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1-(6-oxo-6,9-dihydro-1H-purin-2-yl)urea | 1133814-30-8

中文名称
——
中文别名
——
英文名称
1-(6-oxo-6,9-dihydro-1H-purin-2-yl)urea
英文别名
(6-Oxo-1,7-dihydropurin-2-yl)urea;(6-oxo-1,7-dihydropurin-2-yl)urea
1-(6-oxo-6,9-dihydro-1H-purin-2-yl)urea化学式
CAS
1133814-30-8
化学式
C6H6N6O2
mdl
——
分子量
194.153
InChiKey
MKGBVDDNOLVUGJ-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):
    -1.5
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    125
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

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文献信息

  • Integrated electrode and cell immobilization device equipped with the integrated electrode
    申请人:——
    公开号:US20040209352A1
    公开(公告)日:2004-10-21
    An integrated electrode capable of immobilizing an isolated cell and/or a cultured cell on the electrode without giving any damage to its cell membrane, and capable of detecting an electrophysiological activity of the immobilized cell with sufficient sensitivity is provided. An integrated electrode having a substrate equipped with at least one electric conductor, and a wiring part which leads an electrical signal out from the aforementioned electric conductor, in which the integrated electrode can detect an electrical signal resulting from an electrophysiological change of a cell immobilized on the surface of the aforementioned electric conductor, and at least a part of the surface of the aforementioned electric conductor is coated with a dielectric material, with the aforementioned dielectric material being a positively charged polymer material, and the aforementioned cell being an isolated cell and/or a cultured cell.
    本发明提供了一种集成电极,它能将离体细胞和/或培养细胞固定在电极上而不损伤其细胞膜,并能以足够的灵敏度检测被固定细胞的电生理活动。一种集成电极,其基板上装有至少一个电导体,以及一个将电信号从上述电导体引出的接线部分,其中集成电极可检测固定在上述电导体表面的细胞的电生理变化产生的电信号,上述电导体表面的至少一部分涂有介电材料,上述介电材料为带正电荷的聚合物材料,上述细胞为离体细胞和/或培养细胞。
  • Efficient Synthesis of 2-Ureaguanines via the in situ Reactions of 2-Isocyanatopurines with Amines
    作者:Eric Marsault、Antoine Le Roux
    DOI:10.1055/s-0033-1338482
    日期:——
    The synthesis of 2-ureaguanines is reported. The preparation involves a suitably protected intermediate, formation of a 2-isocyanatopurine and in situ trapping with a diverse range of amines followed by double deprotection. This is the first application of 2-isocyanatopurines for the synthesis of 2-ureaguanines.
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