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2-(benzo[b]thiophen-3-yl)-1H-imidazole | 1393085-27-2

中文名称
——
中文别名
——
英文名称
2-(benzo[b]thiophen-3-yl)-1H-imidazole
英文别名
2-Benzo[b]thien-3-yl-1H-imidazole;2-(1-benzothiophen-3-yl)-1H-imidazole
2-(benzo[b]thiophen-3-yl)-1H-imidazole化学式
CAS
1393085-27-2
化学式
C11H8N2S
mdl
——
分子量
200.264
InChiKey
QXOKVYIWSVMPQN-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):
    2.7
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    56.9
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-(benzo[b]thiophen-3-yl)-1H-imidazole四丁基氟化铵 、 sodium hydride 作用下, 以 四氢呋喃 、 mineral oil 为溶剂, 反应 0.33h, 生成 (2-(benzo[b]thiophen-3-yl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone
    参考文献:
    名称:
    Discovery of Novel 2-Aryl-4-benzoyl-imidazole (ABI-III) Analogues Targeting Tubulin Polymerization As Antiproliferative Agents
    摘要:
    Novel ABI-III compounds were designed and synthesized based on our previously reported ABI-I and ABI-II analogues. ABI-III compounds are highly potent against a panel of melanoma and prostate cancer cell lines, with the best compound having an average IC50 value of 3.8 nM. They are not substrate of Pgp and thus may effectively overcome Pgp-mediated multidrug resistance. ABI-III analogues maintain their mechanisms of action by inhibition of tubulin polymerization.
    DOI:
    10.1021/jm300564b
  • 作为产物:
    描述:
    3-甲醛苯并噻吩草酸醛ammonium hydroxide 作用下, 以 乙醇 为溶剂, 以16.8%的产率得到2-(benzo[b]thiophen-3-yl)-1H-imidazole
    参考文献:
    名称:
    Discovery of Novel 2-Aryl-4-benzoyl-imidazole (ABI-III) Analogues Targeting Tubulin Polymerization As Antiproliferative Agents
    摘要:
    Novel ABI-III compounds were designed and synthesized based on our previously reported ABI-I and ABI-II analogues. ABI-III compounds are highly potent against a panel of melanoma and prostate cancer cell lines, with the best compound having an average IC50 value of 3.8 nM. They are not substrate of Pgp and thus may effectively overcome Pgp-mediated multidrug resistance. ABI-III analogues maintain their mechanisms of action by inhibition of tubulin polymerization.
    DOI:
    10.1021/jm300564b
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文献信息

  • Discovery of Novel 2-Aryl-4-benzoyl-imidazole (ABI-III) Analogues Targeting Tubulin Polymerization As Antiproliferative Agents
    作者:Jianjun Chen、Sunjoo Ahn、Jin Wang、Yan Lu、James T. Dalton、Duane D. Miller、Wei Li
    DOI:10.1021/jm300564b
    日期:2012.8.23
    Novel ABI-III compounds were designed and synthesized based on our previously reported ABI-I and ABI-II analogues. ABI-III compounds are highly potent against a panel of melanoma and prostate cancer cell lines, with the best compound having an average IC50 value of 3.8 nM. They are not substrate of Pgp and thus may effectively overcome Pgp-mediated multidrug resistance. ABI-III analogues maintain their mechanisms of action by inhibition of tubulin polymerization.
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