4-[2-羟基-2-(5-羟基-3,5-二甲基-2-羰基环己基)乙基]哌啶-2,6-二酮 | 143468-15-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 黄酮类化合物
• 中文名称: 4-[2-羟基-2-(5-羟基-3,5-二甲基-2-羰基环己基)乙基]哌啶-2,6-二酮
• 英文名称: 2-(3-Chloro-phenyl)-3-nitro-chromen-4-one
• 英文别名: 2-(3-Chlorophenyl)-3-nitrochromen-4-one
• CAS: 143468-15-9
• 化学式: C₁₅H₈ClNO₄
• 分子量: 301.686
• InChiKey: WSTSSNHIBMUZAP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  21
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  72.1
• 氢给体数：
  0
• 氢受体数：
  4

上下游信息

• 上游原料

  中文名称	英文名称	CAS号	化学式	分子量
  ——	2-(3-chlorophenyl)-4H-chromen-4-one	1849-61-2	C15H9ClO2	256.688

反应信息

• 作为反应物：
  描述：

  4-[2-羟基-2-(5-羟基-3,5-二甲基-2-羰基环己基)乙基]哌啶-2,6-二酮 在 palladium on activated charcoal 盐酸 、 氢气 作用下， 以 1,4-二氧六环 为溶剂， 反应 16.0h， 以85%的产率得到3-Amino-2-(3-chloro-phenyl)-chromen-4-one
  参考文献：
  名称：

  Synthesis and in vitro cytotoxicity of a series of 3-aminoflavones

  摘要：

  To further understand the molecular requirements for the antiproliferative activity of flavonoids, a series of 3-aminoflavones and some of their derivatives were prepared and evaluated using L1210 murine leukemia. Our novel five-step synthetic approach required easily available substituted aromatic aldehydes as starting materials and proved more convenient and more general than previously reported methods. Our results in the 3-aminoflavones series indicated that the 4'-methoxy group is important for cytotoxic activity. Moreover, for the flavone-8-acetic analogs, a marked increase in potency was observed with the addition of a 3-amino or a 3-nitro group, Methoxy groups on the 6 and 7 positions of flavonoids (as in cirsiliol) also appear to be important for antiproliferative activity. These results are essential for the further understanding of the critical molecular requirements that lead to antiproliferative properties in the flavonoid series.

  DOI：

  10.1016/s0223-5234(97)84363-2
• 作为产物：
  描述：

  2-acetylphenyl 3-chlorobenzoate 在 吡啶 、 硝酸铵 、 硫酸 、 溶剂黄146 、 三氟乙酸酐 、 potassium hydroxide 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 2.83h， 生成 4-[2-羟基-2-(5-羟基-3,5-二甲基-2-羰基环己基)乙基]哌啶-2,6-二酮
  参考文献：
  名称：

  伯基特淋巴瘤中硝基苯乙烯及相关化合物的合成，抗增殖和促凋亡作用。

  摘要：

  背景技术淋巴细胞癌（淋巴瘤）约占全世界恶性疾病的12％。硝基苯乙烯支架被认为是开发针对Burkitt淋巴瘤（BL）的特别有效的化合物的主要靶标结构。目的目前的研究目的是合成一组硝基苯乙烯化合物并评估其在伯基特氏淋巴瘤（BL）中的活性。方法使用Henry Knoevenagel缩合反应设计和合成一组结构变化的化合物。单晶X射线分析证实了这些新颖结构的六个实例的E构型。还研究了许多与硝基苯乙烯有关的化合物，包括1，3-双（芳基）-2-硝基丙烯与含有硝基乙烯基药效团的杂环支架，例如3-硝基-2-苯基-2H-色烯。使用BL细胞系EBV-MUTU-1和EBV + DG-75（耐化学性）评估化合物的抗增殖活性，以建立初步的结构活性关系。结果成功建立了具有优化的硝基苯乙烯骨架和3-硝基-2-苯基-2Hchromne结构的铅化合物，在MUTU-1细胞中的典型IC50值分别为0.45 µM和0.47 µM，

