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2-(2-chloro-benzylidene)-benzo[4,5]imidazo[2,1-b]thiazol-3-one | 23983-05-3

中文名称
——
中文别名
——
英文名称
2-(2-chloro-benzylidene)-benzo[4,5]imidazo[2,1-b]thiazol-3-one
英文别名
(E)-2-(2-Chlorobenzylidene)benzo[4,5]imidazo[2,1-b]thiazol-3(2H)-one;(2E)-2-[(2-chlorophenyl)methylidene]-[1,3]thiazolo[3,2-a]benzimidazol-1-one
2-(2-chloro-benzylidene)-benzo[4,5]imidazo[2,1-<i>b</i>]thiazol-3-one化学式
CAS
23983-05-3
化学式
C16H9ClN2OS
mdl
——
分子量
312.779
InChiKey
LSMPFFSYANAQSU-NTEUORMPSA-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):
    4.7
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    60.2
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-(2-chloro-benzylidene)-benzo[4,5]imidazo[2,1-b]thiazol-3-one 、 alkaline earth salt of/the/ methylsulfuric acid 生成 2-(2-chloro-benzhydryl)-benzo[4,5]imidazo[2,1-b]thiazol-3-one
    参考文献:
    名称:
    Mustafa,A. et al., Justus Liebigs Annalen der Chemie, 1970, vol. 740, p. 132 - 141
    摘要:
    DOI:
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文献信息

  • Mechanism-based inhibitors of transthyretin amyloidosis: studies with biphenyl ethers and structural templates
    申请人:Surolia Avadhesha
    公开号:US20100190832A1
    公开(公告)日:2010-07-29
    Transthyretin (TTR), a tetrameric thyroxine (T4) carrier protein, is associated with a variety of amyloid diseases. Derivative of biphenyl ethers (BPE), which are shown to interact with a high affinity to its T4 binding site thereby preventing its aggregation and fibrillogenesis. They prevent fibrillogenesis by stabilizing the tetrameric ground state of transthyretin. Two compounds (2-(5-mercapto-[1,3,4]oxadiazol-2-yl)-phenol and 2,3,6-trichloro-N-(4H-[1,2,4]triazol-3-yl) exhibit the ability to arrest TTR amyloidosis. The dissociation constants for the binding of BPEs and compound 11 and 12 to TTR correlate with their efficacies of inhibiting amyloidosis. They also have the ability to inhibit the elongation of intermediate fibrils as well as show nearly complete (>90%) disruption of the preformed fibrils. Biphenyl ethers and compounds 11 and 12 as very potent inhibitors of TTR fibrillization and inducible cytotoxicity.
  • Mustafa,A. et al., Justus Liebigs Annalen der Chemie, 1970, vol. 740, p. 132 - 141
    作者:Mustafa,A. et al.
    DOI:——
    日期:——
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