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Isotubulosinmethylaether

中文名称
——
中文别名
——
英文名称
Isotubulosinmethylaether
英文别名
10,11,8'-trimethoxy-tubolosane;NZ72;8',10,11-Trimethoxytubulosan;3-ethyl-9,10-dimethoxy-2-[(6-methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)methyl]-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizine
Isotubulosinmethylaether化学式
CAS
——
化学式
C30H39N3O3
mdl
——
分子量
489.658
InChiKey
YQCYWTNBMKOEPG-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):
    4.9
  • 重原子数:
    36
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    58.8
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • Methods for Sensitizing Cancer Cells to Inhibitors
    申请人:Sherman Michael
    公开号:US20090062222A1
    公开(公告)日:2009-03-05
    The present invention is based on the discovery that inactivation of the heat shock response in cancer cells significantly enhances their sensitivity to proteasome and Hsp90 inhibitors. The inventors have discovered novel compounds which exhibit low toxicity, inhibit the heat shock protein response and sensitize cancer cells to anti-cancer therapies. In general, the heat shock protein inhibitors of the present invention share a common structure, namely a 2H-benzo[a]quinolizine tricyclic ring. Also encompassed are methods for a high throughput screen to identify heat shock inhibitors that sensitize cancer cells to anti-cancer therapies.
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