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2-[[(4-Chlorophenyl)thio]-(2,5-difluorophenyl)methyl]-1-methyl-5-chloro-1H-imidazole

中文名称
——
中文别名
——
英文名称
2-[[(4-Chlorophenyl)thio]-(2,5-difluorophenyl)methyl]-1-methyl-5-chloro-1H-imidazole
英文别名
5-chloro-2-[(4-chlorophenyl)sulfanyl-(2,5-difluorophenyl)methyl]-1-methylimidazole
2-[[(4-Chlorophenyl)thio]-(2,5-difluorophenyl)methyl]-1-methyl-5-chloro-1H-imidazole化学式
CAS
——
化学式
C17H12Cl2F2N2S
mdl
——
分子量
385.264
InChiKey
OCPICKCJPGNGQH-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):
    5.5
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    43.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Beta-amyloid protein production. secretion inhibitor
    申请人:Yasukouchi Takanori
    公开号:US20050234109A1
    公开(公告)日:2005-10-20
    Provided are novel compounds having an inhibitory activity against production or secretion of β-amyloid protein. They embrace compounds represented by the following formula (1): and capable of being replaced with a variety of substituents; and salts thereof, and solvates of any one of them.
    提供了一种新型化合物,具有抑制β-淀粉样蛋白产生或分泌的活性。它们包括由以下公式(1)表示的化合物:并且能够被各种取代基所替换;以及它们的盐和任何一个溶剂化物。
  • Morpholine derivatives
    申请人:Kubota Hideki
    公开号:US20060241302A1
    公开(公告)日:2006-10-26
    Provided is a compound capable of inhibiting production or secretion of β amyloid protein. A compound represented by the following formula (1): (wherein, R 1 represents a heterocyclic group which may have a substituent, R 2 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R 3 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R 4 represents a hydrogen atom or a C 1-6 alkyl group, and X represents —S—, —SO— or —SO 2 —); an N-oxide or S-oxide thereof; a salt thereof; or a solvate thereof; and a medicament containing any of them.
    提供了一种能够抑制β淀粉样蛋白产生或分泌的化合物。该化合物由以下公式(1)表示:(其中,R1代表可能具有取代基的杂环基团,R2代表可能具有取代基或杂环基团的环烃基团,R3代表可能具有取代基或杂环基团的环烃基团,R4代表氢原子或C1-6烷基基团,X代表—S—、—SO—或—SO2—);其N-氧化物或S-氧化物;其盐;或其溶剂化物;以及含有任何一种的药物。
  • BETA-AMYLOID PROTEIN PRODUCTION/SECRETION INHIBITORS
    申请人:YASUKOUCHI Takanori
    公开号:US20070293495A1
    公开(公告)日:2007-12-20
    Provided are novel compounds having an inhibitory activity against production or secretion of β-amyloid protein. They embrace compounds represented by the following formula (1): and capable of being replaced with a variety of substituents; and salts thereof, and solvates of any one of them.
    提供了一些新化合物,具有抑制β-淀粉样蛋白的产生或分泌活性。它们包括以下式子(1)所代表的化合物:并且可以被各种取代基所替换;以及它们的盐和任何一个的溶剂化物。
  • Heterocyclic methyl sulfone derivative
    申请人:Daiichi Pharmaceutical Co., Ltd.
    公开号:US07932271B2
    公开(公告)日:2011-04-26
    Provided is a compound capable of inhibiting production or secretion of β amyloid protein. A compound represented by the following formula (1): (wherein, R1 represents a heterocyclic group which may have a substituent, R2 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R3 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R4 represents a hydrogen atom or a C1-6 alkyl group, and X represents —S—, —SO— or —SO2—); an N-oxide or S-oxide thereof; a salt thereof; or a solvate thereof; and a medicament containing any of them.
    提供了一种化合物,能够抑制β淀粉样蛋白的产生或分泌。该化合物由以下式子(1)表示:(其中,R1代表一个杂环基团,可以具有取代基;R2代表一个环烃基团,可以具有取代基或一个杂环基团,可以具有取代基;R3代表一个环烃基团,可以具有取代基或一个杂环基团,可以具有取代基;R4代表一个氢原子或一个C1-6烷基基团,X代表—S—,—SO—或—SO2—);其N-氧化物或S-氧化物;其盐;或其溶剂化物;以及含有它们的药物。
  • HETEROCYCLIC METHYL SULFONE DERIVATIVE
    申请人:DAIICHI PHARMACEUTICAL CO., LTD.
    公开号:EP1640366A1
    公开(公告)日:2006-03-29
    Provided is a compound capable of inhibiting production or secretion of β amyloid protein. A compound represented by the following formula (1): (wherein, R1 represents a heterocyclic group which may have a substituent, R2 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R3 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R4 represents a hydrogen atom or a C1-6 alkyl group, and X represents -S-,-SO- or -SO2-) an N-oxide or S-oxide thereof; a salt thereof; or a solvate thereof; and a medicament containing any of them.
    本发明提供了一种能够抑制β淀粉样蛋白产生或分泌的化合物。 由下式(1)代表的化合物: (其中,R1代表可具有取代基的杂环基团,R2代表可具有取代基的环烃基团或可具有取代基的杂环基团,R3代表可具有取代基的环烃基团或可具有取代基的杂环基团,R4代表氢原子或C1-6烷基,X代表-S-、-SO-或-SO2-)其N-氧化物或S-氧化物;其盐;或其溶液;以及含有其中任何一种的药物。
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