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(2R)-3-[2-(4-butylphenyl)-2-oxoethoxy]-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-2H-furan-5-one | 139870-17-0

中文名称
——
中文别名
——
英文名称
(2R)-3-[2-(4-butylphenyl)-2-oxoethoxy]-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-2H-furan-5-one
英文别名
——
(2R)-3-[2-(4-butylphenyl)-2-oxoethoxy]-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-2H-furan-5-one化学式
CAS
139870-17-0
化学式
C18H22O7
mdl
——
分子量
350.368
InChiKey
QQPKDDUGSFEKAR-XJKSGUPXSA-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):
    1.8
  • 重原子数:
    25
  • 可旋转键数:
    9
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    113
  • 氢给体数:
    3
  • 氢受体数:
    7

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:
    参考文献:
    名称:
    3-O-alkylascorbic acids as free radical quenchers. 3. Protective effect on coronary occlusion-reperfusion induced arrhythmias in anesthetized rats
    摘要:
    Structural modification of ascorbic acid by substitution of the 3-hydroxy group with lipophilic moieties has allowed the development of agents for treating reperfusion injury. These ascorbic acid derivatives inhibited lipid peroxidation, and some of them also reduced coronary reperfusion-induced arrhythmias in anesthetized rats. We found that 3-O-[(dodecylcarbonyl)methyl]ascorbic acid (8) was protective against reperfusion injury without directly influencing hemodynamics. 2-O-Octadecylascorbic acid (19) and 5,6-O-dodecylideneascorbic acid (15) also exhibited a marked effect on reperfusion injury, but significantly reduced the arterial blood pressure and heart rate in rats.
    DOI:
    10.1021/jm00087a017
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文献信息

  • 3-O-alkylascorbic acids as free radical quenchers. 3. Protective effect on coronary occlusion-reperfusion induced arrhythmias in anesthetized rats
    作者:Yasunori Nihro、Satoshi Sogawa、Akihiro Izumi、Akihiro Sasamori、Tadamitsu Sudo、Tokutaro Miki、Hitoshi Matsumoto、Toshio Satoh
    DOI:10.1021/jm00087a017
    日期:1992.5
    Structural modification of ascorbic acid by substitution of the 3-hydroxy group with lipophilic moieties has allowed the development of agents for treating reperfusion injury. These ascorbic acid derivatives inhibited lipid peroxidation, and some of them also reduced coronary reperfusion-induced arrhythmias in anesthetized rats. We found that 3-O-[(dodecylcarbonyl)methyl]ascorbic acid (8) was protective against reperfusion injury without directly influencing hemodynamics. 2-O-Octadecylascorbic acid (19) and 5,6-O-dodecylideneascorbic acid (15) also exhibited a marked effect on reperfusion injury, but significantly reduced the arterial blood pressure and heart rate in rats.
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