Ethyl 2-(4-(4-(2-(dimethylamino)ethyl)piperazin-1-yl)-6-(4-methylpiperazin-1-yl)pyrimidin-2-ylamino)-4-methylthiazole-5-carboxylate | 479228-26-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: Ethyl 2-(4-(4-(2-(dimethylamino)ethyl)piperazin-1-yl)-6-(4-methylpiperazin-1-yl)pyrimidin-2-ylamino)-4-methylthiazole-5-carboxylate
• 英文别名: ethyl 2-[[4-[4-[2-(dimethylamino)ethyl]piperazin-1-yl]-6-(4-methylpiperazin-1-yl)pyrimidin-2-yl]amino]-4-methyl-1,3-thiazole-5-carboxylate
• CAS: 479228-26-7
• 化学式: C₂₄H₃₉N₉O₂S
• 分子量: 517.699
• InChiKey: INTLSFATTZEYKD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  36
• 可旋转键数：
  10
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  121
• 氢给体数：
  1
• 氢受体数：
  12

反应信息

• 作为产物：
  描述：

  1-(2-二甲基氨基乙基)哌嗪 、 Ethyl 2-[[4-chloro-6-(4-methylpiperazin-1-yl)pyrimidin-2-yl]amino]-4-methyl-1,3-thiazole-5-carboxylate 以 正丁醇 为溶剂， 生成 Ethyl 2-(4-(4-(2-(dimethylamino)ethyl)piperazin-1-yl)-6-(4-methylpiperazin-1-yl)pyrimidin-2-ylamino)-4-methylthiazole-5-carboxylate
  参考文献：
  名称：

  Identification of potent pyrimidine inhibitors of phosphodiesterase 7 (PDE7) and their ability to inhibit T cell proliferation

  摘要：

  A series of pyrimidine based inhibitors of PDE7 are discussed. The synthesis, structure-activity relationships (SAR) and selectivity against several other PDE family members as well as activity in T cells are presented. These compounds were found to have effects on T cell proliferation, however it is not clear whether the mechanism is related to PDE7 inhibition. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.02.060

文献信息

• Identification of potent pyrimidine inhibitors of phosphodiesterase 7 (PDE7) and their ability to inhibit T cell proliferation
  作者：Junqing Guo、Andrew Watson、James Kempson、Marianne Carlsen、Joseph Barbosa、Karen Stebbins、Deborah Lee、John Dodd、Steven G. Nadler、Murray McKinnon、Joel Barrish、William J. Pitts

  DOI：10.1016/j.bmcl.2009.02.060

  日期：2009.4

  A series of pyrimidine based inhibitors of PDE7 are discussed. The synthesis, structure-activity relationships (SAR) and selectivity against several other PDE family members as well as activity in T cells are presented. These compounds were found to have effects on T cell proliferation, however it is not clear whether the mechanism is related to PDE7 inhibition. (C) 2009 Elsevier Ltd. All rights reserved.