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

3,5-bis-(4-hydroxy-3-methoxybenzylidene)-4-oxopiperidinium chloride | 886851-95-2

中文名称
——
中文别名
——
英文名称
3,5-bis-(4-hydroxy-3-methoxybenzylidene)-4-oxopiperidinium chloride
英文别名
3,5-bis[(4-hydroxy-3-methoxyphenyl)methylidene]piperidin-4-one;hydrochloride
3,5-bis-(4-hydroxy-3-methoxybenzylidene)-4-oxopiperidinium chloride化学式
CAS
886851-95-2
化学式
C21H21NO5*ClH
mdl
——
分子量
403.862
InChiKey
NRULDJYGPFISDL-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):
    3.18
  • 重原子数:
    28.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    88.02
  • 氢给体数:
    3.0
  • 氢受体数:
    6.0

反应信息

  • 作为产物:
    描述:
    4-哌啶酮香草醛盐酸 作用下, 以 乙醇 为溶剂, 以55%的产率得到3,5-bis-(4-hydroxy-3-methoxybenzylidene)-4-oxopiperidinium chloride
    参考文献:
    名称:
    Synthesis and Evaluation of Bisbenzylidenedioxotetrahydrothiopranones as Activators of Endoplasmic Reticulum (ER) Stress Signaling Pathways and Apoptotic Cell Death in Acute Promyelocytic Leukemic Cells
    摘要:
    Curcumin is known to trigger ER-stress induced cell death of acute promyelocytic leukemic (APL) cells by intercepting the degradation of nuclear co-repressor (N-CoR) protein which has a key role in the pathogenesis of APL. Replacing the heptadienedione moiety of curcumin with a monocarbonyl cross-conjugated dienone embedded in a tetrahydrothiopyranone dioxide ring resulted in thiopyranone dioxides that were more resilient to hydrolysis and had greater growth inhibitory activities than curcumin on APL cells. Several members intercepted the degradation of misfolded N-CoR and triggered the signaling cascade in the unfolded protein response (UPR) which led to apoptotic cell death. Microarray analysis showed that genes involved in protein processing pathways that were germane to the activation of the UPR were preferentially up-regulated in treated APL cells, supporting the notion that the UPR was a consequential mechanistic pathway affected by thiopyranone dioxides. The Michael acceptor reactivity of the scaffold may have a role in exacerbating ER stress in APL cells.
    DOI:
    10.1021/jm401352a
点击查看最新优质反应信息