(3,5-dimethylpyridin-2-yl)methyl methanesulfonate | 1260021-58-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: (3,5-dimethylpyridin-2-yl)methyl methanesulfonate
• 英文别名: (3,5-Dimethylpyridin-2-yl)methyl methanesulfonate
• CAS: 1260021-58-6
• 化学式: C₉H₁₃NO₃S
• 分子量: 215.273
• InChiKey: UDXOSYWEOCTSNA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  64.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (3,5-dimethylpyridin-2-yl)methyl methanesulfonate 、 (S)-methyl 3-(4-hydroxyphenyl)-2-(palmitamido)propanoate 在 18-冠醚-6 、 potassium carbonate 作用下， 以 丙酮 为溶剂， 以400 mg的产率得到(S)-methyl 3-(4-((3,5-dimethylpyridin-2-yl)methoxy)phenyl)-2-palmitamidopropanoate
  参考文献：
  名称：

  Synthesis and structure–activity relationships of tyrosine-based inhibitors of autotaxin (ATX)

  摘要：

  Autotaxin (ATX) is a secreted soluble enzyme that generates lysophosphatidic acid (LPA) through its lysophospholipase D activity. Because of LPA's role in neoplastic diseases, ATX is an attractive therapeutic target due to its involvement in LPA biosynthesis. Here we describe the SAR of ATX inhibitor, VPC8a202, and apply this SAR knowledge towards developing a high potency inhibitor. We found that electron density in the pyridine region greatly influences activity of our inhibitors at ATX. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.09.030
• 作为产物：
  描述：

  3,5-二甲基-2-吡啶甲醇 、 甲基磺酰氯 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 (3,5-dimethylpyridin-2-yl)methyl methanesulfonate
  参考文献：
  名称：

  Synthesis and structure–activity relationships of tyrosine-based inhibitors of autotaxin (ATX)

  摘要：

  Autotaxin (ATX) is a secreted soluble enzyme that generates lysophosphatidic acid (LPA) through its lysophospholipase D activity. Because of LPA's role in neoplastic diseases, ATX is an attractive therapeutic target due to its involvement in LPA biosynthesis. Here we describe the SAR of ATX inhibitor, VPC8a202, and apply this SAR knowledge towards developing a high potency inhibitor. We found that electron density in the pyridine region greatly influences activity of our inhibitors at ATX. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.09.030

文献信息

• Synthesis and structure–activity relationships of tyrosine-based inhibitors of autotaxin (ATX)
  作者：James E. East、Andrew J. Kennedy、Jose L. Tomsig、Alexandra R. De Leon、Kevin R. Lynch、Timothy L. Macdonald

  DOI：10.1016/j.bmcl.2010.09.030

  日期：2010.12

  Autotaxin (ATX) is a secreted soluble enzyme that generates lysophosphatidic acid (LPA) through its lysophospholipase D activity. Because of LPA's role in neoplastic diseases, ATX is an attractive therapeutic target due to its involvement in LPA biosynthesis. Here we describe the SAR of ATX inhibitor, VPC8a202, and apply this SAR knowledge towards developing a high potency inhibitor. We found that electron density in the pyridine region greatly influences activity of our inhibitors at ATX. (C) 2010 Elsevier Ltd. All rights reserved.