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3'-deoxy-3'-fluoroxylo C | 26563-01-9

中文名称
——
中文别名
——
英文名称
3'-deoxy-3'-fluoroxylo C
英文别名
xylo-F C;1-(3-deoxy-3-fluoro-β-D-xylofuranosyl)cytosine;4-amino-1-(3-fluoro-β-D-3-deoxy-xylofuranosyl)-1H-pyrimidin-2-one;4-Amino-1-((2R,3S,4R,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one;4-amino-1-[(2R,3S,4R,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
3'-deoxy-3'-fluoroxylo C化学式
CAS
26563-01-9
化学式
C9H12FN3O4
mdl
——
分子量
245.21
InChiKey
PKOBNLOZXOHYOP-PXBUCIJWSA-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):
    -1.7
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    108
  • 氢给体数:
    3
  • 氢受体数:
    5

反应信息

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文献信息

  • Anti-HCV nucleoside derivatives
    申请人:——
    公开号:US20030008841A1
    公开(公告)日:2003-01-09
    The present invention comprises novel and known purine and pyrimidine nucleoside derivatives which have been discovered to be active against hepatitis C virus (HCV). The use of these derivatives for the treatment of HCV infection is claimed as are the novel nucleoside derivatives disclosed herein.
    本发明涉及新颖和已知的嘌呤和嘧啶核苷衍生物,已发现这些衍生物对丙型肝炎病毒(HCV)具有活性。本发明声明利用这些衍生物治疗HCV感染,以及本文所披露的新颖核苷衍生物。
  • ANTIVIRAL PHOSPHONATE ANALOGS
    申请人:Boojamra Constantine G.
    公开号:US20090275535A1
    公开(公告)日:2009-11-05
    The invention is related to phosphorus substituted compounds with antiviral activity, compositions containing such compounds, and therapeutic methods that include the administration of such compounds, as well as to processes and intermediates useful for preparing such compounds.
    这项发明涉及具有抗病毒活性的磷取代化合物,包含这种化合物的组合物以及包括给予这种化合物的治疗方法,还包括用于制备这种化合物的过程和中间体。
  • NUCLEOSIDE DERIVATIVES FOR THE TREATMENT OF HEPATITIS C
    申请人:F. HOFFMANN-LA ROCHE AG
    公开号:EP1315736A2
    公开(公告)日:2003-06-04
  • Nucleoside Phosphonate Analogs
    申请人:Boojamra Constantine G.
    公开号:US20110071101A1
    公开(公告)日:2011-03-24
    The invention is related to phosphorus substituted nucleoside compounds and therapeutic methods that include the administration of such compounds, as well as to processes and intermediates useful for preparing such compounds.
  • MODIFIED RNAi AGENTS
    申请人:ALNYLAM PHARMACEUTICALS, INC.
    公开号:US20150197746A1
    公开(公告)日:2015-07-16
    One aspect of the present invention relates to double-stranded RNAi (dsRNA) duplex agent capable of inhibiting the expression of a target gene in vivo. The dsRNA duplex comprises one or more xylo modifications in one or both strand. Other aspects of the invention relates to pharmaceutical compositions comprising these dsRNA agents suitable for in vivo therapeutic use, and methods of inhibiting the expression of a target gene by administering these dsRNA agents, e.g., for the treatment of various disease conditions.
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