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13,16,19,22-tetraoxatetratriacontane-1,34-diyl bis(4-methylbenzenesulfonate) | 165191-85-5

中文名称
——
中文别名
——
英文名称
13,16,19,22-tetraoxatetratriacontane-1,34-diyl bis(4-methylbenzenesulfonate)
英文别名
——
13,16,19,22-tetraoxatetratriacontane-1,34-diyl bis(4-methylbenzenesulfonate)化学式
CAS
165191-85-5
化学式
C44H74O10S2
mdl
——
分子量
827.198
InChiKey
KMVAEZSTTTZOEW-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):
    10.28
  • 重原子数:
    56.0
  • 可旋转键数:
    39.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    123.66
  • 氢给体数:
    0.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    描述:
    N-dodecyl-4,13-diaza-18-crown-613,16,19,22-tetraoxatetratriacontane-1,34-diyl bis(4-methylbenzenesulfonate)sodium carbonate 作用下, 以 乙腈 为溶剂, 反应 72.0h, 以35%的产率得到O,O'-bis<12-(N'-dodecyldiaza-18-crown-6)dodecyl>tris(ethylene glycol)
    参考文献:
    名称:
    Synthetic Models for Transmembrane Channels: Structural Variations That Alter Cation Flux
    摘要:
    Twelve novel bis- or tris(macrocyclic) compounds have been designed as models for cation-conducting channels that function in phospholipid bilayer vesicle membranes. In general, the channel model systems have the structure ''sidearm-crown-spacer-crown-spacer-crown-sidearm'', although certain features have been altered from compound to compound to assess the structure-activity relationship. Two additional compounds have been prepared exclusively as controls. The ionophores have been incorporated into the membranes either by warming the compound with the preformed vesicle or by incorporation during vesicle formation. The two methods gave identical results within experimental error. Cation flux was assessed by two different analytical methods. In one case, the fluorescent dye pyranine was encapsulated within vesicles containing ionophore. Proton transport was then monitored by changes in dye fluorescence with time following an acid pulse. Ionophoretic activity far most of the compounds was studied using a dynamic NMR method in which the flux rate of Na-23(+) through the bilayer was monitored. All NMR studies were done in conjunction with gramicidin as a control to minimize experimental variations from run to run. Several of the synthetic ionophores showed cation conduction of as much as 40% of the activity of gramicidin. Apparently, small structural changes significantly altered flux rates and two known carriers closely related to the channel formers failed to exhibit measurable transport under comparable conditions.
    DOI:
    10.1021/ja00134a011
  • 作为产物:
    参考文献:
    名称:
    Synthetic Models for Transmembrane Channels: Structural Variations That Alter Cation Flux
    摘要:
    Twelve novel bis- or tris(macrocyclic) compounds have been designed as models for cation-conducting channels that function in phospholipid bilayer vesicle membranes. In general, the channel model systems have the structure ''sidearm-crown-spacer-crown-spacer-crown-sidearm'', although certain features have been altered from compound to compound to assess the structure-activity relationship. Two additional compounds have been prepared exclusively as controls. The ionophores have been incorporated into the membranes either by warming the compound with the preformed vesicle or by incorporation during vesicle formation. The two methods gave identical results within experimental error. Cation flux was assessed by two different analytical methods. In one case, the fluorescent dye pyranine was encapsulated within vesicles containing ionophore. Proton transport was then monitored by changes in dye fluorescence with time following an acid pulse. Ionophoretic activity far most of the compounds was studied using a dynamic NMR method in which the flux rate of Na-23(+) through the bilayer was monitored. All NMR studies were done in conjunction with gramicidin as a control to minimize experimental variations from run to run. Several of the synthetic ionophores showed cation conduction of as much as 40% of the activity of gramicidin. Apparently, small structural changes significantly altered flux rates and two known carriers closely related to the channel formers failed to exhibit measurable transport under comparable conditions.
    DOI:
    10.1021/ja00134a011
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