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3-(2-amino-6-(benzyloxy)-9H-purin-8-yl)propanoic acid | 1292801-96-7

中文名称
——
中文别名
——
英文名称
3-(2-amino-6-(benzyloxy)-9H-purin-8-yl)propanoic acid
英文别名
——
3-(2-amino-6-(benzyloxy)-9H-purin-8-yl)propanoic acid化学式
CAS
1292801-96-7
化学式
C15H15N5O3
mdl
——
分子量
313.316
InChiKey
DPIPMDMABYODOO-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):
    1.53
  • 重原子数:
    23.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    127.01
  • 氢给体数:
    3.0
  • 氢受体数:
    6.0

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:
    methyl 3-(2-amino-6-(benzyloxy)-9H-purin-8-yl)propanoate 在 potassium hydroxide 、 溶剂黄146 作用下, 以 甲醇 为溶剂, 以76%的产率得到3-(2-amino-6-(benzyloxy)-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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