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2-(1-benzyl-1H-benzoimidazol-2-yl)-4-methyl-thiazole-5-carboxylic acid isopropylamide | 1263903-15-6

中文名称
——
中文别名
——
英文名称
2-(1-benzyl-1H-benzoimidazol-2-yl)-4-methyl-thiazole-5-carboxylic acid isopropylamide
英文别名
2-(1-benzylbenzimidazol-2-yl)-4-methyl-N-propan-2-yl-1,3-thiazole-5-carboxamide
2-(1-benzyl-1H-benzoimidazol-2-yl)-4-methyl-thiazole-5-carboxylic acid isopropylamide化学式
CAS
1263903-15-6
化学式
C22H22N4OS
mdl
——
分子量
390.509
InChiKey
SBFJTZOQBOYDKQ-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):
    4.6
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    88
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    描述:
    2-(1-benzyl-1H-benzoimidazol-2-yl)-4-methyl-thiazole-5-carboxylic acid异丙胺N,N'-羰基二咪唑 作用下, 以 四氢呋喃 为溶剂, 反应 0.5h, 以42%的产率得到2-(1-benzyl-1H-benzoimidazol-2-yl)-4-methyl-thiazole-5-carboxylic acid isopropylamide
    参考文献:
    名称:
    Synthesis and in vitro cytotoxic evaluation of some thiazolylbenzimidazole derivatives
    摘要:
    A novel kind of thiazolylbenzimidazole derivatives were designed and synthesized and evaluated for their antitumor activity against SMMC-7721 and A549 cell lines. Most compounds showed good antitumor activities, and compound lib displayed remarkable in vitro anticancer activity comparable to taxol. The preliminary structure-activity relationship of these benzimidazole derivatives was discussed based on the experimental data obtained. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.11.014
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文献信息

  • Synthesis and in vitro cytotoxic evaluation of some thiazolylbenzimidazole derivatives
    作者:Yu Luo、Feng Xiao、Shijing Qian、Wei Lu、Bo Yang
    DOI:10.1016/j.ejmech.2010.11.014
    日期:2011.1
    A novel kind of thiazolylbenzimidazole derivatives were designed and synthesized and evaluated for their antitumor activity against SMMC-7721 and A549 cell lines. Most compounds showed good antitumor activities, and compound lib displayed remarkable in vitro anticancer activity comparable to taxol. The preliminary structure-activity relationship of these benzimidazole derivatives was discussed based on the experimental data obtained. (C) 2010 Elsevier Masson SAS. All rights reserved.
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