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N2-acetyl-O6-methylguanine | 1061382-73-7

中文名称
——
中文别名
——
英文名称
N2-acetyl-O6-methylguanine
英文别名
N-(6-methoxy-7H-purin-2-yl)acetamide
N<sup>2</sup>-acetyl-O<sup>6</sup>-methylguanine化学式
CAS
1061382-73-7
化学式
C8H9N5O2
mdl
——
分子量
207.192
InChiKey
GKFISIKBQRNOCB-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

  • 密度:
    1.494±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.1
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    92.8
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    N2-acetyl-O6-methylguaninebeta-胸苷 在 purine nucleoside phosphorylase 、 potassium phosphate buffer 作用下, 以95%的产率得到N-[9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-methoxypurin-2-yl]acetamide
    参考文献:
    名称:
    An Enzymatic Transglycosylation of Purine Bases
    摘要:
    An enzymatic transglycosylation of purine heterocyclic bases employing readily available natural nucleosides or sugar-modified nucleosides as donors of the pentofuranose fragment and recombinant nucleoside phosphorylases as biocatalysts has been investigated. An efficient enzymatic method is suggested for the synthesis of purine nucleosides containing diverse substituents at the C6 and C2 carbon atoms. The glycosylation of N-6-benzoyladenine and N-2-acetylguanine and its O-6-derivatives is not accompanied by deacylation of bases.
    DOI:
    10.1080/15257770701506343
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文献信息

  • An Enzymatic Transglycosylation of Purine Bases
    作者:Jarkko Roivainen、Tatiana Elizarova、Seppo Lapinjoki、Igor A. Mikhailopulo、Roman S. Esipov、Anatoly I. Miroshnikov
    DOI:10.1080/15257770701506343
    日期:2007.11.26
    An enzymatic transglycosylation of purine heterocyclic bases employing readily available natural nucleosides or sugar-modified nucleosides as donors of the pentofuranose fragment and recombinant nucleoside phosphorylases as biocatalysts has been investigated. An efficient enzymatic method is suggested for the synthesis of purine nucleosides containing diverse substituents at the C6 and C2 carbon atoms. The glycosylation of N-6-benzoyladenine and N-2-acetylguanine and its O-6-derivatives is not accompanied by deacylation of bases.
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