  DOI：

  10.2174/1573406413666171002123907

文献信息

• Synthesis of 2-Aryl-3-nitro-4<i>H</i>-1-benzopyran-4-ones
  作者：Daniel Dauzonne、Cyrille Grandjean

  DOI：10.1055/s-1992-26198

  日期：——

  2-Aryl-3-nitro-4H-1-benzopyran-4-ones (or 3-nitroflavones) 3 are conveniently prepared in good yields using a two-step approach starting from 2-aryl-3-chloro-3,4-dihydro-4-hydroxy-3-nitro-2H-1-benzopyrans 1. A general synthesis of the novel 2-aryl-3-chloro-2,3-dihydro-3-nitro-4H-1-benzopyran-4-ones 2 employed as intermediates in the procedure is described.

  2-Aryl-3-nitro-4H-1-benzopyran-4-ones (or 3-nitroflavones) 3 are conveniently prepared in good yields using a two-step approach starting from 2-aryl-3-chloro-3,4-dihydro-4-hydroxy-3-nitro-2H-1-benzopyrans 1. A general synthesis of the novel 2-aryl-3-chloro-2,3-dihydro-3-nitro-4H-1-benzopyran-4-ones 2 employed as intermediates in the procedure is described.
• Synthesis and in vitro cytotoxicity of a series of 3-aminoflavones
  作者：D Dauzonne、B Folléas、L Martinez、GG Chabot

  DOI：10.1016/s0223-5234(97)84363-2

  日期：1997.1

  To further understand the molecular requirements for the antiproliferative activity of flavonoids, a series of 3-aminoflavones and some of their derivatives were prepared and evaluated using L1210 murine leukemia. Our novel five-step synthetic approach required easily available substituted aromatic aldehydes as starting materials and proved more convenient and more general than previously reported methods. Our results in the 3-aminoflavones series indicated that the 4'-methoxy group is important for cytotoxic activity. Moreover, for the flavone-8-acetic analogs, a marked increase in potency was observed with the addition of a 3-amino or a 3-nitro group, Methoxy groups on the 6 and 7 positions of flavonoids (as in cirsiliol) also appear to be important for antiproliferative activity. These results are essential for the further understanding of the critical molecular requirements that lead to antiproliferative properties in the flavonoid series.
• Synthesis, Antiproliferative and Pro-Apoptotic Effects of Nitrostyrenes and Related Compounds in Burkitt's Lymphoma
  作者：Andrew J. Byrne、Sandra A. Bright、Darren Fayne、James P. McKeown、Thomas McCabe、Brendan Twamley、Clive Williams、Mary J. Meegan

  DOI：10.2174/1573406413666171002123907

  日期：2018.2.6

  identified as a lead target structure for the development of particularly effective compounds targeting Burkitt's lymphoma (BL). OBJECTIVES The aims of the curent study were to synthesise a panel of nitrostyrene compounds and to evaluate their activity in Burkitt's lymphoma (BL). METHODS A panel of structurally varied compounds were designed and synthesised using Henry Knoevenagel condensation reactions.

  背景技术淋巴细胞癌（淋巴瘤）约占全世界恶性疾病的12％。硝基苯乙烯支架被认为是开发针对Burkitt淋巴瘤（BL）的特别有效的化合物的主要靶标结构。目的目前的研究目的是合成一组硝基苯乙烯化合物并评估其在伯基特氏淋巴瘤（BL）中的活性。方法使用Henry Knoevenagel缩合反应设计和合成一组结构变化的化合物。单晶X射线分析证实了这些新颖结构的六个实例的E构型。还研究了许多与硝基苯乙烯有关的化合物，包括1，3-双（芳基）-2-硝基丙烯与含有硝基乙烯基药效团的杂环支架，例如3-硝基-2-苯基-2H-色烯。使用BL细胞系EBV-MUTU-1和EBV + DG-75（耐化学性）评估化合物的抗增殖活性，以建立初步的结构活性关系。结果成功建立了具有优化的硝基苯乙烯骨架和3-硝基-2-苯基-2Hchromne结构的铅化合物，在MUTU-1细胞中的典型IC50值分别为0.45 µM和0.47 µM，