(Z)-3-(3-chlorobenzyl)-5-(3-nitrobenzylidene)thiazolidine-2,4-dione | 1442655-13-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (Z)-3-(3-chlorobenzyl)-5-(3-nitrobenzylidene)thiazolidine-2,4-dione
• 英文别名: (5Z)-3-[(3-chlorophenyl)methyl]-5-[(3-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dione
• CAS: 1442655-13-1
• 化学式: C₁₇H₁₁ClN₂O₄S
• 分子量: 374.804
• InChiKey: INEBWHNYOLRHBT-DHDCSXOGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  25
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  109
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (Z)-3-(3-chlorobenzyl)-5-(3-nitrobenzylidene)thiazolidine-2,4-dione 在 盐酸 、 铁粉 作用下， 以 乙醇 、 水 为溶剂， 反应 2.0h， 以79%的产率得到(Z)-3-(3-chlorobenzyl)-5-(3-aminobenzylidene)thiazolidine-2,4-dione
  参考文献：
  名称：

  Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione

  摘要：

  Hybridization of two different bioactive molecules with different mechanism of action is one of the methods that are being adopted to treat cancer. Molecules bearing a thiazolidine-2,4-dione scaffold have been recognized as antineoplastic agents with a broad spectrum of activity against many cancer cell lines. In this manuscript we have described the synthesis and biological evaluation of two series of N-3-substituted-5-arylidene thiazolidine-2,4-diones, bearing the alpha-bromoacryloylamido moiety at the para- or meta-position on the phenyl of the arylidene portion. We have observed that selected compounds 5a, 5c and 5g suppress proliferation of human myeloid leukaemia HL-60 and U937 cells by triggering morphological changes and internucleosomal DNA fragmentation, which are well-known features of apoptosis. Finally, our results indicated that the investigated compounds induced apoptotic cell death through a mechanism that involved activation of multiple caspases and was also associated with the release of cytochrome c from the mitochondria. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.02.030
• 作为产物：
  描述：

  (Z)-5-(3-硝基苯亚甲基)噻唑烷-2,4-二酮 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 2.5h， 以77%的产率得到(Z)-3-(3-chlorobenzyl)-5-(3-nitrobenzylidene)thiazolidine-2,4-dione
  参考文献：
  名称：

  Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione

  摘要：

  Hybridization of two different bioactive molecules with different mechanism of action is one of the methods that are being adopted to treat cancer. Molecules bearing a thiazolidine-2,4-dione scaffold have been recognized as antineoplastic agents with a broad spectrum of activity against many cancer cell lines. In this manuscript we have described the synthesis and biological evaluation of two series of N-3-substituted-5-arylidene thiazolidine-2,4-diones, bearing the alpha-bromoacryloylamido moiety at the para- or meta-position on the phenyl of the arylidene portion. We have observed that selected compounds 5a, 5c and 5g suppress proliferation of human myeloid leukaemia HL-60 and U937 cells by triggering morphological changes and internucleosomal DNA fragmentation, which are well-known features of apoptosis. Finally, our results indicated that the investigated compounds induced apoptotic cell death through a mechanism that involved activation of multiple caspases and was also associated with the release of cytochrome c from the mitochondria. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.02.030

文献信息

• Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione
  作者：Romeo Romagnoli、Pier Giovanni Baraldi、Maria Kimatrai Salvador、M. Encarnacion Camacho、Jan Balzarini、Jaime Bermejo、Francisco Estévez

  DOI：10.1016/j.ejmech.2013.02.030

  日期：2013.5

  Hybridization of two different bioactive molecules with different mechanism of action is one of the methods that are being adopted to treat cancer. Molecules bearing a thiazolidine-2,4-dione scaffold have been recognized as antineoplastic agents with a broad spectrum of activity against many cancer cell lines. In this manuscript we have described the synthesis and biological evaluation of two series of N-3-substituted-5-arylidene thiazolidine-2,4-diones, bearing the alpha-bromoacryloylamido moiety at the para- or meta-position on the phenyl of the arylidene portion. We have observed that selected compounds 5a, 5c and 5g suppress proliferation of human myeloid leukaemia HL-60 and U937 cells by triggering morphological changes and internucleosomal DNA fragmentation, which are well-known features of apoptosis. Finally, our results indicated that the investigated compounds induced apoptotic cell death through a mechanism that involved activation of multiple caspases and was also associated with the release of cytochrome c from the mitochondria. (C) 2013 Elsevier Masson SAS. All rights reserved.