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9-<(1-benzyloxy-3-diethylphosphono)-1-propyloxymethyl>guanine | 156569-09-4

中文名称
——
中文别名
——
英文名称
9-<(1-benzyloxy-3-diethylphosphono)-1-propyloxymethyl>guanine
英文别名
——
9-<(1-benzyloxy-3-diethylphosphono)-1-propyloxymethyl>guanine化学式
CAS
156569-09-4
化学式
C21H30N5O6P
mdl
——
分子量
479.473
InChiKey
MQRQHOQVBNZXOD-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):
    2.92
  • 重原子数:
    33.0
  • 可旋转键数:
    14.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    143.58
  • 氢给体数:
    2.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    描述:
    9-<(1-benzyloxy-3-diethylphosphono)-1-propyloxymethyl>guaninesodium hydroxide 作用下, 反应 2.0h, 以582 mg的产率得到9-<(1-benzyloxymethyl-3-ethylphosphono)-1-propyloxymethyl>guanine monosodium salt
    参考文献:
    名称:
    Synthesis of Acyclonucleoside Phosphonates as Antiviral Agents Against Cytomegalovirus
    摘要:
    Phosphonic acid analogs of ACV and DHPG that are isosteric with ACV phosphate and DHPG phosphate have been synthesized and evaluated for antiviral activity against human, murine. and guinea pig strains of cytomegalovirus. The phosphonates showed high activity against all of the strains. They were also evaluated against a DHPG resistant strain of human cytomegalovirus. Although the activity dropped considerably, significant antiviral activity was still evident.
    DOI:
    10.1080/15257779408013261
  • 作为产物:
    参考文献:
    名称:
    Synthesis of Acyclonucleoside Phosphonates as Antiviral Agents Against Cytomegalovirus
    摘要:
    Phosphonic acid analogs of ACV and DHPG that are isosteric with ACV phosphate and DHPG phosphate have been synthesized and evaluated for antiviral activity against human, murine. and guinea pig strains of cytomegalovirus. The phosphonates showed high activity against all of the strains. They were also evaluated against a DHPG resistant strain of human cytomegalovirus. Although the activity dropped considerably, significant antiviral activity was still evident.
    DOI:
    10.1080/15257779408013261
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