3-(2-甲氧基-苯基)-丁酸 | 104216-85-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 苯丙酸
• 中文名称: 3-(2-甲氧基-苯基)-丁酸
• 英文名称: 3-(o-Methoxy-phenyl)-buttersaeure
• 英文别名: 3-(2-methoxy-phenyl)-butyric acid；3-(2-Methoxy-phenyl)-buttersaeure；3-(2-Methoxyphenyl)butanoic acid
• CAS: 104216-85-5
• 化学式: C₁₁H₁₄O₃
• mdl: MFCD00622132
• 分子量: 194.23
• InChiKey: UKDWWUNLNDAURT-UHFFFAOYSA-N

物化性质

• 熔点：
  47 °C
• 沸点：
  171 °C(Press: 11 Torr)
• 密度：
  1.112±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.363
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-(2-甲氧基-苯基)-丁酸 在 盐酸 、 氢氧化钾 、 氯化亚砜 、 PPA 、 氢碘酸 、 sulfur 、 溶剂黄146 、 汞 、 锌 作用下， 以 甲苯 为溶剂， 生成 8-甲基萘-1-醇
  参考文献：
  名称：

  448.在芳构化反应中消除非角烷基。第四部分

  摘要：

  DOI：

  10.1039/jr9600002230
• 作为产物：
  描述：

  methyl 3-(2-methoxyphenyl)but-2-enoate 在 palladium 10% on activated carbon 、 氢气 、 potassium hydroxide 作用下， 以 甲醇 、 乙醇 、 水 为溶剂， 反应 1.0h， 生成 3-(2-甲氧基-苯基)-丁酸
  参考文献：
  名称：

  Development of alkyl glycerone phosphate synthase inhibitors: Structure-activity relationship and effects on ether lipids and epithelial-mesenchymal transition in cancer cells

  摘要：

  In aggressive tumors, alkylglyceronephosphate synthase (AGPS) controls cellular ether phospholipid utilization and metabolism to promote cancer cell proliferation and motility. SAR studies on the first-in-class AGPS inhibitor 1, discovered by our group, led to the 2,6-difluoro analog 2i which showed higher binding affinity than 1 in vitro. In 231MFP cancer cells, 2i reduced ether lipids levels and cell migration rate. When tested in PC-3 and MDA-MB-231 cancer cells, 2i specifically impaired epithelial to mesenchymal transition (EMT) by modulating E-cadherin, Snail and MMP2 expression levels. Moreover, the combination of siRNAs against AGPS and 2i provided no additive effect, confirming that the modulation of 2i on EMT specifically relies on AGPS inhibition. Finally, this compound also affected cancer cell proliferation especially in MDA-MB-231 cells expressing higher AGPS level, whereas it provided negligible effects on MeT5A, a non-tumorigenic cell line, thus showing cancer specificity. (C) 2018 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2018.11.050

文献信息

• Novel Tetrahydropyridothiophenes
  申请人：Pekari Klaus

  公开号：US20080260749A1

  公开（公告）日：2008-10-23

  Compounds of a certain formula (I) in which Ra and Rb have the meanings indicated in the description, are novel effective compounds with anti-proliferative and apoptosis inducing activity.

  具有某种化学式（I）的化合物，在其中Ra和Rb具有描述中指示的含义，是具有抗增殖和诱导凋亡活性的新型有效化合物。
• Tetrahydropyridothiophenes As Antripoliferative Agents For The Treatment Of Cancer
  申请人：Pekari Klaus

  公开号：US20090252706A1

  公开（公告）日：2009-10-08

  The invention relates to compounds of formula (I) wherein Ra is —C(O)ORI, in which R1 is 1-7C-alkyl. 3-7C-cycloakyl, 1-7C-alkyl substituted by Raa, or 2-7C-alkyl substituted by Rab and Rac on different carbon atoms, Rb is -T-Q, in which T is 1-6C-alkylene or 3-7C-cycloalkylene, and Q is substituted by Rba and Rbb and Rbc, and is phenyl, which are useful for the therapy of hyperproliferative diseases, in particular human cancer.

  本发明涉及公式（I）的化合物，其中Ra为—C（O）ORI，其中R1为1-7C-烷基，3-7C-环烷基，1-7C-烷基，被Raa取代的2-7C-烷基或在不同碳原子上被Rab和Rac取代的2-7C-烷基，Rb为-T-Q，其中T为1-6C-烷基或3-7C-环烷基，Q被Rba，Rbb和Rbc取代，并且是苯基，这些化合物对于治疗增生性疾病，特别是人类癌症具有用处。
• NOVEL TETRAHYDROPYRIDOTHIOPHENES
  申请人：Pekari Klaus

  公开号：US20090257977A1

  公开（公告）日：2009-10-15

  Compounds of a certain formula (I), in which Ra and Rb have the meanings indicated in the description, are novel effective compounds with anti-proliferative and apoptosis inducing activity.

  某一公式（I）的化合物，其中Ra和Rb的含义如说明书所示，是具有抗增殖和诱导细胞凋亡活性的新型有效化合物。
• Tetrahydropyridothiophenes as Antiproliferative Agents for the Treatment of Cancer
  申请人：Pekari Klaus

  公开号：US20090098133A1

  公开（公告）日：2009-04-16

  Compounds of a certain formula (I), in which Ra and Rb have the meanings indicated in the description, are novel effective compounds with anti-proliferative and apoptosis inducing activity.

  某一公式（I）的化合物，其中Ra和Rb具有描述中指示的含义，是一种具有抗增殖和诱导凋亡活性的新型有效化合物。
• TETRAHYDROBENZOTHIOPHENE DERIVATIVES
  申请人：Bartels Bjorn

  公开号：US20110044938A1

  公开（公告）日：2011-02-24

  Compounds of a certain formula I, in which Ra and Rb have the meanings indicated in the description, are novel effective compounds with anti-proliferative and apoptosis inducing activity.

  某一公式I的化合物，其中Ra和Rb具有说明中所示的含义，是一种新颖的有效化合物，具有抗增殖和诱导凋亡活性。