1-[2-oxo-2-(10H-phenothiazin-10-yl)ethyl]-4-methylpyridinium chloride | 1422532-41-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻嗪类
• 英文名称: 1-[2-oxo-2-(10H-phenothiazin-10-yl)ethyl]-4-methylpyridinium chloride
• 英文别名: 2-(4-Methylpyridin-1-ium-1-yl)-1-phenothiazin-10-ylethanone;chloride；2-(4-methylpyridin-1-ium-1-yl)-1-phenothiazin-10-ylethanone;chloride
• CAS: 1422532-41-9
• 化学式: C₂₀H₁₇N₂OS*Cl
• 分子量: 368.887
• InChiKey: GLTTZPXRJOFSNR-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  1.12
• 重原子数：
  25
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  49.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-[2-oxo-2-(10H-phenothiazin-10-yl)ethyl]-4-methylpyridinium chloride 、 2-氰基-3-乙氧基丙烯酸乙酯 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 24.0h， 以66%的产率得到ethyl (Z)-2-cyano-4-[1-(2-oxo-2-phenothiazin-10-ylethyl)pyridin-4-ylidene]but-2-enoate
  参考文献：
  名称：

  Synthesis and biological evaluation of a new series of phenothiazine-containing protein farnesyltransferase inhibitors

  摘要：

  Two new families of human farnesyltransferase inhibitors 13a-m and 14a-d, based on a phenothiazine scaffold, were synthesized. Compounds 14a and 14b were the most promising inhibitors of human farnesyltransferase with IC50 values of 0.7 and 0.6 mu M, respectively. (C) 2012 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2012.11.008
• 作为产物：
  描述：

  4-甲基吡啶 、 10-(氯乙酰基)-10H-吩噻嗪 以 丙酮 为溶剂， 生成 1-[2-oxo-2-(10H-phenothiazin-10-yl)ethyl]-4-methylpyridinium chloride
  参考文献：
  名称：

  环亚铵盐和 4-(三甲基甲硅烷基)-3-丁炔-2-酮的 1,3-偶极环加成获得具有潜在细胞生长抑制活性的新型功能化中吲嗪

  摘要：

  该研究表明，4-(trimethylsilyl)-3-butyn-2-one 在与环亚铵盐进行 [3+2] 环加成反应以获得非硅加合物，即 1-acetylindolizines 时是一种有效的亲偶极试剂。在某些情况下，还获得了两种可能的含三甲基甲硅烷基加合物。这些甲硅烷基化加合物的结构已通过 X 射线晶体学发现为 1-acetyl-2-trimethylsilyl-indolizines 和 1-trimethylsilyl-2-acetylindolizines。比较了 4-(trimethylsilyl)-3-butyn-2-one 与 3-butyn-2-one 在 [3+2] 环加成反应中的性能。就抑制 NCI-60 癌细胞体外生长的生物学潜力而言，将所得 1-乙酰基或 2-乙酰基二氢吲嗪与先前描述的 3-乙酰基或 1-羧乙基二氢吲嗪进行了比较。

  DOI：

  10.1039/d2nj05257a

文献信息

• Synthesis and biological evaluation of a new series of N-ylides as protein farnesyltransferase inhibitors
  作者：Cristina-Maria Abuhaie、Alina Ghinet、Amaury Farce、Joëlle Dubois、Benoît Rigo、Elena Bîcu

  DOI：10.1016/j.bmcl.2013.08.088

  日期：2013.11

  A new family of 30 benzoylated N-ylides 4 and 5 was synthesized and evaluated for the inhibitory activity on human protein farnesyltransferase. Most of these novel compounds possessed in vitro inhibition potencies in the micromolar range. The nature of the substituents on the pyridine and phenyl units proved to be important in determining inhibitory activity and generally, the replacement of the cyanoacrylonitrile function by a cyanoethylacrylate group decreased the biological potential on farnesyltransferase. These results completed our SAR study on this original class of N-ylides. (C) 2013 Elsevier Ltd. All rights reserved.
• Synthesis and biological evaluation of a new series of phenothiazine-containing protein farnesyltransferase inhibitors
  作者：Cristina-Maria Abuhaie、Alina Ghinet、Amaury Farce、Joëlle Dubois、Philippe Gautret、Benoît Rigo、Dalila Belei、Elena Bîcu

  DOI：10.1016/j.ejmech.2012.11.008

  日期：2013.1

  Two new families of human farnesyltransferase inhibitors 13a-m and 14a-d, based on a phenothiazine scaffold, were synthesized. Compounds 14a and 14b were the most promising inhibitors of human farnesyltransferase with IC50 values of 0.7 and 0.6 mu M, respectively. (C) 2012 Elsevier Masson SAS. All rights reserved.
• 1,3-Dipolar cycloaddition of cycloimmonium salts and 4-(trimethylsilyl)-3-butyn-2-one to access new functionalized indolizines with potential cytostatic activity
  作者：Andreea Zubaş、Alina Ghinet、Sergiu Shova、Elena Bîcu

  DOI：10.1039/d2nj05257a

  日期：——

  4-(trimethylsilyl)-3-butyn-2-one was an effective dipolarophile in the [3+2] cycloaddition reaction with cycloimmonium salts to obtain non-silicon adducts, namely 1-acetylindolizines. In some cases, two possible isomeric trimethylsilyl-containing adducts were also obtained. The structure of these silylated adducts has been found by X-ray crystallography to be 1-acetyl-2-trimethylsilyl-indolizines and

  该研究表明，4-(trimethylsilyl)-3-butyn-2-one 在与环亚铵盐进行 [3+2] 环加成反应以获得非硅加合物，即 1-acetylindolizines 时是一种有效的亲偶极试剂。在某些情况下，还获得了两种可能的含三甲基甲硅烷基加合物。这些甲硅烷基化加合物的结构已通过 X 射线晶体学发现为 1-acetyl-2-trimethylsilyl-indolizines 和 1-trimethylsilyl-2-acetylindolizines。比较了 4-(trimethylsilyl)-3-butyn-2-one 与 3-butyn-2-one 在 [3+2] 环加成反应中的性能。就抑制 NCI-60 癌细胞体外生长的生物学潜力而言，将所得 1-乙酰基或 2-乙酰基二氢吲嗪与先前描述的 3-乙酰基或 1-羧乙基二氢吲嗪进行了比较。