5-硫代吗啉基磺酰基靛红 | 1144853-48-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 5-硫代吗啉基磺酰基靛红
• 英文名称: 5-(thiomorpholine-4-sulfonyl)indoline-2,3-dione
• 英文别名: 5-Thiomorpholinosulfonyl Isatin；5-thiomorpholin-4-ylsulfonyl-1H-indole-2,3-dione
• CAS: 1144853-48-4
• 化学式: C₁₂H₁₂N₂O₄S₂
• 分子量: 312.37
• InChiKey: UYTDODWBVJYAQH-UHFFFAOYSA-N

物化性质

• 溶解度：
  可溶于二氯甲烷、乙酸乙酯、甲醇

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  117
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  5-硫代吗啉基磺酰基靛红 、 4-甲氧基溴苄 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 1.25h， 以55%的产率得到1-(4-methoxybenzyl)-5-(thiomorpholine-4-sulfonyl)indoline-2,3-dione
  参考文献：
  名称：

  Synthesis and in Vitro Evaluation of Sulfonamide Isatin Michael Acceptors as Small Molecule Inhibitors of Caspase-6

  摘要：

  A key step in the onset of Huntington's disease is the caspase-6 mediated cleavage of the protein huntingtin into toxic fragments. Therefore. the inhibition of caspase-6 has been identified as a target for therapeutic drug development for the treatment of this disease. In this study a series of isatin sulfonamide Michael acceptors having a high nanomolar potency for inhibiting caspase-6 and increased selectivity for caspase-6 versus caspase-3 inhibition is reported.

  DOI：

  10.1021/jm900135r
• 作为产物：
  描述：

  硫代吗啉 、 2,3-二氧代-2,3-二氢-1H-吲哚-5-磺酰氯 在 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 以75%的产率得到5-硫代吗啉基磺酰基靛红
  参考文献：
  名称：

  Synthesis and in Vitro Evaluation of Sulfonamide Isatin Michael Acceptors as Small Molecule Inhibitors of Caspase-6

  摘要：

  A key step in the onset of Huntington's disease is the caspase-6 mediated cleavage of the protein huntingtin into toxic fragments. Therefore. the inhibition of caspase-6 has been identified as a target for therapeutic drug development for the treatment of this disease. In this study a series of isatin sulfonamide Michael acceptors having a high nanomolar potency for inhibiting caspase-6 and increased selectivity for caspase-6 versus caspase-3 inhibition is reported.

  DOI：

  10.1021/jm900135r

文献信息

• Synthesis and in Vitro Evaluation of Sulfonamide Isatin Michael Acceptors as Small Molecule Inhibitors of Caspase-6
  作者：Wenhua Chu、Justin Rothfuss、Yunxiang Chu、Dong Zhou、Robert H. Mach

  DOI：10.1021/jm900135r

  日期：2009.4.23

  A key step in the onset of Huntington's disease is the caspase-6 mediated cleavage of the protein huntingtin into toxic fragments. Therefore. the inhibition of caspase-6 has been identified as a target for therapeutic drug development for the treatment of this disease. In this study a series of isatin sulfonamide Michael acceptors having a high nanomolar potency for inhibiting caspase-6 and increased selectivity for caspase-6 versus caspase-3 inhibition is reported.