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N6-(4-fluoro-phenyl)-adenosine | 29305-74-6

中文名称
——
中文别名
——
英文名称
N6-(4-fluoro-phenyl)-adenosine
英文别名
N(6)-( 4-Fluoro-phenyl)-adenosine;(2R,3R,4S,5R)-2-[6-(4-fluoroanilino)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol
<i>N</i><sup>6</sup>-(4-fluoro-phenyl)-adenosine化学式
CAS
29305-74-6
化学式
C16H16FN5O4
mdl
——
分子量
361.333
InChiKey
LFUHYAZTIWDXOX-XNIJJKJLSA-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

物化性质

  • 沸点:
    688.3±65.0 °C(Predicted)
  • 密度:
    1.74±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    126
  • 氢给体数:
    4
  • 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:
    描述:
    参考文献:
    名称:
    N6-Phenyladenosines: pronounced effect of phenyl substituents on affinity for A2 adenosine receptors
    摘要:
    A number of N6-phenyladenosines with various substitutions on the phenyl ring have been synthesized and tested for their affinities toward brain A1 and A2 adenosine receptors. Compounds with meta substituents, such as (m-hydroxy- and m-iodophenyl)adenosine, were found to have high A1 selectivity. Meta substitution caused a selective decrease in the affinity of these compounds for A2 receptors. The results suggest that, in contrast to what is commonly held, certain N6-substituents have pronounced effects on affinity for brain A2 adenosine receptors. Thus, brain A2 receptors may have a well-defined region that recognizes N6-substitutions.
    DOI:
    10.1021/jm00388a039
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文献信息

  • N6-Phenyladenosines: pronounced effect of phenyl substituents on affinity for A2 adenosine receptors
    作者:Madan M. Kwatra、Edward Leung、M. Marlene Hosey、Richard D. Green
    DOI:10.1021/jm00388a039
    日期:1987.5
    A number of N6-phenyladenosines with various substitutions on the phenyl ring have been synthesized and tested for their affinities toward brain A1 and A2 adenosine receptors. Compounds with meta substituents, such as (m-hydroxy- and m-iodophenyl)adenosine, were found to have high A1 selectivity. Meta substitution caused a selective decrease in the affinity of these compounds for A2 receptors. The results suggest that, in contrast to what is commonly held, certain N6-substituents have pronounced effects on affinity for brain A2 adenosine receptors. Thus, brain A2 receptors may have a well-defined region that recognizes N6-substitutions.
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