4-(4-(3-(4-Methylpiperazin-1-yl)propoxy)-3-(trifluoromethyl)phenyl)pyrimidine-2-carbonitrile | 1243143-34-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 4-(4-(3-(4-Methylpiperazin-1-yl)propoxy)-3-(trifluoromethyl)phenyl)pyrimidine-2-carbonitrile
• 英文别名: 4-[4-[3-(4-methylpiperazin-1-yl)propoxy]-3-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrile
• CAS: 1243143-34-1
• 化学式: C₂₀H₂₂F₃N₅O
• 分子量: 405.423
• InChiKey: LZLJBBHMBQJUSF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  29
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  65.3
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  N-甲基哌嗪 、 以 N-甲基吡咯烷酮 为溶剂， 反应 0.33h， 生成 4-(4-(3-(4-Methylpiperazin-1-yl)propoxy)-3-(trifluoromethyl)phenyl)pyrimidine-2-carbonitrile
  参考文献：
  名称：

  4-(3-Trifluoromethylphenyl)-pyrimidine-2-carbonitrile as cathepsin S inhibitors: N3, not N1 is critically important

  摘要：

  Using computer aided modelling studies, a new extended P2/S2 interaction was identified. This extended region can accommodate a variety of functional groups, such as aryls and basic amines. It was discovered that the N3 nitrogen of the pyrimidine-2-carbonitrile is critical for its cathepsin cysteine protease inhibition. N1 nitrogen also contributes to the inhibitory activity, but to a very limited degree. An 'in situ double activation' mechanism was proposed to explain these results. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.06.043

文献信息

• 4-(3-Trifluoromethylphenyl)-pyrimidine-2-carbonitrile as cathepsin S inhibitors: N3, not N1 is critically important
  作者：Jiaqiang Cai、Xavier Fradera、Mario van Zeeland、Maureen Dempster、Kenneth S. Cameron、D. Jonathan Bennett、John Robinson、Lucy Popplestone、Mark Baugh、Paul Westwood、John Bruin、William Hamilton、Emma Kinghorn、Clive Long、Joost C.M. Uitdehaag

  DOI：10.1016/j.bmcl.2010.06.043

  日期：2010.8

  Using computer aided modelling studies, a new extended P2/S2 interaction was identified. This extended region can accommodate a variety of functional groups, such as aryls and basic amines. It was discovered that the N3 nitrogen of the pyrimidine-2-carbonitrile is critical for its cathepsin cysteine protease inhibition. N1 nitrogen also contributes to the inhibitory activity, but to a very limited degree. An 'in situ double activation' mechanism was proposed to explain these results. (C) 2010 Elsevier Ltd. All rights reserved.