3-(p-Tolyl)-2-hydroxyiminopropionic acid | 133712-82-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 苯丙酸
• 英文名称: 3-(p-Tolyl)-2-hydroxyiminopropionic acid
• 英文别名: 2-(hydroxyimino)-3-p-tolylpropanoic acid；2-Hydroxyimino-3-(4-methylphenyl)propanoic acid；2-hydroxyimino-3-(4-methylphenyl)propanoic acid
• CAS: 133712-82-0
• 化学式: C₁₀H₁₁NO₃
• 分子量: 193.202
• InChiKey: NYMHAOMOFDKRFB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  69.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-(p-Tolyl)-2-hydroxyiminopropionic acid 在 草酰基二咪唑 作用下， 以 苯 为溶剂， 以95%的产率得到对甲基苯乙腈
  参考文献：
  名称：

  An improved method for the synthesis of arylacetonitriles from 3-aryl-2-hydroxyiminopropionic acids using 1,1'-oxalyldiimidazole.

  摘要：

  1，1'-草二亚胺（ODI，3）是一种有效的试剂，可在基本中性条件下将3-芳基-2-羟基亚胺丙酸（2）降解为相应的芳基乙腈（1）。

  DOI：

  10.1248/cpb.39.187
• 作为产物：
  描述：

  5-(4-methyl-benzylidene)-imidazolidine-2,4-dione 在 盐酸羟胺 、 水 、 sodium hydroxide 作用下， 以 水 为溶剂， 反应 15.0h， 生成 3-(p-Tolyl)-2-hydroxyiminopropionic acid
  参考文献：
  名称：

  Design, synthesis, and biological evaluation of substrate-competitive inhibitors of C-terminal Binding Protein (CtBP)

  摘要：

  C-terminal Binding Protein (CtBP) is a transcriptional co-regulator that downregulates the expression of many tumor-suppressor genes. Utilizing a crystal structure of CtBP with its substrate 4-methylthio-2-oxobutyric acid (MTOB) and NAD(+) as a guide, we have designed, synthesized, and tested a series of small molecule inhibitors of CtBP. From our first round of compounds, we identified 2-(hydroxyimino)-3-phenylpropanoic acid as a potent CtBP inhibitor (IC50 = 0.24 mu M). A structure-activity relationship study of this compound further identified the 4-chloro- (IC50 = 0.18 mu M) and 3-chloro- (IC50 = 0.17 mu M) analogues as additional potent CtBP inhibitors. Evaluation of the hydroxyimine analogues in a short-term cell growth/viability assay showed that the 4-chloro- and 3-chloro-analogues are 2-fold and 4-fold more potent, respectively, than the MTOB control. A functional cellular assay using a CtBP-specific transcriptional readout revealed that the 4-chloro- and 3-chloro-hydroxyimine analogues were able to block CtBP transcriptional repression activity. This data suggests that substrate-competitive inhibition of CtBP dehydrogenase activity is a potential mechanism to reactivate tumor-suppressor gene expression as a therapeutic strategy for cancer. (C) 2016 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2016.04.037

文献信息

• Synthesis of the Marine Bromotyrosine Psammaplin F and Crystal Structure of a Psammaplin A Analogue
  作者：Qianjiao Yang、Dan Liu、Deyang Sun、Sen Yang、Guodong Hu、Zuti Wu、Linxiang Zhao

  DOI：10.3390/molecules15128784

  日期：——

  Psammaplin F, an unsymmetrical disulfide bromotyrosine, was isolated from the sponge Pseudoceratina purpurea in 2003. We reported here the first total synthesis of psammaplin F in 12% overall yield by employing Cleland’s reagent reduction as key step. The longest linear synthetic sequence starting from 3-bromo-4-hydroxybenzaldehyde and hydantoin was seven steps. In addition, a detailed X-ray crystal structure analysis of psammaplin A analogue 8b is given for the first time.

  在2003年，从海绵Pseudoceratina purpurea中分离出了不对称二硫化物溴酪氨酸Psammaplin F。我们在这里报告了Psammaplin F的首次总合成，整体产率为12%，关键步骤采用了Cleland试剂还原。从3-溴-4-羟基苯甲醛和氢噻嗪开始的最长线性合成序列为七步。此外，首次提供了Psammaplin A类似物8b的详细X射线晶体结构分析。
• An improved method for the synthesis of arylacetonitriles from 3-aryl-2-hydroxyiminopropionic acids using 1,1'-oxalyldiimidazole.
  作者：Tokujiro KITAGAWA、Megumi KAWAGUCHI、Misuzu IKIUCHI

  DOI：10.1248/cpb.39.187

  日期：——

  1, 1'-Oxalyldiimidazole (ODI, 3) is a useful reagent for the degradation of 3-aryl-2-hydroxyiminopropionic acids (2) into the corresponding arylacetonitriles (1) under essentially neutral conditions.

  1，1'-草二亚胺（ODI，3）是一种有效的试剂，可在基本中性条件下将3-芳基-2-羟基亚胺丙酸（2）降解为相应的芳基乙腈（1）。
• Design, synthesis, and biological evaluation of substrate-competitive inhibitors of C-terminal Binding Protein (CtBP)
  作者：Sudha Korwar、Benjamin L. Morris、Hardik I. Parikh、Robert A. Coover、Tyler W. Doughty、Ian M. Love、Brendan J. Hilbert、William E. Royer、Glen E. Kellogg、Steven R. Grossman、Keith C. Ellis

  DOI：10.1016/j.bmc.2016.04.037

  日期：2016.6

  C-terminal Binding Protein (CtBP) is a transcriptional co-regulator that downregulates the expression of many tumor-suppressor genes. Utilizing a crystal structure of CtBP with its substrate 4-methylthio-2-oxobutyric acid (MTOB) and NAD(+) as a guide, we have designed, synthesized, and tested a series of small molecule inhibitors of CtBP. From our first round of compounds, we identified 2-(hydroxyimino)-3-phenylpropanoic acid as a potent CtBP inhibitor (IC50 = 0.24 mu M). A structure-activity relationship study of this compound further identified the 4-chloro- (IC50 = 0.18 mu M) and 3-chloro- (IC50 = 0.17 mu M) analogues as additional potent CtBP inhibitors. Evaluation of the hydroxyimine analogues in a short-term cell growth/viability assay showed that the 4-chloro- and 3-chloro-analogues are 2-fold and 4-fold more potent, respectively, than the MTOB control. A functional cellular assay using a CtBP-specific transcriptional readout revealed that the 4-chloro- and 3-chloro-hydroxyimine analogues were able to block CtBP transcriptional repression activity. This data suggests that substrate-competitive inhibition of CtBP dehydrogenase activity is a potential mechanism to reactivate tumor-suppressor gene expression as a therapeutic strategy for cancer. (C) 2016 Elsevier Ltd. All rights reserved.