1-(4-methoxybenzyl)-5-(morpholine-4-sulfonyl)indoline-2,3-dione | 1144853-55-3

• 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
• 英文名称: 1-(4-methoxybenzyl)-5-(morpholine-4-sulfonyl)indoline-2,3-dione
• 英文别名: 1-[(4-Methoxyphenyl)methyl]-5-morpholin-4-ylsulfonylindole-2,3-dione
• CAS: 1144853-55-3
• 化学式: C₂₀H₂₀N₂O₆S
• 分子量: 416.455
• InChiKey: JFHCPVCIDURGGU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  29
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  102
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  1-(4-methoxybenzyl)-5-(morpholine-4-sulfonyl)indoline-2,3-dione 、 丙二腈 以 甲醇 为溶剂， 反应 0.5h， 以58%的产率得到2-(1-(4-methoxybenzyl)-5-(morpholine-4-sulfonyl)-2-oxoindolin-3-ylidene)malononitrile
  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：

  5-(4-吗啉磺酰基)-1H-吲哚-2,3-二酮 、 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59%的产率得到1-(4-methoxybenzyl)-5-(morpholine-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

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.