methyl 3-methoxy-4-(4-oxo-3-(5-(4-(phenylsulfonyl)piperazin-1-yl)pyridin-2-yl)thiazolidin-2-yl)benzoate | 1615687-48-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: methyl 3-methoxy-4-(4-oxo-3-(5-(4-(phenylsulfonyl)piperazin-1-yl)pyridin-2-yl)thiazolidin-2-yl)benzoate
• 英文别名: Methyl 4-[3-[5-[4-(benzenesulfonyl)piperazin-1-yl]pyridin-2-yl]-4-oxo-1,3-thiazolidin-2-yl]-3-methoxybenzoate；methyl 4-[3-[5-[4-(benzenesulfonyl)piperazin-1-yl]pyridin-2-yl]-4-oxo-1,3-thiazolidin-2-yl]-3-methoxybenzoate
• CAS: 1615687-48-3
• 化学式: C₂₇H₂₈N₄O₆S₂
• 分子量: 568.675
• InChiKey: BNFMAWNLNURHHW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  39
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  143
• 氢给体数：
  0
• 氢受体数：
  10

反应信息

• 作为产物：
  描述：

  5-溴-2-硝基吡啶 在 盐酸 、 palladium 10% on activated carbon 、 氢气 、 1-丙基磷酸酐 、 三乙胺 作用下， 以 1,4-二氧六环 、 N-甲基吡咯烷酮 、 乙醇 、 二氯甲烷 、 乙酸乙酯 为溶剂， 反应 10.0h， 生成 methyl 3-methoxy-4-(4-oxo-3-(5-(4-(phenylsulfonyl)piperazin-1-yl)pyridin-2-yl)thiazolidin-2-yl)benzoate
  参考文献：
  名称：

  Synthesis and antiproliferative effect of novel 4-thiazolidinone-, pyridine- and piperazine-based conjugates on human leukemic cells

  摘要：

  The present work reveals the synthesis and antiproliferative effect of a series of 2, 3 disubstituted 4-thiazolidinone analogues on human leukemic cells. The chemical structures of newly synthesized compounds were confirmed by IR, H-1 NMR, C-13 NMR and mass spectral analysis. Compound methyl 3-methoxy-4-(4-oxo-3-(5-(piperazin-1-yl)pyridin-2-yl)thiazolidin-2-yl)benzoate (5) displayed potent activity (IC50 9.71, 15.24 and 19.29 mu M) against Nalm6, K562, Jurkat cells. Cell cycle analysis and mitochondrial membrane potential further confirmed that compound 5 is cytotoxic and able to induce cell death. (C) 2014 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2014.05.009

文献信息

• Synthesis and antiproliferative effect of novel 4-thiazolidinone-, pyridine- and piperazine-based conjugates on human leukemic cells
  作者：Kothanahally S. Sharath Kumar、Ananda Hanumappa、Mahesh Hegde、Kereyagalahally H. Narasimhamurthy、Sathees C. Raghavan、Kanchugarakoppal S. Rangappa

  DOI：10.1016/j.ejmech.2014.05.009

  日期：2014.6

  The present work reveals the synthesis and antiproliferative effect of a series of 2, 3 disubstituted 4-thiazolidinone analogues on human leukemic cells. The chemical structures of newly synthesized compounds were confirmed by IR, H-1 NMR, C-13 NMR and mass spectral analysis. Compound methyl 3-methoxy-4-(4-oxo-3-(5-(piperazin-1-yl)pyridin-2-yl)thiazolidin-2-yl)benzoate (5) displayed potent activity (IC50 9.71, 15.24 and 19.29 mu M) against Nalm6, K562, Jurkat cells. Cell cycle analysis and mitochondrial membrane potential further confirmed that compound 5 is cytotoxic and able to induce cell death. (C) 2014 Elsevier Masson SAS. All rights reserved.