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benzyl (tert-butoxycarbonyl)glycyl-2,2-d2-L-prolylglycylglycylglycinate | 874305-97-2

中文名称
——
中文别名
——
英文名称
benzyl (tert-butoxycarbonyl)glycyl-2,2-d2-L-prolylglycylglycylglycinate
英文别名
——
benzyl (tert-butoxycarbonyl)glycyl-2,2-d2-L-prolylglycylglycylglycinate化学式
CAS
874305-97-2
化学式
C25H35N5O8
mdl
——
分子量
535.566
InChiKey
HQTVTLDCSXNEBO-NALVIQTBSA-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):
    -0.41
  • 重原子数:
    38.0
  • 可旋转键数:
    11.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    172.24
  • 氢给体数:
    4.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Cation Dependence of Chloride Ion Complexation by Open-Chained Receptor Molecules in Chloroform Solution
    摘要:
    Seventeen peptides, most having the sequence GGGPGGG, but differing in the C- and N-terminal ends, have been studied as anion-complexing agents. These relatively simple, open-chained peptide systems interact with both chloride and the associated cation. Changes, in the N- and C-terminal side chains appear to make little difference in the efficacy of binding. NMR studies suggest that the primary interactions involve amide NH contacts with the chloride anion, and CD spectral analyses suggest a concomitant conformational change upon binding. Changes in binding constants, which are expected in different solvents, also suggest selective solvent interactions with the unbound host that helps to preorganize the open-chained peptide system. Significant differences are apparent in complexation strengths when the heptapeptide chain is shortened or lengthened or when the relative position of proline within the heptapeptide is varied.
    DOI:
    10.1021/ja0558894
  • 作为产物:
    参考文献:
    名称:
    Cation Dependence of Chloride Ion Complexation by Open-Chained Receptor Molecules in Chloroform Solution
    摘要:
    Seventeen peptides, most having the sequence GGGPGGG, but differing in the C- and N-terminal ends, have been studied as anion-complexing agents. These relatively simple, open-chained peptide systems interact with both chloride and the associated cation. Changes, in the N- and C-terminal side chains appear to make little difference in the efficacy of binding. NMR studies suggest that the primary interactions involve amide NH contacts with the chloride anion, and CD spectral analyses suggest a concomitant conformational change upon binding. Changes in binding constants, which are expected in different solvents, also suggest selective solvent interactions with the unbound host that helps to preorganize the open-chained peptide system. Significant differences are apparent in complexation strengths when the heptapeptide chain is shortened or lengthened or when the relative position of proline within the heptapeptide is varied.
    DOI:
    10.1021/ja0558894
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