4-[2-(3,4-二甲氧基苯基)乙基]苯胺 | 110997-83-6

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 中文名称: 4-[2-(3,4-二甲氧基苯基)乙基]苯胺
• 英文名称: 4-[2-(3,4-dimethoxyphenyl)ethyl]aniline
• 英文别名: 4-(3,4-dimethoxyphenethyl)aniline；4-[2-(3,4-Dimethoxy-phenyl)ethyl]-phenylamine；4-[2-(3,4-dimethoxyphenyl)ethyl]benzeneamine
• CAS: 110997-83-6
• 化学式: C₁₆H₁₉NO₂
• 分子量: 257.332
• InChiKey: MEJNYOQOZUXCOG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  44.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-[2-(3,4-二甲氧基苯基)乙基]苯胺 在 sodium hydroxide 、 三乙胺 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 生成 4-chloro-N-[4-[2-(3,4-dimethoxyphenyl)ethyl]phenyl]-2-hydroxybenzamide
  参考文献：
  名称：

  Catechol based inhibitors of 15-lipoxygenase

  摘要：

  A potent 15-lipoxygenase (15-LO) inhibitor, compound 6, was identified by mass screening the Parke-Davis compound portfolio. The active moiety of compound 6 was determined to be the catechol functionality. Additional analogs were prepared and analyzed for inhibitory activity against 5-, 12-, and 15-lipoxygenase.

  DOI：

  10.1016/0960-894x(95)00565-b
• 作为产物：
  描述：

  2-(4-硝基苯基)乙酰氯 在 palladium on activated charcoal 三氯化铝 、 硫酸 、 氢气 、 溶剂黄146 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 生成 4-[2-(3,4-二甲氧基苯基)乙基]苯胺
  参考文献：
  名称：

  Catechol based inhibitors of 15-lipoxygenase

  摘要：

  A potent 15-lipoxygenase (15-LO) inhibitor, compound 6, was identified by mass screening the Parke-Davis compound portfolio. The active moiety of compound 6 was determined to be the catechol functionality. Additional analogs were prepared and analyzed for inhibitory activity against 5-, 12-, and 15-lipoxygenase.

  DOI：

  10.1016/0960-894x(95)00565-b

文献信息

• Anti-influenza activity of phenethylphenylphthalimide analogs derived from thalidomide
  作者：Yuma Iwai、Hitoshi Takahashi、Dai Hatakeyama、Kazunori Motoshima、Minoru Ishikawa、Kazuyuki Sugita、Yuichi Hashimoto、Yuichi Harada、Shigeyuki Itamura、Takato Odagiri、Masato Tashiro、Yoshihisa Sei、Kentaro Yamaguchi、Takashi Kuzuhara

  DOI：10.1016/j.bmc.2010.05.035

  日期：2010.7

  subunits. We identified potential novel anti-influenza agents from a screen of 34 synthesized phenethylphenylphthalimide analogs derived from thalidomide (PPT analogs). For this screen we used a PA endonuclease inhibition assay, a PB2 pathogenicity-determinant domain-binding assay, and an anti-influenza A virus assay. Three PPT analogs, PPT-65, PPT-66, and PPT-67, were found to both inhibit PA endonuclease

  源自猪的甲型流感病毒已在​​全世界引起大流行，甲型流感被认为是严重的全球健康问题。因此，非常需要靶向这些病毒的新型药物。甲型流感病毒表达对其转录和复制必不可少的RNA聚合酶，该酶包含PA，PB1和PB2亚基。我们从34种合成的来自沙利度胺的苯乙基苯基邻苯二甲酰亚胺类似物（PPT类似物）的筛选中鉴定出潜在的新型抗流感药。对于此筛选，我们使用了PA核酸内切酶抑制测定，PB2致病性决定域结合测定和抗A型流感病毒测定。发现三种PPT类似物PPT-65，PPT-66和PPT-67均能抑制PA核酸内切酶活性并延缓甲型流感的生长，表明它们的活性之间存在相关性。还发现PPT-28抑制甲型流感的生长。这四个类似物共有3,4-二羟基苯乙基。我们还讨论了3,4-二羟基苯乙基柔韧性可能在PA核酸内切酶抑制中起重要功能作用的可能性。另一个带有二甲氧基苯乙基的类似物PPT-62具有PB2致病性决定域结合活性，但没有抑
• Enolamides, pharmaceutical compositions and methods for treating
  申请人：Warner-Lambert Company

  公开号：US04761424A1

  公开（公告）日：1988-08-02

  The present invention relates to novel enolamide type compounds, pharmaceutical compositions, and methods of use thereof, useful in the treatment of diseases in which products of lipoxygenase enzyme activity or the action of leukotrienes contribute to the pathological condition.

  本发明涉及新型烯酰胺类化合物、药物组合物及其使用方法，适用于治疗疾病，其中脂氧酶酶活性产物或白三烯的作用促成了病理状况。
• N-substituted-2-hydroxy-.alpha.-oxo-benzeneacetamides and pharmaceutical
  申请人：Warner-Lambert Company

  公开号：US04939133A1

  公开（公告）日：1990-07-03

  The present invention relates to novel N-substituted 2-hydroxybenzamide and N-substituted 2-hydroxy-.alpha.-oxo-benezene acetamide compounds pharmaceutical compositions, and methods of use for therefore for the treatment of diseases in which products having lipoxygenase enzyme activity contribute to the pathological condition. Selected novel intermediates are also the present invention.

  本发明涉及新型N-取代的2-羟基苯甲酰胺和N-取代的2-羟基-α-氧代苯乙酰胺化合物药物组合物，以及用于治疗病变中脂氧合酶酶活性产物导致病理状况的方法。所述发明还涉及选定的新型中间体。
• Method of inhibiting amyloid protein aggregation and imaging amyloid deposits
  申请人：——

  公开号：US20040220235A1

  公开（公告）日：2004-11-04

  The present invention provides a method of treating Alzheimer's disease using a compound of Formula I 1 Also provided is a method of inhibiting the aggregation of amyloid proteins using a compound of Formula I and a method of imaging amyloid deposits, as well as new compounds of Formula I.

  本发明提供了一种利用I1式化合物治疗阿尔茨海默病的方法。还提供了一种利用I式化合物抑制淀粉样蛋白聚集的方法，以及一种成像淀粉样沉积物的方法，以及新的I式化合物。
• Enolamides, pharmaceutical compositions and methods of use thereof for
  申请人：Warner-Lambert Company

  公开号：US04921871A1

  公开（公告）日：1990-05-01

  The present invention relates to novel enolamide type compounds, pharmaceutical compositions, and methods of use thereof, useful in the treatment of diseases in which products of lipoxygenase enzyme activity or the action of leukotrienes contribute to the pathological condition.

  本发明涉及新型烯酰胺类化合物、制药组合物及其使用方法，用于治疗病态条件中脂氧酶酶活性产物或白三烯作用有贡献的疾病。