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austrasulfone | 76928-46-6

中文名称
——
中文别名
——
英文名称
austrasulfone
英文别名
4-ethenylsulfonylbutan-2-one
austrasulfone化学式
CAS
76928-46-6
化学式
C6H10O3S
mdl
——
分子量
162.21
InChiKey
YKCAPWJWQQTXTB-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):
    -0.3
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    59.6
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    描述:
    dihydroaustrasulfone alcohol4-二甲氨基吡啶三乙胺对甲苯磺酰氯 作用下, 以 二氯甲烷 为溶剂, 反应 5.0h, 以90%的产率得到austrasulfone
    参考文献:
    名称:
    A neuroprotective sulfone of marine origin and the in vivo anti-inflammatory activity of an analogue
    摘要:
    Our continuing effort of searching bioactive substances from the Formosan soft coral Cladiella australis has led to the isolation of a bioactive substance austrasulfone (1), which possesses significant neuroprotective activities. A straightforward synthesis of 1 was achieved by a two-step reaction sequence. Dihydroaustrasulfone alcohol (3), the synthetic precursor of 1, not only exhibited in vitro anti-inflammatory activity, but also showed potent therapeutic ability in the treatment of neuropathic pain, atherosclerosis, and multiple sclerosis in rats. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.09.067
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文献信息

  • A neuroprotective sulfone of marine origin and the in vivo anti-inflammatory activity of an analogue
    作者:Zhi-Hong Wen、Chih-Hua Chao、Ming-Hsuan Wu、Jyh-Horng Sheu
    DOI:10.1016/j.ejmech.2010.09.067
    日期:2010.12
    Our continuing effort of searching bioactive substances from the Formosan soft coral Cladiella australis has led to the isolation of a bioactive substance austrasulfone (1), which possesses significant neuroprotective activities. A straightforward synthesis of 1 was achieved by a two-step reaction sequence. Dihydroaustrasulfone alcohol (3), the synthetic precursor of 1, not only exhibited in vitro anti-inflammatory activity, but also showed potent therapeutic ability in the treatment of neuropathic pain, atherosclerosis, and multiple sclerosis in rats. (C) 2010 Elsevier Masson SAS. All rights reserved.
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