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4-(cyclopropylamino)-6-[N-3-(trimethylacetyloxypropoxy)amino]-5-nitropyrimidine

中文名称
——
中文别名
——
英文名称
4-(cyclopropylamino)-6-[N-3-(trimethylacetyloxypropoxy)amino]-5-nitropyrimidine
英文别名
3-[[6-(Cyclopropylamino)-5-nitropyrimidin-4-yl]amino]oxypropyl 2,2-dimethylpropanoate;3-[[6-(cyclopropylamino)-5-nitropyrimidin-4-yl]amino]oxypropyl 2,2-dimethylpropanoate
4-(cyclopropylamino)-6-[N-3-(trimethylacetyloxypropoxy)amino]-5-nitropyrimidine化学式
CAS
——
化学式
C15H23N5O5
mdl
——
分子量
353.378
InChiKey
AGEZTIWNKHOIDD-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):
    4
  • 重原子数:
    25
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    131
  • 氢给体数:
    2
  • 氢受体数:
    9

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis and Biological Activities of New Carbaacyclonucleosides and 1′-Oxaacyclonucleosides Related to Clitocine
    摘要:
    We describe the synthesis of two series of acyclonucleosides : carbaacyclonucleosides and 1'-oxaacyclonucleosides which possess the same aglycone as clitocine 3 which is a natural nucleoside exhibiting interesting biological properties. These compounds have been obtained by condensation of 4-aminobutanol or 3-silyloxypropoxyamine with 4,6-dichloro-5-nitropyrimidine. Structural modifications have been made on the heterocyclic base and the side chain to enhance their potential activity.All these compounds have been tested against different viruses : HIV-1, HSV-1, HSV-2, CMV, VZV, EBV. The carbaacyclonucleoside 10 was associated with an anti-EBV activity (EC50 = 0.86 mu g/mL).
    DOI:
    10.1080/15257770008035008
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文献信息

  • Synthesis and Biological Activities of New Carbaacyclonucleosides and 1′-Oxaacyclonucleosides Related to Clitocine
    作者:Corinne Bacchelli、Roger Condom、Nadia Patino、Anne-Marie Aubertin
    DOI:10.1080/15257770008035008
    日期:2000.3
    We describe the synthesis of two series of acyclonucleosides : carbaacyclonucleosides and 1'-oxaacyclonucleosides which possess the same aglycone as clitocine 3 which is a natural nucleoside exhibiting interesting biological properties. These compounds have been obtained by condensation of 4-aminobutanol or 3-silyloxypropoxyamine with 4,6-dichloro-5-nitropyrimidine. Structural modifications have been made on the heterocyclic base and the side chain to enhance their potential activity.All these compounds have been tested against different viruses : HIV-1, HSV-1, HSV-2, CMV, VZV, EBV. The carbaacyclonucleoside 10 was associated with an anti-EBV activity (EC50 = 0.86 mu g/mL).
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