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3-(2-amino-6-((4-(aminomethyl)benzyl)oxy)-9H-purin-8-yl)propanoic acid | 1292802-13-1

中文名称
——
中文别名
——
英文名称
3-(2-amino-6-((4-(aminomethyl)benzyl)oxy)-9H-purin-8-yl)propanoic acid
英文别名
——
3-(2-amino-6-((4-(aminomethyl)benzyl)oxy)-9H-purin-8-yl)propanoic acid化学式
CAS
1292802-13-1
化学式
C16H18N6O3
mdl
——
分子量
342.357
InChiKey
GNUOMPPNEBXCPR-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

物化性质

  • 沸点:
    764.2±70.0 °C(Predicted)
  • 密度:
    1.472±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.99
  • 重原子数:
    25.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    153.03
  • 氢给体数:
    4.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Real-Time Measurements of Protein Dynamics Using Fluorescence Activation-Coupled Protein Labeling Method
    摘要:
    We present a fluorescence activation-coupled protein labeling (FAPL) method, which employs small-molecular probes that exhibit almost no basal fluorescence but acquire strong fluorescence upon covalent binding to tag-proteins. This method enables real-time imaging of protein labeling without any washout process and is uniquely suitable for real-time imaging of protein dynamics on the cell surface. We applied this method to address the spatiotemporal dynamics of the EGF receptor during cell migration.
    DOI:
    10.1021/ja200225m
  • 作为产物:
    描述:
    6-(4-(aminomethyl)benzyloxy)pyrimidine-2,4-diaminepotassium carbonate溶剂黄146N,N-二异丙基乙胺 、 potassium hydroxide 、 sodium nitrite 作用下, 以 甲醇乙醇丙酮 为溶剂, 反应 7.5h, 生成 3-(2-amino-6-((4-(aminomethyl)benzyl)oxy)-9H-purin-8-yl)propanoic acid
    参考文献:
    名称:
    Real-Time Measurements of Protein Dynamics Using Fluorescence Activation-Coupled Protein Labeling Method
    摘要:
    We present a fluorescence activation-coupled protein labeling (FAPL) method, which employs small-molecular probes that exhibit almost no basal fluorescence but acquire strong fluorescence upon covalent binding to tag-proteins. This method enables real-time imaging of protein labeling without any washout process and is uniquely suitable for real-time imaging of protein dynamics on the cell surface. We applied this method to address the spatiotemporal dynamics of the EGF receptor during cell migration.
    DOI:
    10.1021/ja200225m
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