1-(2-bromophenyl)-3-(2,3-di-(furan-2-yl)quinoxalin-6-yl)urea | 1369352-04-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 1-(2-bromophenyl)-3-(2,3-di-(furan-2-yl)quinoxalin-6-yl)urea
• 英文别名: 1-[2,3-Bis(furan-2-yl)quinoxalin-6-yl]-3-(2-bromophenyl)urea；1-[2,3-bis(furan-2-yl)quinoxalin-6-yl]-3-(2-bromophenyl)urea
• CAS: 1369352-04-4
• 化学式: C₂₃H₁₅BrN₄O₃
• 分子量: 475.301
• InChiKey: YSKROLDVMROANF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  31
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  93.2
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  糠偶酰 在 palladium on activated charcoal 、 氢气 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 生成 1-(2-bromophenyl)-3-(2,3-di-(furan-2-yl)quinoxalin-6-yl)urea
  参考文献：
  名称：

  Perturbing pro-survival proteins using quinoxaline derivatives: A structure–activity relationship study

  摘要：

  In HeLa cells the combinatorial knockdown of Bcl-xL and Mcl-1 is sufficient to induce spontaneous apoptosis. Quinoxaline derivatives were screened for the induction of Mcl-1 dependent apoptosis using a cell line without functional Bcl-xL. Quinoxaline urea analog 1h was able to specifically induce apoptosis in an Mcl-1 dependent manner. We demonstrate that even small changes to 1h results in dramatic loss of activity. In addition, 1h and ABT-737 synergistically inhibit cell growth and induce apoptosis. Our results also suggest that 1h could have therapeutic potential against ABT-737 refractory cancer. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.02.022

文献信息

• QUINOXALINE COMPOUNDS AND USES THEREOF
  申请人：Natarajan Amarnath

  公开号：US20130289041A1

  公开（公告）日：2013-10-31

  Disclosed herein are compounds of formula (I) and methods of inhibiting IKKβ and the NF-κB signaling and mTOR pathways.

  本文披露了式(I)化合物以及抑制IKKβ、NF-κB信号通路和mTOR途径的方法。
• US8993758B2
  申请人：——

  公开号：US8993758B2

  公开（公告）日：2015-03-31
• US9353094B2
  申请人：——

  公开号：US9353094B2

  公开（公告）日：2016-05-31
• [EN] QUINOXALINE COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS DE QUINOXALINE ET LEURS UTILISATIONS
  申请人：UNIV NEBRASKA

  公开号：WO2012071414A2

  公开（公告）日：2012-05-31

  Disclosed herein are compounds of formula (I) and methods of inhibiting ΙΚΚβ and the NF-κB signaling and mTOR pathways.
• Perturbing pro-survival proteins using quinoxaline derivatives: A structure–activity relationship study
  作者：Rajkumar Rajule、Vashti C. Bryant、Hernando Lopez、Xu Luo、Amarnath Natarajan

  DOI：10.1016/j.bmc.2012.02.022

  日期：2012.4

  In HeLa cells the combinatorial knockdown of Bcl-xL and Mcl-1 is sufficient to induce spontaneous apoptosis. Quinoxaline derivatives were screened for the induction of Mcl-1 dependent apoptosis using a cell line without functional Bcl-xL. Quinoxaline urea analog 1h was able to specifically induce apoptosis in an Mcl-1 dependent manner. We demonstrate that even small changes to 1h results in dramatic loss of activity. In addition, 1h and ABT-737 synergistically inhibit cell growth and induce apoptosis. Our results also suggest that 1h could have therapeutic potential against ABT-737 refractory cancer. (C) 2012 Elsevier Ltd. All rights reserved.