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methyl <(6'-(((naphthylmethyl)amino)carbonyl)hexyl) 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-nonulopyranosid>onate | 144226-36-8

中文名称
——
中文别名
——
英文名称
methyl <(6'-(((naphthylmethyl)amino)carbonyl)hexyl) 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-nonulopyranosid>onate
英文别名
——
methyl <(6'-(((naphthylmethyl)amino)carbonyl)hexyl) 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-nonulopyranosid>onate化学式
CAS
144226-36-8
化学式
C30H42N2O10
mdl
——
分子量
590.671
InChiKey
UPKXENWUJSHVGB-UYUPAEIESA-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):
    0.66
  • 重原子数:
    42.0
  • 可旋转键数:
    15.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    183.88
  • 氢给体数:
    6.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Design and evaluation of a tightly binding fluorescent ligand for influenza A hemagglutinin
    摘要:
    Attachment of influenza virus to susceptible cells is mediated by the viral protein hemagglutinin, which recognizes cell-membrane-bound glycoconjugates that terminate in alpha-sialosides. We have synthesized a fluorescent alpha-sialoside that has the highest affinity of any reported monovalent ligand for hemagglutinin, and it is not a substrate for the viral neuraminidase. This alpha-sialoside provides a convenient fluorescence competition assay for the binding of other ligands. Since each of the currently used binding assays has significant disadvantages, such a simple assay is of great importance for the study of potential inhibitors of viral attachment.
    DOI:
    10.1021/ja00050a004
  • 作为产物:
    描述:
    (2R,4S,5R,6R)-4-Acetoxy-5-acetylamino-2-{6-[(naphthalen-1-ylmethyl)-carbamoyl]-hexyloxy}-6-((1R,2R)-1,2,3-triacetoxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl estersodium methylate 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以99%的产率得到methyl <(6'-(((naphthylmethyl)amino)carbonyl)hexyl) 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-nonulopyranosid>onate
    参考文献:
    名称:
    Design and evaluation of a tightly binding fluorescent ligand for influenza A hemagglutinin
    摘要:
    Attachment of influenza virus to susceptible cells is mediated by the viral protein hemagglutinin, which recognizes cell-membrane-bound glycoconjugates that terminate in alpha-sialosides. We have synthesized a fluorescent alpha-sialoside that has the highest affinity of any reported monovalent ligand for hemagglutinin, and it is not a substrate for the viral neuraminidase. This alpha-sialoside provides a convenient fluorescence competition assay for the binding of other ligands. Since each of the currently used binding assays has significant disadvantages, such a simple assay is of great importance for the study of potential inhibitors of viral attachment.
    DOI:
    10.1021/ja00050a004
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