methyl 4-[(Z)-3-oxoprop-1-enyl]sulfanylbutanoate | 125197-82-2

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: methyl 4-[(Z)-3-oxoprop-1-enyl]sulfanylbutanoate
• CAS: 125197-82-2
• 化学式: C₈H₁₂O₃S
• 分子量: 188.247
• InChiKey: DAVREXXRZZMQCL-CLTKARDFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.39
• 重原子数：
  12.0
• 可旋转键数：
  6.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  43.37
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  Γ--硫代丁内酯 、 丙炔醛 生成 methyl 4-[(Z)-3-oxoprop-1-enyl]sulfanylbutanoate
  参考文献：
  名称：

  HANKO, RUDOLF;HAMMOND, MICHAEL D.;FRUCHTMANN, ROMANIS;PFITZNER, JOERG;PLA+, J. MED. CHEM., 33,(1990) N, C. 1163-1170

  摘要：

  DOI：

文献信息

• Design, synthesis, and 5-lipoxygenase-inhibiting properties of 1-thio-substituted butadienes
  作者：Rudolf Hanko、Michael D. Hammond、Romanis Fruchtmann、Joerg Pfitzner、Graham A. Place

  DOI：10.1021/jm00166a013

  日期：1990.4

  The synthesis of novel 1-thio-substituted butadienes, designed as mechanism-based 5-lipoxygenase inhibitors, is described. The structure of these compounds closely resembles a proposed high-energy intermediate during the lipoxygenation of arachidonic acid. They demonstrate 5-lipoxygenase inhibition in vitro and in vivo. The most potent compound is 15a with an IC50 of 1.8 microM in vitro. LTC4 release was inhibited by 80% after intraperitoneal administration of 15c at a dose of 2 mg/kg.