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4-(2,4-bis(benzyloxy)quinolin-3-yl)benzaldehyde | 1609645-82-0

中文名称
——
中文别名
——
英文名称
4-(2,4-bis(benzyloxy)quinolin-3-yl)benzaldehyde
英文别名
——
4-(2,4-bis(benzyloxy)quinolin-3-yl)benzaldehyde化学式
CAS
1609645-82-0
化学式
C30H23NO3
mdl
——
分子量
445.518
InChiKey
VGVIDCSJESWMOP-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):
    6.87
  • 重原子数:
    34.0
  • 可旋转键数:
    8.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    48.42
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(2,4-bis(benzyloxy)quinolin-3-yl)benzaldehyde 在 palladium 10% on activated carbon 、 氢气 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 17.0h, 生成
    参考文献:
    名称:
    Design, synthesis and biological evaluation of Pontin ATPase inhibitors through a molecular docking approach
    摘要:
    A virtual screening strategy, through molecular docking, for the elaboration of an electronic library of Pontin inhibitors has resulted in the identification of two original scaffolds. The chemical synthesis of four candidates allowed extensive biological evaluations for their anticancer activity. Two compounds displayed an effect on Pontin ATPase activity, and one of them also exhibited a noticeable effect on cell growth. Further biological studies revealed that the most active compound induced apoptotic cell death together with necrosis, this latter effect being likely related to the cellular balance of ATP regulation. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.04.003
  • 作为产物:
    描述:
    methyl 4-[2,4-bis(benzyloxy)quinolin-3-yl]benzoate 在 lithium aluminium tetrahydride 、 2-碘酰基苯甲酸 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以98%的产率得到4-(2,4-bis(benzyloxy)quinolin-3-yl)benzaldehyde
    参考文献:
    名称:
    Design, synthesis and biological evaluation of Pontin ATPase inhibitors through a molecular docking approach
    摘要:
    A virtual screening strategy, through molecular docking, for the elaboration of an electronic library of Pontin inhibitors has resulted in the identification of two original scaffolds. The chemical synthesis of four candidates allowed extensive biological evaluations for their anticancer activity. Two compounds displayed an effect on Pontin ATPase activity, and one of them also exhibited a noticeable effect on cell growth. Further biological studies revealed that the most active compound induced apoptotic cell death together with necrosis, this latter effect being likely related to the cellular balance of ATP regulation. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.04.003
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