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Biflavonyl-(6,6'') | 20081-46-3

中文名称
——
中文别名
——
英文名称
Biflavonyl-(6,6'')
英文别名
6-(4-Oxo-2-phenyl-chromen-6-yl)-2-phenyl-chromen-4-one;6-(4-oxo-2-phenylchromen-6-yl)-2-phenylchromen-4-one
Biflavonyl-(6,6'')化学式
CAS
20081-46-3
化学式
C30H18O4
mdl
——
分子量
442.471
InChiKey
RFRYEGZKLVLBMV-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):
    6.1
  • 重原子数:
    34
  • 可旋转键数:
    3
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    6-溴-2-苯基-(4H)-4-苯并吡喃酮 在 bis-triphenylphosphine-palladium(II) chloride 、 四(三苯基膦)钯 、 sodium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 22.0h, 生成 Biflavonyl-(6,6'')
    参考文献:
    名称:
    Efficient Synthesis of Biflavones Having A Ring-A Ring of Two Flavone Units Using Suzuki Cross-Coupling Reactions
    摘要:
    Biflavones having a A ring-A ring of two flavone units were easily prepared by using Suzuki cross-coupling reaction of borylated flavones with bromoflavones or flavone-5-triflate in good to excellent yields.
    DOI:
    10.3987/com-10-s(e)36
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文献信息

  • Synthesis of phospholipase A2 inhibitory biflavonoids
    作者:Jianjun Chen、Hyeun Wook Chang、Hyun Pyo Kim、Haeil Park
    DOI:10.1016/j.bmcl.2006.01.117
    日期:2006.5
    A series of C-C biflavones was designed to investigate the relationship between structural array of different flavone-flavone subunit linkage and the inhibitory activity against phospholipase A(2) (PLA(2)). Among six classes of C-C biflavones designed, four classes of C-C biflavones, which have flavone-flavone subunit linkages at A ring-A ring, A ring-B ring, B ring-B ring, and B ring-C ring, were synthesized. The synthetic biflavones exhibited somewhat different inhibitory activities against sPLA(2)-IIA. Among them, the biflavone a having a C-C 4'-4' linkage showed comparable inhibitory activity with that of the natural biflavonoid, ochnaflavone, and 7-fold stronger activity than that of amentoflavone. Further chemical modification is being carried out in order to obtain the chemically optimized biflavonoids. (C) 2006 Elsevier Ltd. All rights reserved.
  • Efficient Synthesis of Biflavones Having A Ring-A Ring of Two Flavone Units Using Suzuki Cross-Coupling Reactions
    作者:Hiroto Nakano、Yukio Hoshino、Haruo Matsuyama、Yoshihito Kohari
    DOI:10.3987/com-10-s(e)36
    日期:——
    Biflavones having a A ring-A ring of two flavone units were easily prepared by using Suzuki cross-coupling reaction of borylated flavones with bromoflavones or flavone-5-triflate in good to excellent yields.
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