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

S-(7-(hydroxyamino)-7-oxoheptyl)methanesulfonothioate | 1155413-98-1

中文名称
——
中文别名
——
英文名称
S-(7-(hydroxyamino)-7-oxoheptyl)methanesulfonothioate
英文别名
N-hydroxy-7-methylsulfonylsulfanylheptanamide
S-(7-(hydroxyamino)-7-oxoheptyl)methanesulfonothioate化学式
CAS
1155413-98-1
化学式
C8H17NO4S2
mdl
——
分子量
255.359
InChiKey
FIBDRAVGKQUGIV-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

物化性质

  • 密度:
    1.282±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    15
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    117
  • 氢给体数:
    2
  • 氢受体数:
    5

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:
    7-溴庚酸4-甲基苯磺酸吡啶N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 反应 5.03h, 生成 S-(7-(hydroxyamino)-7-oxoheptyl)methanesulfonothioate
    参考文献:
    名称:
    Catch and Anchor Approach To Combat Both Toxicity and Longevity of Botulinum Toxin A
    摘要:
    Botulinum neurotoxins have remarkable persistence (similar to weeks to months in cells), outlasting the small-molecule inhibitors designed to target them. To address this disconnect, inhibitors bearing two pharmacophores.a zinc binding group and a Cys-reactive warhead.were designed to leverage both affinity and reactivity. A series of first-generation bifunctional inhibitors was achieved through structure-based inhibitor design. Through X-ray crystallography, engagement of both the catalytic Zn2+ and Cys165 was confirmed. A second-generation series improved on affinity by incorporating known reversible inhibitor pharmacophores; the mechanism was confirmed by exhaustive dialysis, mass spectrometry, and in vitro evaluation against the C165S mutant. Finally, a third-generation inhibitor was shown to have good cellular activity and low toxicity. In addition to our findings, an alternative method of modeling time-dependent inhibition that simplifies assay setup and allows comparison of inhibition models is discussed.
    DOI:
    10.1021/acs.jmedchem.0c01006
点击查看最新优质反应信息

文献信息

  • [EN] NEW ANTICANCER COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS ANTICANCERS
    申请人:SULFIDRIS S R L
    公开号:WO2009065926A2
    公开(公告)日:2009-05-28
    The present invention relates to new polysulf urated compounds containing 2 or more sulphur atoms belonging to the class of organic thiosulf onates, or dithiole-thione derivatives cyclic or linear, or trithiocarbonates for the use alone or in combination with other anticancer treatments for the treatment and/or prevention of cancer and inflammatory diseases.
查看更多