sodium O-3-methoxy-2-((Z)-octadec-9-enyloxy)propyl O-hydrogen phosphorothioate | 1426539-20-9

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 甘油脂
• 英文名称: sodium O-3-methoxy-2-((Z)-octadec-9-enyloxy)propyl O-hydrogen phosphorothioate
• CAS: 1426539-20-9
• 化学式: C₂₂H₄₄O₅PS*Na
• 分子量: 474.618
• InChiKey: VTLZHAWKWTYBNA-GMFCBQQYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  2.65
• 重原子数：
  30.0
• 可旋转键数：
  22.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  70.98
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  在 吡啶 、 二硫化碳 、 N,O-双三甲硅基乙酰胺 、 sulfur 、 叔丁胺 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 2.0h， 生成 sodium O-3-methoxy-2-((Z)-octadec-9-enyloxy)propyl O-hydrogen phosphorothioate
  参考文献：
  名称：

  Phosphorothioate analogs of sn-2 radyl lysophosphatidic acid (LPA): Metabolically stabilized LPA receptor agonists

  摘要：

  We describe an efficient synthesis of metabolically stabilized sn-2 radyl phosphorothioate analogs of lysophosphatidic acid (LPA), and the determination of the agonist activity of each analog for the six LPA receptors (LPA(1-6)) using a recently developed TGF alpha shedding assay. In general, the sn-2 radyl OMPT analogs showed similar agonist activities to the previous 1-oleoyl-2-O-methyl-glycerophosphothioate (sn-1 OMPT) analogs for LPA(1-6) receptors. In most cases, the sn-2 radyl-OMPT analogs were more potent agonists than LPA itself. Most importantly, sn-2 alkyl OMPT analogs were very potent LPA(5) and LPA(6) agonists. The availability of sn-2 radyl OPMT analogs further refines the structure-activity relationships for ligand-receptor interactions for this class of GPCRs. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.01.002