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3-(4-methoxypyridin-3-yl)propionicacid | 1171923-11-7

中文名称
——
中文别名
——
英文名称
3-(4-methoxypyridin-3-yl)propionicacid
英文别名
3-(4-Methoxypyridin-3-yl)propanoic acid;3-(4-methoxypyridin-3-yl)propanoic acid
3-(4-methoxypyridin-3-yl)propionicacid化学式
CAS
1171923-11-7
化学式
C9H11NO3
mdl
——
分子量
181.191
InChiKey
MFVWUQGKUKKNFB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    59.4
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-(bis[tert-butoxycarbonyl]amino)-6-amino-2-methylquinoline 、 3-(4-methoxypyridin-3-yl)propionicacidN,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 生成 N-(4-amino-2-methylquinolin-6-yl)-3-(4-methoxypyridin-3-yl)propionamide
    参考文献:
    名称:
    Small molecule inhibitors of anthrax lethal factor toxin
    摘要:
    This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.11.009
  • 作为产物:
    描述:
    4-甲氧基-3-吡啶甲醛 在 5%-palladium/activated carbon 、 potassium tert-butylate氢气 、 potassium hydroxide 作用下, 以 四氢呋喃甲醇乙酸乙酯 为溶剂, 60.0 ℃ 、262.01 kPa 条件下, 反应 65.75h, 生成 3-(4-methoxypyridin-3-yl)propionicacid
    参考文献:
    名称:
    Small molecule inhibitors of anthrax lethal factor toxin
    摘要:
    This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.11.009
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文献信息

  • Small molecule inhibitors of anthrax lethal factor toxin
    作者:John D. Williams、Atiyya R. Khan、Steven C. Cardinale、Michelle M. Butler、Terry L. Bowlin、Norton P. Peet
    DOI:10.1016/j.bmc.2013.11.009
    日期:2014.1
    This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds. (C) 2013 Elsevier Ltd. All rights reserved.
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