| 1369465-55-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• CAS: 1369465-55-3
• 化学式: C₁₂H₈ClNO₂S
• 分子量: 265.72
• InChiKey: NXOYHJRCISUHHA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.56
• 重原子数：
  17.0
• 可旋转键数：
  3.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  50.19
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  在 氯甲酸乙酯 、 三乙胺 、 sodium azide 作用下， 以 丙酮 为溶剂， 反应 0.83h， 生成
  参考文献：
  名称：

  Design, synthesis and SAR of thienopyridines as potent CHK1 inhibitors

  摘要：

  A novel series of CHK1 inhibitors based on thienopyridine template has been designed and synthesized. These inhibitors maintain critical hydrogen bonding with the hinge and conserved water in the ATP binding site. Several compounds show single digit nanomolar CHK1 activities. Compound 70 shows excellent enzymatic activity of 1 nM. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.10.105
• 作为产物：
  描述：

  2-(4-氯苯基)噻唑-5-甲醛 、 丙二酸 在 哌啶 、 吡啶 作用下， 生成
  参考文献：
  名称：

  Design, synthesis and SAR of thienopyridines as potent CHK1 inhibitors

  摘要：

  A novel series of CHK1 inhibitors based on thienopyridine template has been designed and synthesized. These inhibitors maintain critical hydrogen bonding with the hinge and conserved water in the ATP binding site. Several compounds show single digit nanomolar CHK1 activities. Compound 70 shows excellent enzymatic activity of 1 nM. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.10.105