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2-{4-[4-(4-Methyl-piperazin-1-yl)-butyl]-phenyl}-1H-benzoimidazole | 919088-47-4

中文名称
——
中文别名
——
英文名称
2-{4-[4-(4-Methyl-piperazin-1-yl)-butyl]-phenyl}-1H-benzoimidazole
英文别名
2-{4-[4-(4-Methylpiperazin-1-yl)butyl]phenyl}-1H-benzimidazole;2-[4-[4-(4-methylpiperazin-1-yl)butyl]phenyl]-1H-benzimidazole
2-{4-[4-(4-Methyl-piperazin-1-yl)-butyl]-phenyl}-1H-benzoimidazole化学式
CAS
919088-47-4
化学式
C22H28N4
mdl
——
分子量
348.491
InChiKey
WLZWOGCDAPRJBB-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):
    4.1
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    35.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-(4-羟基丁-1-炔-1-基)苯甲醛 在 Lindlar's catalyst sodium disulfite 、 氢气三乙胺 作用下, 以 乙醇二氯甲烷N,N-二甲基乙酰胺乙酸乙酯 为溶剂, 80.0 ℃ 、101.33 kPa 条件下, 反应 3.0h, 生成 2-{4-[4-(4-Methyl-piperazin-1-yl)-butyl]-phenyl}-1H-benzoimidazole
    参考文献:
    名称:
    Identification of 2-arylbenzimidazoles as potent human histamine H4 receptor ligands
    摘要:
    A series of 2-arylbenzimidazoles was synthesized and found to bind with high affinity to the human histamine H(4) receptor. Structure-activity relationships were investigated through library preparation and evaluation as well as traditional medicinal chemistry approaches, leading to the discovery of compounds with single-digit nanomolar affinity for the H(4) receptor.
    DOI:
    10.1016/j.bmcl.2006.08.117
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文献信息

  • Identification of 2-arylbenzimidazoles as potent human histamine H4 receptor ligands
    作者:Alice Lee-Dutra、Kristen L. Arienti、Daniel J. Buzard、Michael D. Hack、Haripada Khatuya、Pragnya J. Desai、Steven Nguyen、Robin L. Thurmond、Lars Karlsson、James P. Edwards、J. Guy Breitenbucher
    DOI:10.1016/j.bmcl.2006.08.117
    日期:2006.12
    A series of 2-arylbenzimidazoles was synthesized and found to bind with high affinity to the human histamine H(4) receptor. Structure-activity relationships were investigated through library preparation and evaluation as well as traditional medicinal chemistry approaches, leading to the discovery of compounds with single-digit nanomolar affinity for the H(4) receptor.
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