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2-(4-chlorophenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole | 313519-04-9

中文名称
——
中文别名
——
英文名称
2-(4-chlorophenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole
英文别名
——
2-(4-chlorophenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole化学式
CAS
313519-04-9
化学式
C12H11ClN2
mdl
MFCD00572023
分子量
218.686
InChiKey
GFJNNGKTSOPVAY-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:
    15
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Regulation of stress-induced cytokine production by pyridinylimidazoles; inhibition of CSBP kinase
    摘要:
    Members of three classes of pyridinylimidazoles bind with varying affinities to CSBP (p38) kinase which is a member of a stress-induced signal transduction pathway. Based upon SAR and protein homology modeling, the pharmacophore and three potential modes of binding to the enzyme are presented. For a subset of pyridinylimidazoles, binding is shown to correlate with inhibition of CSBP kinase activity, whereas no significant inhibition of PKA, PKC alpha and ERK kinase activity is observed. Copyright (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0968-0896(96)00212-x
  • 作为产物:
    描述:
    参考文献:
    名称:
    Regulation of stress-induced cytokine production by pyridinylimidazoles; inhibition of CSBP kinase
    摘要:
    Members of three classes of pyridinylimidazoles bind with varying affinities to CSBP (p38) kinase which is a member of a stress-induced signal transduction pathway. Based upon SAR and protein homology modeling, the pharmacophore and three potential modes of binding to the enzyme are presented. For a subset of pyridinylimidazoles, binding is shown to correlate with inhibition of CSBP kinase activity, whereas no significant inhibition of PKA, PKC alpha and ERK kinase activity is observed. Copyright (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0968-0896(96)00212-x
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