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2-(3-benzyloxy-4-methoxyphenyl)-3-hydroxy-6,7-dimethyl-4H-chromen-4-one | 1353224-16-4

中文名称
——
中文别名
——
英文名称
2-(3-benzyloxy-4-methoxyphenyl)-3-hydroxy-6,7-dimethyl-4H-chromen-4-one
英文别名
3-Hydroxy-2-(4-methoxy-3-phenylmethoxyphenyl)-6,7-dimethylchromen-4-one
2-(3-benzyloxy-4-methoxyphenyl)-3-hydroxy-6,7-dimethyl-4H-chromen-4-one化学式
CAS
1353224-16-4
化学式
C25H22O5
mdl
——
分子量
402.447
InChiKey
LMPJDSPDLNLGLS-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):
    5.2
  • 重原子数:
    30
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    2-(3-benzyloxy-4-methoxyphenyl)-3-hydroxy-6,7-dimethyl-4H-chromen-4-one 在 5%-palladium/activated carbon 、 氢气 作用下, 以 甲醇乙酸乙酯 为溶剂, 以89%的产率得到3-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,7-dimethyl-4H-chromen-4-one
    参考文献:
    名称:
    Chemical Modification of the Multitarget Neuroprotective Compound Fisetin
    摘要:
    Many factors are implicated in age-related central nervous system (CNS) disorders, making it unlikely that modulating only a single factor will provide effective treatment. Perhaps a better approach is to identify small molecules that have multiple biological activities relevant to the maintenance of brain function. Recently, we identified an orally active, neuroprotective, and cognition-enhancing molecule, the flavonoid fisetin, that is effective in several animal models of CNS disorders. Fisetin has direct antioxidant activity and can also increase the intracellular levels of glutathione (GSH), the major endogenous antioxidant. In addition, fisetin has both neurotrophic and anti-inflammatory activity. However, its relatively high EC50 in cell based assays, low lipophilicity, high topological polar surface area (tPSA), and poor bioavailability suggest that there is room for medicinal chemical improvement. Here we describe a multitiered approach to screening that has allowed us to identify fisetin derivatives with significantly enhanced activity in an in vitro neuroprotection model while at the same time maintaining other key activities.
    DOI:
    10.1021/jm2012563
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