3-(4-methyl-piperidin-1-yl)-10,10-dioxo-10H-10lambda*6*-thioxanthen-9-one | 958872-79-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻喃类
• 英文名称: 3-(4-methyl-piperidin-1-yl)-10,10-dioxo-10H-10lambda*6*-thioxanthen-9-one
• 英文别名: 3-(4-methylpiperidin-1-yl)-10,10-dioxothioxanthen-9-one
• CAS: 958872-79-2
• 化学式: C₁₉H₁₉NO₃S
• 分子量: 341.431
• InChiKey: JETQDUBHADSBQE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  24
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  62.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  4-甲基哌啶 、 3-chlorothioxanthen-9-one-10,10-dioxide 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 0.5h， 生成 3-(4-methyl-piperidin-1-yl)-10,10-dioxo-10H-10lambda*6*-thioxanthen-9-one
  参考文献：
  名称：

  Synthesis and screening of 3-substituted thioxanthen-9-one-10,10-dioxides

  摘要：

  This manuscript describes methods appropriate for the parallel synthesis of libraries based on the tricyclic thioxanthen-9one-10,10-dioxide scaffold. The novel compounds were synthesized from previously reported 3-chlorothioxanthen-9-one-10,10-dioxide and commercially available 3-carboxylic acid thioxanthen-9-oiie-10,10-dioxide. The library members were screened for activity in a fluorescence polarization assay for inhibitors of BRCT domains of breast cancer gene I and in cell-based secreted alkaline phosphatase reported replicon system for activity against hepatitis C virus. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.07.103

文献信息

• Synthesis and screening of 3-substituted thioxanthen-9-one-10,10-dioxides
  作者：Pedro M.J. Lory、Maria E. Estrella-Jimenez、Matthew J. Shashack、Ganesh L. Lokesh、Amarnath Natarajan、Scott R. Gilbertson

  DOI：10.1016/j.bmcl.2007.07.103

  日期：2007.11

  This manuscript describes methods appropriate for the parallel synthesis of libraries based on the tricyclic thioxanthen-9one-10,10-dioxide scaffold. The novel compounds were synthesized from previously reported 3-chlorothioxanthen-9-one-10,10-dioxide and commercially available 3-carboxylic acid thioxanthen-9-oiie-10,10-dioxide. The library members were screened for activity in a fluorescence polarization assay for inhibitors of BRCT domains of breast cancer gene I and in cell-based secreted alkaline phosphatase reported replicon system for activity against hepatitis C virus. (c) 2007 Elsevier Ltd. All rights reserved.