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3-[3-(2-Cyanothien-3-yl)phenyl]imidazo[1,2-alpha]pyridine-7-carboxylic acid methyl ester

中文名称
——
中文别名
——
英文名称
3-[3-(2-Cyanothien-3-yl)phenyl]imidazo[1,2-alpha]pyridine-7-carboxylic acid methyl ester
英文别名
methyl 3-[3-(2-cyanothiophen-3-yl)phenyl]imidazo[1,2-a]pyridine-7-carboxylate
3-[3-(2-Cyanothien-3-yl)phenyl]imidazo[1,2-alpha]pyridine-7-carboxylic acid methyl ester化学式
CAS
——
化学式
C20H13N3O2S
mdl
——
分子量
359.4
InChiKey
WDSRYMFUXGPTIA-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:
    26
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    95.6
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

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文献信息

  • Imidazo-pyridine derivatives as ligands for gaba receptors
    申请人:——
    公开号:US20020188000A1
    公开(公告)日:2002-12-12
    A class of 3-phenylimidazo[1,2-a]pyridine derivatives, substituted at the meta position of the phenyl ring by an optionally substituted aryl or heteroaryl group which is directly attached or bridged by an oxygen atom or a —NH— linkage, are selective ligands for GABA A receptors, in particular having high affinity for the &agr;2 and/or &agr;3 subunit thereof, and are accordingly of benefit in the treatment and/or prevention of disorders of the central nervous system, including anxiety and convulsions.
    一类3-苯基咪唑[1,2-a]吡啶衍生物,苯环的间位取代一个可选取代芳基或杂环芳基,该芳基或杂环芳基直接连接或通过氧原子或-NH-键桥接,是选择性的GABAA受体配体,特别是对其α2和/或α3亚基具有高亲和力,因此对于治疗和/或预防中枢神经系统疾病,包括焦虑和惊厥,具有益处。
  • IMIDAZO-PYRIDINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS
    申请人:MERCK SHARP & DOHME LTD.
    公开号:EP1235827A2
    公开(公告)日:2002-09-04
  • [EN] IMIDAZO-PYRIDINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS<br/>[FR] DERIVES D'IMIDAZO-PYRIDINE UTILISES COMME LIGANDS POUR RECEPTEURS DE GABA
    申请人:MERCK SHARP & DOHME
    公开号:WO2001038326A2
    公开(公告)日:2001-05-31
    A class of 3-phenylimidazo[1,2-a]pyridine derivatives, substituted at the meta position of the phenyl ring by an optionally substituted aryl or heteroaryl group which is directly attached or bridged by an oxygen atom or a -NH- linkage, are selective ligands for GABAA receptors, in particular having high affinity for the α2 and/or α3 subunit thereof, and are accordingly of benefit in the treatment and/or prevention of disorders of the central nervous system, including anxiety and convulsions.
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