1-(3-((3-methylbenzyl)oxy)phenyl)ethanone | 1019445-78-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(3-((3-methylbenzyl)oxy)phenyl)ethanone
• 英文别名: 1-[3-[(3-Methylphenyl)methoxy]phenyl]ethanone
• CAS: 1019445-78-3
• 化学式: C₁₆H₁₆O₂
• mdl: MFCD11522624
• 分子量: 240.302
• InChiKey: IMKUKAGKDGDPSW-UHFFFAOYSA-N

物化性质

• 沸点：
  369.3±22.0 °C(Predicted)
• 密度：
  1.082±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.187
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(3-((3-methylbenzyl)oxy)phenyl)ethanone 在 sodium hydride 、 二异丁基氢化铝 、 三苯基膦 、 三氟乙酸 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成
  参考文献：
  名称：

  Design and synthesis of oxadiazolidinediones as inhibitors of plasminogen activator inhibitor-1

  摘要：

  A novel series of PAI-1 inhibitors containing an oxadiazolidinedione moiety were identified by high through-put screening. Optimization of substituents by parallel synthesis and the iterative design toward understanding structure-activity relationship to improve potency are described. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.04.058
• 作为产物：
  描述：

  3-甲基苄溴 在 正丁基锂 、 jones reagent 、 potassium carbonate 作用下， 以 丙酮 为溶剂， 生成 1-(3-((3-methylbenzyl)oxy)phenyl)ethanone
  参考文献：
  名称：

  Design and synthesis of oxadiazolidinediones as inhibitors of plasminogen activator inhibitor-1

  摘要：

  A novel series of PAI-1 inhibitors containing an oxadiazolidinedione moiety were identified by high through-put screening. Optimization of substituents by parallel synthesis and the iterative design toward understanding structure-activity relationship to improve potency are described. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.04.058

文献信息

• Acetophenone derivatives: novel and potent small molecule inhibitors of monoamine oxidase B
  作者：Zhi-Min Wang、Xue-Mei Li、Wei Xu、Fan Li、Jin Wang、Ling-Yi Kong、Xiao-Bing Wang

  DOI：10.1039/c5md00357a

  日期：——

  series of acetophenone derivatives have been designed, synthesized and evaluated for human monoamine oxidase A and B inhibitory activity in vitro. Most of the tested compounds acted preferentially on MAO-B with IC50 values in the nanomolar range and weak or no inhibition of MAO-A. In particular, compounds 1j (IC50 = 12.9 nM) and 2e (IC50 = 11.7 nM) were the most potent MAO-B inhibitors being 2.76- and 2

  已经设计，合成和评估了两个系列的苯乙酮衍生物在体外对人单胺氧化酶A和B的抑制活性。大多数测试的化合物优先以30纳摩尔范围的IC 50值对MAO-B起作用，对MAO-A的抑制作用弱或无抑制作用。特别是化合物1j（IC 50 = 12.9 nM）和2e（IC 50= 11.7 nM）是最有效的MAO-B抑制剂，其活性比司来吉兰高2.76倍和2.99倍。此外，MAO-B抑制的结构-活性关系表明，苯乙酮部分C3和C4处的取代基，特别是被卤素取代的苄氧基取代，对MAO-B抑制更有利。已经进行了分子对接和动力学研究以解释MAO-B与苯乙酮衍生物的结合模式。此外，代表性化合物1j和2e在SH-SY5Y细胞中显示出低神经毒性。可以得出结论，苯乙酮衍生物可用于开发有望用于治疗神经退行性疾病的先导化合物。
• Design and synthesis of oxadiazolidinediones as inhibitors of plasminogen activator inhibitor-1
  作者：Ariamala Gopalsamy、Scott L. Kincaid、John W. Ellingboe、Thomas M. Groeling、Thomas M. Antrilli、Girija Krishnamurthy、Ann Aulabaugh、Gregory S. Friedrichs、David L. Crandall

  DOI：10.1016/j.bmcl.2004.04.058

  日期：2004.7

  A novel series of PAI-1 inhibitors containing an oxadiazolidinedione moiety were identified by high through-put screening. Optimization of substituents by parallel synthesis and the iterative design toward understanding structure-activity relationship to improve potency are described. (C) 2004 Elsevier Ltd. All rights reserved.