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| 1072838-41-5

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1072838-41-5
化学式
C51H89NO7SSi3
mdl
——
分子量
944.593
InChiKey
AYARXLNNJJWUPT-ZDBWYGPUSA-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

物化性质

  • 沸点:
    826.9±65.0 °C(predicted)
  • 密度:
    1.007±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    14.68
  • 重原子数:
    63.0
  • 可旋转键数:
    25.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    104.18
  • 氢给体数:
    1.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    四丁基氟化铵 作用下, 以48%的产率得到
    参考文献:
    名称:
    Total synthesis and evaluation of C25-benzyloxyepothilone C for tubulin assembly and cytotoxicity against MCF-7 breast cancer cells
    摘要:
    The total synthesis of C25-benzyloxy epothilone C is described. A sequential Suzuki-Aldol-Yamaguchi macrolactonization strategy was utilized employing a novel derivatized C8-C12 fragment. The C25-benzyloxy analog exhibited significantly reduced biological activity in microtubule assembly and cytotoxicity assays. Molecular modeling simulations indicated that excessive steric bulk in the C25 position may reduce activity by disrupting key hydrogen bonds that are crucial for epothilone binding to beta-tubulin. (C) 2008 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2008.07.024
  • 作为产物:
    描述:
    sodium chloritedisodium hydrogenphosphate 作用下, 以59%的产率得到
    参考文献:
    名称:
    Total synthesis and evaluation of C25-benzyloxyepothilone C for tubulin assembly and cytotoxicity against MCF-7 breast cancer cells
    摘要:
    The total synthesis of C25-benzyloxy epothilone C is described. A sequential Suzuki-Aldol-Yamaguchi macrolactonization strategy was utilized employing a novel derivatized C8-C12 fragment. The C25-benzyloxy analog exhibited significantly reduced biological activity in microtubule assembly and cytotoxicity assays. Molecular modeling simulations indicated that excessive steric bulk in the C25 position may reduce activity by disrupting key hydrogen bonds that are crucial for epothilone binding to beta-tubulin. (C) 2008 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2008.07.024
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