bis(4-fluorophenyl)-2-fluorophenylacetamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: bis(4-fluorophenyl)-2-fluorophenylacetamide
• 英文别名: 2-(2-fluorophenyl)-2,2-bis(4-fluorophenyl)acetamide
• 化学式: C₂₀H₁₄F₃NO
• 分子量: 341.332
• InChiKey: VDPKWHHLYDETTO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  43.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  bis(4-fluorophenyl)-2-fluorophenylacetonitrile 在 硫酸 、 溶剂黄146 作用下， 反应 3.0h， 以4.98 g的产率得到bis(4-fluorophenyl)-2-fluorophenylacetamide
  参考文献：
  名称：

  Novel Inhibitors of the Gardos Channel for the Treatment of Sickle Cell Disease

  摘要：

  Sickle cell disease (SCD) is a hereditary condition characterized by deformation of red blood cells (RBCs). This phenomenon is due to the presence of abnormal hemoglobin that polymerizes upon deoxygenation. This effect is exacerbated when dehydrated RBCs experience a loss of both water and potassium salts. One critical pathway for the regulation of potassium efflux from RBCs is the Gardos channel, a calcium-activated potassium channel. This paper describes the synthesis and biological evaluation of a series of potent inhibitors of the Gardos channel. The goal was to identify compounds that were potent and selective inhibitors of the channel but had improved pharmacokinetic properties compared to 1, Clotrimazole. Several triarylamides such as 10 and 21 were potent inhibitors of the Gardos channel (IC50 of < 10 nM) and active in a mouse model of SCD. Compound 21 (ICA-17043) was advanced into phase 3 clinical trials for SCD.

  DOI：

  10.1021/jm070663s
• 作为试剂：
  描述：

  硫酸 、 溶剂黄146 、 bis(4-fluorophenyl)-2-fluorophenylacetonitrile 、 ammonium hydroxide 在 ice 、 二氯甲烷 、 水 、 Brine 、 Sodium sulfate-III 、 正己烷 、 dichloromethane hexane 、 bis(4-fluorophenyl)-2-fluorophenylacetamide 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以gave the desired product bis(4-fluorophenyl)-2-fluorophenylacetamide 5 as a white crystalline solid (4.98 g, 0.0145 mol, 94%)的产率得到bis(4-fluorophenyl)-2-fluorophenylacetamide
  参考文献：
  名称：

  TREATMENT METHODS USING TRIARYL METHANE COMPOUNDS

  摘要：

  本发明提供了治疗或预防哮喘或炎症性疾病的方法。在一种实施方案中，本发明提供了用于治疗哮喘或炎症性疾病的化合物和配方。

  公开号：

  US20100056637A1

文献信息

• Treatment methods using triaryl methane compounds
  申请人：Castle A. Neil

  公开号：US20070185209A1

  公开（公告）日：2007-08-09

  The use of novel inhibitors of potassium flux is disclosed for the treatment of inflammatory processes, such as multiple sclerosis, insulin-dependent (type I) diabetes mellitus, rheumatoid arthritis, peripheral neuritis and pulmonary hypertension. The compounds are also of use in treating and preventing stroke. These inhibitors have a high specificity for the IK1 channel and greater stability relative to non-fluorine substituted homologues.

  本发明揭示了使用新型钾通量抑制剂治疗炎症过程，例如多发性硬化症、胰岛素依赖性（I型）糖尿病、类风湿性关节炎、周围神经炎和肺动脉高压。这些化合物还可用于治疗和预防中风。这些抑制剂对IK1通道具有高度特异性，相对于非氟取代同源物具有更高的稳定性。
• Carbonylamino derivatives useful for the treatment of inflammatory bowel disease
  申请人：NeuroSearch A/S

  公开号：EP2322164A2

  公开（公告）日：2011-05-18

  The present invention relates to the use of a particular group of carbonylamino derivatives for the treatment or alleviation of a disease or condition relating to certain inflammatory disorders.

  本发明涉及使用一组特定的羰基氨基衍生物来治疗或缓解与某些炎症有关的疾病或病症。
• WO2007/75849
  申请人：——

  公开号：——

  公开（公告）日：——
• EP1158971A4
  申请人：——

  公开号：EP1158971A4

  公开（公告）日：2003-04-16
• GARDOS CHANNEL ANTAGONISTS
  申请人：Icagen, Inc.

  公开号：EP1158971A1

  公开（公告）日：2001-12-05