4-chlorothiophene-3-carboaldehyde | 36155-89-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-chlorothiophene-3-carboaldehyde
• 英文别名: 4-Chlorothiophene-3-carbaldehyde
• CAS: 36155-89-2
• 化学式: C₅H₃ClOS
• mdl: MFCD04971312
• 分子量: 146.597
• InChiKey: MXDGWCVDBWFTMC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  8
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  45.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-chlorothiophene-3-carboaldehyde 在 sodium hydroxide 、 potassium permanganate 作用下， 生成 4-chlorothiophene-3-carboxylic acid
  参考文献：
  名称：

  Novel thienopyrrole glycogen phosphorylase inhibitors: Synthesis, in vitro SAR and crystallographic studies

  摘要：

  Two series of novel thienopyrrole inhibitors of recombinant human liver glycogen phosphorylase a (GPa) which are effective in reducing glucose output from rat hepatocytes are described. Representative compounds have been shown to bind at the dimer interface site of the rabbit muscle enzyme by X-ray crystallography.

  DOI：

  10.1016/j.bmcl.2006.08.047

文献信息

• Halogen-substituted heterocyclic compound
  申请人：UBE INDUSTRIES, LTD.

  公开号：US10000463B2

  公开（公告）日：2018-06-19

  A novel α-halogen-substituted thiophene compound or a pharmacologically acceptable salt thereof, which has a potent LPA receptor-antagonist activity and is useful as a medicament is provided.

  本研究提供了一种新型α-卤代噻吩化合物或其药理学上可接受的盐，该化合物具有强效的 LPA 受体拮抗剂活性，可用作药物。
• HALOGEN-SUBSTITUTED HETEROCYCLIC COMPOUND
  申请人：UBE INDUSTRIES, LTD.

  公开号：EP2940013B1

  公开（公告）日：2018-02-21
• HALOGEN-SUBSTITUTED HETEROCYCLIC COMPOUND USEFUL FOR THE TREATMENT OF DISEASES CAUSED BY LPA.
  申请人：UBE INDUSTRIES, LTD.

  公开号：EP3360869B1

  公开（公告）日：2020-07-29
• Novel thienopyrrole glycogen phosphorylase inhibitors: Synthesis, in vitro SAR and crystallographic studies
  作者：Paul R.O. Whittamore、Matthew S. Addie、Stuart N.L. Bennett、Alan M. Birch、Michael Butters、Linda Godfrey、Peter W. Kenny、Andrew D. Morley、Paul M. Murray、Nikos G. Oikonomakos、Ludovic R. Otterbein、Andrew D. Pannifer、Jeremy S. Parker、Kristy Readman、Pawel S. Siedlecki、Paul Schofield、Andy Stocker、Melvyn J. Taylor、Linda A. Townsend、David P. Whalley、Jennifer Whitehouse

  DOI：10.1016/j.bmcl.2006.08.047

  日期：2006.11

  Two series of novel thienopyrrole inhibitors of recombinant human liver glycogen phosphorylase a (GPa) which are effective in reducing glucose output from rat hepatocytes are described. Representative compounds have been shown to bind at the dimer interface site of the rabbit muscle enzyme by X-ray crystallography.