1-(4-(4-(5-acetyl-2-hydroxybenzyl)piperazin-1-yl)phenyl)ethanone | 1292319-35-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(4-(4-(5-acetyl-2-hydroxybenzyl)piperazin-1-yl)phenyl)ethanone
• 英文别名: 1-[4-[4-[(5-Acetyl-2-hydroxyphenyl)methyl]piperazin-1-yl]phenyl]ethanone
• CAS: 1292319-35-7
• 化学式: C₂₁H₂₄N₂O₃
• 分子量: 352.433
• InChiKey: JSYRFQDCWGVFEV-UHFFFAOYSA-N

物化性质

• 熔点：
  146-148 °C
• 沸点：
  572.0±50.0 °C(Predicted)
• 密度：
  1.204±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  26
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  60.8
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  胡椒醛 、 1-(4-(4-(5-acetyl-2-hydroxybenzyl)piperazin-1-yl)phenyl)ethanone 在 potassium hydroxide 作用下， 以 甲醇 为溶剂， 反应 24.5h， 以62%的产率得到(E)-3-(benzo[d][1,3]dioxol-5-yl)-1-(4-(4-(5-((E)-3-(benzo[d][1,3]dioxol-5-yl)acryloyl)-2-hydroxybenzyl)piperazin-1-yl)phenyl)prop-2-en-1-one
  参考文献：
  名称：

  New bichalcone analogs as NF-κB inhibitors and as cytotoxic agents inducing Fas/CD95-dependent apoptosis

  摘要：

  A series of novel bichalcone analogs were synthesized and evaluated in lipopolysaccharide (LPS)-activated microglial cells as inhibitors of nitric oxide (NO) and for in vitro anticancer activity using a limited panel of four human cancer cell lines. All analogs inhibited NO production. Compounds 4 and 11 exhibited optimal activity with IC50 values of 0.3 and 0.5 mu M, respectively, and were at least 38-fold better than the positive control. A mechanism of action study showed that both compounds significantly blocked the nuclear translocation of NF-kappa B p65 and up-regulation of iNOS at 1.0 mu M. Compound 4 and three other analogs (3, 20, and 23) exerted significant in vitro anticancer activity GI(50) values ranging from 0.70 to 13.10 mu M. A mode of action study using HT-29 colon cancer cells showed that 23 acts by inducing apoptosis signaling. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.02.004
• 作为产物：
  描述：

  聚合甲醛 、 对羟基苯乙酮 、 4-哌嗪苯乙酮 以 乙醇 为溶剂， 以69.6%的产率得到1-(4-(4-(5-acetyl-2-hydroxybenzyl)piperazin-1-yl)phenyl)ethanone
  参考文献：
  名称：

  New bichalcone analogs as NF-κB inhibitors and as cytotoxic agents inducing Fas/CD95-dependent apoptosis

  摘要：

  A series of novel bichalcone analogs were synthesized and evaluated in lipopolysaccharide (LPS)-activated microglial cells as inhibitors of nitric oxide (NO) and for in vitro anticancer activity using a limited panel of four human cancer cell lines. All analogs inhibited NO production. Compounds 4 and 11 exhibited optimal activity with IC50 values of 0.3 and 0.5 mu M, respectively, and were at least 38-fold better than the positive control. A mechanism of action study showed that both compounds significantly blocked the nuclear translocation of NF-kappa B p65 and up-regulation of iNOS at 1.0 mu M. Compound 4 and three other analogs (3, 20, and 23) exerted significant in vitro anticancer activity GI(50) values ranging from 0.70 to 13.10 mu M. A mode of action study using HT-29 colon cancer cells showed that 23 acts by inducing apoptosis signaling. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.02.004

文献信息

• New bichalcone analogs as NF-κB inhibitors and as cytotoxic agents inducing Fas/CD95-dependent apoptosis
  作者：M. Vijaya Bhaskar Reddy、Yuh-Chiang Shen、Jai-Sing Yang、Tsong-Long Hwang、Kenneth F. Bastow、Keduo Qian、Kuo-Hsiung Lee、Tian-Shung Wu

  DOI：10.1016/j.bmc.2011.02.004

  日期：2011.3

  A series of novel bichalcone analogs were synthesized and evaluated in lipopolysaccharide (LPS)-activated microglial cells as inhibitors of nitric oxide (NO) and for in vitro anticancer activity using a limited panel of four human cancer cell lines. All analogs inhibited NO production. Compounds 4 and 11 exhibited optimal activity with IC50 values of 0.3 and 0.5 mu M, respectively, and were at least 38-fold better than the positive control. A mechanism of action study showed that both compounds significantly blocked the nuclear translocation of NF-kappa B p65 and up-regulation of iNOS at 1.0 mu M. Compound 4 and three other analogs (3, 20, and 23) exerted significant in vitro anticancer activity GI(50) values ranging from 0.70 to 13.10 mu M. A mode of action study using HT-29 colon cancer cells showed that 23 acts by inducing apoptosis signaling. (C) 2011 Elsevier Ltd. All rights reserved.