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5-Methoxy-3-methyl-1-[(3,4,5-trimethoxyphenyl)methyl]benzimidazol-2-one | 1447364-14-8

中文名称
——
中文别名
——
英文名称
5-Methoxy-3-methyl-1-[(3,4,5-trimethoxyphenyl)methyl]benzimidazol-2-one
英文别名
5-methoxy-3-methyl-1-[(3,4,5-trimethoxyphenyl)methyl]benzimidazol-2-one
5-Methoxy-3-methyl-1-[(3,4,5-trimethoxyphenyl)methyl]benzimidazol-2-one化学式
CAS
1447364-14-8
化学式
C19H22N2O5
mdl
——
分子量
358.394
InChiKey
NOEWIJLTGNWIEG-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):
    2.3
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    60.5
  • 氢给体数:
    0
  • 氢受体数:
    5

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:
    参考文献:
    名称:
    Design, synthesis and biological studies of novel tubulin inhibitors
    摘要:
    A series of compounds originally derived from the vascular endothelial growth factor receptor tyrosine kinase inhibitor, SU5416, were synthesized and evaluated. The most potent compound in this series, compound 3, which structurally resembles the potent anti-microtubule agent combretastatin A-4, inhibited tubulin polymerization and showed potent growth inhibitory activities on both prostate and breast cancer lines with IC50 values in the low nanomolar range. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.04.078
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文献信息

  • Design, synthesis and biological studies of novel tubulin inhibitors
    作者:Yanjun Sun、Bulbul Pandit、Somsundaram N. Chettiar、Jonathan P. Etter、Andrew Lewis、Jayasekar Johnsamuel、Pui-Kai Li
    DOI:10.1016/j.bmcl.2013.04.078
    日期:2013.8
    A series of compounds originally derived from the vascular endothelial growth factor receptor tyrosine kinase inhibitor, SU5416, were synthesized and evaluated. The most potent compound in this series, compound 3, which structurally resembles the potent anti-microtubule agent combretastatin A-4, inhibited tubulin polymerization and showed potent growth inhibitory activities on both prostate and breast cancer lines with IC50 values in the low nanomolar range. (C) 2013 Elsevier Ltd. All rights reserved.
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