N¹-methoxy-N¹-methyl-N⁸-phenyloctanediamide | 651768-07-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N¹-methoxy-N¹-methyl-N⁸-phenyloctanediamide
• 英文别名: N~1~-Methoxy-N~1~-methyl-N~8~-phenyloctanediamide；N'-methoxy-N'-methyl-N-phenyloctanediamide
• CAS: 651768-07-9
• 化学式: C₁₆H₂₄N₂O₃
• 分子量: 292.378
• InChiKey: WAUYUNVIUOUMFQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  21
• 可旋转键数：
  9
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  58.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N¹-methoxy-N¹-methyl-N⁸-phenyloctanediamide 在 吡啶 、 正丁基锂 、 盐酸羟胺 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 生成 8-[(E)-Hydroxyimino]-8-pyridin-2-yl-octanoic acid phenylamide
  参考文献：
  名称：

  Novel histone deacetylase inhibitors: design, synthesis, enzyme inhibition, and binding mode study of SAHA-Based non-hydroxamates

  摘要：

  In order to find novel non-hydroxamate histone deacetylase (HDAC) inhibitors, a series of compounds modeled after suberoylanilide hydroxamic acid (SAHA) were designed and synthesized as (i) substrate (acetyl lysine) analogues (compounds 3-7), (ii) analogues bearing various functional groups expected to chelate zinc ion (compounds 8-15), and (iii) analogues bearing nucleophilic functional groups which could bind covalently to HDACs (compounds 16-18). In this series, semicarbazide 8b and bromoacetamides 18b,c were found to be potent HDAC inhibitors for non-hydroxamates. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.09.048
• 作为产物：
  描述：

  辛二酸 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 N¹-methoxy-N¹-methyl-N⁸-phenyloctanediamide
  参考文献：
  名称：

  Novel histone deacetylase inhibitors: design, synthesis, enzyme inhibition, and binding mode study of SAHA-Based non-hydroxamates

  摘要：

  In order to find novel non-hydroxamate histone deacetylase (HDAC) inhibitors, a series of compounds modeled after suberoylanilide hydroxamic acid (SAHA) were designed and synthesized as (i) substrate (acetyl lysine) analogues (compounds 3-7), (ii) analogues bearing various functional groups expected to chelate zinc ion (compounds 8-15), and (iii) analogues bearing nucleophilic functional groups which could bind covalently to HDACs (compounds 16-18). In this series, semicarbazide 8b and bromoacetamides 18b,c were found to be potent HDAC inhibitors for non-hydroxamates. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.09.048

文献信息

• The Effect of Various Zinc Binding Groups on Inhibition of Histone Deacetylases 1-11
  作者：Andreas S. Madsen、Helle M. E. Kristensen、Gyrithe Lanz、Christian A. Olsen

  DOI：10.1002/cmdc.201300433

  日期：2014.3

  putative new zinc binding domains. By evaluating the compound collection against all 11 recombinant human HDACs, we found that the trifluoromethyl ketone functionality provides potent inhibition of all four subclasses of the Zn2+‐dependent HDACs. Potent inhibition was observed with two different scaffolds, demonstrating the efficiency of the trifluoromethyl ketone moiety as a zinc binding motif. Interestingly

  组蛋白脱乙酰基酶（HDAC）具有裂解多种蛋白质中ε - N-乙酰化赖氨酸残基的乙酰基的能力。鉴于人类细胞包含成千上万个不同的乙酰化赖氨酸残基，HDACS可以调节多种过程，包括某些与癌症和神经退行性疾病等疾病有关的过程。在这里，我们报告了一系列化合物的合成和体外生化分析，包括已知的抑制剂以及新颖的化学型，这些化合物结合了新的锌结合域。通过评估针对所有11种重组人HDAC的化合物集合，我们发现三氟甲基酮官能团可有效抑制Zn 2+的所有四个亚类依赖的HDAC。用两种不同的支架观察到有效的抑制作用，证明了三氟甲基酮部分作为锌结合基序的效率。有趣的是，我们还将硅烷二醇确定为锌结合基团，对于将来开发非I-异羟肟酸酯I类和IIb B类HDAC抑制剂具有潜力。