ethyl 5-amino-1-(phenylsulfonyl)-1H-pyrazole-4-carboxylate | 1349199-14-9

• 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: ethyl 5-amino-1-(phenylsulfonyl)-1H-pyrazole-4-carboxylate
• 英文别名: Ethyl 5-amino-1-(benzenesulfonyl)pyrazole-4-carboxylate；ethyl 5-amino-1-(benzenesulfonyl)pyrazole-4-carboxylate
• CAS: 1349199-14-9
• 化学式: C₁₂H₁₃N₃O₄S
• 分子量: 295.319
• InChiKey: ANWCGSYCXVRESE-UHFFFAOYSA-N

物化性质

• 熔点：
  149-151 °C(Solv: acetonitrile (75-05-8))
• 沸点：
  505.8±53.0 °C(Predicted)
• 密度：
  1.44±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  113
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  苯磺酰肼 、 2-氰基-3-乙氧基丙烯酸乙酯 以 乙腈 为溶剂， 反应 6.0h， 以93%的产率得到ethyl 5-amino-1-(phenylsulfonyl)-1H-pyrazole-4-carboxylate
  参考文献：
  名称：

  Synthesis and in vitro cytotoxic activity of novel pyrazolo[3,4-d]pyrimidines and related pyrazole hydrazones toward breast adenocarcinoma MCF-7 cell line

  摘要：

  New series of pyrazolo[3,4-d]pyrimidines (7a-e and 13a-d) and pyrazole hydrazones 17a-d were synthesized and evaluated for their antiproliferative activity against human breast adenocarcinoma MCF-7 cell line. Most of the tested compounds exploited potent to moderate growth inhibitory activity, in particular compound 7e exhibited superior potency to the reference drug cisplatin (IC50 = 7.60 and 13.29 mu M, respectively). The antitumor activity of the new compounds was accompanied by significant increase in the activity of superoxide dismutase with concomitant decrease in the activities of catalase and glutathione peroxidase and reduced glutathione level. Accordingly, the overproduction of hydrogen peroxide, nitric oxide and other free radicals allowed reactive oxygen species (ROS)-mediated tumor cells death, as monitored by reduction in the synthesis of protein and nucleic acids. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.09.036

文献信息

• Synthesis and in vitro cytotoxic activity of novel pyrazolo[3,4-d]pyrimidines and related pyrazole hydrazones toward breast adenocarcinoma MCF-7 cell line
  作者：Ghaneya Sayed Hassan、Hanan Hassan Kadry、Sahar Mahmoud Abou-Seri、Mamdouh Moawad Ali、Abeer Essam El-Din Mahmoud

  DOI：10.1016/j.bmc.2011.09.036

  日期：2011.11

  New series of pyrazolo[3,4-d]pyrimidines (7a-e and 13a-d) and pyrazole hydrazones 17a-d were synthesized and evaluated for their antiproliferative activity against human breast adenocarcinoma MCF-7 cell line. Most of the tested compounds exploited potent to moderate growth inhibitory activity, in particular compound 7e exhibited superior potency to the reference drug cisplatin (IC50 = 7.60 and 13.29 mu M, respectively). The antitumor activity of the new compounds was accompanied by significant increase in the activity of superoxide dismutase with concomitant decrease in the activities of catalase and glutathione peroxidase and reduced glutathione level. Accordingly, the overproduction of hydrogen peroxide, nitric oxide and other free radicals allowed reactive oxygen species (ROS)-mediated tumor cells death, as monitored by reduction in the synthesis of protein and nucleic acids. (C) 2011 Elsevier Ltd. All rights reserved.