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[1',2',3',4',5',6'-13C6]-(β-D-glucopyranosyl)-(6-13C,1,3,4-15N3)-cytosine | 373366-02-0

中文名称
——
中文别名
——
英文名称
[1',2',3',4',5',6'-13C6]-(β-D-glucopyranosyl)-(6-13C,1,3,4-15N3)-cytosine
英文别名
4-(15N)azanyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxy(113C)methyl)(2,3,4,5,6-13C5)oxan-2-yl](613C,1,3-15N2)pyrimidin-2-one
[1',2',3',4',5',6'-13C6]-(β-D-glucopyranosyl)-(6-13C,1,3,4-15N3)-cytosine化学式
CAS
373366-02-0
化学式
C10H15N3O6
mdl
——
分子量
283.149
InChiKey
YYUQXKHCNLFJNF-IXJAFUFMSA-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):
    -2.7
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    149
  • 氢给体数:
    5
  • 氢受体数:
    6

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    苯甲酰氯[1',2',3',4',5',6'-13C6]-(β-D-glucopyranosyl)-(6-13C,1,3,4-15N3)-cytosine三甲基氯硅烷 、 ammonium chloride 作用下, 以 吡啶甲醇 为溶剂, 反应 22.0h, 以90%的产率得到N4-benzoyl-[1',2',3',4',5',6'-13C6]-(β-D-glucopyranosyl)-(6-13C,1,3,4-15N3)-cytosine
    参考文献:
    名称:
    A Short Path Synthesis of [13C/15N] Multilabeled Pyrimidine Nucleosides Starting from Glucopyranose Nucleosides
    摘要:
    The synthesis of fully [C-13/N-15] labeled pyrimidine nucleosides has been achieved from C-13-glucose and labeled nucleobases. The reaction scheme leads directly to the protected nucleosides without the need for the inversion of configuration of C-3 of C-13-glucose. This was achieved by an oxitative ring-opening reaction removing the carbon with the wrong configuration.
    DOI:
    10.1021/jo0205098
  • 作为产物:
    描述:
    [(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-[4-(benzoyl(15N)amino)-2-oxo(613C,1,3-15N2)pyrimidin-1-yl](2,3,4,5,6-13C5)oxan-2-yl](113C)methyl acetate 在 作用下, 以 甲醇 为溶剂, 生成 [1',2',3',4',5',6'-13C6]-(β-D-glucopyranosyl)-(6-13C,1,3,4-15N3)-cytosine
    参考文献:
    名称:
    A Short Path Synthesis of [13C/15N] Multilabeled Pyrimidine Nucleosides Starting from Glucopyranose Nucleosides
    摘要:
    The synthesis of fully [C-13/N-15] labeled pyrimidine nucleosides has been achieved from C-13-glucose and labeled nucleobases. The reaction scheme leads directly to the protected nucleosides without the need for the inversion of configuration of C-3 of C-13-glucose. This was achieved by an oxitative ring-opening reaction removing the carbon with the wrong configuration.
    DOI:
    10.1021/jo0205098
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文献信息

  • A Short Path Synthesis of [<sup>13</sup>C/<sup>15</sup>N] Multilabeled Pyrimidine Nucleosides Starting from Glucopyranose Nucleosides
    作者:Irene M. Lagoja、Sylvie Pochet、Valerie Boudou、Roy Little、Eveline Lescrinier、Jef Rozenski、Piet Herdewijn
    DOI:10.1021/jo0205098
    日期:2003.3.1
    The synthesis of fully [C-13/N-15] labeled pyrimidine nucleosides has been achieved from C-13-glucose and labeled nucleobases. The reaction scheme leads directly to the protected nucleosides without the need for the inversion of configuration of C-3 of C-13-glucose. This was achieved by an oxitative ring-opening reaction removing the carbon with the wrong configuration.
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