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N-[2-(4-Hydroxyphenyl)ethyl]-3-methylbutanamide | 921607-20-7

中文名称
——
中文别名
——
英文名称
N-[2-(4-Hydroxyphenyl)ethyl]-3-methylbutanamide
英文别名
——
N-[2-(4-Hydroxyphenyl)ethyl]-3-methylbutanamide化学式
CAS
921607-20-7
化学式
C13H19NO2
mdl
——
分子量
221.29
InChiKey
WEZYUYBFOZNOHM-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):
    2.4
  • 重原子数:
    16
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    49.3
  • 氢给体数:
    2
  • 氢受体数:
    2

文献信息

  • SMALL MOLECULE PRINTING
    申请人:Park Seung Bum
    公开号:US20120021933A1
    公开(公告)日:2012-01-26
    The present invention provides compositions and methods to facilitate the identification of compounds that are capable of interacting with a biological macromolecule of interest. In one aspect, a composition is provided that comprises an array of one or more types of chemical compounds attached to a solid support, wherein the density of the array of compounds is at least 1000 spots per cm 2 . In particularly preferred embodiments, these compounds are attached to the solid support through a covalent interaction. In general, these inventive arrays are generated by: (1) providing a solid support, wherein said solid support is functionalized with a selected chemical moiety capable of interacting with a desired chemical compound to form an attachment; (2) providing one or more solutions of one or more types of compounds to be attached to the solid support; and (3) delivering said one or more types of compounds to the solid support, whereby an array is formed and the array of compounds has a density of at least 1000 spots per cm 2 . In another aspect, the present invention provides methods for utilizing these arrays to identify small molecule partners for biological macromolecules of interest comprising: (1) providing an array of compounds, wherein the array has a density of at least 1000 spots per cm 2 ; (2) contacting the array with one of more types of biological macromolecules of interest; and (3) determining the interaction of specific small molecule-biological macromolecule partners.
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