2-(4-hydroxyphenyl)-1-[4-(2-piperidin-1-ylethoxy)benzyl]-1H-benzimidazole | 1240736-67-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: 2-(4-hydroxyphenyl)-1-[4-(2-piperidin-1-ylethoxy)benzyl]-1H-benzimidazole
• 英文别名: 2-(4-Hydroxyphenyl)-1-[4-(2-piperidin-1-ylethoxy)benzyl]-1H-benzimidazole；4-[1-[[4-(2-piperidin-1-ylethoxy)phenyl]methyl]benzimidazol-2-yl]phenol
• CAS: 1240736-67-7
• 化学式: C₂₇H₂₉N₃O₂
• 分子量: 427.546
• InChiKey: MDJKJVUFUPBARW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  32
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  50.5
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-(4-methoxyphenyl)-1-[4-(2-piperidin-1-ylethoxy)benzyl]-1H-benzimidazole 在 aluminum (III) chloride 、 乙硫醇 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以75%的产率得到2-(4-hydroxyphenyl)-1-[4-(2-piperidin-1-ylethoxy)benzyl]-1H-benzimidazole
  参考文献：
  名称：

  2-Phenyl-1-[4-(2-piperidine-1-yl-ethoxy)benzyl]-1H-benzimidazoles as ligands for the estrogen receptor: Synthesis and pharmacological evaluation

  摘要：

  2-Phenyl-1H-benzimidazoles 7a-e were synthesized and tested for gene activation on ERa-positive MCF-7 breast cancer cells, stably transfected with the reporter plasmid ERE(wtc)luc (MCF-7-2a cells). None of the compounds showed agonistic properties, but they antagonized dependent on hydroxyl groups at the benzimidazole core (5- or 6-OH) and at the aromatic ring in the 2-position (4-OH) in high concentrations the gene activation induced by estradiol (E2, 1 nM). All compounds exhibited significant antiproliferative properties on MCF-7 cells but they were inactive against hormone independent, ER negative MDA-MB-231 cells. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.06.016