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3-(β-D-ribofuranosyl)-6-pentyl-2,3-dihydrofurano[2,3-d]pyrimidin-2-one | 1058167-76-2

中文名称
——
中文别名
——
英文名称
3-(β-D-ribofuranosyl)-6-pentyl-2,3-dihydrofurano[2,3-d]pyrimidin-2-one
英文别名
——
3-(β-D-ribofuranosyl)-6-pentyl-2,3-dihydrofurano[2,3-d]pyrimidin-2-one化学式
CAS
1058167-76-2
化学式
C16H22N2O6
mdl
——
分子量
338.36
InChiKey
LBKSGMNEHKJECO-RGCMKSIDSA-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):
    0.33
  • 重原子数:
    24.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    117.95
  • 氢给体数:
    3.0
  • 氢受体数:
    8.0

反应信息

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文献信息

  • New furano- and pyrrolo[2,3-d]pyrimidine nucleosides and their 5′-O-triphosphates: Synthesis and biological properties
    作者:M. A. Ivanov、A. V. Ivanov、I. A. Krasnitskaya、O. A. Smirnova、I. L. Karpenko、E. F. Belanov、V. S. Prasolov、V. L. Tunitskaya、L. A. Alexandrova
    DOI:10.1134/s1068162008050099
    日期:2008.9
    Bicyclic furano[2,3-d]pyrimidine ribonucleosides were synthesized by Pd(0)-and CuI-catalyzed coupling of 5-iodouridine with terminal alkynes. The treatment of the resulting nucleosides with ammonia or methylamine solution in aqueous alcohol resulted in pyrrolo-and N-7-methylpyrrolo[2,3-d]pyrimidine nucleosides. 5'-O-Triphosphates of bicyclic nucleosides were obtained by the treatment of the nucleosides with POCl3 in the presence of a "proton sponge." The 5'-O-triphosphates are not substrates for HCV RNA-dependent RNA polymerase, but are effective substrates for HCV RNA helicase/NTPase and did not inhibit ATP hydrolysis. Only 3-(beta-D-ribofuranosyl)-6-decyl-2,3-dihydrofuro-[2,3-d]pyrimidin-2-one showed a moderate anti-HCV activity in the HCV replicon system and efficiently inhibited replication of bovine viral diarrhea virus (BVDV) in KCT-cells, other compounds being inactive. None of the compounds were cytotoxic within the tested range of concentrations.
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