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2-(4-chlorophenyl)-5-hydroxy-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide | 135429-09-3

中文名称
——
中文别名
——
英文名称
2-(4-chlorophenyl)-5-hydroxy-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide
英文别名
2-[2-(4-chlorophenyl)-5-oxo-4H-imidazo[4,5-b]pyridin-3-yl]-N,N-dimethylacetamide
2-(4-chlorophenyl)-5-hydroxy-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide化学式
CAS
135429-09-3
化学式
C16H15ClN4O2
mdl
——
分子量
330.774
InChiKey
IJYBYRAICQVVJO-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):
    1.7
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    67.2
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    参考文献:
    名称:
    2-Phenyl-3H-imidazo[4,5-b]pyridine-3-acetamides as nonbenzodiazepine anticonvulsants and anxiolytics
    摘要:
    A series of 2-phenyl-3H-imidazo[4,5-b]pyridine-3-acetamides were designed and synthesized as non-benzodiazepine anxiolytics based on a molecular disconnection of a typical 1,4-benzodiazepine (BZD). A number of these compounds showed submicromolar potency in a [H-3]benzodiazepine binding assay in vitro and good potency in protecting rodents against pentylenetetrazole-induced seizures. Compound 84 appears to be a selective anticonvulsant (pentylenetetrazole) agent when tested against a profile of chemically and electrically induced seizures in mice. In addition, compound 148 appears to be a selective anxiolytic/hypnotic agent on the basis of biochemical and pharmacological characterization. It appears to be a full BZD agonist as assessed by GABA shift ratio and to be effective in punishment and nonpunishment animal models of anxiety. In addition, it shows a lower side-effect profile than diazepam as assessed by rotorod neurotoxicity and potentiation of ethanol-induced sleep time in mice. The chemistry and structure-activity relationships of this series is discussed.
    DOI:
    10.1021/jm00114a007
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