摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-(phenyltetrasulfanyl)propanoic acid | 1443749-96-9

中文名称
——
中文别名
——
英文名称
3-(phenyltetrasulfanyl)propanoic acid
英文别名
——
3-(phenyltetrasulfanyl)propanoic acid化学式
CAS
1443749-96-9
化学式
C10H12O2S4
mdl
——
分子量
292.468
InChiKey
QYNXEJGVTXNXSL-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):
    4.34
  • 重原子数:
    16.0
  • 可旋转键数:
    8.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    37.3
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为产物:
    描述:
    苄硫醇3-巯基丙酸吡啶二氯化二硫 作用下, 以 乙醚 为溶剂, 反应 2.0h, 以75%的产率得到3-(phenyltetrasulfanyl)propanoic acid
    参考文献:
    名称:
    Tetrasulfanes as Selective Modulators of the Cellular Thiolstat
    摘要:
    Naturally occurring polysulfanes often exhibit a wide spectrum of biological activity, which results from their ability to react with, and hence modify cysteine residues in key proteins and enzymes of the cellular thiolstat. Such interactions frequently proceed via S-thiolation of cysteine residues and subsequent formation of Reactive Oxygen Species. Polysulfanes are highly effective, yet also surprisingly selective for cysteine residues and enable the control of numerous cellular processes ranging from an activation of antioxidant defenses to the induction of programed cell death. Unfortunately, the arsenal of natural tri- and tetrasulfanes is limited. Here, we showcase the synthesis of asymmetric tetrasulfanes, which exhibit an interesting nematocidal activity and represent a new generation of tailor-made polysulfanes with potential applications in the field of agriculture and medicine. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus Sulfur and Silicon and the Related Elements.
    DOI:
    10.1080/10426507.2012.746691
点击查看最新优质反应信息