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4-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)-N-(6-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)hexyl)butanamide | 1146684-88-9

中文名称
——
中文别名
——
英文名称
4-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)-N-(6-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)hexyl)butanamide
英文别名
——
4-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)-N-(6-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)hexyl)butanamide化学式
CAS
1146684-88-9
化学式
C46H49N5O9S2
mdl
——
分子量
880.055
InChiKey
OWKPVNJEVZOJCF-KKKWNNDSSA-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

物化性质

  • 密度:
    1.30±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    8.5
  • 重原子数:
    62.0
  • 可旋转键数:
    19.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    171.82
  • 氢给体数:
    3.0
  • 氢受体数:
    13.0

反应信息

  • 作为产物:
    描述:
    、 在 N-羟基-7-氮杂苯并三氮唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺N,N-二异丙基乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以13.8 mg的产率得到4-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)-N-(6-((2Z,5Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)hexyl)butanamide
    参考文献:
    名称:
    Tethered thiazolidinone dimers as inhibitors of the bacterial type III secretion system
    摘要:
    Disruption of protein-protein interactions by small molecules is achievable but presents significant hurdles for effective compound design. In earlier work we identified a series of thiazolidinone inhibitors of the bacterial type III secretion system (T3SS) and demonstrated that this scaffold had the potential to be expanded into molecules with broad-spectrum anti-Gram negative activity. We now report on one series of thiazolidinone analogs in which the heterocycle is presented as a dimer at the termini of a series of linkers. Many of these dimers inhibited the T3SS-dependent secretion of a virulence protein at concentrations lower than that of the original monomeric compound identified in our screen. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.01.047
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文献信息

  • US8252940B2
    申请人:——
    公开号:US8252940B2
    公开(公告)日:2012-08-28
  • [EN] 5-SUBSTITUTED-2-IMINO-THIAZOLIDINONE COMPOUNDS AND THEIR USE AS INHIBITORS OF BACTERIAL INFECTION<br/>[FR] COMPOSÉS 2-IMINO-THIAZOLIDINONE SUBSTITUÉS EN POSITION 5 ET LEUR UTILISATION COMME INHIBITEURS D'INFECTION BACTÉRIENNE
    申请人:UNIV WASHINGTON
    公开号:WO2009137133A2
    公开(公告)日:2009-11-12
    A method for inhibiting Gram-negative bacterial pathogenesis, a method of screening for compounds that inhibit type III secretion in Gram-negative bacteria, and compounds that inhibit type III secretion in Gram-negative bacteria.
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