Keap1-Nrf2相互作用活性相关的疾病或症状的方法。

  公开号：

  US20180148408A1

文献信息

• [EN] DIRECT INHIBITORS OF KEAP1-NRF2 INTERACTION AS ANTIOXIDANT INFLAMMATION MODULATORS<br/>[FR] INHIBITEURS DIRECTS DE L'INTERACTION KEAP1-NRF2 EN TANT QUE MODULATEURS DE L'INFLAMMATION PAR ANTI-OXYDANT
  申请人：UNIV RUTGERS

  公开号：WO2013067036A1

  公开（公告）日：2013-05-10

  A method of identifying compounds as direct inhibitors of Keap1-Nrf2 interaction through high-throughput screening and lead development. The direct inhibitors of Keap1-Nrf2 interaction are more specific and free of various undesirable effects than existing indirect inhibitors, and are potential drug candidates of chemopreventive and therapeutic agents for treatment of various diseases or conditions involving oxidative stress and/or inflammation, including but not limited to cancers, diabetes, Alzheimer's, and Parkinson's. Novel compounds are identified and methods of preventing or treating diseases or conditions related to Keapl-Nrf2 interaction activity by use of the novel compounds identified or compositions containing such compounds are also disclosed.

  一种通过高通量筛选和引物开发将化合物识别为直接抑制Keap1-Nrf2相互作用的方法。Keap1-Nrf2相互作用的直接抑制剂比现有的间接抑制剂更具特异性，且不受各种不良效应的影响，是潜在的化学预防和治疗剂的候选药物，可用于治疗涉及氧化应激和/或炎症的各种疾病或病症，包括但不限于癌症、糖尿病、阿尔茨海默病和帕金森病。还披露了识别新化合物和利用所识别的新化合物或含有这些化合物的组合物预防或治疗与Keap1-Nrf2相互作用活性相关的疾病或病症的方法。
• Direct inhibitors of Keap1-Nrf2 interaction as antioxidant inflammation modulators
  申请人：Rutgers, The State University of New Jersey

  公开号：US10106502B2

  公开（公告）日：2018-10-23

  A method of identifying compounds as direct inhibitors of Keap1-Nrf2 interaction through high-throughput screening and lead development. The direct inhibitors of Keap1-Nrf2 interaction are more specific and free of various undesirable effects than existing indirect inhibitors, and are potential drug candidates of chemopreventive and therapeutic agents for treatment of various diseases or conditions involving oxidative stress and/or inflammation, including but not limited to cancers, diabetes, Alzheimer's, and Parkinson's. Novel compounds are identified and methods of preventing or treating diseases or conditions related to Keap1-Nrf2 interaction activity by use of the novel compounds identified or compositions containing such compounds are also disclosed.

  一种通过高通量筛选和先导化合物开发来确定作为 Keap1-Nrf2 相互作用直接抑制剂的化合物的方法。与现有的间接抑制剂相比，Keap1-Nrf2 相互作用的直接抑制剂更具特异性且无各种不良反应，是潜在的化学预防和治疗候选药物，可用于治疗涉及氧化应激和/或炎症的各种疾病或病症，包括但不限于癌症、糖尿病、阿尔茨海默氏症和帕金森氏症。本文鉴定了新型化合物，还公开了通过使用鉴定的新型化合物或含有此类化合物的组合物预防或治疗与Keap1-Nrf2相互作用活性有关的疾病或病症的方法。
• US20140256767A1
  申请人：——

  公开号：US20140256767A1

  公开（公告）日：2014-09-11
• DIRECT INHIBITORS OF KEAP1-NRF2 INTERACTION AS ANTIOXIDANT INFLAMMATION MODULATORS
  申请人：Rutgers, The State University of New Jersey

  公开号：US20180148408A1

  公开（公告）日：2018-05-31

  A method of identifying compounds as direct inhibitors of Keap1-Nrf2 interaction through high-throughput screening and lead development. The direct inhibitors of Keap1-Nrf2 interaction are more specific and free of various undesirable effects than existing indirect inhibitors, and are potential drug candidates of chemopreventive and therapeutic agents for treatment of various diseases or conditions involving oxidative stress and/or inflammation, including but not limited to cancers, diabetes, Alzheimer's, and Parkinson's. Novel compounds are identified and methods of preventing or treating diseases or conditions related to Keap1-Nrf2 interaction activity by use of the novel compounds identified or compositions containing such compounds are also disclosed.

  通过高通量筛选和引物开发的方法，识别化合物作为Keap1-Nrf2相互作用的直接抑制剂。Keap1-Nrf2相互作用的直接抑制剂比现有的间接抑制剂更具特异性，不受各种不良影响，并且是化学预防和治疗各种涉及氧化应激和/或炎症的疾病或症状的潜在药物候选者，包括但不限于癌症、糖尿病、阿尔茨海默病和帕金森病。还公开了识别新化合物以及使用所识别的新化合物或含有这些化合物的组合物来预防或治疗与Keap1-Nrf2相互作用活性相关的疾病或症状的方法。