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(1S,3aS,41R,4a1S,5R,10aR,12aS)-1-(furan-3-yl)-5-hydroxy-4a1,7,7,10a,12a-pentamethyl-4a1,5,6,6a,7,10a,10b,11,12,12a-decahydronaphtho[2,1-f][9,10]dioxireno[2,3-d]isochromene-3,8(1H,3aH)-dione | 62279-68-9

中文名称
——
中文别名
——
英文名称
(1S,3aS,41R,4a1S,5R,10aR,12aS)-1-(furan-3-yl)-5-hydroxy-4a1,7,7,10a,12a-pentamethyl-4a1,5,6,6a,7,10a,10b,11,12,12a-decahydronaphtho[2,1-f][9,10]dioxireno[2,3-d]isochromene-3,8(1H,3aH)-dione
英文别名
——
(1S,3aS,41R,4a1S,5R,10aR,12aS)-1-(furan-3-yl)-5-hydroxy-4a1,7,7,10a,12a-pentamethyl-4a1,5,6,6a,7,10a,10b,11,12,12a-decahydronaphtho[2,1-f][9,10]dioxireno[2,3-d]isochromene-3,8(1H,3aH)-dione化学式
CAS
62279-68-9
化学式
C26H30O7
mdl
——
分子量
454.52
InChiKey
QIAYKQSCKSMIJW-KJNGQSBESA-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):
    3.41
  • 重原子数:
    33.0
  • 可旋转键数:
    1.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    98.64
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

反应信息

  • 作为产物:
    描述:
    7-去乙酰基葛杜宁sodium hydroxide双氧水 作用下, 以 丙酮 为溶剂, 以68%的产率得到(1S,3aS,41R,4a1S,5R,10aR,12aS)-1-(furan-3-yl)-5-hydroxy-4a1,7,7,10a,12a-pentamethyl-4a1,5,6,6a,7,10a,10b,11,12,12a-decahydronaphtho[2,1-f][9,10]dioxireno[2,3-d]isochromene-3,8(1H,3aH)-dione
    参考文献:
    名称:
    Gedunin, a Novel Hsp90 Inhibitor: Semisynthesis of Derivatives and Preliminary Structure−Activity Relationships
    摘要:
    Gedunin (1), a tetranortriterpenoid isolated from the Indian neern tree (Azadirachta indica), was recently shown to manifest anticancer activity via inhibition of the 90 kDa heat shock protein (Hsp90) folding machinery and to induce the degradation of Hsp90-dependent client proteins similar to other Hsp90 inhibitors. The mechanism of action by which gedunin induces client protein degradation remains undetermined, however, prior studies have demonstrated that it does not bind competitively versus ATP. In an effort to further probe the mechanism of action, 19 semisynthetic derivatives of gedunin were prepared and their antiproliferative activity against MCF-7 and SkBr3 breast cancer cells determined. Although no compound was found to exhibit antiproliferative activity more effective than the natural product, functionalities critical for antiproliferative activity have been identified.
    DOI:
    10.1021/jm8007486
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