2-Methyl-3-pyridin-4-yl-1H-indol-6-ylamine | 887615-83-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 2-Methyl-3-pyridin-4-yl-1H-indol-6-ylamine
• 英文别名: 2-methyl-3-(pyridin-4-yl)-1H-indol-6-amine；2-methyl-3-pyridin-4-yl-1H-indol-6-amine
• CAS: 887615-83-0
• 化学式: C₁₄H₁₃N₃
• 分子量: 223.277
• InChiKey: AAIHLDQORIUJKB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  17
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  54.7
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-Methyl-3-pyridin-4-yl-1H-indol-6-ylamine 以 四氢呋喃 为溶剂， 生成 1-Methyl-3-(2-methyl-3-pyridin-4-yl-1H-indol-6-yl)-1-phenyl-urea
  参考文献：
  名称：

  Novel indole inhibitors of IMPDH from fragments: Synthesis and initial structure–activity relationships

  摘要：

  The elaboration of previously reported indole fragments as inhibitors of inosine monophosphate dehydrogenase (IMPDH) is described. The synthesis, in vitro inhibitory values for IMPDH II, PBMC proliferation and physicochemical properties are discussed. (C) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.01.090
• 作为产物：
  描述：

  1-benzenesulfonyl-3-bromo-2-methyl-1H-indol-6-ylamine 在 氢氧化钾 、 四(三苯基膦)钯 、 sodium carbonate 作用下， 以 甲醇 、 乙二醇二甲醚 为溶剂， 生成 2-Methyl-3-pyridin-4-yl-1H-indol-6-ylamine
  参考文献：
  名称：

  Low molecular weight indole fragments as IMPDH inhibitors

  摘要：

  The study of non-oxazole containing indole fragments as inhibitors of inosine monophosphate dehydrogenase (I MPDH) is described. The synthesis and in vitro inhibitory values for IMPDH II are discussed. (C) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.01.089

文献信息

• Low molecular weight indole fragments as IMPDH inhibitors
  作者：Rebekah E. Beevers、George M. Buckley、Natasha Davies、Joanne L. Fraser、Francis C. Galvin、Duncan R. Hannah、Alan F. Haughan、Kerry Jenkins、Stephen R. Mack、William R. Pitt、Andrew J. Ratcliffe、Marianna D. Richard、Verity Sabin、Andrew Sharpe、Sophie C. Williams

  DOI：10.1016/j.bmcl.2006.01.089

  日期：2006.5

  The study of non-oxazole containing indole fragments as inhibitors of inosine monophosphate dehydrogenase (I MPDH) is described. The synthesis and in vitro inhibitory values for IMPDH II are discussed. (C) 2006 Elsevier Ltd. All rights reserved.
• Novel indole inhibitors of IMPDH from fragments: Synthesis and initial structure–activity relationships
  作者：Rebekah E. Beevers、George M. Buckley、Natasha Davies、Joanne L. Fraser、Francis C. Galvin、Duncan R. Hannah、Alan F. Haughan、Kerry Jenkins、Stephen R. Mack、William R. Pitt、Andrew J. Ratcliffe、Marianna D. Richard、Verity Sabin、Andrew Sharpe、Sophie C. Williams

  DOI：10.1016/j.bmcl.2006.01.090

  日期：2006.5

  The elaboration of previously reported indole fragments as inhibitors of inosine monophosphate dehydrogenase (IMPDH) is described. The synthesis, in vitro inhibitory values for IMPDH II, PBMC proliferation and physicochemical properties are discussed. (C) 2006 Elsevier Ltd. All rights reserved.