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8-Hydroxy-1,3,6-trimethoxy-1,7-bis(3-methylbut-2-enyl)xanthene-2,9-dione | 1146966-49-5

中文名称
——
中文别名
——
英文名称
8-Hydroxy-1,3,6-trimethoxy-1,7-bis(3-methylbut-2-enyl)xanthene-2,9-dione
英文别名
——
8-Hydroxy-1,3,6-trimethoxy-1,7-bis(3-methylbut-2-enyl)xanthene-2,9-dione化学式
CAS
1146966-49-5
化学式
C26H30O7
mdl
——
分子量
454.52
InChiKey
IYMLBRVJNBIMJK-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):
    5.6
  • 重原子数:
    33
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    91.3
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    3,6,8-Trihydroxy-1-methoxy-1,7-bis(3-methylbut-2-enyl)xanthene-2,9-dione 、 碘甲烷potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以66%的产率得到8-Hydroxy-1,3,6-trimethoxy-1,7-bis(3-methylbut-2-enyl)xanthene-2,9-dione
    参考文献:
    名称:
    Synthetic Studies of Mangostin Derivatives with an Inhibitory Activity on PDGF-Induced Human Aortic Smooth Cells Proliferation
    摘要:
    The mangostin derivatives 3-10, were synthesized by halogenation, electrochemical oxidation, and mCPBA oxidation of alpha- and gamma-mangostins (1, 2). Among them, the hydroxyl 9 and the benzopyran 10 derivatives produced by mCPBA, showed remarkable antiproliferative activities against human aortic smooth muscle cells (HASMC) induced by platelet-derived growth factor (PDGF).
    DOI:
    10.3987/com-08-s(f)65
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文献信息

  • Synthetic Studies of Mangostin Derivatives with an Inhibitory Activity on PDGF-Induced Human Aortic Smooth Cells Proliferation
    作者:Shigeru Nishiyama、Yuko Nishihama、Takahisa Ogamino、Wen Lei Shi、Byung-Yoon Cha、Takayuki Yonezawa、Toshiaki Teruya、Kazuo Nagai、Kiyotake Suenaga、Je-Tae Woo
    DOI:10.3987/com-08-s(f)65
    日期:——
    The mangostin derivatives 3-10, were synthesized by halogenation, electrochemical oxidation, and mCPBA oxidation of alpha- and gamma-mangostins (1, 2). Among them, the hydroxyl 9 and the benzopyran 10 derivatives produced by mCPBA, showed remarkable antiproliferative activities against human aortic smooth muscle cells (HASMC) induced by platelet-derived growth factor (PDGF).
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